Aandachtsgebieden

Hoofdpijn, genetica

Proefschrift

Hereditary cerebral hemorrhage with amyloidosis – Dutch type (1990).

Lidmaatschappen

• Dutch migraine genetics research group
• Dutch research group on amyloidosis
• Nederlands Hoofdpijnvereniging (oprichtingslid)
• Nederlandse vereniging voor Neurologie
• International Headache Society
• Nevenfuncties: Parttime aanstelling als onderzoeker in he LUMC    

NEVENFUNCTIES

Onderzoek clusterhoofdpijn, genetica migraine, HCHWA-D, CADASIL.

Redacteur Nascholingstijdschrift Nervus;

Editorial board J Headache Pain;

Lid wetenschappelijke adviesraad Nederlandse Hoofdpijnvereniging.

BIG nummer

89021277401

BOEKEN

Ik schreef samen met prof. dr. M.D. Ferrari het boek “Alles over hoofdpijn en aangezichtspijn” en ben redacteur van “Tante krijgt een zenuwtoeval en andere essays over Neurologie en Literatuur”. Samen met de publicist F. Meulenberg schreef ik in 2009 “Migraine als Muze” over migraine in de literatuur en “De trillende Tuinman en andere Parkinsonbeelden”, over de ziekte van Parkinson in de literatuur. Vanwege deze hobby (de relatie tussen neurologie en literatuur) ben ik in Leiden Film- en Literatuurwetenschap gaan studeren en heb vorig jaar mijn bachelor gehaald. Momenteel ben ik bezig met een (2^e) proefschrift getiteld “The Diagnosis of Migraine in the Borderland of Neurology and Literary Studies. The patient as text – the text as patient.”

PUBLICATIES

Rasker JJ, Jansen ENH, Haan J, Oostrom J. Normal pressure hydrocephalus in rheumatic patients. A diagnostic pitfall. N Engl J Med 312: 1239-1241, 1985.

Haan J, Jansen ENH, Oostrom J, Roos RAC. Falling spells in normal pressure hydrocephalus: A favourable prognostic sign? Eur Neurol 27: 216-220, 1987.

Haan J, Thomeer RTWM. Predictive value of external lumbar drainage in normal pressure hydrocephalus. Neurosurg 22: 388-391, 1988.

Haan J, Roos RAC, Buruma OJS. Dementie bij de ziekte van Parkinson. Ned Tijdschr Geneesk 132: 383-386, 1988.

Haan J, Roos RAC, Goekoop JG, Buruma OJS. Depressie bij de ziekte van Parkinson. Ned T Geneesk 132: 1228-1231, 1988.

Bernsen PLJA, Haan J, Vielvoye GJ, Peerlinck KMJ. Spinal epidural hematoma visualized by magnetic resonance imaging. Neuroradiol 30: 280, 1988.

Ferrari MD, Haan J, Seters AP van. Bromocriptine-induced trigeminal neuralgia attacks in a patient with a pituitary tumor. Neurology 38: 1482-1484, 1988.

Haan J, Ferrari MD, Brouwer OF. Acute confusional migraine. Case report and review of the literature. Clin Neurol Neurosurg 90: 275-278, 1988.

Haan J, Caekebeke JFV, Meer F van der, Wintzen AR. Cerebral venous thrombosis as presenting sign of myeloproliferative disorders. J Neurol Neurosurg Psychiat, 51: 1219-1220, 1988.

Hilten JJ van, Haan J, Wintzen AR. Elevated spinal fluid pressure as only sign of cerebral venous thrombosis. Can J Neurol Sci 15: 439, 1988.

Haan J, Kremer HPH, Padberg GWAM. Paroxysmal choreoathetosis as presenting sign of diabetes mellitus. J Neurol Neurosurg Psychiat, 52: 133, 1989.

Haan J, Bakker HM de. Brain abscess as a complication of Halo traction. Role of CT scan in diagnosing penetration of the skull. Am J Neuroradiol, 10: 446, 1989.

Haan J, Thomeer RTWM. Tijdelijke lumbale externe drainage bij 'Normal Pressure Hydrocephalus'. T Geriat Geront 20: 25-28, 1989.

Marcusse HM, Haan J, Tan WD, Breedveld FC. Anterior spinal artery syndrome in Systemic Lupus Erythematosus. Brit J Rheumat 28: 344-346, 1989.

Haan J, Roos RAC, Briet PE, Herpers MJHM, Luyendijk W, Bots GTAM. Hereditary cerebral hemorrhage with amyloidosis - Dutch type. Clin Neurol Neurosurg 91: 285-290, 1989.

Hilten JJ, Haan J, Wintzen AR, Nes JCM van de, Heuvelmans JHA, Aarts PAMM, Goslinga H. Cerebral infarction in hereditary spherocytosis. Stroke 20: 1755-1756, 1989.

Bloem BR, Lagaay AM, Beek W van, Haan J, Roos RAC, Wintzen AR. Prevalence of subjective dysphagia in community residents over 87 years of age. Brit Med J 300: 721-722, 1990.

Haan J, Demmers RT, Buruma OJS, Roos RAC. Lymphocyte concanavalin A capping in hereditary cerebral hemorrhage with amyloidosis - Dutch type. J Neurol 237:117-119, 1990.

Haan J, Kroonenburgh MJPG van, Algra PR, Buruma OJS, Pauwels EKJ, Roos RAC. Hereditary cerebral hemorrhage with amyloidosis - Dutch type: Tc-99m HM-PAO single photon emission computed tomography. Neuroradiol 32:142-145, 1990.

Ferrari MD, Peeters EAJ, Haan J, Roos RAC, Vermey P, de Wolff FA, Buruma OJS. Cytochrome P450 and Parkinson's disease. Poor parahydroxylation of phenytoin. J Neurol Sci 96:153-157, 1990.

Broeckhoven C van, Haan J, Bakker E, Hardy JA, Hul W van, Wehnert A, Vegter-van der Vlis M, Roos RAC. The genetic defect in hereditary cerebral hemorrhage with amyloidosis of Dutch type is tightly linked to the ß-amyloid gene on chromosome 21. Science 248:1120-1122, 1990.

Haan J, Algra PR, Roos RAC. Hereditary cerebral hemorrhage with amyloidosis - Dutch type: Clinical and CT analysis of 24 cases. Arch Neurol 47:649-653, 1990.

Bloem BR, Irwin I, Buruma OJS, Haan J, Roos RAC, Tetrud JW, Langston JW. The MPTP model: Versatile contributions to the treatment of idiopathic Parkinson's disease. J Neurol Sci 97:273-293, 1990.

Haan J, Lanser JBK, Zijderveld I, Does IGF van der, Roos RAC. Dementia in hereditary cerebral hemorrhage with amyloidosis - Dutch type. Arch Neurol 47:965-967, 1990.

Haan J, Roos RAC, Algra PR, Lanser JBK, Bots GTAM, Vegter-van der Vlis M. Hereditary cerebral hemorrhage with amyloidosis - Dutch type: Magnetic resonance imaging findings of seven cases. Brain 113: 1251-1267, 1990.

Haan J, Roos RAC. Amyloid in central nervous system disease. Clin Neurol Neurosurg 92: 305-310, 1990.

Weinstein HC, Haan J, van Royen EA, Derix MMA, Lanser JBK, van der Zant F, Dunnewold RJW, van Kroonenburgh MJPG, Pauwels EKJ, van der Velde EA, Buruma OJS. SPECT in the diagnosis of Alzheimer's disease and multi-infarct-dementia. Clin Neurol Neurosurg 93: 39-43, 1991.

Haan J, Timmers-den Hollander L, Timmers WF, Timmers J, Roos RAC. Hereditaire cerebrale amyloïde angiopathie: recente ontwikkelingen. Ned T Geneesk 135 83-87, 1991.

Haan J, Van Kleef JW, Zwartendijk J, Lanser JBK, Brand R, Van Der Does IGF, Bloem BR, Krul EJT, Elshove HM, Moll AC, Buruma OJS, Roos RAC. Cognitive function after spinal or general anaesthesia for transurethral prostatectomy in elderly men. J Am Geriatr Soc 39: 596-600, 1991.

Dijk JG van, Koenderink M, Zwinderman AH, Haan J, Kramer CGS, den Heijer JC. Autonomic nervous system tests depend on resting heart rate and blood pressure. J Autonom Nerv Syst 35: 15-24, 1991.

Dijk JG van, Haan J, Koenderink M, Roos RAC. Autonomic nervous function in progressive supranuclear palsy. Arch Neurol 48: 1083-1084, 1991.

