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Neurogenetics
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December 3, 2015
Refining the phenotype associated with CASC5 mutation
Abdelkrim Saadi, Florine Verny, Karine Siquier-Pernet, et al.
Neurogenetics
|
February 17, 2016
Recessive mutations of TMC1 associated with moderate to severe hearing loss
Ayesha Imtiaz, Azra Maqsood, Atteeq U Rehman, et al.
Neurogenetics
|
August 17, 2019
VPS53 gene is associated with a new phenotype of complicated hereditary spastic paraparesis
Moran 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 hotspot
Margaret K King, Enrico Leipold, Jessica M Goehringer, et al.
Neurogenetics
|
December 23, 2003
Friedreich ataxia-update on pathogenesis and possible therapies
Max Voncken, Panos Ioannou, Martin B Delatycki
Neurogenetics
|
December 24, 2004
The urokinase-plasminogen activator (PLAU) gene is not associated with late onset Alzheimer's disease
Silvia 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 disease
E Grasbon-Frodl, R Schmalzbauer, P Weber, et al.
Neurogenetics
|
October 14, 2004
Alternative splicing in the N-terminus of Alzheimer's presenilin 1
Wiep Scheper, Rob Zwart, Frank Baas
Neurogenetics
|
January 1, 2005
Epsilon-sarcoglycan is not involved in sporadic Gilles de la Tourette syndrome
Friedrich 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 Turkey
Andrea M Richter, Riza Koksal Ozgul, Virginie C Poisson, et al.
Page
of 108
Search research articles
Search
Showing results (21-30 of 1,080) with videos related to
Sort By:
Page
of 108
Neurogenetics
|
December 3, 2015
Refining the phenotype associated with CASC5 mutation
Abdelkrim Saadi, Florine Verny, Karine Siquier-Pernet, et al.
Neurogenetics
|
February 17, 2016
Recessive mutations of TMC1 associated with moderate to severe hearing loss
Ayesha Imtiaz, Azra Maqsood, Atteeq U Rehman, et al.
Neurogenetics
|
August 17, 2019
VPS53 gene is associated with a new phenotype of complicated hereditary spastic paraparesis
Moran 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 hotspot
Margaret K King, Enrico Leipold, Jessica M Goehringer, et al.
Neurogenetics
|
December 23, 2003
Friedreich ataxia-update on pathogenesis and possible therapies
Max Voncken, Panos Ioannou, Martin B Delatycki
Neurogenetics
|
December 24, 2004
The urokinase-plasminogen activator (PLAU) gene is not associated with late onset Alzheimer's disease
Silvia 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 disease
E Grasbon-Frodl, R Schmalzbauer, P Weber, et al.
Neurogenetics
|
October 14, 2004
Alternative splicing in the N-terminus of Alzheimer's presenilin 1
Wiep Scheper, Rob Zwart, Frank Baas
Neurogenetics
|
January 1, 2005
Epsilon-sarcoglycan is not involved in sporadic Gilles de la Tourette syndrome
Friedrich 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 Turkey
Andrea M Richter, Riza Koksal Ozgul, Virginie C Poisson, et al.
Page
of 108