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Neurogenetics

Showing results (591-600 of 949) with videos related to

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Neurogenetics|January 28, 2004
Genetic and environmental factors in the pathogenesis of Huntington's diseaseAnton van Dellen, Anthony J Hannan
Neurogenetics|May 11, 2004
A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2M A Kaunisto, H Harno, K R J Vanmolkot, et al.
Neurogenetics|May 11, 2004
The estrogen receptor 1 G594A polymorphism is associated with migraine susceptibility in two independent case/control groupsNatalie J Colson, Rod A Lea, Sharon Quinlan, et al.
Neurogenetics|March 27, 2004
Mitotic impairment by doublecortin is diminished by doublecortin mutations found in patientsSebastien Couillard-Despres, Goekhan Uyanik, Sonja Ploetz, et al.
Neurogenetics|January 18, 2005
Investigation of hormone receptor genes in migraineNatalie J Colson, Rod A Lea, Sharon Quinlan, et al.
Neurogenetics|September 30, 2004
Fine mapping of 16q-linked autosomal dominant cerebellar ataxia type III in Japanese familiesRyuki Hirano, Hiroshi Takashima, Ryuichi Okubo, et al.
Neurogenetics|June 19, 2004
A novel PMP22 mutation Ser22Phe in a family with hereditary neuropathy with liability to pressure palsies and CMT1A phenotypesKleopas A Kleopa, Domna-Maria Georgiou, Paschalis Nicolaou, et al.
Neurogenetics|October 22, 2005
A novel 3-bp deletion in the PANK2 gene of Dutch patients with pantothenate kinase-associated neurodegeneration: evidence for a founder effectP Rump, H H Lemmink, C C Verschuuren-Bemelmans, et al.
Neurogenetics|February 18, 2010
Atypical, perhaps under-recognized? An unusual phenotype of Friedreich ataxiaBeate Diehl, Michael S Lee, Janet R Reid, et al.
Neurogenetics|December 17, 2009
Analysis of exon dosage using MLPA in South African Parkinson's disease patientsRowena J Keyser, Debbie Lombard, Rene Veikondis, et al.
Pageof 95

Showing results (591-600 of 949) with videos related to

Sort By:
Pageof 95
Neurogenetics|January 28, 2004
Genetic and environmental factors in the pathogenesis of Huntington's diseaseAnton van Dellen, Anthony J Hannan
Neurogenetics|May 11, 2004
A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2M A Kaunisto, H Harno, K R J Vanmolkot, et al.
Neurogenetics|May 11, 2004
The estrogen receptor 1 G594A polymorphism is associated with migraine susceptibility in two independent case/control groupsNatalie J Colson, Rod A Lea, Sharon Quinlan, et al.
Neurogenetics|March 27, 2004
Mitotic impairment by doublecortin is diminished by doublecortin mutations found in patientsSebastien Couillard-Despres, Goekhan Uyanik, Sonja Ploetz, et al.
Neurogenetics|January 18, 2005
Investigation of hormone receptor genes in migraineNatalie J Colson, Rod A Lea, Sharon Quinlan, et al.
Neurogenetics|September 30, 2004
Fine mapping of 16q-linked autosomal dominant cerebellar ataxia type III in Japanese familiesRyuki Hirano, Hiroshi Takashima, Ryuichi Okubo, et al.
Neurogenetics|June 19, 2004
A novel PMP22 mutation Ser22Phe in a family with hereditary neuropathy with liability to pressure palsies and CMT1A phenotypesKleopas A Kleopa, Domna-Maria Georgiou, Paschalis Nicolaou, et al.
Neurogenetics|October 22, 2005
A novel 3-bp deletion in the PANK2 gene of Dutch patients with pantothenate kinase-associated neurodegeneration: evidence for a founder effectP Rump, H H Lemmink, C C Verschuuren-Bemelmans, et al.
Neurogenetics|February 18, 2010
Atypical, perhaps under-recognized? An unusual phenotype of Friedreich ataxiaBeate Diehl, Michael S Lee, Janet R Reid, et al.
Neurogenetics|December 17, 2009
Analysis of exon dosage using MLPA in South African Parkinson's disease patientsRowena J Keyser, Debbie Lombard, Rene Veikondis, et al.
Pageof 95