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Neurology. Genetics

Showing results (651-660 of 842) with videos related to

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Neurology. Genetics|April 12, 2016
Respiratory chain deficiency in nonmitochondrial diseaseAngela Pyle, Helen J Nightingale, Helen Griffin, et al.
Neurology. Genetics|April 12, 2016
Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson diseaseSuzanne Lesage, Jose Bras, Florence Cormier-Dequaire, et al.
Neurology. Genetics|April 12, 2016
Posterior reversible encephalopathy syndrome is not associated with mutations in aquaporin-4Marcelo Matiello, Rajanandini Muralidharan, David Sun, et al.
Neurology. Genetics|April 12, 2016
Alzheimer risk genes modulate the relationship between plasma apoE and cortical PiB bindingAndreas Lazaris, Kristy S Hwang, Naira Goukasian, et al.
Neurology. Genetics|April 12, 2016
Novel mutations highlight the key role of the ankyrin repeat domain in TRPV4-mediated neuropathyJeremy M Sullivan, Christina M Zimanyi, William Aisenberg, et al.
Neurology. Genetics|April 12, 2016
Recessive REEP1 mutation is associated with congenital axonal neuropathy and diaphragmatic palsyGudrun Schottmann, Dominik Seelow, Franziska Seifert, et al.
Neurology. Genetics|April 12, 2016
Mutation in the sixth immunoglobulin domain of L1CAM is associated with migrational brain anomaliesChristine Shieh, Franklin Moser, John M Graham, et al.
Neurology. Genetics|April 12, 2016
Whole-exome sequencing in neurologic practice: Reducing the diagnostic odysseyNicholas E Johnson
Neurology. Genetics|April 12, 2016
Benign hereditary chorea related to NKX2-1 with ataxia and dystoniaClaudio M de Gusmao, Fernando Kok, Erasmo Barbante Casella, et al.
Neurology. Genetics|April 12, 2016
X-inactivation in the clinical phenotype of fragile X premutation carrier sistersDeborah A Hall, Erin E Robertson-Dick, Joan A O'Keefe, et al.
Pageof 85

Showing results (651-660 of 842) with videos related to

Sort By:
Pageof 85
Neurology. Genetics|April 12, 2016
Respiratory chain deficiency in nonmitochondrial diseaseAngela Pyle, Helen J Nightingale, Helen Griffin, et al.
Neurology. Genetics|April 12, 2016
Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson diseaseSuzanne Lesage, Jose Bras, Florence Cormier-Dequaire, et al.
Neurology. Genetics|April 12, 2016
Posterior reversible encephalopathy syndrome is not associated with mutations in aquaporin-4Marcelo Matiello, Rajanandini Muralidharan, David Sun, et al.
Neurology. Genetics|April 12, 2016
Alzheimer risk genes modulate the relationship between plasma apoE and cortical PiB bindingAndreas Lazaris, Kristy S Hwang, Naira Goukasian, et al.
Neurology. Genetics|April 12, 2016
Novel mutations highlight the key role of the ankyrin repeat domain in TRPV4-mediated neuropathyJeremy M Sullivan, Christina M Zimanyi, William Aisenberg, et al.
Neurology. Genetics|April 12, 2016
Recessive REEP1 mutation is associated with congenital axonal neuropathy and diaphragmatic palsyGudrun Schottmann, Dominik Seelow, Franziska Seifert, et al.
Neurology. Genetics|April 12, 2016
Mutation in the sixth immunoglobulin domain of L1CAM is associated with migrational brain anomaliesChristine Shieh, Franklin Moser, John M Graham, et al.
Neurology. Genetics|April 12, 2016
Whole-exome sequencing in neurologic practice: Reducing the diagnostic odysseyNicholas E Johnson
Neurology. Genetics|April 12, 2016
Benign hereditary chorea related to NKX2-1 with ataxia and dystoniaClaudio M de Gusmao, Fernando Kok, Erasmo Barbante Casella, et al.
Neurology. Genetics|April 12, 2016
X-inactivation in the clinical phenotype of fragile X premutation carrier sistersDeborah A Hall, Erin E Robertson-Dick, Joan A O'Keefe, et al.
Pageof 85