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Gisela Terwindt

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Chromosomes, Human, Pair 19

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Polymorphism, Single-Stranded Conformational

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Publications

TOP 3
Else Eising; Michel D Ferrari; Gisela M Terwindt; Boukje De Vries; Arn Mjm van den Maagdenberg
Pearls and pitfalls in genetic studies of migraine.
W P J van Oosterhout; E W van Zwet; R Zielman; Michel D Ferrari; Arie van der Plas; Gisela M Terwindt
Postdural puncture headache in migraineurs and nonheadache subjects: a prospective study.
Nadine Pelzer; Anine H Stam; Michel D Ferrari; Joost Haan; Gisela M Terwindt
Familial and sporadic hemiplegic migraine: diagnosis and treatment.

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All Publications

2013: Else Eising; Michel D Ferrari; Gisela M Terwindt; Boukje De Vries; Arn Mjm van den Maagdenberg
Pearls and pitfalls in genetic studies of migraine.
Cephalalgia : an international journal of headache 2013;33(8):614-25.
2013: W P J van Oosterhout; E W van Zwet; R Zielman; Michel D Ferrari; Arie van der Plas; Gisela M Terwindt
Postdural puncture headache in migraineurs and nonheadache subjects: a prospective study.
Neurology 2013;80(10):941-8.
2013: Nadine Pelzer; Anine H Stam; Michel D Ferrari; Joost Haan; Gisela M Terwindt
Familial and sporadic hemiplegic migraine: diagnosis and treatment.
Current treatment options in neurology 2013;15(1):13-27.
2012: Inge H Palm-Meinders; Gisela M Terwindt; Mark A Van Buchem; Baldur van Lew; Jacobus T N Bakkers; Michel D Ferrari; Paul A M Hofman; Junya Konishi; Hille Koppen; Lenore J Launer; H A M Middelkoop; Juliette M E Moonen; Mark C Kruit
Structural brain changes in migraine.
JAMA : the journal of the American Medical Association 2012;308(18):1889-97.
2011: W P J van Oosterhout; C M Weller; F Bakels; T Stijnen; M D Ferrari; A H Stam; Gisela M Terwindt
Validation of the web-based LUMINA questionnaire for recruiting large cohorts of migraineurs.
Cephalalgia : an international journal of headache 2011;31(13):1359-67.
2011: Hille Koppen; Mark C Kruit; Vera Lim; Aryo Nugroho; Inge Palm-Meinders; Gisela M Terwindt; Mark van Buchem; Iris Westhof; Michel Ferrari; Bernhard Hommel
The impact of a migraine attack and its after-effects on perceptual organization, attention, and working memory.
Cephalalgia : an international journal of headache 2011;31(14):1419-27.
2011: Lannie Ligthart; Grant W Montgomery; Dale R Nyholt; Ben A Oostra; Brenda W J H Penninx; Johannes H Smit; Albert V Smith; Gisela M Terwindt; André G Uitterlinden; Arn M J M van den Maagdenberg; Cornelia M van Duijn; Gonneke Willemsen; Frans G Zitman; Monique Breteler; Eco J C de Geus; Marleen H M de Moor; Boukje de Vries; Michel D Ferrari; Vilmundur Gudnason; Albert Hofman; Jouke-Jan Hottenga; M Arfan Ikram; A Cecile J W Janssens; V Mathijs Kattenberg; Stephany C Koelewijn; Lenore J Launer; Najaf Amin; Yurii S Aulchenko; Dorret I Boomsma
Meta-analysis of genome-wide association for migraine in six population-based European cohorts.
European journal of human genetics : EJHG 2011;19(8):901-7.
2011: Daniel I Chasman; Boukje De Vries; Florian Ernst; Konstanze Fendrich; Michel D Ferrari; Tobias Freilinger; Lyn R Griffiths; Wolfgang Hoffmann; Mikko Kallela; Christian Kubisch; Lenore J Launer; Aarno Palotie; Paul M Ridker; Ulf Schminke; Markus Schürks; Gisela M Terwindt; Arn M J M van den Maagdenberg; Henry Völzke; Robert Y L Zee; Verneri Anttila; Julie E Buring; Tobias Kurth
Genome-wide association study reveals three susceptibility loci for common migraine in the general population.
Nature genetics 2011;43(7):695-8.