Haan J, Hardy JA, Roos RAC. Hereditary cerebral hemorrhage with amyloidosis - Dutch type: Its importance for Alzheimer research. Trends Neurosci 14: 231-234, 1991.

Bakker E, Van Broeckhoven C, Haan J, Voorhoeve E, Van Hul W, Levy E, Lieberburg I, Carman MD, Van Ommen GJB, Frangione B, Roos RAC. DNA-diagnosis for hereditary cerebral hemorrhage with amyloido­sis (Dutch type). Am J Hum Genet 49: 518-521, 1991.

Dijk JG van, Dorresteijn M, Haan J, Ferrari MD. No confirmation of visual evoked potential diagnostic test for migraine. Lancet I: 517-518, 1991.

Dijk JG van, Dorresteijn M, Haan J, Ferrari MD. Visual evoked potentials and background EEG activity in migraine. Headache 31: 392-395, 1991.

Roos RAC, Haan J, Maat-Schieman MLC. Hereditary cerebral hemorrhage with amyloidosis - Dutch type: Brief overview and description of recent developments. Bull Clin Neurosci 56: 34-38, 1991.

Klop C, Roos RAC, Haan J. De ziekte van Parkinson en depressie. TGO/JDR 16: 241-243, 1991.

Roos RAC, Haan J, Van Broeckhoven C. HCHWA-D: A congophilic angiopathy. An Overview. Ann NY Acad Sci 640: 155-161, 1991.

Haan J, Roos RAC. Comparison between the Icelandic and Dutch forms of hereditary cerebral amyloid angiopathy. Clin Neurol Neurosurg 94 (Suppl) S82-S83, 1992.

Roos RAC, Haan J. Function of amyloid and amyloid protein precursor. Clin Neurol Neurosurg 94 (Suppl) S1-S3, 1992.

Haan J, Kluft C, Leebeek FWG, Bart ACW de, Buruma OJS, Roos RAC. Hereditary cerebral hemorrhage with amyloidosis - Dutch type: A study of fibrinoly­sis. Thromb Haemost 67: 16-18, 1992.

Bloem BR, Haan J, Lagaay AM, van Beek W, Wintzen AR, Roos RAC. Investigation of gait in elderly subjects over 88 years of age. J Geriatr Psych Neurol 5: 78-84, 1992.

Dijk JG van, Haan J, Ferrari MD. Photic stimulation and the diagnosis of migraine. Headache Quart. Current treatment and diagnosis.3: 387-397, 1992.

Nostrand WE van, Wagner SL, Haan J, Bakker E, Roos RAC. Alzheimer's disease and HCHWA-D share a decrease in cerebrosp­inal fluid levels of amyloid precursor. Ann Neurol 32: 215-218, 1992.

Maat-Schieman MLC, Van Duinen SG, Haan J, Roos RAC. Morphology of cerebral plaque-like lesions in hereditary cerebral hemorrhage with amyloidosis (Dutch). Acta Neuropathol 84: 674-679, 1992.

Haan J, Bakker B, Jennekens-Schinkel A, Roos RAC. Progressive dementia, without cerebral hemorrhage in a patient with hereditary cerebral amyloid angiopathy. Clin Neurol Neurosurg 94: 317-318, 1992.

Dijk JG van, Haan J, Zwinderman AH, Kremer HPH, Roos RAC. Autonomic nervous system dysfunction in Parkinson's disease. Relationships with age, medication, duration and severity. J Neurol Neurosurg Psych 56: 1090-1095, 1993.

Ferrari MD, Haan J, Visser WH, Saxena PR, Bax WA, Mulder LJMM. Sumatriptan in de klinische praktijk. Ned T Geneesk 137: 850-855, 1993.

Ferrari MD, Haan J, Bax WA, Van Coevorden RS, Timmerman H, Meijler WJ. Onterechte gelijkschakeling van sumatriptan met ergotamine en dihydroergotamine in het geneesmiddelen vergoedingssysteem. Ned T Geneesk 137: 846-850, 1993.

Haan J, Ferrari MD. Behandeling van migraine en cluster hoofdpijn. Mod Med 17: 685-688, 1993.

Haan J, Peters WG. Amyloid and peripheral nervous system disease. Clin Neurol Neurosurg 96: 1-9, 1994.

Haan J, Maat-Schieman MLC, Roos RAC. Clinical effects of cerebral amyloid angiopathy. Dementia 5: 210-213, 1994.

Haan J, Maat-Schieman MLC, Van Duinen SG, Jensson O, Thorsteinsson L, Roos RAC. Co-localization of ß/A4 and cystatin C in cortical blood vessels in Dutch, but not in Icelandic hereditary cerebral hemorrhage with amyloidosis. Acta Neurol Scand 89: 367-371, 1994.

Haan J, Van Broeckhoven C, van Duijn CM, Voorhoeve E, van Harskamp F, van Swieten JC, Maat-Schieman MLC, Roos RAC, Bakker E. The apolipoprotein E ε4 allele does not influence the clinical expression of the amyloid precursor protein-gene codon 693 or 692 mutations. Ann Neurol 36: 434-437, 1994.

Ophoff RA, Van Eijk R, Sandkuijl LA, Terwindt GM, Grubben CPM, Haan J, Lindhout D, Ferrari MD, Frants RR. Genetic heterogeneity of familial hemiplegic migraine. Genomics, 22: 21-26, 1994.

Maat-Schieman MLC, Rozemuller AJ, Van Duinen SG, Haan J, Eikelenboom P, Roos RAC. Microglia in diffuse plaques in hereditary cerebral hemorrhage with amyloidosis (Dutch). An immunohistochemical study. J Neuropathol Exp Neurol 53: 483-491, 1994.

Maat-Schieman MLC, Radder CM, Van Duinen SG, Haan J, Roos RAC. Hereditary cerebral hemorrhage with amyloidosis (Dutch): A model for congophilic plaque-formation without neurofibrillary pathology. Acta Neuropathol 88: 371-378, 1994.

Haan J, Terwindt GM, Bos PLJM Ophoff RA, Frants RR, Ferrari MD. Familial hemiplegic migraine in the Netherlands. Clin Neurol Neurosurg, 96:244-249, 1994.

Haan J, Roos RAC, Bakker E. No protective effect of apolipoprotein E eps 2 allele in Dutch hereditary cerebral amyloid angiopathy. Ann Neurol 37:282, 1995.

Ferrari MD, Haan J, Blokland JAK, Arndt JW, Minnee P, Zwinderman AH, Pauwels EJK, Saxena PRS. Cerebral blood flow during migraine attacks without aura and effect of sumatriptan. Arch Neurol 52: 135-139, 1995.

Ferrari MD, Haan J. Acute treatment of migraine attacks. Curr Opinion Neurol 8: 237-242, 1995.

Duinen SG van, Maat-Schieman MLC, Bruijn JA, Haan J, Roos RAC. Cortical tissue of patients with hereditary cerebral hemorrhage with amyloidosis (Dutch) contains various extracellular matrix deposits. Lab Invest 73: 183-189, 1995.

May A, Ophoff RA, Terwindt GM, Urban C, van Eijk R, Haan J, Diener HC, Lindhout D, Frants RR, Sandkuijl LA, Ferrari MD. Familial hemiplegic migraine locus on 19p13 is involved in the common forms of migraine with and without aura. Hum Genet 96: 604-608, 1995.

Haan J, Terwindt G, Ophof R, Bos P, Frants RR, Ferrari MD. Is familial hemiplegic migraine a hereditary form of basilar migraine? Cephalalgia 15:477-481, 1995.

Wielaard R, Bornebroek M, Ophoff RA, Winter-Warnars HAO, Scheltens P, Frants RR, Ferrari MD, Haan J. A four-generation Dutch family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), linked to chromsome 19p13. Clin Neurol Neurosurg 97: 307-313, 1995.

Haan J, Ferrari MD. Epilepsie en migraine. Episcript 1:3-7, 1996.

Haan J, Ferrari MD. Hoofdpijnen. Bijblijven. 12: 41-50, 1996.

Bornebroek M, Haan J, Van Buchem MA, Lanser JBK, De Vries-van de Weerd MACS, Zoeteweij M, Roos RAC. White matter lesions and cognitive deterioration in presymptomatic carriers of the amyloid precursor protein gene codon 693 mutation. Arch Neurol 53: 43-48, 1996.

Terwindt GM, Ophoff RA, Haan J, Frants RR, Ferrari MD. Familial hemiplegic migraine: A clinical comparison of families linked and unlinked to chromosome 19. Cephalalgia 16:153-155, 1996.

