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Stephan Züchner

Showing results (1-10 of 198) with videos related to

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Gene Therapy|June 8, 2021
Schwann cell gene therapies in sightStephan Züchner
Expert Opinion on Pharmacotherapy|July 31, 2007
The genetics of hereditary spastic paraplegia and implications for drug therapyStephan Züchner
Nature Reviews. Neurology|August 7, 2010
Peripheral neuropathies: whole genome sequencing identifies causal variants in CMTStephan Züchner
Journal of the Peripheral Nervous System : JPNS|June 7, 2022
Charcot-Marie-Tooth disease in AfricaStephan Züchner, Davide Pareyson
Neuromuscular Disorders : NMD|January 27, 2019
Replication studies of MIR149 association in Charcot-Marie-Tooth disease type 1A in a European populationFeifei Tao, , Stephan Züchner
Journal of Molecular Medicine (Berlin, Germany)|September 1, 2005
Emerging pathways for hereditary axonopathiesStephan Züchner, Jeffery M Vance
Neuromolecular Medicine|June 16, 2006
Molecular genetics of autosomal-dominant axonal Charcot-Marie-Tooth diseaseStephan Züchner, Jeffery M Vance
Nature Clinical Practice. Neurology|August 26, 2006
Mechanisms of disease: a molecular genetic update on hereditary axonal neuropathiesStephan Züchner, Jeffery M Vance
Frontiers in Neurology|December 12, 2018
Perspectives on the Genomics of HSP Beyond Mendelian InheritanceDana M Bis-Brewer, Stephan Züchner
Genes|April 8, 2014
Genetics of Charcot-Marie-Tooth (CMT) Disease within the Frame of the Human Genome Project SuccessVincent Timmerman, Alleene V Strickland, Stephan Züchner
Pageof 20

Showing results (1-10 of 198) with videos related to

Sort By:
Pageof 20
Gene Therapy|June 8, 2021
Schwann cell gene therapies in sightStephan Züchner
Expert Opinion on Pharmacotherapy|July 31, 2007
The genetics of hereditary spastic paraplegia and implications for drug therapyStephan Züchner
Nature Reviews. Neurology|August 7, 2010
Peripheral neuropathies: whole genome sequencing identifies causal variants in CMTStephan Züchner
Journal of the Peripheral Nervous System : JPNS|June 7, 2022
Charcot-Marie-Tooth disease in AfricaStephan Züchner, Davide Pareyson
Neuromuscular Disorders : NMD|January 27, 2019
Replication studies of MIR149 association in Charcot-Marie-Tooth disease type 1A in a European populationFeifei Tao, , Stephan Züchner
Journal of Molecular Medicine (Berlin, Germany)|September 1, 2005
Emerging pathways for hereditary axonopathiesStephan Züchner, Jeffery M Vance
Neuromolecular Medicine|June 16, 2006
Molecular genetics of autosomal-dominant axonal Charcot-Marie-Tooth diseaseStephan Züchner, Jeffery M Vance
Nature Clinical Practice. Neurology|August 26, 2006
Mechanisms of disease: a molecular genetic update on hereditary axonal neuropathiesStephan Züchner, Jeffery M Vance
Frontiers in Neurology|December 12, 2018
Perspectives on the Genomics of HSP Beyond Mendelian InheritanceDana M Bis-Brewer, Stephan Züchner
Genes|April 8, 2014
Genetics of Charcot-Marie-Tooth (CMT) Disease within the Frame of the Human Genome Project SuccessVincent Timmerman, Alleene V Strickland, Stephan Züchner
Pageof 20