-
2009
-
Schoonman GG, van Oosterhout WR, Ferrari MD, van der Grond J
Anatomical Variations in the Circle of Willis and Migraine Susceptibility: Is There an Association?
Headache. 2009 Oct 21
Bekijk de publicatie
-
- Erfelijkheidsonderzoek
- Migraine
Eikermann-Haerter K, Baum MJ, Ferrari MD, van den Maagdenberg AM, Moskowitz MA, Ayata C
Androgenic suppression of spreading depression in familial hemiplegic migraine type 1 mutant mice
Ann Neurol. 2009 Oct;66(4):564-8
Bekijk de publicatie
-
de Vries B, Steup-Beekman G, Haan J, Bollen E, Luyendijk J, Frants R, Terwindt G, van Buchem M, Huizinga T, van den Maagdenberg A, Ferrari M
TREX1 Gene Variant in Neuropsychiatric Systemic Lupus Erythematosus
Ann Rheum Dis. 2009 Oct 28
Bekijk de publicatie
-
- Erfelijkheidsonderzoek
- Migraine
de Vries B, Stam AH, Kirkpatrick M,Vanmolkot KR, Koenderink JB, van den Heuvel JJ, Stunnenberg B, Goudie D, Shetty J, Jain V, van Vark J, Terwindt GM, Frants RR, Haan J, van den Maagdenberg AM, Ferrari MD
Familial hemiplegic migraine is associated with febrile seizures in an FHM2 family with a novel de novo ATP1A2 mutation
Epilepsia. 2009 Nov;50(11):2503-4
Bekijk de publicatie
-
Koek MM, Bakel F, Engel W, van den Maagdenberg A, Ferrari MD, Coulier L, Hankemeier T
Metabolic Profiling of Ultrasmall Sample Volumes with GC/MS: From Microliter to Nanoliter Samples
Anal Chem. 2009 Nov 30
Bekijk de publicatie
-
2007
-
- Erfelijkheidsonderzoek
- Overig
Richards A, van den Maagdenberg AMJM , Jen JC, Kavanagh D, Bertram P, Spitzer D, Liszewski MK, Barilla-Labarca M, Terwindt GM, Kasai Y, McLellan M, Grand MG, Vanmolkot KRJ, de Vries B, Wan J, Kane MJ, Mamsa H, Schäfer 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 RF, 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. September 2007.
Bekijk de publicatie
-
1998
-
- Erfelijkheidsonderzoek
- Overig
Terwindt GM, Haan J, Ophoff RA , Groenen SM, Storimans CW, Lanser JB, Roos RA, Bleeker-Wagemakers EM, Frants RR, Ferrari MD
Clinical and genetic analysis of a large Dutch family with autosomal dominant vascular retinopathy, migraine and Raynaud's phenomenon
Brain . 1998 Feb;121 ( Pt 2):303-16.
Bekijk de publicatie