Bornebroek M, Van Buchem MA, Haan J, Brand R, Lanser JBK, De Bruine FT, Roos RAC. Hereditary cerebral hemorrhage with amyloidosis - Dutch type: Better correlation of cognitive deterioration with advancing age than with the number of focal lesions or white matter hyperintensities. Alz Dis Assoc Dis 10:224-231,1996

Bornebroek M, Haan J, Maat-Schieman MLC, Van Duinen SG, Roos RAC. Hereditary cerebral hemorrhage with amyloidosis - Dutch type (HCHWA-D): I - A review of clinical, radiologic and genetic aspects. Brain Pathol 6: 111-114, 1996.

Maat-Schieman MLC, Van Duinen SG, Bornebroek M, Haan J, Roos RAC. Hereditary cerebral hemorrhage with amyloidosis - Dutch type (HCHWA-D): II - A review of histopathological aspects. Brain Pathol 6: 115-120, 1996.

Maas JJ, Beersma MFC, Haan J, Jonkers GJPM, Kroes ACM. Bilateral brachial plexus neuritis following parvovirus B19 and cytomegalo­virus infection. Ann Neurol 40:928-932, 1996.

Bornebroek M, Verzijlbergen JF, Haan J, van Scheyen EJ, Verhoeff NPLG, Pauwels EJK, Roos RAC. Potential imaging of cerebral amyloid deposits using 123I-labeled amyloid P component and SPECT. Nucl Med Comm 17: 929-933, 1996.

Ophoff RA, Terwindt GM, Vergouwe MN, van Eijk R, Oefner PJ, Hoffman SMG, Lamerdin JE, Mohrenweiser HW, Bulman DE, Ferrari M, Haan J, Lindhout D, van Ommen GJB, Hofker MH, Ferrari MD, Frants RR. Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4. Cell 87: 543-552, 1996.

Haan J, Hollander JMR, van Duinen SG, Saxena PR, Wintzen AR. Reversible sever myopathy during treatment with finasteride. Muscle Nerve 20: 502-504, 1997.

Haan J, Terwindt GW, Ferrari MD. Genetics of migraine. Neurol Clin 15: 43-60, 1997.

Haan J, Ferrari MD. Treatment of acute migraine. Neurol Rev Int 1: 1-4, 1997.

Bornebroek M, Haan J, Backhovens H, Deutz P, Van Buchem MA, Van Den Broeck M, Bakker E, Roos RAC, Van Broeckhoven C. Presenilin-1 polmorphism and hereditary cerebral hemorrhage with amyloidosis, Dutch type. Ann Neurol 42: 108-110, 1997.

Bornebroek M, Haan J, Van Duinen SG, Maat-Schieman MLC, Van Buchem MA, Bakker E, Van Broeckhoven C, Roos RAC. Dutch hereditary cerebral amyloid angiopathy: Structural lesions and Apolipoprotein E genotype. Ann Neurol 41: 695-698, 1997.

Maat-Schieman MLC, Van Duinen SG, Rozemuller AJM, Haan J, Roos RAC. Association of vascular amyloid ß and cells of the mononuclear phagocyte system in hereditary cerebral hemorrhage with amyloidosis (Dutch) and Alzheimer disease. J Neuropathol Exp Neurol 56: 273-284, 1997.

Haan J, Kappelle LJ, de Ronde H, Ferrari MD, Bertina RM. The factor V Leiden mutation (R506Q) is not a major risk factor for migrainous cerebral infarction. Cephalalgia 17: 605-607, 1997.

Terwindt GM, Ophoff RA, Lindhout D, Haan J, Halley DJJ, Sandkuijl LA, Brouwer OF, Frants RR, Ferrari MD. Partial cosegregation of hemiplegic migraine and benign infantile convulsions. Epilepsia 38:915-921, 1997.

Bloem BR, Boers I, Lagaay AM, Haan J, Wintzen AR, Roos RAC. Loopbeperkingen bij de alleroudsten. T Gerontol Geriatr 28: 76-81, 1997

Haan J, Terwindt GM, Maassen JA,'t Hart LM, Ferrari MD. Screening for mtDNA mutations in migraine patients. Cephalalgia 17: 329-330, 1997

Terwindt GM, Haan J, Ophoff RA, Frants RR, Ferrari MD. The quest for migraine genes. Curr Opin Neurol 10: 221-225, 1997.

Bornebroek M, Westendorp RGJ, Haan J, Bakker E, Timmers WF, Broeckhoven C van, Roos RAC. Mortality from hereditary cerebral hemorrhage with amyloidosis - Dutch type. The impact of sex, parental transmission and year of birth. Brain 120: 2243-2249,1997.

Terwindt GM, Haan J, Ophoff RA, Groenen SMA, Storimans CWJM, Lanser JBK, Roos RAC, Bleeker-Wagemakers EM, Frants RR, Ferrari M. Clinical and genetic analysis of a large Dutch family with autosomal dominant vascular retinopathy, migraine, and Raynaud's phenomenon. Brain 121: 303-316, 1998.

Kamphuisen PW, Haan J, Rosekrans PCM, Van Der Meer FJM. Deep vein thrombosis and coumarin skin necrosis associated with a Factor V inhibitor with lupus-like features. Am J Hemat 57: 176-178, 1998.

Vinters HV, Natte R, Maat-Schieman MLC, van Duinen SG, Hegeman-Kleinn I, Welling-Graafland C, Haan J, Roos RAC. Secondary microvascular degeneration in amyloid angiopathy of patients with hereditary cerebral hemorrhage with amyloidosis, Dutch type (HCHWA-D). Acta Neuropathol 95: 235-244, 1998.

Bornebroek M, von dem Borne PAK, Haan J, Meijers JCM, van Nostrand WE, Roos RAC. Binding of amyloid ß precursor protein to coagulation factor XIa in vivo may favour haemorrhagic stroke. J Neurol 245: 111-115, 1998.

Terwindt GM, Ophoff RA, Haan J, Vergouwe MN, Van Eijk R, Frants RR, Ferrari MD. Variable clinical expression of mutations in the P/Q-type calcium channel gene in familial hemiplegic migraine. Neurology 50: 1105-1110, 1998.

Terwindt GM, Ophoff RA, Haan J, Frants RR, Ferrari MD. Kanalopathieen: Genetische verklaring voor migraine en andere paroxismale neurologische aandoeningen. Ned T Geneesk 142: 1015-1019, 1998.

Terwindt GM, Ophoff RA, Haan J, Sandkuijl LA, Frants RR, Ferrari MD. Migraine, ataxia and epilepsy: A challenging spectrum of genetically determined calcium channelopathies. Eur J Hum Genet 6: 297-307, 1998.

Natte R, Vinters HV, Maat-Schieman MLC, Bornebroek M, Haan J, Roos RAC, Duinen SG van. Microvasculopathy is associated with the number of cerebrovascular lesions in hereditary cerebral hemorrhage with amyloidosis, Dutch type. Stroke 29: 1588-1594, 1998.

Haan J, Kappelle LJ, Ferrari MD, Bertina RM. The transition G to A at position 20210 in the 3'-untranslated region of the prothrombin gene is not associated with migrai­nous infarction. Cephalalgia 18: 229-230, 1998.

Haan J, Schoonman GG, Bertina RM, Kappelle LJ, Terwindt GM, Ferrari MD. Prothrombotic mutations and ischemic stroke at a young age in two sisters. J Neurol Neurosurg Psych 65:958-959, 1998.

Kors EE, Terwindt GM, Ferrari MD, Haan J. Migraine: Een genetische ziekte? Mod Med 22: 40-43, 1998

Kors EE, Terwindt GM, Ferrari MD, Haan J. Migraine, een erfelijke ziekte. Ned T Neurol 2:5-9, 1999

Haan J, Terwindt GM, Maassen JA, t Hart LM, Frants RR, Ferrari MD. Search for mitochondrial DNA mutations in migraine subgroups. Cephalagia 1999;19:20-22.

Haan J, Ferrari MD. Migraine behandeling: Stapsgewijs of "stratified: met behulp van MIDAS? Mod Med 1999;23:45-48

Kors E, Haan J, Ferrari MD. Genetics of primary headache. Curr Opinion Neurol 1999;12:249-254

Lesnik Oberstein SAJ, Ferrari MD, Bakker E, van Gestel J, Kneppers ALJ, Frants RR, Breuning MH, Haan J. Diagnostic Notch3 sequence analysis in CADASIL: Three new mutations in Dutch patients. Neurology 1999;52:1913-1915.