2011: Anine H Stam; Mark A Louter; Joost Haan; Boukje De Vries; Arn M J M van den Maagdenberg; Rune R Frants; Michel D Ferrari; Gisela M Terwindt
A long-term follow-up study of 18 patients with sporadic hemiplegic migraine.
Cephalalgia : an international journal of headache 2011;31(2):199-205.
2010: Lonneke M L de Lau; Dorine A M Siepman; Michel J M Remmers; Gisela M Terwindt; Rogier Q Hintzen
Acute disseminating encephalomyelitis following legionnaires disease.
Archives of neurology 2010;67(5):623-6.
2010: Mark C Kruit; Mark A Van Buchem; Lenore J Launer; Gisela M Terwindt; Michel D Ferrari
Migraine is associated with an increased risk of deep white matter lesions, subclinical posterior circulation infarcts and brain iron accumulation: the population-based MRI CAMERA study.
Cephalalgia : an international journal of headache 2010;30(2):129-36.
2010: Anine H Stam; Boukje De Vries; A C J W Janssens; Kaate R J Vanmolkot; Yurii Aulchenko; Peter Henneman; Ben A Oostra; Rune R Frants; Arn van den Maagdenberg; Michel D Ferrari; C.M. Duijn; Gisela M Terwindt
Shared genetic factors in migraine and depression: evidence from a genetic isolate.
Neurology 2010;74(4):288-94.
2010: Arn M J M Van Den Maagdenberg; Gisela M Terwindt; Joost Haan; Rune R Frants; Michel D Ferrari
Genetics of headaches.
Handbook of clinical neurology 2010;97():85-97.
2010: Mark A Louter; Gerthe Veen; Michel D Ferrari; Frans Zitman; Gisela M Terwindt
[Migraine and depression should be treated concurrently].
Nederlands tijdschrift voor geneeskunde 2010;154():A1044.
2009: Boukje De Vries; Anine H Stam; Martin Kirkpatrick; Kaate R J Vanmolkot; Jan B Koenderink; Jeroen J M W van den Heuvel; Bas Stunnenberg; David Goudie; Jay Shetty; VIVEK JAIN; Judith van Vark; Gisela M Terwindt; Rune R Frants; Joost Haan; Arn van den Maagdenberg; Michel D Ferrari
Familial hemiplegic migraine is associated with febrile seizures in an FHM2 family with a novel de novo ATP1A2 mutation.
Epilepsia 2009;50(11):2503-4.
2009: Anine H Stam; Gert-Jan Luijckx; B T Poll-Thé; Ieke B Ginjaar; Rune R Frants; Joost Haan; Michel D Ferrari; Gisela M Terwindt; Arn van den Maagdenberg
Early seizures and cerebral oedema after trivial head trauma associated with the CACNA1A S218L mutation.
Journal of neurology, neurosurgery, and psychiatry 2009;80(10):1125-9.
2009: Anine H Stam; Joost Haan; Arn van den Maagdenberg; Michel D Ferrari; Gisela M Terwindt
Migraine and genetic and acquired vasculopathies.
Cephalalgia : an international journal of headache 2009;29(9):1006-17.
2009: Boukje De Vries; Hafsa Mamsa; Anine H Stam; Jijun Wan; Stef L M Bakker; Kaate R J Vanmolkot; Joost Haan; Gisela M Terwindt; Elles M J Boon; Bruce D Howard; Rune R Frants; Robert W Baloh; Michel D Ferrari; Joanna C Jen; Arn van den Maagdenberg
Episodic ataxia associated with EAAT1 mutation C186S affecting glutamate reuptake.
Archives of neurology 2009;66(1):97-101.
2008: Tracey D Graves; Paola Imbrici; Esther E Kors; Gisela M Terwindt; Louise H Eunson; Rune R Frants; Joost Haan; Michel D Ferrari; Peter J Goadsby; Michael G Hanna; Arn van den Maagdenberg; Dimitri M Kullmann
Premature stop codons in a facilitating EF-hand splice variant of CaV2.1 cause episodic ataxia type 2.
Neurobiology of disease 2008;32(1):10-5.
2008: Guus G Schoonman; Jeroen van der Grond; C Kortmann; Rob J van der Geest; Gisela M Terwindt; Michel D Ferrari
Migraine headache is not associated with cerebral or meningeal vasodilatation--a 3T magnetic resonance angiography study.
