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Neurogenetics

Showing results (41-50 of 1,080) with videos related to

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Neurogenetics|April 1, 2025
Multi-target approach to Alzheimer's disease prevention and treatment: antioxidant, anti-inflammatory, and amyloid- modulating mechanismsKashif Abbas, Mohd Mustafa, Mudassir Alam, et al.
Neurogenetics|January 16, 2026
ADK deficiency without hypermethioninemia presenting as intractable epilepsy: a rare neurometabolic case and literature reviewAgung Triono, Kristy Iskandar, Neti Nurani, et al.
Neurogenetics|October 10, 2003
Absence of pathogenic mutations in presenilin homologue 2 in a conclusively 17-linked tau-negative dementia familyR Rademakers, M Van den Broeck, K Sleegers, et al.
Neurogenetics|January 22, 2013
Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcificationSandy Chan Hsu, Renee L Sears, Roberta R Lemos, et al.
Neurogenetics|February 26, 2013
Application of long-range polymerase chain reaction in the diagnosis of X-linked dystonia-parkinsonismToshitaka Kawarai, Paul Matthew D Pasco, Rosalia A Teleg, et al.
Neurogenetics|March 5, 2013
Dominant GDAP1 founder mutation is a common cause of axonal Charcot-Marie-Tooth disease in FinlandMari Auranen, Emil Ylikallio, Jussi Toppila, et al.
Neurogenetics|April 19, 2013
CCM molecular screening in a diagnosis context: novel unclassified variants leading to abnormal splicing and importance of large deletionsFlorence Riant, Michaelle Cecillon, Pascale Saugier-Veber, et al.
Neurogenetics|June 12, 2013
Genetic modifiers in Huntington's disease: fiction or fact?Larissa Arning, Jörg T Epplen
Neurogenetics|December 6, 2005
Early-onset Parkinson's disease caused by a novel parkin mutation in a genetic isolate from north-eastern BrazilHsin F Chien, Christan F Rohé, Maria D L Costa, et al.
Neurogenetics|November 15, 2005
Introducing a novel human mtDNA mutation into the Paracoccus denitrificans COX I gene explains functional deficits in a patientSimona Lucioli, Klaus Hoffmeier, Rosalba Carrozzo, et al.
Pageof 108

Showing results (41-50 of 1,080) with videos related to

Sort By:
Pageof 108
Neurogenetics|April 1, 2025
Multi-target approach to Alzheimer's disease prevention and treatment: antioxidant, anti-inflammatory, and amyloid- modulating mechanismsKashif Abbas, Mohd Mustafa, Mudassir Alam, et al.
Neurogenetics|January 16, 2026
ADK deficiency without hypermethioninemia presenting as intractable epilepsy: a rare neurometabolic case and literature reviewAgung Triono, Kristy Iskandar, Neti Nurani, et al.
Neurogenetics|October 10, 2003
Absence of pathogenic mutations in presenilin homologue 2 in a conclusively 17-linked tau-negative dementia familyR Rademakers, M Van den Broeck, K Sleegers, et al.
Neurogenetics|January 22, 2013
Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcificationSandy Chan Hsu, Renee L Sears, Roberta R Lemos, et al.
Neurogenetics|February 26, 2013
Application of long-range polymerase chain reaction in the diagnosis of X-linked dystonia-parkinsonismToshitaka Kawarai, Paul Matthew D Pasco, Rosalia A Teleg, et al.
Neurogenetics|March 5, 2013
Dominant GDAP1 founder mutation is a common cause of axonal Charcot-Marie-Tooth disease in FinlandMari Auranen, Emil Ylikallio, Jussi Toppila, et al.
Neurogenetics|April 19, 2013
CCM molecular screening in a diagnosis context: novel unclassified variants leading to abnormal splicing and importance of large deletionsFlorence Riant, Michaelle Cecillon, Pascale Saugier-Veber, et al.
Neurogenetics|June 12, 2013
Genetic modifiers in Huntington's disease: fiction or fact?Larissa Arning, Jörg T Epplen
Neurogenetics|December 6, 2005
Early-onset Parkinson's disease caused by a novel parkin mutation in a genetic isolate from north-eastern BrazilHsin F Chien, Christan F Rohé, Maria D L Costa, et al.
Neurogenetics|November 15, 2005
Introducing a novel human mtDNA mutation into the Paracoccus denitrificans COX I gene explains functional deficits in a patientSimona Lucioli, Klaus Hoffmeier, Rosalba Carrozzo, et al.
Pageof 108