Haan J, Ferrari MD. Migraine behandeling: De triptanen toegepast? Elseviers themabijlage bij Medisch contact. 3-7, 1999

Lesnik Oberstein SAJ, Haan J, Ferrari MD, Breuning MH. CADASIL: Een erfelijke oorzaak voor herseninfarcten, dementia en migraine. Ned T Neurol 1999;4:237-241

Bornebroek M, Haan J, Roos RAC. HCHWA-D: A review of the variety in phenotypic expression. Amyloid: Int J Exp Clin Invest 6;215-224, 1999.

Vliet J van, Ferrari MD, Haan J. Diagnostiek en behandeling van cluster hoofdpijn. Zuiver zuurstof of subcutaan sumatriptan als acuut redmiddel. Pharmaceut Weekbl 1999;134:1476-1481

Bloem BR, Gussekloo J, Lagaay AM, Remarque EJ, Haan J, Westendorp RGJ. Idiopathic senile gait disorders are signs of subclinical disease. J Am Geriatr Soc 48:1098-1101, 2000.

Haan J, Ferrari MD. Mahler's migraine. Cephalalgia 2000;20:254.

Haan J, Sluis P, Sluis EL, Ferrari MD. Acetazolamide treatment for migraine aura status. Neurology 55:1588-1589,2000.

Ferrari MD, Haan J. Migraine aura, illusory vertical splitting, and Picasso. Cephalagia 20:686, 2000.

Haan J, Kors EE, Terwindt GM, Vermeulen FLMG, Vergouwe MN, van den Maagdenberg AMJM, Gill DS, Pascual J, Ophoff RA, Frants RR, Ferrari MD. Alternating hemiplegia of childhood: No mutations in the familial hemiplegic migraine CACNA1A gene. Cephalalgia 20:696-700, 2000.

Terwindt GM, Ophoff RA, van Eijk R, Vergouwe MN, Haan J, Frants RR, Sandkuijl LA, Ferrari MD. Involvement of the P/Q type calcium channel α1A-subunit (CACNA1A) gene region on 19p13 in migraine with and without aura. Neurology 56:1028-1032, 2001.

Lesnik Oberstein SAJ, Bakker E, Ferrari MD, Haan J. Van gen naar ziekte: Van Notch3 naar cerebrale autosomaal dominante arteriopathie met subcorticale infarcten en leuko-encephalopathie. Ned T Geneesk 145:359-360, 2001

Kors E, Terwindt GM, Vermeulen FLMG, Fitzsimons RB, Jardine PE, Heywood P, Love S, Van den Maagdenberg AMJM, Haan J, Frants RR, Ferrari MD. Delayed cerebral edema and fatal coma after minor head trauma: Role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine. Ann Neurol 49:753-760, 2001.

Van Vliet JA, Haan J, Ferrari MD. Clusterhoofdpijn en cerebellair meningeoom: Toeval of causaal verband? Ned T Neurol 4: 84-85, 2001

Haan J, Ferrari MD. Lisinopril heeft geen relevant preventief effect bij migraine. Ned T Geneesk 145: 755, 2001

Lesnik Oberstein SAJ, van den Boom R, van Buchem MA, van Houwelingen HC, Bakker E, Vollebregt E, Ferrari MD, Breuning MH, Haan J. Cerebral microbleeds in CADASIL. Neurology 57: 1066-1070, 2001

Eekers PJ, Vliet JA van, Haan J, Koehler PJ, Ferrari MD. Prodromal symptoms and aura in cluster headache: A nation-wide study in 1844 Dutch patients. Cephalalgia 21: 265-266, 2001

Vliet JA van, Haan J, Ferrari MD. Cluster headache and cluster-headache-like syndromes in the Netherlands: a nationwide study in 1377 patients. Clin Neurol Neurosurg 103: 132-133, 2001

Ophoff RA, DeYoung J, Service SK, Joosse M, Caffo NA, Sandkuijl LA, Terwindt GM, Haan J, van den Maagdenberg AMJM, Jen J, Baloh RW, Barilla-LaBarca ML, Saccone NL, Atkinson JP, Ferrari MD, Freimer NB, Frants RR. Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy and stroke map to a single locus on chromosome 3p21.1-p21.3. Am J Hum Genet 69: 447-453, 2001

Haan J, van Vliet JA, Kors EE, Terwindt GM, Vermeulen FLMG, van de Maagdenberg AMJM, Frants RR, Ferrari MD. No involvement of the calcium channel gene (CACNA1A) in a family with cluster headache. Cephalalgia 2001;21:959-962

Haan J, Bakker E, Bornebroek M, Roos RAC. Van gen naar ziekte; Het gen voor amyloid-beta-precursorproteine betrokken bij erfelijke cerebrale amyloidangiopathie. Ned T Geneesk 145: 1639-1641, 2001

Natte R, Maat-Schieman MLC, Haan J, Bornebroek M, Roos RAC, van Duinen SG. Dementia in hereditary cerebral hemorrhage with amyloidosis-Dutch type is associated with cerebral amyloid angiopathy but is independent of plaques and neurofibrillary tangles. Ann Neurol 2001;50:765-772

Wiendels NJ, Haan J, Knuistingh Neven A, Ferrari MD. Chronische dagelijkse hoofdpijn en overmatig gebruik van hoofdpijnmedicatie. Mod Med 2001;12:1216-1222

Boom R van den, Lesnik Oberstein SAJ, Duinen SG van, Bornebroek M, Ferrari MD, Haan J, Buchem MA van. Subcortical lacunar lesions: An MRI finding in patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. Radiology 2002;224:791-796.

Bornebroek M, Haan J, Maat-Schieman MLC, Roos RAC. Erfelijke cerebrale amyloid angiopathie van het Nederlandse type: De stand van zaken. Ned T Neurol 2002;5:4-11

Terwindt GM, Kors EE, Haan J, Vermeulen FLMG, van den Maagdenberg AMJM, Frants RR, Ferrari MD. Mutation analysis of the CACNA1A calcium channel subunit gene in 27 patients with sporadic hemiplegic migraine. Arch Neurol 2002;59:1016-1018.

van den Maagdenberg AMJM, Kors EE, Brunt ER, van Paesschen W, Pascual J, Ravine D, Keeling S, Vanmolkot KRJ, Vermeulen FLMG, Terwindt GM, Haan J, Frants RR and Ferrari MD. Three novel truncating mutations and one novel missense mutation in the CACNA1A gene causing episodic ataxia type 2. J Neurol 2002;249:1515-9.

Haan J, Kors EE, Ferrari MD. Familial cyclic vomiting syndrome. Cephalalgia 2002;22:552-554.

Ferrari MD, Haan J. The genetics of migraine: Implications for treatment approaches. J Neurl Transm 2002; [Suppl] 63:111-127.

Haan J. The CACNA1A gene: Why was it a good candidate gene for AHC? Rev Neurol 2003; 36: 472.

Van Vliet JA, Ferrari MD, Haan J. SUNCT syndrome resolving after contralateral hemispheric ischaemic stroke. Cephalalgia 23: 235-237, 2003

Van Vliet JA, Ferrari MD, Haan J, Laan LAEM, Voormolen JHC. Trigeminal autonomic cephalalgia-tic-like syndrome associated with a pontine tumour in a one year old girl. J Neurol Neurosurg Psychiatr 2003;74:291-392

Kors E, Haan J, Ferrari MD. Migraine genetics. Curr Pain Headache Reports. 7: 212-217, 2003

Kors EE, Haan J, Giffin NJ, Pazdera L, Schnittger C, Lennox GG, Terwindt GM, Vermeuelen FLMJ, van den Maagdenberg AMJM, Frants RR, Ferrari MD. Expanding the phenotypic spectrum of the CACNA1A gene T666M mutation. A description of 5 families with familial hemiplegic migraine. Arch Neurol 60: 684-688, 2003.

Lesnik Oberstein SAJ, van den Boom R, Middelkoop HAM, Ferrari MD, Knaap YM, van Houwelingen HC, Breuning MH, van Buchem MA, Haan J. Incipient CADASIL. Arch Neurol 60: 707-712, 2003.

Boom R van den, Lesnik Oberstein SA, Spilt A, Behloul F, Ferrari MD, Haan J, Westendorp RG, Buchem MA van. Cerebral hemodynamics and white matter hyperintensities in CADASIL. J Cerebral Blood Flow Metab 23: 599-604, 2003.

Ferrari MD, Haan J. Genetics of migraine and cluster headache. Continuum 9:48-57, 2003.