Brain : a journal of neurology 2008;131(Pt 8):2192-200.
2008: Anine H Stam; Arn van den Maagdenberg; Joost Haan; Gisela M Terwindt; Michel D Ferrari
Genetics of migraine: an update with special attention to genetic comorbidity.
Current opinion in neurology 2008;21(3):288-93.
2008: Joost Haan; Gisela M Terwindt; Arn van den Maagdenberg; Anine H Stam; Michel D Ferrari
A review of the genetic relation between migraine and epilepsy.
Cephalalgia : an international journal of headache 2008;28(2):105-13.
2007: Boukje De Vries; Tobias Freilinger; Kaate R J Vanmolkot; Jan B Koenderink; Anine H Stam; Gisela M Terwindt; Elena Babini; Eelke H van den Boogerd; Jeroen J M W van den Heuvel; Rune R Frants; Joost Haan; Michael Pusch; Arn van den Maagdenberg; Michel D Ferrari; Martin Dichgans
Systematic analysis of three FHM genes in 39 sporadic patients with hemiplegic migraine.
Neurology 2007;69(23):2170-6.
2007: Kaate R J Vanmolkot; Anine H Stam; Ashok Raman; Jan B Koenderink; Boukje De Vries; Eelke H van den Boogerd; Judith van Vark; Jeroen J M W van den Heuvel; Nin Bajaj; Gisela M Terwindt; Joost Haan; Rune R Frants; Michel D Ferrari; Arn van den Maagdenberg
First case of compound heterozygosity in Na,K-ATPase gene ATP1A2 in familial hemiplegic migraine.
European journal of human genetics : EJHG 2007;15(8):884-8.
2007: Maija Wessman; Gisela M Terwindt; Mari A Kaunisto; Aarno Palotie; Roel A Ophoff
Migraine: a complex genetic disorder.
Lancet neurology 2007;6(6):521-32.
2007: Arn van den Maagdenberg; Joost Haan; Gisela M Terwindt; Michel D Ferrari
Migraine: gene mutations and functional consequences.
Current opinion in neurology 2007;20(3):299-305.
2007: Guus G Schoonman; D J Evers; B E P B Ballieux; E J de Geus; Ron de Kloet; Gisela M Terwindt; J Gert van Dijk; Michel D Ferrari
Is stress a trigger factor for migraine?
Psychoneuroendocrinology 2007;32(5):532-8.
2007: Kaate R J Vanmolkot; Elena Babini; Boukje De Vries; Anine H Stam; Tobias Freilinger; Gisela M Terwindt; Lisa Norris; Joost Haan; Rune R Frants; Nabih M Ramadan; Michel D Ferrari; Michael Pusch; Arn van den Maagdenberg; Martin Dichgans
The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies. Mutation in brief #957. Online.
Human mutation 2007;28(5):522.
2006: Guus G Schoonman; D J Evers; Gisela M Terwindt; J Gert van Dijk; Michel D Ferrari
The prevalence of premonitory symptoms in migraine: a questionnaire study in 461 patients.
Cephalalgia : an international journal of headache 2006;26(10):1209-13.
2006: Kaate R J Vanmolkot; Hans Stroink; Jan B Koenderink; Esther E Kors; Jeroen J M W van den Heuvel; Eelke H van den Boogerd; Anine H Stam; Joost Haan; Bert B A de Vries; Gisela M Terwindt; Rune R Frants; Michel D Ferrari; Arn van den Maagdenberg
Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 ATP1A2 mutation.
Annals of neurology 2006;59(2):310-4.
2006: Ann I Scher; Gisela M Terwindt; W M Monique Verschuren; Mark C Kruit; Henk J Blom; Hisanori Kowa; Rune R Frants; Arn van den Maagdenberg; Mark A Van Buchem; Michel D Ferrari; Lenore J Launer
Migraine and MTHFR C677T genotype in a population-based sample.
Annals of neurology 2006;59(2):372-5.
2005: Jouke-Jan Hottenga; Kaate R J Vanmolkot; Esther E Kors; S Kheradmand Kia; Paulus T V M de Jong; Joost Haan; Gisela M Terwindt; Rune R Frants; Michel D Ferrari; Arn van den Maagdenberg
The 3p21.1-p21.3 hereditary vascular retinopathy locus increases the risk for Raynaud's phenomenon and migraine.
