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European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology
|
March 16, 2010
The involvement of GSK3beta in bipolar disorder: integrating evidence from multiple types of genetic studies
J J Luykx, M P M Boks, A P R Terwindt, et al.
Molecular Psychiatry
|
March 25, 2009
Network analysis of positional candidate genes of schizophrenia highlights myelin-related pathways
T Rietkerk, M P M Boks, I E C Sommer, et al.
Neurology
|
May 5, 1998
Variable clinical expression of mutations in the P/Q-type calcium channel gene in familial hemiplegic migraine. Dutch Migraine Genetics Research Group
G M Terwindt, R A Ophoff, J Haan, et al.
Clinical Neurology and Neurosurgery
|
August 1, 1997
Hyperekplexia-like syndromes without mutations in the GLRA1 gene
M N Vergouwe, M A Tijssen, R Shiang, et al.
Clinical Neurology and Neurosurgery
|
November 1, 1995
A four-generation Dutch family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), linked to chromosome 19p13
R Wielaard, M Bornebroek, R A Ophoff, et al.
Molecular Psychiatry
|
March 11, 2015
Evaluating historical candidate genes for schizophrenia
M S Farrell, T Werge, P Sklar, et al.
Neurology
|
April 26, 2001
Involvement of the CACNA1A gene containing region on 19p13 in migraine with and without aura
G M Terwindt, R A Ophoff, R van Eijk, et al.
American Journal of Medical Genetics
|
June 19, 1998
Chromosomal localization of the 5-HT1F receptor gene: no evidence for involvement in response to sumatriptan in migraine patients
A Maassen VanDenBrink, M N Vergouwe, R A Ophoff, et al.
American Journal of Human Genetics
|
February 1, 1995
Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 caucasian families
A Elbaz, J Vale-Santos, K Jurkat-Rott, et al.
Genomics
|
July 1, 1994
Genetic heterogeneity of familial hemiplegic migraine
R A Ophoff, R van Eijk, L A Sandkuijl, et al.
Page
of 7
Search research articles
Search
Showing results (21-30 of 68) with videos related to
Sort By:
Page
of 7
European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology
|
March 16, 2010
The involvement of GSK3beta in bipolar disorder: integrating evidence from multiple types of genetic studies
J J Luykx, M P M Boks, A P R Terwindt, et al.
Molecular Psychiatry
|
March 25, 2009
Network analysis of positional candidate genes of schizophrenia highlights myelin-related pathways
T Rietkerk, M P M Boks, I E C Sommer, et al.
Neurology
|
May 5, 1998
Variable clinical expression of mutations in the P/Q-type calcium channel gene in familial hemiplegic migraine. Dutch Migraine Genetics Research Group
G M Terwindt, R A Ophoff, J Haan, et al.
Clinical Neurology and Neurosurgery
|
August 1, 1997
Hyperekplexia-like syndromes without mutations in the GLRA1 gene
M N Vergouwe, M A Tijssen, R Shiang, et al.
Clinical Neurology and Neurosurgery
|
November 1, 1995
A four-generation Dutch family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), linked to chromosome 19p13
R Wielaard, M Bornebroek, R A Ophoff, et al.
Molecular Psychiatry
|
March 11, 2015
Evaluating historical candidate genes for schizophrenia
M S Farrell, T Werge, P Sklar, et al.
Neurology
|
April 26, 2001
Involvement of the CACNA1A gene containing region on 19p13 in migraine with and without aura
G M Terwindt, R A Ophoff, R van Eijk, et al.
American Journal of Medical Genetics
|
June 19, 1998
Chromosomal localization of the 5-HT1F receptor gene: no evidence for involvement in response to sumatriptan in migraine patients
A Maassen VanDenBrink, M N Vergouwe, R A Ophoff, et al.
American Journal of Human Genetics
|
February 1, 1995
Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 caucasian families
A Elbaz, J Vale-Santos, K Jurkat-Rott, et al.
Genomics
|
July 1, 1994
Genetic heterogeneity of familial hemiplegic migraine
R A Ophoff, R van Eijk, L A Sandkuijl, et al.
Page
of 7