Van Vliet JA, Eekers PJE, Haan J, Ferrari MD. Features involved in the diagnostic delay of cluster headache. J Neurol Neurosurg Psychiatr. 74: 1123-1125, 2003.

Van Vliet JA, Zijlker TD, Haan J. Pijn in het aangezicht met neus- of oogverschijnselen: KNO of Neurologie? Mod Med 3: 199-204, 2003

Lesnik Oberstein SAJ, Jukema JW, Van Duinen SG, Macfarlane PW, Houwelingen HC, Breuning MH, Ferrari MD, Haan J. Myocardial infarction in CADASIL. Medicine (Baltimore) 82: 251-256, 2003.

Lesnik Oberstein SA, Duinen SG van, Boom R van den, Maat-Scieman ML, Buchem MA van, Houwelingen HC van, Hegeman-Kleinn IM, Ferrari MD, Breuning MH, Haan J. Evaluation of diagnostic NOTCH3 immunostaining in CADASIL. Acta Neuropathol 106: 107-111, 2003.

Vanmolkot KRJ, Kors EE, Hottenga JJ, Terwindt GM, Haan J, Hoefnagels WAJ, Black DF, Sandkuijl LA, Frants RR, Ferrari MD, van den Maagdenberg AMJM. Novel mutations in the Na⁺,K⁺-ATPase pump gene ATP1A2 associated with Familial Hemiplegic Migraine and Benign Familial Infantile Convulsions. Ann Neurol 54: 360-366, 2003.

Bornebroek M, De Jonghe C, Haan J, Kumar-Singh S, Younkin S, Roos RAC, Van Broeckhoven C. Hereditary cerebral hemorrhage with amyloidosis dutch type (AbetaPP 693): decreased plasma amyloid-beta 42 concentration. Neurobiol Dis 14:619-623, 2003.

Van Vliet JA, Haan J, Ferrari MD. A patient with long-lasting attacks of bilateral blepharospasm, photophobia, lacrimation and rhinorrhoea. Cephalalgia 24: 143-146, 2004.

Haan J, Kors EE, Van Den Maagdenberg AMJM, Vanmolkot KR, Terwindt GM, Frants RR, Ferrari MD. Towards a molecular genetic classification of familial hemiplegic migraine. Curr Pain Headache Rep 2004; 8: 238-243.

Kors EE, Vanmolkot KRJ, Haan J, Frants RR, van den Maagdenberg AMJM, Ferrari MD. Recent findings in headache genetics. Curr Opinion Neurol 2004;17:283-288.

Kors EE, Vanmolkot KRJ, Haan J, van den Maagdenberg AMJM, Frants RR, Ferrari MD. Van gen naar ziekte: Familiaire hemiplegische migraine ten gevolge van stoornissen in een natrium-kaliumpompgen. NTVG 2004;148:1919-1921.

Kors EE, Melberg A, Vanmolkot KRJ, Kumlien E, Haan J, Raininko R, Flink R, Ginjaar HB,Frants RR, Ferrari MD, van den Maagdenberg AMJM. Childhood epilepsy, familial hemiplegic migraine, cerebellar ataxia, and a new CACNA1A mutaton. Neurology 2004;63:1136-7

Kors EE, Vanmolkot KRJ, Haan J, Kheradmand Kia S, Stroink H, Laan LAEM, Gill DS, Pascual J, van den Maagdenberg AMJM, Frants RR, Ferrari MD. Alternating hemiplegia of childhood: No mutations in the second familial hemiplegic migraine gene ATP1A2. Neuropediatrics 2004;35:293-296.

Hottenga JJ, Vanmolkot KRJ, Kors EE, Kheradmand Kia S, de Jong PTVM, Haan J, Terwindt GM, Frants RR, Ferrari MD, van den Maagdenberg AMJM. The 3p21.1-p21.3 hereditary vascular retinopathy locus increases the risk for Raynaud phenomenon and migraine. Cephalalgia 2005;251168-1172.

Overbeek OM, van der Mast RC, Lesnik Oberstein SAJ, Haan J. CADASIL, een erfelijk neuropsychiatrisch ziektebeeld. T Psychiatr 2005;47:167-173.

Van den Boom R, Bornebroek M, Behloul F, van den Berg-Huysmans AA, Haan J, van Buchem MA. Microbleeds in hereditary cerebral hemorrhage with amyloidosis – Dutch type. Neurology 2005;64:1288-9.

Favier I, Haan J, Ferrari MD. Chronic Cluster Headache: a Review. J Headache Pain 2005;6:3-9

Haan J, Kors EE, Vanmolkot KR, van den Maagdenberg AM, Frants RR, Ferrari MD. Migraine genetics: an update. Curr Pain Headache Rep. 2005;9:213-20

Stam AH, Haan J, Frants RR, Ferrari MD, van den Maagdenberg AMJM. Migraine New treatment options from molecular biology. Expert Rev Neurotherapeutics 2005;5653-661.

Vanmolkot KRJ, Stroink H, Koenderink JB, Kors EE, van den Heuvel JJMW, van den Boogerd EH, Stam H, Haan J, de Vries BBA, Terwindt GM, Frants RR, Ferrari MD, van den Maagdenberg AMJM. Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 TP12 mutation. Ann Neurol 2006;59:310-314.

Vliet JA van, Eekers PJE, Haan J, Ferrari MD. Evaluating the IHS criteria for cluster headache. A comparison between patients meeting all criteria and patients failing one criterion. Cephalalgia 2006;26:241-245.

Boom R van den, Lesnik Oberstein SAJ, Berg-Huysmans AA van den, Ferrari MD, Buchem MA van, Haan J. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephaloptahy: Structural MR imaging and Apolipoprotein E genotype. Am J Neurorad 2006; 27: 359-362.

Vanmolkot KRJ, Kors EE, Turk U, Turkdogan D, Keyser A, Broos LAM, Kheradmand Kia S, Heuvel JJMW van den, Black DF, Haan J, Frants RR, Barone V, Ferrari MD, Casari G, Koenderink B, Maagdenberg AMJM van den. Two de novo mutations in the Na,K-ATPase gene ATP1A2 associated with pure familial hemiplegic migraine. Eur J Hum Genet 2006;14:555-560.

Favier I, Haan J. Clusterhoofdpijn. T Neurol Neurochir 2006;107:83-89.

Vliet JA van, Favier I, Helmerhorst FM, Haan J, Ferrari MD. Cluster headache in women: Relation with menstruation, use of oral contraceptives, pregnancy and menopause. J Neurol Neurosurg Psychiatr 2006;77:690-692.

Terwindt GM, Haan J, Bax JJ, de Bruijn SFTM, Ferrari MD. Migraine en het gaatje in het hart: Oorzakelijk verband tussen migraine en foramen ovale persistens niet aangetoond. Ned T Geneesk 2006;150:1050-1052.

Haan J, Tonk M, Lesnik Oberstein SAJ. Genetic causes of stroke and vascular dementia. Aging Health 2006;2:497-504.

Vries B de, Haan J, Frants RR, Maagdenberg AMJM Van den, Ferrari MD. Genetic biomarkers for migraine. Headache 2006;46:1059-1068.

Haan J, Terwindt GM, Ferrari MD. Migraine en epilepsie: Een (genetische) relatie? T Neurol Neurosurg 2006;107:216-221

Terwindt GM, Haan J, Ferrari MD. Hemiplegic and basilar-type migraine: Current and future treatment. Headache Currents 2006;3:97-100.

De Thije-Kors E, Haan J. Hemiplegic and basilar-type migraine: Epidemiology, genetics and mechanisms. Headache Currents 2006;3:73-81.

De Vries B, Haan J, Stam AH, Vanmolkot KR, Stroink H, Laan LA, Gill DS, Pascual J, Frants RR, van den Maagdenberg AM, Ferrari MD. Alternating hemiplegia of childhood: No mutations in the glutamate transporter EAAT1. Neuropediatrics 2006;37:302-304.

Favier I, van Vliet JA, Roon KI, Witteveen RJW, Verschuuren JJGM, Ferrari MD, Haan J. Trigeminal autonomic cephalgias due to structural lesions. A review of 31 cases. Arch Neurol 2007;64:12-14.

Haan J, Hollander J, Ferrari MD. Migraine in the elderly: A review. Cephalalgia 2007;27:97-106.

Favier I, Haan J, van Duinen SG, Ferrari MD. Typical cluster headache caused by granulomatous pituitary involvement. Cephalalgia 2007;27:173-176.

