Works matching AU Frants RR

Results: 11

Two novel functional mutations in the Na<sup>+</sup>,K<sup>+</sup>-ATPase α2-subunit ATP1A2 gene in patients with familial hemiplegic migraine and associated neurological phenotypes.

Published in:

Clinical Genetics, 2008, v. 73, n. 1, p. 37, doi. 10.1111/j.1399-0004.2007.00918.x

By:

Castro, M-J;
Nunes, B;
de Vries, B;
Lemos, C;
Vanmolkot, KRJ;
van den Heuvel, JJMW;
Temudo, T;
Barros, J;
Sequeiros, J;
Frants, RR;
Koenderink, JB;
Pereira-Monteiro, JM;
van den Maagdenberg, AMJM

Publication type:

Article

Clinical and genetic analysis of a large Dutch family with autosomal dominant vascular retinopathy, migraine and Raynaud's phenomenon.

Published in:

Brain: A Journal of Neurology, 1998, v. 121, n. 2, p. 303, doi. 10.1093/brain/121.2.303

By:

Terwindt, GM;
Haan, J;
Ophoff, RA;
Groenen, SMA;
Storimans, CWJM;
Lanser, JBK;
Roos, RAC;
Bleeker-Wagemakers, EM;
Frants, RR;
Ferrari, MD

Publication type:

Article

Migraine and MTHFR C677T genotype in a population-based sample.

Published in:

2006

By:

Scher AI;
Terwindt GM;
Verschuren WM;
Kruit MC;
Blom HJ;
Kowa H;
Frants RR;
van den Maagdenberg AM;
van Buchem M;
Ferrari MD;
Launer LJ

Publication type:

Journal Article

Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 ATP1A2 mutation.

Published in:

2006

By:

Vanmolkot KR;
Stroink H;
Koenderink JB;
Kors EE;
van den Heuvel JJ;
van den Boogerd EH;
Stam AH;
Haan J;
De Vries BB;
Terwindt GM;
Frants RR;
Ferrari MD;
van den Maagdenberg AM

Publication type:

Journal Article

Variable hypomethylation of D4Z4 in facioscapulohumeral muscular dystrophy.

Published in:

2005

By:

van Overveld PGM;
Enthoven L;
Ricci E;
Rossi M;
Felicetti L;
Jeanpierre M;
Winokur ST;
Frants RR;
Padberg GW;
van der Maarel SM

Publication type:

Journal Article

The Phe-124-Cys and A-161T variants of the human 5-HT(1B) receptor gene are not major determinants of the clinical response to sumatriptan.

Published in:

2007

By:

Mehrotra S;
Vanmolkot KR;
Frants RR;
van den Maagdenberg AM;
Ferrari MD;
Maassenvandenbrink A

Publication type:

Journal Article

High cortical spreading depression susceptibility and migraine-associated symptoms in Ca(v)2.1 S218L mice.

Published in:

2010

By:

van den Maagdenberg AM;
Pizzorusso T;
Kaja S;
Terpolilli N;
Shapovalova M;
Hoebeek FE;
Barrett CF;
Gherardini L;
van de Ven RC;
Todorov B;
Broos LA;
Tottene A;
Gao Z;
Fodor M;
De Zeeuw CI;
Frants RR;
Plesnila N;
Plomp JJ;
Pietrobon D;
Ferrari MD

Publication type:

journal article

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

Published in:

Cephalalgia, 2000, v. 20, n. 8, p. 696, doi. 10.1046/j.0333-1024.2000.00095.x

By:

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

Publication type:

Article

Search for mitochondrial DNA mutations in migraine subgroups.

Published in:

1999

By:

Haan, J;
Terwindt, GM;
Maassen, JA;
Hart, LM 't;
Frants, RR;
Ferrari, MD;
Terwindt, G M;
Maassen, J A;
Hart, L M;
Frants, R R;
Ferrari, M D

Publication type:

journal article

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

Published in:

1996

By:

Terwindt, GM;
Ophoff, RA;
Haan, J;
Frants, RR;
Ferrari, MD;
Terwindt, G M;
Ophoff, R A;
Frants, R R;
Ferrari, M D

Publication type:

journal article

A long-term follow-up study of 18 patients with sporadic hemiplegic migraine.

Published in:

2011

By:

Stam AH;
Louter MA;
Haan J;
de Vries B;
van den Maagdenberg AM;
Frants RR;
Ferrari MD;
Terwindt GM

Publication type:

Journal Article