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Neurogenetics

Showing results (801-810 of 949) with videos related to

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Neurogenetics|May 18, 1999
Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies: a SacI polymorphism in the proximal CMT1A-REP elements may lead to genetic misdiagnosisC Fuchs, T Liehr, S Ozbey, et al.
Neurogenetics|May 18, 1999
Mapping, genomic structure, and polymorphisms of the human GABABR1 receptor gene: evaluation of its involvement in idiopathic generalized epilepsyH C Peters, G Kämmer, A Volz, et al.
Neurogenetics|December 22, 2007
RNA interference of LRRK2-microarray expression analysis of a Parkinson's disease key playerK Häbig, M Walter, S Poths, et al.
Neurogenetics|February 12, 2014
The documentation of consent and disclosure of neurogenetic testing outside clinical geneticsC Lo, J Martindale, M Hadjivassiliou, et al.
Neurogenetics|March 24, 2025
Repeated clear benefits of immunotherapy in a patient with Charcot-Marie-Tooth disease carrying a rare point mutation in PMP22Honami Kawai, Yoichiro Nishida, Takashi Kanda, et al.
Neurogenetics|March 5, 2025
Investigating the gut microbiome in schizophrenia cases versus controls: South Africa's versionCarlien Rust, Laila Asmal, Michaela O'Hare, et al.
Neurogenetics|November 28, 2024
Three Iranian patients with rare subtypes of hereditary spastic paraplegia (HSP): SPG76, SPG56, and SPG69Zahra Sadr, Aida Ghasemi, Mohammad Rohani, et al.
Neurogenetics|November 25, 2024
Understanding pathophysiology in fragile X syndrome: a comprehensive reviewJuan Carlos Castillo Juárez, Alejandro Aguilar Gómez, Adrian Esteban Salatino Díaz, et al.
Neurogenetics|November 27, 2024
Giant axonal neuropathy: a rare inherited neuropathy with a novel mutationBita Poorshiri, Neda Jabbarpour, Mohammad Barzegar, et al.
Neurogenetics|February 15, 2025
Early-onset Parkinson's disease in a patient with a rare homozygous pathogenic GBA1 variant and no Gaucher disease symptomsJuliana Cordovil Cotrin, Rafael Mina Piergiorge, Andressa Pereira Gonçalves, et al.
Pageof 95

Showing results (801-810 of 949) with videos related to

Sort By:
Pageof 95
Neurogenetics|May 18, 1999
Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies: a SacI polymorphism in the proximal CMT1A-REP elements may lead to genetic misdiagnosisC Fuchs, T Liehr, S Ozbey, et al.
Neurogenetics|May 18, 1999
Mapping, genomic structure, and polymorphisms of the human GABABR1 receptor gene: evaluation of its involvement in idiopathic generalized epilepsyH C Peters, G Kämmer, A Volz, et al.
Neurogenetics|December 22, 2007
RNA interference of LRRK2-microarray expression analysis of a Parkinson's disease key playerK Häbig, M Walter, S Poths, et al.
Neurogenetics|February 12, 2014
The documentation of consent and disclosure of neurogenetic testing outside clinical geneticsC Lo, J Martindale, M Hadjivassiliou, et al.
Neurogenetics|March 24, 2025
Repeated clear benefits of immunotherapy in a patient with Charcot-Marie-Tooth disease carrying a rare point mutation in PMP22Honami Kawai, Yoichiro Nishida, Takashi Kanda, et al.
Neurogenetics|March 5, 2025
Investigating the gut microbiome in schizophrenia cases versus controls: South Africa's versionCarlien Rust, Laila Asmal, Michaela O'Hare, et al.
Neurogenetics|November 28, 2024
Three Iranian patients with rare subtypes of hereditary spastic paraplegia (HSP): SPG76, SPG56, and SPG69Zahra Sadr, Aida Ghasemi, Mohammad Rohani, et al.
Neurogenetics|November 25, 2024
Understanding pathophysiology in fragile X syndrome: a comprehensive reviewJuan Carlos Castillo Juárez, Alejandro Aguilar Gómez, Adrian Esteban Salatino Díaz, et al.
Neurogenetics|November 27, 2024
Giant axonal neuropathy: a rare inherited neuropathy with a novel mutationBita Poorshiri, Neda Jabbarpour, Mohammad Barzegar, et al.
Neurogenetics|February 15, 2025
Early-onset Parkinson's disease in a patient with a rare homozygous pathogenic GBA1 variant and no Gaucher disease symptomsJuliana Cordovil Cotrin, Rafael Mina Piergiorge, Andressa Pereira Gonçalves, et al.
Pageof 95