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Neurogenetics

Showing results (31-40 of 1,080) with videos related to

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Neurogenetics|March 19, 2005
Creutzfeldt-Jakob disease associated with an R148H mutation of the prion protein geneBjarne Krebs, Rosa-Maria Lederer, Otto Windl, et al.
Neurogenetics|November 2, 2004
Early onset autosomal dominant spastic paraplegia caused by novel mutations in SPG3AAnnette Abel, Nuria Fonknechten, Anne Hofer, et al.
Neurogenetics|May 27, 2005
Identification of a VPS13A founder mutation in French Canadian families with chorea-acanthocytosisCarol Dobson-Stone, Antonio Velayos-Baeza, An Jansen, et al.
Neurogenetics|December 7, 2007
Different spectra of genomic deletions within the CCM genes between Italian and American CCM patient cohortsChristina L Liquori, Silvana Penco, Judith Gault, et al.
Neurogenetics|December 7, 2007
Myotonic dystrophy type 2 in Japan: ancestral origin distinct from Caucasian familiesTsukasa Saito, Yoshinobu Amakusa, Takashi Kimura, et al.
Neurogenetics|May 18, 1999
HLA typing in the United Kingdom multiple sclerosis genome screenF Coraddu, S Sawcer, R Feakes, et al.
Neurogenetics|May 18, 1999
Mutations in the Caenorhabditis elegans dystrophin-like gene dys-1 lead to hyperactivity and suggest a link with cholinergic transmissionC Bessou, J B Giugia, C J Franks, et al.
Neurogenetics|May 10, 2008
ARSACS in the Dutch population: a frequent cause of early-onset cerebellar ataxiaSascha Vermeer, Rowdy P P Meijer, Benjamin J Pijl, et al.
Neurogenetics|April 3, 2025
The association of SCN1A polymorphisms with epilepsy and drug resistance: a systematic review and meta-analysisIda Mohammadi, Shahryar Rajai Firouzabadi, Aryan Aarabi, et al.
Neurogenetics|April 3, 2025
Genetic variants associated with idiopathic Parkinson's disease in Latin America: A systematic reviewFelipe Duarte-Zambrano, David Felipe Alfonso-Cedeño, Jorge A Barrero, et al.
Pageof 108

Showing results (31-40 of 1,080) with videos related to

Sort By:
Pageof 108
Neurogenetics|March 19, 2005
Creutzfeldt-Jakob disease associated with an R148H mutation of the prion protein geneBjarne Krebs, Rosa-Maria Lederer, Otto Windl, et al.
Neurogenetics|November 2, 2004
Early onset autosomal dominant spastic paraplegia caused by novel mutations in SPG3AAnnette Abel, Nuria Fonknechten, Anne Hofer, et al.
Neurogenetics|May 27, 2005
Identification of a VPS13A founder mutation in French Canadian families with chorea-acanthocytosisCarol Dobson-Stone, Antonio Velayos-Baeza, An Jansen, et al.
Neurogenetics|December 7, 2007
Different spectra of genomic deletions within the CCM genes between Italian and American CCM patient cohortsChristina L Liquori, Silvana Penco, Judith Gault, et al.
Neurogenetics|December 7, 2007
Myotonic dystrophy type 2 in Japan: ancestral origin distinct from Caucasian familiesTsukasa Saito, Yoshinobu Amakusa, Takashi Kimura, et al.
Neurogenetics|May 18, 1999
HLA typing in the United Kingdom multiple sclerosis genome screenF Coraddu, S Sawcer, R Feakes, et al.
Neurogenetics|May 18, 1999
Mutations in the Caenorhabditis elegans dystrophin-like gene dys-1 lead to hyperactivity and suggest a link with cholinergic transmissionC Bessou, J B Giugia, C J Franks, et al.
Neurogenetics|May 10, 2008
ARSACS in the Dutch population: a frequent cause of early-onset cerebellar ataxiaSascha Vermeer, Rowdy P P Meijer, Benjamin J Pijl, et al.
Neurogenetics|April 3, 2025
The association of SCN1A polymorphisms with epilepsy and drug resistance: a systematic review and meta-analysisIda Mohammadi, Shahryar Rajai Firouzabadi, Aryan Aarabi, et al.
Neurogenetics|April 3, 2025
Genetic variants associated with idiopathic Parkinson's disease in Latin America: A systematic reviewFelipe Duarte-Zambrano, David Felipe Alfonso-Cedeño, Jorge A Barrero, et al.
Pageof 108