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Neurogenetics

Showing results (841-850 of 949) with videos related to

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Neurogenetics|December 10, 2013
Repeat interruptions in spinocerebellar ataxia type 10 expansions are strongly associated with epileptic seizuresKaren N McFarland, Jilin Liu, Ivette Landrian, et al.
Neurogenetics|October 9, 2013
Neuroligin modulates the locomotory dopaminergic and serotonergic neuronal pathways of C. elegansPatricia G Izquierdo, Fernando Calahorro, Manuel Ruiz-Rubio
Neurogenetics|February 26, 2010
Meta-analysis of association between variation in the PDE4D gene and ischemic cerebral infarction risk in Asian populationsXiaowei Xu, Xia Li, Jiejie Li, et al.
Neurogenetics|October 20, 2005
Familial risks for migraine and other headaches among siblings based on hospitalizations in SwedenKari Hemminki, Xinjun Li, Sven-Erik Johansson, et al.
Neurogenetics|October 20, 2005
Functional analysis of novel KCNQ2 and KCNQ3 gene variants found in a large pedigree with benign familial neonatal convulsions (BFNC)Maria T Bassi, Umberto Balottin, Chris Panzeri, et al.
Neurogenetics|November 1, 2005
Immunoglobulin KM allotypes are associated with the prevalence of autoantibodies to GD1a ganglioside, but not with susceptibility to the disease, in Japanese patients with Guillain-Barré syndromeJanardan P Pandey, Michiaki Koga, Nobuhiro Yuki
Neurogenetics|October 13, 2005
Nonsense mutation in TITF1 in a Portuguese family with benign hereditary choreaMaria do Carmo Costa, Cristina Costa, Ana Paula Silva, et al.
Neurogenetics|October 12, 2005
Association of sporadic Creutzfeldt-Jakob disease with homozygous genotypes at PRNP codons 129 and 219 in the Korean populationByung-Hoon Jeong, Kyung-Hee Lee, Nam-Ho Kim, et al.
Neurogenetics|November 19, 2009
Novel variants identified in methyl-CpG-binding domain genes in autistic individualsHolly N Cukier, Raquel Rabionet, Ioanna Konidari, et al.
Neurogenetics|July 1, 2017
Rare causes of early-onset dystonia-parkinsonism with cognitive impairment: a de novo PSEN-1 mutationMiryam Carecchio, Marina Picillo, Lorella Valletta, et al.
Pageof 95

Showing results (841-850 of 949) with videos related to

Sort By:
Pageof 95
Neurogenetics|December 10, 2013
Repeat interruptions in spinocerebellar ataxia type 10 expansions are strongly associated with epileptic seizuresKaren N McFarland, Jilin Liu, Ivette Landrian, et al.
Neurogenetics|October 9, 2013
Neuroligin modulates the locomotory dopaminergic and serotonergic neuronal pathways of C. elegansPatricia G Izquierdo, Fernando Calahorro, Manuel Ruiz-Rubio
Neurogenetics|February 26, 2010
Meta-analysis of association between variation in the PDE4D gene and ischemic cerebral infarction risk in Asian populationsXiaowei Xu, Xia Li, Jiejie Li, et al.
Neurogenetics|October 20, 2005
Familial risks for migraine and other headaches among siblings based on hospitalizations in SwedenKari Hemminki, Xinjun Li, Sven-Erik Johansson, et al.
Neurogenetics|October 20, 2005
Functional analysis of novel KCNQ2 and KCNQ3 gene variants found in a large pedigree with benign familial neonatal convulsions (BFNC)Maria T Bassi, Umberto Balottin, Chris Panzeri, et al.
Neurogenetics|November 1, 2005
Immunoglobulin KM allotypes are associated with the prevalence of autoantibodies to GD1a ganglioside, but not with susceptibility to the disease, in Japanese patients with Guillain-Barré syndromeJanardan P Pandey, Michiaki Koga, Nobuhiro Yuki
Neurogenetics|October 13, 2005
Nonsense mutation in TITF1 in a Portuguese family with benign hereditary choreaMaria do Carmo Costa, Cristina Costa, Ana Paula Silva, et al.
Neurogenetics|October 12, 2005
Association of sporadic Creutzfeldt-Jakob disease with homozygous genotypes at PRNP codons 129 and 219 in the Korean populationByung-Hoon Jeong, Kyung-Hee Lee, Nam-Ho Kim, et al.
Neurogenetics|November 19, 2009
Novel variants identified in methyl-CpG-binding domain genes in autistic individualsHolly N Cukier, Raquel Rabionet, Ioanna Konidari, et al.
Neurogenetics|July 1, 2017
Rare causes of early-onset dystonia-parkinsonism with cognitive impairment: a de novo PSEN-1 mutationMiryam Carecchio, Marina Picillo, Lorella Valletta, et al.
Pageof 95