Liem MK, van der Grond J, Haan J, van den Boom R, Ferrari MD, Knaap YM, Breuning MH, van Buchem MA, Middelkoop HAM, Lesnik Oberstein SAJ. Lacunar infarcts are the main correlate with cognitive dysfunction in CADASIL. Stroke 2007;38: 923 – 928.

Vanmolkot KRJ, Babini E, de Vries B, Stam AH, Freilinger T, Terwindt GM, Norris L, Haan J, Frants RR, Ramadan NM, Ferrari MD, Pusch M, van den Maagdenberg AMJM, Dichgans M. The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: Genetic and functional studies. Hum Mut 2007;28:522-530.

Vanmolkot KRJ, Stam AH, Raman A, Koenderink JB, de Vries B, van den Boogerd EH, van Vark J, van den Heuvel JJMW, Bajaj N, Terwindt GM, Haam J, Frants RR, Ferrari MD, van den Maagdenberg AMJM. First case of compound heterozygosity in Na,K-ATPase gene ATP1A2 in familial hemiplegic migraine. Eur J Hum Genet 2007;15:884-888.

Maagdenberg AMJM van den, Haan J, Terwindt GM, Ferrari MD. Migraine: gene mutations and functional consequences. Curr Opin Neurol 2007;20:299-305.

Haan J. De garderobe van de dokter. Beelden van de arts in fictie. Een angstaanjagend boek. De Neuroloog 3,

Richards A, van den Maagdenberg AMJM, Jen JC, Kavanagh D, Bertram P, Spitzer D, Liszewski MK, Barilla-LaBarca ML, Terwindt GM, Kasai Y, McLellan M, Grand MG, Vanmolkot KJR, de Vries B, Wan J, Kane MJ, Mamsa H, Schaefer R, Stam AH, Haan J, de Jong PTVM, Storimans CW, van Schooneveld MJ, Oosterhuis JA, Gschwendter A, Dichgans M, Kotschet KE, Hodgkinson S, Hardy TA, Delatycki MB, Hajj-Ali RA, Kothari PH, Nelson SF, Frants RR, Baloh RW, Ferrari MD, Atkinson JP. C-terminal truncations in human 3’-5’ DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy. Nat Genet 2007; 39:1068-1070.

Haan J, Lesnik-Oberstein SAJ, Ferrari MD. Epilepsy in CADASIL. Cerebrovasc Dis 2007;24:316-317.

Terwindt GM, Haan J, Koppen H, Ferrari MD. Migraine en cardiovasculair risico. NTvG 2007;151:2029-2031.

De Vries B, Freilinger T, Vanmolkot KRJ, Stam AH, Terwindt GM, Babini E, van den Boogerd EH, van den Heuvel JJMW, Frants RR, Haan J, Pusch M, van den Maagdenberg AMJM, Ferrari MD, Dichgans M. Systematic analysis of three FHM genes in sporadic patients with hemiplegic migraine. Neurology 2007;69:2170-2176.

Haan J, Meulenberg F. Locked-in syndroom. T Neuropsychiatr Gedragsneuro 2007;6:212-215.

Haan J, Terwindt GM, van den Maagdenberg AMJM, Stam AH, Ferrari MD. A review of the genetic relation between migraine and epilepsy. Cephalagia 2008;28:105-113.

Favier I, Ferrari MD, Haan J. Trigeminale autonome cefalalgie: Drie vormen van eenzijdige, kortdurende hoofdpijn met faciale autonome verschijnselen. NTvG 2008;152:139-142.

Lesnik Oberstein SA, Maat-Schieman ML, Boon EM, Haan J, Breuning MH, van Duinen SG. No vessel wall abnormailities in a human foetus with a Notch3 mutation. Acta Neuropathol 2008;115:369-370.

Favier I, Haan J, Ferrari MD. Cluster headache: To scan or not to scan. Curr Pain Headache Rep 2008;12:128-131.

Vanmolkot KJR, Terwindt GM, Frants RR, Haan J, van den Maagdenberg AMJM, Ferrari MD. A gene for a new monogenic neurovascular migraine syndrome: A next step in unraveling molecular pathways for migraine? Cephalalgia 2008;28:471-473.

Stam AH, Vanmolkot KR, Kremer HP, Gartner J, Brown J, Leshinsky-Silver E, Gilad R, Kors EE, Frankenhuizen WS, Ginjaar HB, Haan J, Frants RR, Ferrari MD, van den Maagdenberg AM, Terwindt GM. CACNA1A R1347Q: A frequent recurring mutation in hemiplegic migraine. Clin Genet 2008;74:481-485.

Stam AH, van den Maagdenberg AMJM, Haan J, Terwindt GM, Ferrari MD. Genetics of migraine: An update with special attention to genetic comorbidity. Curr Opin Neurol 2008;21:288-293.

De Vries B, Stam AH, Beker F, van den Maagdenberg AMJM, Vanmolkot KRJ, Laan LAEM, Ginjaar IB, Frants RR, Lauffer H, Haan J, Haas JP, Terwindt GM, Ferrari MD. CACNA1A mutation linking hemiplegic migraine and alternating hemiplegia of childhood. Cephalalgia 2008;28:887-891.

Graves TD, Imbrici P, Kors EE, Terwindt GM, Eunson LH, Frants RR, Haan J, Ferrari MD, Goadsby PJ, Hanna MG, van den Maagdenberg AM, Kullmann DM. Premature stop codons in a facilitating EF-hand splice variant of Ca(V)2.1 causes episodic ataxia type 2. Neurobiol Dis 2008;32:10-5.

Haan J, van den Maagdenberg AM, Brouwer OF, Ferrari MD. Migraine and epilepsy: Genetically linked? Expert Rev Neurother 2008;8:1307-1311.

Liem MK, Lesnik Oberstein SAJ, Haan J, van der Neut IL, van den Boom R, Ferrari MD, van Buchem MA, van der Grond J. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: Progression of MR abnormalities in a prospective 7-year follow-up study^. Radiology 2008;249:964-971.

De Vries B, Mamsa H, Stam AH, Wan J, Bakker SLM, Vanmolkot KRJ, Haan J, Terwindt GM, Boon EMJ, Howard BD, Frants RR, Baloh RW, Ferrari MD, Jen JC, van den Maagdenberg AMJM. Episodic ataxia associated with EAAT1 mutation C186S affecting glutamate reuptake. Arch Neurol 2009;66:97-101.

Liem MK, Lesnik Oberstein SAJ, Haan J, van der Neut IL, Ferrari MD, van Buchem MA, Middelkoop HAM, van der Grond J. MRI correlates of cognitive decline in CADASIL. A 7-year follow-up study. Neurology 2009;72:143-148.

Vein AA, Koppen H, Haan J, Terwindt GM, Ferrari MD. Space headache: A new secondary headache. Cephalalgia 2009;29:683-686.

Liem MK, Lesnik Oberstein MA, Haan J, van den Boom R, Ferrari MD, van Buchem MA, van der Grond J. Cerebrovascular reactivity is a main determinant of white matter hyperintensity progression in CADASIL. AJNR Am J Neurorad 2009;30:1244-1247.

Wilbrink LA, Ferrari MD, Kruit MC, Haan J. Neuroimaging in trigeminal autonomic cephalgias: When, how, and of what? Curr Opinion Neurol 2009;22:247-253.

Ter Meulen BC, Haan J, Meulenberg F. Narratieve Neurologie: Toegang tot de belevingswereld van de patient. NTvG 2009;153:1036-1039.

Stam AH, Luijckx GJ, Poll-The BT, Ginjaar I, Frants RR, Haan J, Ferrari MD, Terwindt GM, van den Maagdenberg AMJM. Early seizures and cerebral edema after trivial head trauma associated with the CACNA1A S218L mutation. J Neurol Neusosurg Pychiatry 2009;80:1125-1129.

Van Rooden S, van der Grond J, van den Boom R, Haan J, Linn J, Greenberg SM, van Buchem MA. Descreptive analysis of the Boston criteria applied to a Dutch cerebral amyloid angiopathy population. Stroke 2009;40:3022-3027.

Stam AH, Haan J, vand den Maagdenberg AMJM, Ferrari MD, Terwindt GM. Migraine and genetic and acquired vasculopathies. Cephalalgia; Headache Currents 2009;29:1006-1017.

Koppen H, Terwindt GM, Haan J, de Bruijn SFTM, Bax JJ, Ferrari MD. No indication for patent foramen ovale closure in migraine. Neth Heart J 2009;17:320-321.

