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Neurogenetics

Showing results (921-930 of 949) with videos related to

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Neurogenetics|September 18, 2016
A customized high-resolution array-comparative genomic hybridization to explore copy number variations in Parkinson's diseaseValentina La Cognata, Giovanna Morello, Giulia Gentile, et al.
Neurogenetics|January 29, 2014
Partial deletions of the GRN gene are a cause of frontotemporal lobar degenerationFabienne Clot, Anne Rovelet-Lecrux, Foudil Lamari, et al.
Neurogenetics|February 10, 2015
Milestones in Friedreich ataxia: more than a century and still learningAgessandro Abrahão, José Luiz Pedroso, Pedro Braga-Neto, et al.
Neurogenetics|January 31, 2015
Association of a common genetic variant within ANKK1 with six-month cognitive performance after traumatic brain injuryJohn K Yue, Angela M Pronger, Adam R Ferguson, et al.
Neurogenetics|February 15, 2023
Neurodegeneration with brain iron accumulation: a case series highlighting phenotypic and genotypic diversity in 20 Indian familiesHaseena Sait, Somya Srivastava, Manmohan Pandey, et al.
Neurogenetics|March 9, 2023
A novel KRIT1/CCM1 mutation accompanied by a NOTCH3 mutation in a Chinese family with multiple cerebral cavernous malformationsChunwang Li, Penghui Liu, Weilin Huang, et al.
Neurogenetics|May 3, 2021
Dravet syndrome and Dravet syndrome-like phenotype: a systematic review of the SCN1A and PCDH19 variantsAna Carla Mondek Rampazzo, Rafael Rodrigues Pinheiro Dos Santos, Fernando Arfux Maluf, et al.
Neurogenetics|May 8, 2021
Genotype-phenotype correlations of heterozygous HTRA1-related cerebral small vessel disease: case report and systematic reviewHaohan Zhang, Xiaoming Qin, Yingying Shi, et al.
Neurogenetics|August 18, 2021
NTRK1 gene-related congenital insensitivity to pain with anhidrosis: a nationwide multicenter retrospective studyAndoni Echaniz-Laguna, Cecilia Altuzarra, Alain Verloes, et al.
Neurogenetics|August 20, 2021
Novel variants in the NARS2 gene as a cause of infantile-onset severe epilepsy leading to fatal refractory status epilepticus: case study and literature reviewK Štěrbová, M Vlčková, H Hansíková, et al.
Pageof 95

Showing results (921-930 of 949) with videos related to

Sort By:
Pageof 95
Neurogenetics|September 18, 2016
A customized high-resolution array-comparative genomic hybridization to explore copy number variations in Parkinson's diseaseValentina La Cognata, Giovanna Morello, Giulia Gentile, et al.
Neurogenetics|January 29, 2014
Partial deletions of the GRN gene are a cause of frontotemporal lobar degenerationFabienne Clot, Anne Rovelet-Lecrux, Foudil Lamari, et al.
Neurogenetics|February 10, 2015
Milestones in Friedreich ataxia: more than a century and still learningAgessandro Abrahão, José Luiz Pedroso, Pedro Braga-Neto, et al.
Neurogenetics|January 31, 2015
Association of a common genetic variant within ANKK1 with six-month cognitive performance after traumatic brain injuryJohn K Yue, Angela M Pronger, Adam R Ferguson, et al.
Neurogenetics|February 15, 2023
Neurodegeneration with brain iron accumulation: a case series highlighting phenotypic and genotypic diversity in 20 Indian familiesHaseena Sait, Somya Srivastava, Manmohan Pandey, et al.
Neurogenetics|March 9, 2023
A novel KRIT1/CCM1 mutation accompanied by a NOTCH3 mutation in a Chinese family with multiple cerebral cavernous malformationsChunwang Li, Penghui Liu, Weilin Huang, et al.
Neurogenetics|May 3, 2021
Dravet syndrome and Dravet syndrome-like phenotype: a systematic review of the SCN1A and PCDH19 variantsAna Carla Mondek Rampazzo, Rafael Rodrigues Pinheiro Dos Santos, Fernando Arfux Maluf, et al.
Neurogenetics|May 8, 2021
Genotype-phenotype correlations of heterozygous HTRA1-related cerebral small vessel disease: case report and systematic reviewHaohan Zhang, Xiaoming Qin, Yingying Shi, et al.
Neurogenetics|August 18, 2021
NTRK1 gene-related congenital insensitivity to pain with anhidrosis: a nationwide multicenter retrospective studyAndoni Echaniz-Laguna, Cecilia Altuzarra, Alain Verloes, et al.
Neurogenetics|August 20, 2021
Novel variants in the NARS2 gene as a cause of infantile-onset severe epilepsy leading to fatal refractory status epilepticus: case study and literature reviewK Štěrbová, M Vlčková, H Hansíková, et al.
Pageof 95