Cephalalgia : an international journal of headache 2005;25(12):1168-72.
2005: Mark C Kruit; Lenore J Launer; Mark A Van Buchem; Gisela M Terwindt; Michel D Ferrari
MRI findings in migraine.
Revue neurologique 2005;161(6-7):661-5.
2005: Ann I Scher; Gisela M Terwindt; H Susan J Picavet; W M Monique Verschuren; Michel D Ferrari; Lenore J Launer
Cardiovascular risk factors and migraine: the GEM population-based study.
Neurology 2005;64(4):614-20.
2004: Gisela M Terwindt; Esther E Kors; Alla Vein; Michel D Ferrari; J Gert van Dijk
Single-fiber EMG in familial hemiplegic migraine.
Neurology 2004;63(10):1942-3.
2004: Joost Haan; Esther E Kors; Arn van den Maagdenberg; Kaate R J Vanmolkot; Gisela M Terwindt; Rune R Frants; Michel D Ferrari
Toward a molecular genetic classification of familial hemiplegic migraine.
Current pain and headache reports 2004;8(3):238-43.
2004: Mark C Kruit; Mark A Van Buchem; Paul A M Hofman; Jacobus T N Bakkers; Gisela M Terwindt; Michel D Ferrari; Lenore J Launer
Migraine as a risk factor for subclinical brain lesions.
JAMA : the journal of the American Medical Association 2004;291(4):427-34.
2003: Kaate R J Vanmolkot; Esther E Kors; Jouke-Jan Hottenga; Gisela M Terwindt; Joost Haan; Wil A J Hoefnagels; David F Black; Lodewijk A Sandkuijl; Rune R Frants; Michel D Ferrari; Arn van den Maagdenberg
Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions.
Annals of neurology 2003;54(3):360-6.
2003: Esther E Kors; Joost Haan; N J Giffin; L Pazdera; C Schnittger; G G Lennox; Gisela M Terwindt; F L M J Vermeulen; Arn van den Maagdenberg; Rune R Frants; Michel D Ferrari
Expanding the phenotypic spectrum of the CACNA1A gene T666M mutation: a description of 5 families with familial hemiplegic migraine.
Archives of neurology 2003;60(5):684-8.
2002: Arn van den Maagdenberg; Esther E Kors; E R Brunt; W van Paesschen; J Pascual; David Ravine; S Keeling; Kaate R J Vanmolkot; F L M J Vermeulen; Gisela M Terwindt; Joost Haan; Rune R Frants; Michel D Ferrari
Episodic ataxia type 2. Three novel truncating mutations and one novel missense mutation in the CACNA1A gene.
Journal of neurology 2002;249(11):1515-9.
2002: Gisela M Terwindt; Esther E Kors; Joost Haan; F L M J Vermeulen; Arn van den Maagdenberg; Rune R Frants; Michel Ferrari
Mutation analysis of the CACNA1A calcium channel subunit gene in 27 patients with sporadic hemiplegic migraine.
Archives of neurology 2002;59(6):1016-8.
2002: Petra M.C. Callenbach; René F M de Coo; Alla A Vein; W F M Arts; Jan C Oosterwijk; Gerard Hageman; Robert ten Houten; Gisela M Terwindt; Dick Lindhout; Rune R Frants; Oebele F Brouwer
Benign familial infantile convulsions: a clinical study of seven Dutch families.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 2002;6(5):269-83.
2001: Joost Haan; Jorine A van Vliet; Esther E Kors; Gisela M Terwindt; F L M J Vermeulen; Arn van den Maagdenberg; Rune R Frants; Michel D Ferrari
No involvement of the calcium channel gene (CACNA1A) in a family with cluster headache.
Cephalalgia : an international journal of headache 2001;21(10):959-62.
2001: Roel A Ophoff; Joseph DeYoung; Susan K Service; Marijke Joosse; N A Caffo; Lodewijk A Sandkuijl; Gisela M Terwindt; Joost Haan; Arn van den Maagdenberg; J Jen; R W Baloh; Maria-Louise Barilla-LaBarca; N L Saccone; J P Atkinson; Michel D Ferrari; Nelson B Freimer; Rune R Frants
Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3.
American journal of human genetics 2001;69(2):447-53.
