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Neurology. Genetics

Showing results (391-400 of 1,012) with videos related to

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Neurology. Genetics|April 12, 2016
Novel GABRG2 mutations cause familial febrile seizuresMorgane Boillot, Mélanie Morin-Brureau, Fabienne Picard, et al.
Neurology. Genetics|April 12, 2016
Genetic profile for suspected dysferlinopathy identified by targeted next-generation sequencingRumiko Izumi, Tetsuya Niihori, Toshiaki Takahashi, et al.
Neurology. Genetics|April 12, 2016
Polyneuropathy in a young Belgian patient: A novel heterozygous mutation in the WNK1/HSN2 geneJeroen de Filette, Danielle Hasaerts, Sara Seneca, et al.
Neurology. Genetics|April 12, 2016
Overlap between Parkinson disease and Alzheimer disease in ABCA7 functional variantsKaren Nuytemans, Lizmarie Maldonado, Aleena Ali, et al.
Neurology. Genetics|April 12, 2016
In silico prioritization based on coexpression can aid epileptic encephalopathy gene discoveryKaren L Oliver, Vesna Lukic, Saskia Freytag, et al.
Neurology. Genetics|April 12, 2016
Genetics of neurodegenerative diseasesStefan M Pulst
Neurology. Genetics|July 28, 2017
Functionally pathogenic <i>EARS2</i> variants in vitro may not manifest a phenotype in vivoNathan McNeill, Alessia Nasca, Aurelio Reyes, et al.
Neurology. Genetics|July 28, 2017
This variant alters protein function, but is it pathogenic?Massimo Pandolfo
Neurology. Genetics|August 16, 2017
Whole-exome sequencing associates novel <i>CSMD1</i> gene mutations with familial Parkinson diseaseJavier Ruiz-Martínez, Luis J Azcona, Alberto Bergareche, et al.
Neurology. Genetics|August 2, 2017
Prevalence of spinocerebellar ataxia 36 in a US populationJuliana M Valera, Tatyana Diaz, Lauren E Petty, et al.
Pageof 102

Showing results (391-400 of 1,012) with videos related to

Sort By:
Pageof 102
Neurology. Genetics|April 12, 2016
Novel GABRG2 mutations cause familial febrile seizuresMorgane Boillot, Mélanie Morin-Brureau, Fabienne Picard, et al.
Neurology. Genetics|April 12, 2016
Genetic profile for suspected dysferlinopathy identified by targeted next-generation sequencingRumiko Izumi, Tetsuya Niihori, Toshiaki Takahashi, et al.
Neurology. Genetics|April 12, 2016
Polyneuropathy in a young Belgian patient: A novel heterozygous mutation in the WNK1/HSN2 geneJeroen de Filette, Danielle Hasaerts, Sara Seneca, et al.
Neurology. Genetics|April 12, 2016
Overlap between Parkinson disease and Alzheimer disease in ABCA7 functional variantsKaren Nuytemans, Lizmarie Maldonado, Aleena Ali, et al.
Neurology. Genetics|April 12, 2016
In silico prioritization based on coexpression can aid epileptic encephalopathy gene discoveryKaren L Oliver, Vesna Lukic, Saskia Freytag, et al.
Neurology. Genetics|April 12, 2016
Genetics of neurodegenerative diseasesStefan M Pulst
Neurology. Genetics|July 28, 2017
Functionally pathogenic <i>EARS2</i> variants in vitro may not manifest a phenotype in vivoNathan McNeill, Alessia Nasca, Aurelio Reyes, et al.
Neurology. Genetics|July 28, 2017
This variant alters protein function, but is it pathogenic?Massimo Pandolfo
Neurology. Genetics|August 16, 2017
Whole-exome sequencing associates novel <i>CSMD1</i> gene mutations with familial Parkinson diseaseJavier Ruiz-Martínez, Luis J Azcona, Alberto Bergareche, et al.
Neurology. Genetics|August 2, 2017
Prevalence of spinocerebellar ataxia 36 in a US populationJuliana M Valera, Tatyana Diaz, Lauren E Petty, et al.
Pageof 102