De Vries B, Stam AH, Kirkpatrick M, Vanmolkot KRJ, Koenderink JB, van den Heuvel JJMW, Stunnenberg B, Goudie D, Shetty J, Jain V, van Vark J, Terwindt GM, Frants RR, Haan J, van den Maagdenberg AMJM, Ferrari MD. Familial hemiplegic migraine is associated with febrile seizures in an FHM2 family with a novel de novo ATP1A2 mutation. Epilepsia 2009;50:2503-2504.

De Vries B, Steup-Beekman G, Haan J, Bollen E, Luyendijk J, Frants RR, Terwindt GM, van Buchem M, Huizinga T, van den Maagdenberg AMJM, Ferrari MD. TREX1 gene variant in neuropsychiatric systemic lupus erythematosus. Ann Rheum Dis 2010;69:1886-1887.

Liem MK, Lesnik Oberstein SAJ, van der Grond J, Ferrari MD, Haan J. CADASIL and migraine: A narrative review. Cephalalgia 2010;30:1284-1289.

Arkink EB, van Buchem MA, Haan J, Ferrari MD, Kruit MC. An early 18th century case description of cluster headache. Cephalalgia 2010;30:1392-1395.

Mulleners WM, Haan J, Dekker F, Ferrari MD. Preventieve behandeling van migraine. NTvG 2010;154:1381-1387.

Haan J, Santbrink H van, Ferrari MD. Controverse over term ‘retinale migraine’. NTvG 2010;154:1376-1380.

van den Maagdenberg AMJM, Terwindt GM, Haan J, Frants RR, Ferrari MD. Genetics of headache. Handb Clin Neurol 2010;97:85-97.

Liem MK, van der Grond J, Versluis MJ, Haan J, Webb AG, Ferrari MD, van Buchem MA, Lesnik Oberstein SA. Lenticulostriate arterial lumina are normal in cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy. A high-field in vivo MRI study. Stroke 2010;41:2812-2816.

Das T, Kaptein AA, Haan J. The turbid crystal ball: Life plans affected by multiple sclerosis. Int MS J 2011;3:12-15.

Stam AH, Louter MA, Haan J, de Vries B, van den Maagdenberg AMJM, Frants RR, Ferrari MD, Terwindt GM. A long-term follow-up study of 18 patients with sporadic hemiplegic migraine. Cephalalgia 2011;31:199-205.

Tannemaat MR, Vries EP, Molendijk WJ, Haan J. Fatal ischemic stroke in a patient receiving lenalidomide for multiple myeloma. Clin Neurol Neurosurg 2011;113:488-489.

Haan J, Wilbrink LA, Haan R, Ferrari MD. Het cluster-tic-syndroom en andere tic-TAC-combinaties. Tijdschr Neurol Neurosurg 2011;112:62-68.

Haan J, Smithuis RHM, Haan R, Ferrari MD. Glandula-pinealisafwijkingen en hoofdpijn. Tijdschr Neurol Neurosurg 2011;112:101-108.

Haan J, Ferrari MD. Picasso’s migraine: Illusory cubist splitting or illusion? Cephalalgia 2011;31:1057-1060.

Geerlings RPJ, Koehler PJ, Haane DYP, Stam AH, de Vries B, Boon EMJ, Haan J. Head tremor related to CACNA1A mutations. Cephalalgia 2011;31:1315-1319.

Benit C, Haan J. Nummulaire of munthoofdpijn. Tijdschr Neurol Neurosurg 2011;112:161-165.

Briët MC, Haan J, Kaptein AA. Hermann Hesse and L: two narratives of sciatica. Clin Neurol Neurosurg 2012;114:9-11.

Haan J, Koehler PJ, Bogousslavsky J. Neurology and surrealism: André Breton and Joseph Babinski. Brain 2012;135:3830-3838.

Liem MK, Lesnik Oberstein SA, Versluis MJ, Maat-Schieman ML, Haan J, Webb AG, Ferrari MD, van Buchem MA,. Van der Grond J. 7T MRI reveals diffuse iron deposition in putamen and caudate nucleus in CADASIL. J Neurol Neurosurg Psychiatr 2012;83:1180-1185.

Heinzen EL, Swoboda KJ, Hitomi Y, Gurrieri F, Nicole S, de Vries B, Danilo Tizano F, Fontaine B, Walley NM, Heavin S, Panagiotakaki E, Fiori S, Abiusi E, Di Pietro L, Sweney MT, Shianna KV, Gumbs CE, Little L, Silver K, Ptacek LJ, Haan J, Ferrari MD, Bye AM, Herkes GK, Whitelaw CM, Webb D, Lynch BJ, Uldall P, King MD, Scheffer IE, Neri G, Arzimanoglou A, van den Maagdenberg AMJM, Sisodya SM, Mikati MA, Goldstein DB. De novo mutations in ATP1A3 cause alternating hemiplegia of childhood. Nat Genet 2012;44:1030-1034.

Kaptein AA, Lyons AC, Pearson AS, van der Geest S, Haan J, Meulenberg F, Smyth JM. Storying stories. Med Educ Dev 2012;2:24-26.

Pelzer N, Stam AH, Haan J, Ferrari MD, Terwindt GM. Familial and sporadic hemiplegic migraine: Diagnosis and treatment. Curr Treatment Options Neurology 2013;

Oosterhout WPJ van, Haan J. Migraine after sneezing: Pathophysiological considerations, focused on the difference with coughing. Headache 2013;53:1147-1151.

Haan J. Faked headaches becoming real. An analysis of headache attacks in James Cagney’s last gangster movie White Heat. Headache 2013;53:998-1002.

Wilbrink LA, Weller CM, Cheung C, Stijnen T, Haan J, Ferrari MD, Terwindt GM. Stepwise web-based questionnaires for diagnosing cluster headache: LUCA and QATCH. Cephalalgia 2013;33:924-931.

Bauer PR, Carpay JA, Terwindt GM, Sander JW, Thijs RJ, Haan J, Visser GH. Headache and epilepsy. Curr Pain Headache Rep 2013;

Wilbrink LA, Weller CM, Cheung C, Haan J, Ferrari MD. Cluster-tic syndrome: A cross-sectional study of cluster headache patients. Headache 2013;53:1334-1340.

Pelzer N, de Vries B, Boon EMJ, Kruit MC, Haan J, Ferrari MD, van den Maagdenberg AMJM, Terwindt GM. Heterozygous TREX1 mutations in early-onset cerebrovascular disease. J Neurol 2013;260:2188-2190.

Eysink Smeets MM, Verhagen JMA, Kamphuis DJ, Rozemuller AJM, Haan J. Familiaire cerebrale caverneuze malformaties. Tijdschr Neurol Neurosurg 2013;114:95-104.

Pelzer N, Stam AH, Carpay JA, de Vries B, van den Maagdenberg AMJM, Ferrari MD, Haan J, Terwindt GM. Familial hemiplegic migraine treated by sodium valproate and lamotrigine. Cephalalgia 2014;34:708-711.

Weller CM, Pelzer N, de Vries B, Artigas López M, De Fàbregues O, Pascual J, Ramos Arroyo MA, Koelewijn SC, Stam AH, Haan J, Ferrari MD, Terwindt GM, van den Maagdenberg AMJM. Two novel SCN1A mutations identified in families with familial hemiplegic migraine Cephalalgia 2014;34:1062-1069.

Kamp J, Moursel LG, Haan J, Terwindt GM, Lesnik Oberstein SA, van Duinen SG, van Roon- Mom WM. Amyloid β in hereditary cerebral haemorrhage with amyloidosis - Dutch type. Rev Neurosci 2014;25:641-51.

Rutten JW, Haan J, van Duinen SG, Boon EMJ. Lesnik Oberstein SAJ. Interpretation of NOTCH3 mutations in the diagnosis of CADASIL. Expert Rev Mol Diagn 2014;14:593-603.

Pelzer N, de Vries B, Kamphorst JT, Vijfhuizen LS, Ferrari MD, Haan J, van den Maagdenberg AMJM, Terwindt GM. PRRT2 and hemiplegic migraine: A complex association. Neurology 2014;83:288-290.

Lansink JG, van Oosterhout WP, Borggreve AG, Haan J. [Footballer's migraine instead of concussion]. Ned Tijdschr Geneeskd. 2014;158:A8434. PMID: 25424634.

Weller CM, Wilbrink LA, Houwing-Duistermaat JJ, Koelewijn SC, Vijfhuizen LS, Haan J, Ferrari MD, Terwindt GM, van den Maagdenberg AM, de Vries B. Cluster headache and the hypocretin receptor 2 reconsidered: A genetic association study and meta-analysis. Cephalalgia. 2015;35: 741-747

Weller CM, Leen WG, Neville BGR, Duncan JS, de Vries B, Geilenkirchen MA, Haan J, Kamsteeg EJ, Ferrari MD, van den Maagdenberg AMJM, Willemsen MAAP, Scheffer H, Terwindt GM. A novel SLC2A1 mutation linking hemiplegic migraine with alternating hemiplegia of childhood. Cephalalgia 2015;35:10-15.

