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S Züchner

Showing results (1-10 of 12) with videos related to

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Neuromuscular Disorders : NMD|October 4, 2005
Marked phenotypic variation in a family with a new myelin protein zero mutationA Szabo, S Züchner, E Siska, et al.
Acta Neuropathologica|December 6, 2005
Peripheral nerve and skeletal muscle involvement in CADASILJ M Schröder, S Züchner, M Dichgans, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 18, 2003
A case of gliosarcoma appearing as ischaemic strokeS Züchner, W Kawohl, B Sellhaus, et al.
Sleep|January 6, 2001
RTMS induces brief events of muscle atonia in patients with narcolepsyM Hungs, F M Mottaghy, R Sparing, et al.
Neuroradiology|November 13, 2002
Hypertrophic nerve roots in a case of Roussy-Lévy syndromeC Haubrich, T Krings, J Senderek, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|November 25, 2000
Sleep stage dependant changes of the high-frequency part of the somatosensory evoked potentials at the thalamus and cortexP Halboni, R Kaminski, R Gobbelé, et al.
Clinical Genetics|August 20, 2010
Mutation screening of spastin, atlastin, and REEP1 in hereditary spastic paraplegiaD S McCorquodale, U Ozomaro, J Huang, et al.
Neuromuscular Disorders : NMD|April 17, 2007
GDAP1 mutations in Czech families with early-onset CMTL Baránková, E Vyhnálková, S Züchner, et al.
Neurology|May 12, 2004
Absence of KIF1B mutation in a large Turkish CMT2A family suggests involvement of a second geneN Bissar-Tadmouri, E Nelis, S Züchner, et al.
Annals of Human Genetics|September 3, 2008
Linkage and association study of late-onset Alzheimer disease families linked to 9p21.3S Züchner, J R Gilbert, E R Martin, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Neuromuscular Disorders : NMD|October 4, 2005
Marked phenotypic variation in a family with a new myelin protein zero mutationA Szabo, S Züchner, E Siska, et al.
Acta Neuropathologica|December 6, 2005
Peripheral nerve and skeletal muscle involvement in CADASILJ M Schröder, S Züchner, M Dichgans, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 18, 2003
A case of gliosarcoma appearing as ischaemic strokeS Züchner, W Kawohl, B Sellhaus, et al.
Sleep|January 6, 2001
RTMS induces brief events of muscle atonia in patients with narcolepsyM Hungs, F M Mottaghy, R Sparing, et al.
Neuroradiology|November 13, 2002
Hypertrophic nerve roots in a case of Roussy-Lévy syndromeC Haubrich, T Krings, J Senderek, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|November 25, 2000
Sleep stage dependant changes of the high-frequency part of the somatosensory evoked potentials at the thalamus and cortexP Halboni, R Kaminski, R Gobbelé, et al.
Clinical Genetics|August 20, 2010
Mutation screening of spastin, atlastin, and REEP1 in hereditary spastic paraplegiaD S McCorquodale, U Ozomaro, J Huang, et al.
Neuromuscular Disorders : NMD|April 17, 2007
GDAP1 mutations in Czech families with early-onset CMTL Baránková, E Vyhnálková, S Züchner, et al.
Neurology|May 12, 2004
Absence of KIF1B mutation in a large Turkish CMT2A family suggests involvement of a second geneN Bissar-Tadmouri, E Nelis, S Züchner, et al.
Annals of Human Genetics|September 3, 2008
Linkage and association study of late-onset Alzheimer disease families linked to 9p21.3S Züchner, J R Gilbert, E R Martin, et al.
Pageof 2