2001: Esther E Kors; Gisela M Terwindt; F L M J Vermeulen; R B Fitzsimons; P E Jardine; P Heywood; S Love; Arn van den Maagdenberg; Joost Haan; Rune R Frants; Michel D Ferrari
Delayed cerebral edema and fatal coma after minor head trauma: role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine.
Annals of neurology 2001;49(6):753-60.
2001: Gisela M Terwindt; Roel A Ophoff; Ronald van Eijk; Monique N Vergouwe; Joost Haan; Rune R Frants; Lodewijk A Sandkuijl; Michel D Ferrari
Involvement of the CACNA1A gene containing region on 19p13 in migraine with and without aura.
Neurology 2001;56(8):1028-32.
2000: Joost Haan; Esther E Kors; Gisela M Terwindt; F L M J Vermeulen; Monique N Vergouwe; Arn van den Maagdenberg; DS Gill; J Pascual; Roel A Ophoff; Rune R Frants
Alternating hemiplegia of childhood: no mutations in the familial hemiplegic migraine CACNA1A gene.
Cephalalgia : an international journal of headache 2000;20(8):696-700.
2000: Gisela M Terwindt; Michel D Ferrari; Marja Tijhuis; S M Groenen; H Susan J Picavet; Lenore J Launer
The impact of migraine on quality of life in the general population: the GEM study.
Neurology 2000;55(5):624-9.
1999: Lenore J Launer; Gisela M Terwindt; Michel D Ferrari
The prevalence and characteristics of migraine in a population-based cohort: the GEM study.
Neurology 1999;53(3):537-42.
1999: Joost Haan; Gisela M Terwindt; J Antonie Maassen; LM Hart; Rune R Frants; Michel D Ferrari
Search for mitochondrial DNA mutations in migraine subgroups.
Cephalalgia : an international journal of headache 1999;19(1):20-2.
1998: J Haan; Guus G Schoonman; Gisela M Terwindt; Michel D Ferrari; R M Bertina; L J Kappelle; J Haan
Prothrombotic mutations and ischaemic stroke at a young age in two sisters.
Journal of neurology, neurosurgery, and psychiatry 1998;65(6):958-9.
1998: Gisela M Terwindt; Roel A Ophoff; Joost Haan; Lodewijk A Sandkuijl; Rune R Frants; Michel D Ferrari
Migraine, ataxia and epilepsy: a challenging spectrum of genetically determined calcium channelopathies. Dutch Migraine Genetics Research Group.
European journal of human genetics : EJHG 1998;6(4):297-307.
1998: Roel A Ophoff; Gisela M Terwindt; M D Ferrari; R R Frants
Genetics and pathology of voltage-gated Ca2+ channels.
Histology and histopathology 1998;13(3):827-36.
1998: Gisela M Terwindt; Roel A Ophoff; Joost Haan; Rune R Frants; Michel D Ferrari
[Channelopathies: a genetic explanation of migraine and other paroxysmal neurologic disorders].
Nederlands tijdschrift voor geneeskunde 1998;142(18):1015-9.
1998: Roel A Ophoff; Gisela M Terwindt; R R Frants; M D Ferrari
P/Q-type Ca2+ channel defects in migraine, ataxia and epilepsy.
Trends in pharmacological sciences 1998;19(4):121-7.
1998: Gisela M Terwindt; Roel A Ophoff; Joost Haan; Monique N Vergouwe; Ronald van Eijk; Rune R Frants; Michel D Ferrari
Variable clinical expression of mutations in the P/Q-type calcium channel gene in familial hemiplegic migraine. Dutch Migraine Genetics Research Group.
Neurology 1998;50(4):1105-10.
1998: Gisela M Terwindt; Joost Haan; Roel A Ophoff; S M Groenen; C W Storimans; Jan B K Lanser; Raymund A C Roos; E M Bleeker-Wagemakers; Rune R Frants; Michel D Ferrari
Clinical and genetic analysis of a large Dutch family with autosomal dominant vascular retinopathy, migraine and Raynaud's phenomenon.
Brain : a journal of neurology 1998;121 ( Pt 2)():303-16.
1997: Roel A Ophoff; Gisela M Terwindt; Monique N Vergouwe; Rune R Frants; Michel D Ferrari
Familial hemiplegic migraine: involvement of a calcium neuronal channel.
