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1

Is familial hemiplegic migraine a hereditary form of basilar migraine?

J Haan, GM Terwindt, RA Ophoff, PLJM Bos, RR Frants, MD Ferrari

Journal:

Year:

1995

Language:

english

File:

PDF, 43 KB

english, 1995

2

Space headache: a new secondary headache

AA Vein, H Koppen, J Haan, GM Terwindt, MD Ferrari

Journal:

Year:

2009

Language:

english

File:

PDF, 122 KB

english, 2009

3

Alternating hemiplegia of childhood: no mutations in the familial hemiplegic migraine CACNA1A gene

J Haan, Ee Kors, Gm Terwindt, Flmg Vermeulen, Mn Vergouwe, Amjm Van Den Maagdenberg, Ds Gill, J Pascual, Ra Ophoff, Rr Frants, Md Ferrari

Journal:

Year:

2000

Language:

english

File:

PDF, 65 KB

english, 2000

4

Familial hemiplegic migraine: a clinical comparison of families linked and unlinked to chromosome 19

GM Terwindt, RA Ophoff, J Haan, RR Frants, MD Ferrari

Journal:

Year:

1996

File:

PDF, 63 KB

1996

5

No involvement of the calcium channel gene (CACNA1A) in a family with cluster headache

J Haan, JA Van Vliet, EE Kors, GM Terwindt, FLMG Vermeulen, AMJM Van Den Maagdenberg, RR Frants, MD Ferrari

Journal:

Year:

2001

Language:

english

File:

PDF, 64 KB

english, 2001

6

CACNA1A R1347Q: a frequent recurrent mutation in hemiplegic migraine

AH Stam, KRJ Vanmolkot, HPH Kremer, J Gärtner, J Brown, E Leshinsky-Silver, R Gilad, EE Kors, WS Frankhuizen, HB Ginjaar, J Haan, RR Frants, MD Ferrari, AMJM Van Den Maagdenberg, GM Terwindt

Journal:

Clinical Genetics

Year:

2008

Language:

english

File:

PDF, 212 KB

english, 2008

7

Search for mitochondrial DNA mutations in migraine subgroups

J Haan, GM Terwindt, JA Maassen, LM 't Hart, RR Frants, MD Ferrari

Journal:

Year:

1999

Language:

english

File:

PDF, 537 KB

english, 1999

8

The 3p21.1-p21.3 hereditary vascular retinopathy locus increases the risk for Raynaud's phenomenon and migraine

JJ Hottenga, KRJ Vanmolkot, EE Kors, S Kheradmand Kia, PTVM De Jong, J Haan, GM Terwindt, RR Frants, MD Ferrari, AMJM Van Den Maagdenberg

Journal:

Year:

2005

Language:

english

File:

PDF, 67 KB

english, 2005

9

The prevalence of premonitory symptoms in migraine: a questionnaire study in 461 patients

GG Schoonman, DJ Evers, GM Terwindt, JG Van Dijk, MD Ferrari

Journal:

Year:

2006

Language:

english

File:

PDF, 77 KB

english, 2006

10

A gene for a new monogenic neurovascular migraine syndrome: a next step in unravelling molecular pathways for migraine?

KRJ Vanmolkot, GM Terwindt, RR Frants, J Haan, AMJM Van Den Maagdenberg, MD Ferrari

Journal:

Year:

2008

Language:

english

File:

PDF, 44 KB

english, 2008

11

A review of the genetic relation between migraine and epilepsy

J Haan, GM Terwindt, AMJM Van Den Maagdenberg, AH Stam, MD Ferrari

Journal:

Year:

2008

Language:

english

File:

PDF, 83 KB

english, 2008

12

CACNA1A mutation linking hemiplegic migraine and alternating hemiplegia of childhood

B De Vries, AH Stam, F Beker, AMJM Van Den Maagdenberg, KRJ Vanmolkot, LAEM Laan, IB Ginjaar, RR Frants, H Lauffer, J Haan, JP Haas, GM Terwindt, MD Ferrari

Journal:

Year:

2008

Language:

english

File:

PDF, 240 KB

english, 2008

13

First mutation in the voltage-gated NaV1.1 subunit gene SCN1A with co-occurring familial hemiplegic migraine and epilepsy

M-J Castro, AH Stam, C Lemos, B De Vries, KRJ Vanmolkot, J Barros, GM Terwindt, RR Frants, J Sequeiros, MD Ferrari, JM Pereira-Monteiro, AMJM Van Den Maagdenberg

Journal:

Year:

2009

Language:

english

File:

PDF, 183 KB

english, 2009

14

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

MC Kruit, MA Van Buchem, LJ Launer, GM Terwindt, MD Ferrari

Journal:

Year:

2012

Language:

english

File:

PDF, 124 KB

english, 2012

15

Migraine and genetic and acquired vasculopathies

AH Stam, J Haan, AMJM Van Den Maagdenberg, MD Ferrari, GM Terwindt

Journal:

Year:

2009

Language:

english

File:

PDF, 118 KB

english, 2009

16

Novel SCN1A mutation in the IFMT motif of the α1 subunit of the voltage-gated NaV1.1 channel causing familial hemiplegic migraine

De Vries, B, Weller, CM, De Fàbregues, O, Koelewijn, SC, Stam, AH, Haan, J, Ferrari, MD, Terwindt, GM, van den Maagdenberg, AMJ

Journal:

The Journal of Headache and Pain

Year:

2013

Language:

english

File:

PDF, 54 KB

english, 2013

17

Mitteilungen der DGPPN 10/2013

De Vries, B, Freilinger, T, Anttila, V, Malik, R, Terwindt, GM, Pozo-Rosich, P, Winsvold, B, Nyholt, D, van Oosterhout, WPJ, Artto, V, Todt, M, Hämäläinen, E, Fernandez-Moralez, J, Louter, M, Kaunisto

Journal:

Year:

2013

Language:

german

File:

PDF, 496 KB

german, 2013

18

Migraine without aura: genome-wide association analysis identifies several novel susceptibility

De Vries, B, Freilinger, T, Anttila, V, Malik, R, Terwindt, GM, Pozo-Rosich, P, Winsvold, B, Nyholt, D, van Oosterhout, WPJ, Artto, V, Todt, M, Hämäläinen, E, Fernandez-Moralez, J, Louter, M, Kaunisto

Journal:

The Journal of Headache and Pain

Year:

2013

Language:

english

File:

PDF, 74 KB

english, 2013

19

Postural sway in migraine patients and controls, results from a population based CAMERA-2 study

Koppen, H, Palm-Meinders, IH, Horlings, CGC, Terwindt, GM, Launer, LJ, van Buchem, MA, Kruit, MC, Bloem, MR, Ferrari, MD

Journal:

The Journal of Headache and Pain

Year:

2013

Language:

english

File:

PDF, 54 KB

english, 2013

20

Search for mitochondrial DNA mutations in migraine subgroups

Haan, J, Terwindt, GM, Maassen, JA, Hart, LM 't, Frants, RR, Ferrari, MD

Journal:

Year:

1999

Language:

english

File:

PDF, 531 KB

english, 1999

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