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S Brandner

Showing results (91-100 of 95) with videos related to

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Neuromuscular Disorders : NMD|January 4, 2011
Variable phenotypes are associated with PMP22 missense mutationsM Russo, M Laurá, J M Polke, et al.
Advances in Virus Research|July 14, 2001
Spongiform encephalopathies: insights from transgenic modelsA Aguzzi, S Brandner, M B Fischer, et al.
Neuromuscular Disorders : NMD|March 31, 2015
Transthyretin V122I amyloidosis with clinical and histological evidence of amyloid neuropathy and myopathyA S Carr, A L Pelayo-Negro, Z Jaunmuktane, et al.
Journal of Neurology|February 4, 2012
Frequency of mutations in the genes associated with hereditary sensory and autonomic neuropathy in a UK cohortG L Davidson, S M Murphy, J M Polke, et al.
Brain : a Journal of Neurology|September 2, 2008
Phenotypic heterogeneity and genetic modification of P102L inherited prion disease in an international seriesT E F Webb, M Poulter, J Beck, et al.
Pageof 10

Showing results (91-100 of 95) with videos related to

Sort By:
Pageof 10
You have reached the last page of results.This site can display upto 95 results.
Neuromuscular Disorders : NMD|January 4, 2011
Variable phenotypes are associated with PMP22 missense mutationsM Russo, M Laurá, J M Polke, et al.
Advances in Virus Research|July 14, 2001
Spongiform encephalopathies: insights from transgenic modelsA Aguzzi, S Brandner, M B Fischer, et al.
Neuromuscular Disorders : NMD|March 31, 2015
Transthyretin V122I amyloidosis with clinical and histological evidence of amyloid neuropathy and myopathyA S Carr, A L Pelayo-Negro, Z Jaunmuktane, et al.
Journal of Neurology|February 4, 2012
Frequency of mutations in the genes associated with hereditary sensory and autonomic neuropathy in a UK cohortG L Davidson, S M Murphy, J M Polke, et al.
Brain : a Journal of Neurology|September 2, 2008
Phenotypic heterogeneity and genetic modification of P102L inherited prion disease in an international seriesT E F Webb, M Poulter, J Beck, et al.
Pageof 10