Neurología (Barcelona, Spain) 1997;12 Suppl 5():31-7.
1997: Roel A Ophoff; Gisela M Terwindt; Monique N Vergouwe; Rune R Frants; Michel D Ferrari
Wolff Award 1997. Involvement of a Ca2+ channel gene in familial hemiplegic migraine and migraine with and without aura. Dutch Migraine Genetics Research Group.
Headache 1997;37(8):479-85.
1997: Gisela M Terwindt; Roel A Ophoff; Dick Lindhout; Joost Haan; D J J Halley; Lodewijk A Sandkuijl; Oebele F Brouwer; Rune R Frants; Michel D Ferrari
Partial cosegregation of familial hemiplegic migraine and a benign familial infantile epileptic syndrome.
Epilepsia 1997;38(8):915-21.
1997: Gisela M Terwindt; Joost Haan; Roel A Ophoff; Rune R Frants; Michel D Ferrari
The quest for migraine genes.
Current opinion in neurology 1997;10(3):221-5.
1997: Joost Haan; Gisela M Terwindt; Michel D Ferrari
Genetics of migraine.
Neurologic clinics 1997;15(1):43-60.
1996: W Hester Visser; Gisela M Terwindt; Scott A Reines; K Jiang; C R Lines; Michel D Ferrari
Rizatriptan vs sumatriptan in the acute treatment of migraine. A placebo-controlled, dose-ranging study. Dutch/US Rizatriptan Study Group.
Archives of neurology 1996;53(11):1132-7.
1996: Roel A Ophoff; Gisela M Terwindt; Monique N Vergouwe; Ronald van Eijk; P J Oefner; S M Hoffman; Jane Lamerdin; Harvey W Mohrenweiser; D E Bulman; M Ferrari; Joost Haan; Dick Lindhout; Gert-Jan B van Ommen; M H Hofker; Michel D Ferrari; Rune R Frants
Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4.
Cell 1996;87(3):543-52.
1996: Gisela M Terwindt; Roel A Ophoff; Joost Haan; R R Frants; Michel D Ferrari
Familial hemiplegic migraine: a clinical comparison of families linked and unlinked to chromosome 19.DMG RG.
Cephalalgia : an international journal of headache 1996;16(3):153-5.
1996: Roel A Ophoff; Gisela M Terwindt; Monique N Vergouwe; Ronald van Eijk; Harvey W Mohrenweiser; M Litt; M H Hofker; Joost Haan; Michel D Ferrari; Rune R Frants
A 3-Mb region for the familial hemiplegic migraine locus on 19p13.1-p13.2: exclusion of PRKCSH as a candidate gene. Dutch Migraine Genetic Research Group.
European journal of human genetics : EJHG 1996;4(6):321-8.
1995: Joost Haan; Gisela M Terwindt; Roel A Ophoff; P L Bos; Rune R Frants; Michel D Ferrari; T Krommenhoek; Dick Lindhout; L A Sandkuyl; Ronald van Eijk
Is familial hemiplegic migraine a hereditary form of basilar migraine?
Cephalalgia : an international journal of headache 1995;15(6):477-81.
1995: A May; Roel A Ophoff; Gisela M Terwindt; C Urban; Ronald van Eijk; Joost Haan; H C Diener; Dick Lindhout; Rune R Frants; Lodewijk A Sandkuijl
Familial hemiplegic migraine locus on 19p13 is involved in the common forms of migraine with and without aura.
Human genetics 1995;96(5):604-8.
1994: Joost Haan; Gisela M Terwindt; P L Bos; Roel A Ophoff; R R Frants; Michel D Ferrari
Familial hemiplegic migraine in The Netherlands. Dutch Migraine Genetics Research Group.
Clinical neurology and neurosurgery 1994;96(3):244-9.
1994: Roel A Ophoff; Ronald van Eijk; Lodewijk A Sandkuijl; Gisela M Terwindt; C P Grubben; Joost Haan; Dick Lindhout; Michel D Ferrari; Rune R Frants
Genetic heterogeneity of familial hemiplegic migraine.
Genomics 1994;22(1):21-6.
1994: L A Blonden; Gisela M Terwindt; Johan T den Dunnen; Gert-Jan B van Ommen
A polymorphic STS in intron 44 of the dystrophin gene.
Human genetics 1994;93(4):479-80.