Oosterhout WPJ van, Cheung C, Haan J. Primaire hoofdpijnsyndromen bij ouderen: Epidemiologie, diagnostiek en behandeling. Tijdschr Neurol Neurosurg 2015;116:174-179.

de Coo IF, Wilbrink LA, Haan J. Symptomatic Trigeminal Autonomic Cephalalgias. Curr Pain Headache Rep. 2015;19(8):514.

De Coo IF, Wilbrink LA, Haan J. Effective occipital nerve stimulation during pregnancy in a cluster headache patient. Cephalalgia 2016; 36: 98-99.

De Coo IF, Wilbrink LA, Haan J, Ferrari MD, Terwindt GM. Evaluation of the new ICHD-III beta cluster headache criteria. Cephalalgia 2016;36:547-551.

Oosterhout WPJ van, Cheung C, Haan J. Primary headache syndromes in the elderly: epidemiology, diagnosis and treatment. Journal of Clinical and Translational Research 2016; 2 (2): 1.

Koppen H, Stolwijk J, Wilms EB, van Driel V, Ferrari MD, Haan J. Cardiac monitoring of high-dose verapamil in cluster headache: An international Delphi study. Cephalalgia 2016;36:1385-1388.

De Coo IF, Haan J. Long lasting impairment of taste and smell as side effect of lithium carbonate in a cluster headache patient. Headache 2016;56:1201-1203.

Van Etten ES, Edip Gurol M, van der Grond J, Haan J, Viswanathan A, Schwab KM, Ayres AM, Algra A, Rosand J, van Buchem MA, Terwindt GM, Greenberg SM, Wermer MJH. Recurrent Hemorrhage Risk and Mortality in Hereditary and Sporadic Cerebral Amyloid Angiopathy. Neurology 2016; 87:1482-1487.

Stam AH, Kothari PH, Shaikh A, Gschwendter A, Jen JC, Hodgkinson S, Hardy TA, Hayes M, Kempster PA, Kotschet KE, Bajema IM, van Duinen SG, Maat-Schieman MLC, Jong PTVM, de Smet MD, de Wolff-Rouendaal D, Dijkman G, Pelzer N, Kolar GR, Schmidt RE, Lacey JA, Joseph D, Fintak DR, Grand G, Brunt EM, Liapis H, Hajj-Ali RA, Kruit MC, van Buchem MA, Dichgans M, Frants R, van den Maagdenberg AMJM, Haan J, Baloh RW, Atkinson JP, Terwindt GM, Ferrari MD. Retinal Vasculopathy with Cerebral Leukoencephalopathy and Systemic Manifestations (RVCL-S). Brain 2016;139: 2909-2922.

Louter MA, Wilbrink LA, Haan J, van Zwet EW, van Oosterhout WP, Zitman FG, Ferrari MD, Terwindt GM. Cluster headache and depression. Neurology 2016;1899-1906.

De Coo IF, Wilbrink LA, Haan J, Ferrari MD, Huygen FJPM, Ferrari MD. Occipitale zenuwstimulatie bij medicamenteus onbehandelbare chronische clusterhoofdpijn. Tijdschr Neurol Neurchir 2016;117:145-148.

Oosterhout WPJ van, Haan J. Atypical presentation of an apoplexy in a pineal cyst. J Clin Case Rep 2015; S3-002

De Coo IF, van Dijk MC, Metzemaekers JDM, Haan J. A case report about cluster-tic sydrome due to venous compression of the trigeminal nerve. Headache 2017;57:654-657.

Oosterhout WPJ, Haan J, Kruyt ND. Een patiënt met het syndroom van Melkersson-Rosenthal. Ned T Geneesk 2016;160:D427.

van Etten ES, Verbeek MM, van der Grond J, Zielman R, van Rooden S, van Zwet EW, van Opstal AM, Haan J, Greenberg SM, van Buchem MA, Wermer MJ, Terwindt GM. β-Amyloid in CSF: Biomarker for preclinical cerebral amyloid angiopathy. Neurology 2017;88:169-176.

Wilbrink LA, Louter MA, Teernstra OP, van Zwet EW, Huygen FJ, Haan J, Ferrari MD, Terwindt GM. Allodynia in cluster headache. Pain 2017;158:1113-1117.

Doesborg PGG, Fronczek R, Ferrari MD, Haan J. Trigeminale autonome cefalalgieën. Nervus 2017;2:6-14.

Haan J. Epicrania fugax. Bestaat het? Nervus 2017;2:56-58.

Arkink EB, Schoonman GG, van Vliet JA, Bakels HS, Sneeboer MAM, Haan J, van Buchem MA, Ferrari MD, Kruit MC. The cavernous sinus in cluster headache – a quantitative structural magnetic resonance imaging study. Cephalalgia 2017;37:208-213.

Pelzer N, Blom DE, Stam AH, Vijfhuizen LS, Hageman ATM, van Vliet JA, Ferrari MD, van den Maagdenberg AMJM, Haan J, Terwindt GM. Recurrent coma and fever in familial hemiplegic migraine type 2. A prospective 15-year follow-up of a large family with a novel ATP1A2 mutation. Cephalalgia 2017;37:737-755.

Arkink EB, Schmitz N, Schoonman GG, van Vliet JA, Haan J, van Buchem MA, Ferrari MD, Kruit MC. The anterior hypothalamus in cluster headache. Cephalalgia 2017;1039-1050.

Haan J, Kaptein AA, Ter Meulen BC. Oliver Sacks and migraine. Cephalalgia 2017;37:990-997.

Pijpers JA, Wiendels NJ, Koppen H, Ferrari MD, Haan J, Terwindt GM. Medicatie-afhankelijke Hoofdpijn. Ned Tijdschr Geneeskd. 2018;162(0):D1749

Pelzer N, Haan J, Stam AH, Vijfhuizen LS, Koelewijn SC, Smagge A, de Vries B, Ferrari MD, van den Maagdenberg AMJM, Terwindt GM. Clinical spectrum of hemiplegic migraine and chances of finding a pathogenic mutation. Neurology 2018; 90(7):e575-e582

Haan J. Hoofdredactioneel. Hersenbloedingen: defaitisme voorbij? Nervus 2018;3:1.

Etten ES van, Haan J, Terwindt GM, Wermer MJH. Cerebrale amyloïdangiopathie. Een uitbreidend klinisch spectrum. Nervus 2018;3:6-13.

Oosterhout WPJ van, Haan J. Een bloeding in een pijnappelkliercyste. Nervus 2018;3:41-44.

Oosterhout WPJ van, Haan J. Bestaat het? Een migraineuze hersenbloeding. Nervus 2018;3:58-60.

Doesborg P, Haan J. Cluster headache: New targets and options for treatment. F1000 Research 2018;7:339

de Coo IF, Wilbrink LA, Ie GD, Haan J, Ferrari MD. Aura in Cluster Headache: A Cross-Sectional Study. Headache. 2018; 58: 1203-1210.

Etten ES van, Haan J, Terwindt GM, Wermer MJH. Cerebrale amyloïdangiopathie. Een uitbreidend klinisch spectrum. Focus Vasculair 2018;3:14-20.

Pelzer N, Haan J. Het einde van de traumatische spinale naald. Nervus 2018;3:51-55.

de Coo IF, Naber WC, Wilbrink LA, Haan J, Ferrari MD, Fronczek R. Increased use of illicit drugs in a Dutch cluster headache population. Cephalalgia 2019;39:626-634.

Pelzer N, Louter MA, van Zwet EW, Nyholt DR, Ferrari MD, van den Maagdenberg AM, Haan J, Terwindt GM. Linking migraine frequency with family history of migraine. Cephalalgia. 2019;39:229-236.

Etten ES van, Haan J, Terwindt GM, Wermer MJH. Cerebrale amyloïdangiopathie. Een uitbreidend klinisch spectrum. Imago 2019;5:38-45.

Pelzer N, Hoogeveen E, Haan J, Bunnik R, Poot C, van Zwet E, Inderson A, Fogteloo A, Reinders M, Middelkoop H, Kruit M, van den Maagdenberg A, Ferrari M, Terwindt G. Systemic features of retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations (RVCL-S): a monogenic small vessel disease. J Int Med 2019;285:317-332.