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Stephan Züchner

Showing results (11-20 of 198) with videos related to

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Annual Review of Nutrition|May 15, 2015
Regulation of the Epigenome by Vitamin CJuan I Young, Stephan Züchner, Gaofeng Wang
Mayo Clinic Proceedings|June 1, 2010
A potential novel variant of hereditary sensory neuropathy in a 61-year-old man with cough-induced syncope and vertebral artery dissectionEmil Lou, Stephan Züchner, Jeffery Vance, et al.
Neurology. Genetics|August 18, 2020
Isoform-specific loss of dystonin causes hereditary motor and sensory neuropathyWilliam W Motley, Stephan Züchner, Steven S Scherer
Brain Research|September 17, 2019
Genetic modifiers and non-Mendelian aspects of CMTDana M Bis-Brewer, Sarah Fazal, Stephan Züchner
Neuromuscular Disorders : NMD|January 22, 2004
The novel neurofilament light (NEFL) mutation Glu397Lys is associated with a clinically and morphologically heterogeneous type of Charcot-Marie-Tooth neuropathyStephan Züchner, Matthias Vorgerd, Eckhart Sindern, et al.
Journal of Neuromuscular Diseases|April 10, 2025
The continued promise of genomic technologies and software in neurogeneticsIsaac R L Xu, Matt C Danzi, Jacquelyn Raposo, et al.
Plos Genetics|December 17, 2013
Somatic mtDNA mutation spectra in the aging human putamenSiôn L Williams, Deborah C Mash, Stephan Züchner, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 19, 2007
Update on psychiatric geneticsStephan Züchner, Sushma T Roberts, Marcy C Speer, et al.
Scientific Reports|February 10, 2019
A network biology approach to unraveling inherited axonopathiesDana M Bis-Brewer, Matt C Danzi, Stefan Wuchty, et al.
Journal of the Peripheral Nervous System : JPNS|January 18, 2018
A mutation in the heptad repeat 2 domain of MFN2 in a large CMT2A familyLois Dankwa, Jessica Richardson, William W Motley, et al.
Pageof 20

Showing results (11-20 of 198) with videos related to

Sort By:
Pageof 20
Annual Review of Nutrition|May 15, 2015
Regulation of the Epigenome by Vitamin CJuan I Young, Stephan Züchner, Gaofeng Wang
Mayo Clinic Proceedings|June 1, 2010
A potential novel variant of hereditary sensory neuropathy in a 61-year-old man with cough-induced syncope and vertebral artery dissectionEmil Lou, Stephan Züchner, Jeffery Vance, et al.
Neurology. Genetics|August 18, 2020
Isoform-specific loss of dystonin causes hereditary motor and sensory neuropathyWilliam W Motley, Stephan Züchner, Steven S Scherer
Brain Research|September 17, 2019
Genetic modifiers and non-Mendelian aspects of CMTDana M Bis-Brewer, Sarah Fazal, Stephan Züchner
Neuromuscular Disorders : NMD|January 22, 2004
The novel neurofilament light (NEFL) mutation Glu397Lys is associated with a clinically and morphologically heterogeneous type of Charcot-Marie-Tooth neuropathyStephan Züchner, Matthias Vorgerd, Eckhart Sindern, et al.
Journal of Neuromuscular Diseases|April 10, 2025
The continued promise of genomic technologies and software in neurogeneticsIsaac R L Xu, Matt C Danzi, Jacquelyn Raposo, et al.
Plos Genetics|December 17, 2013
Somatic mtDNA mutation spectra in the aging human putamenSiôn L Williams, Deborah C Mash, Stephan Züchner, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 19, 2007
Update on psychiatric geneticsStephan Züchner, Sushma T Roberts, Marcy C Speer, et al.
Scientific Reports|February 10, 2019
A network biology approach to unraveling inherited axonopathiesDana M Bis-Brewer, Matt C Danzi, Stefan Wuchty, et al.
Journal of the Peripheral Nervous System : JPNS|January 18, 2018
A mutation in the heptad repeat 2 domain of MFN2 in a large CMT2A familyLois Dankwa, Jessica Richardson, William W Motley, et al.
Pageof 20