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Neurogenetics

Showing results (21-30 of 1,080) with videos related to

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Neurogenetics|December 3, 2015
Refining the phenotype associated with CASC5 mutationAbdelkrim Saadi, Florine Verny, Karine Siquier-Pernet, et al.
Neurogenetics|February 17, 2016
Recessive mutations of TMC1 associated with moderate to severe hearing lossAyesha Imtiaz, Azra Maqsood, Atteeq U Rehman, et al.
Neurogenetics|August 17, 2019
VPS53 gene is associated with a new phenotype of complicated hereditary spastic paraparesisMoran Hausman-Kedem, Shay Ben-Shachar, Shay Menascu, et al.
Neurogenetics|March 15, 2017
Pain insensitivity: distal S6-segment mutations in Na<sub>V</sub>1.9 emerge as critical hotspotMargaret K King, Enrico Leipold, Jessica M Goehringer, et al.
Neurogenetics|December 23, 2003
Friedreich ataxia-update on pathogenesis and possible therapiesMax Voncken, Panos Ioannou, Martin B Delatycki
Neurogenetics|December 24, 2004
The urokinase-plasminogen activator (PLAU) gene is not associated with late onset Alzheimer's diseaseSilvia Bagnoli, Andrea Tedde, Elena Cellini, et al.
Neurogenetics|October 14, 2004
A novel three extra-repeat insertion in the prion protein gene (PRNP) in a patient with Creutzfeldt-Jakob diseaseE Grasbon-Frodl, R Schmalzbauer, P Weber, et al.
Neurogenetics|October 14, 2004
Alternative splicing in the N-terminus of Alzheimer's presenilin 1Wiep Scheper, Rob Zwart, Frank Baas
Neurogenetics|January 1, 2005
Epsilon-sarcoglycan is not involved in sporadic Gilles de la Tourette syndromeFriedrich Asmus, Sarah Schoenian, Peter Lichtner, et al.
Neurogenetics|May 25, 2004
Private SACS mutations in autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) families from TurkeyAndrea M Richter, Riza Koksal Ozgul, Virginie C Poisson, et al.
Pageof 108

Showing results (21-30 of 1,080) with videos related to

Sort By:
Pageof 108
Neurogenetics|December 3, 2015
Refining the phenotype associated with CASC5 mutationAbdelkrim Saadi, Florine Verny, Karine Siquier-Pernet, et al.
Neurogenetics|February 17, 2016
Recessive mutations of TMC1 associated with moderate to severe hearing lossAyesha Imtiaz, Azra Maqsood, Atteeq U Rehman, et al.
Neurogenetics|August 17, 2019
VPS53 gene is associated with a new phenotype of complicated hereditary spastic paraparesisMoran Hausman-Kedem, Shay Ben-Shachar, Shay Menascu, et al.
Neurogenetics|March 15, 2017
Pain insensitivity: distal S6-segment mutations in Na<sub>V</sub>1.9 emerge as critical hotspotMargaret K King, Enrico Leipold, Jessica M Goehringer, et al.
Neurogenetics|December 23, 2003
Friedreich ataxia-update on pathogenesis and possible therapiesMax Voncken, Panos Ioannou, Martin B Delatycki
Neurogenetics|December 24, 2004
The urokinase-plasminogen activator (PLAU) gene is not associated with late onset Alzheimer's diseaseSilvia Bagnoli, Andrea Tedde, Elena Cellini, et al.
Neurogenetics|October 14, 2004
A novel three extra-repeat insertion in the prion protein gene (PRNP) in a patient with Creutzfeldt-Jakob diseaseE Grasbon-Frodl, R Schmalzbauer, P Weber, et al.
Neurogenetics|October 14, 2004
Alternative splicing in the N-terminus of Alzheimer's presenilin 1Wiep Scheper, Rob Zwart, Frank Baas
Neurogenetics|January 1, 2005
Epsilon-sarcoglycan is not involved in sporadic Gilles de la Tourette syndromeFriedrich Asmus, Sarah Schoenian, Peter Lichtner, et al.
Neurogenetics|May 25, 2004
Private SACS mutations in autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) families from TurkeyAndrea M Richter, Riza Koksal Ozgul, Virginie C Poisson, et al.
Pageof 108