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Beate Schlotter-Weigel

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Fortschritte Der Neurologie-Psychiatrie|September 25, 2018
[Immune-mediated / inflammatory and hereditary neuropathies - overview and diagnostic algorithm]Beate Schlotter-Weigel, Jan Senderek
Case Reports in Neurology|June 20, 2017
HIV-Associated Cerebellar Dysfunction and Improvement with Aminopyridine Therapy: A Case ReportCarolin Hoyer, Angelika Alonso, Beate Schlotter-Weigel, et al.
Brain Communications|September 21, 2020
Intraepidermal nerve fibre density as biomarker in Charcot-Marie-Tooth disease type 1ABeate Hartmannsberger, Kathrin Doppler, Julia Stauber, et al.
Journal of Neurology|July 20, 2004
The long-term outcome of anti-Jo-1-positive inflammatory myopathiesMichael Späth, Mira Schröder, Beate Schlotter-Weigel, et al.
Neuromuscular Disorders : NMD|January 11, 2005
Deletion of the LMNA initiator codon leading to a neurogenic variant of autosomal dominant Emery-Dreifuss muscular dystrophyMaggie C Walter, Thomas N Witt, Beate Schlotter Weigel, et al.
Neuromuscular Disorders : NMD|December 18, 2003
A novel homozygous missense mutation in the GNE gene of a patient with quadriceps-sparing hereditary inclusion body myopathy associated with muscle inflammationSabine Krause, Beate Schlotter-Weigel, Maggie C Walter, et al.
Neuromuscular Disorders : NMD|July 24, 2007
Late onset Pompe disease: clinical and neurophysiological spectrum of 38 patients including long-term follow-up in 18 patientsWolfgang Müller-Felber, Rita Horvath, Klaus Gempel, et al.
Neuromuscular Disorders : NMD|May 30, 2006
Novel splice site mutation in the caveolin-3 gene leading to autosomal recessive limb girdle muscular dystrophyJuliane S Müller, Henriett Piko, Benedikt G H Schoser, et al.
Clinical Genetics|October 10, 2018
MPV17 mutations in juvenile- and adult-onset axonal sensorimotor polyneuropathyMatthias Baumann, Herbert Schreiber, Beate Schlotter-Weigel, et al.
Acta Neuropathologica|September 19, 2025
Complement profiling of sural nerves in chronic-inflammatory demyelinating polyneuropathyFrauke Stascheit, Andreas Roos, Christina B Schroeter, et al.
Pageof 3

Showing results (1-10 of 30) with videos related to

Sort By:
Pageof 3
Fortschritte Der Neurologie-Psychiatrie|September 25, 2018
[Immune-mediated / inflammatory and hereditary neuropathies - overview and diagnostic algorithm]Beate Schlotter-Weigel, Jan Senderek
Case Reports in Neurology|June 20, 2017
HIV-Associated Cerebellar Dysfunction and Improvement with Aminopyridine Therapy: A Case ReportCarolin Hoyer, Angelika Alonso, Beate Schlotter-Weigel, et al.
Brain Communications|September 21, 2020
Intraepidermal nerve fibre density as biomarker in Charcot-Marie-Tooth disease type 1ABeate Hartmannsberger, Kathrin Doppler, Julia Stauber, et al.
Journal of Neurology|July 20, 2004
The long-term outcome of anti-Jo-1-positive inflammatory myopathiesMichael Späth, Mira Schröder, Beate Schlotter-Weigel, et al.
Neuromuscular Disorders : NMD|January 11, 2005
Deletion of the LMNA initiator codon leading to a neurogenic variant of autosomal dominant Emery-Dreifuss muscular dystrophyMaggie C Walter, Thomas N Witt, Beate Schlotter Weigel, et al.
Neuromuscular Disorders : NMD|December 18, 2003
A novel homozygous missense mutation in the GNE gene of a patient with quadriceps-sparing hereditary inclusion body myopathy associated with muscle inflammationSabine Krause, Beate Schlotter-Weigel, Maggie C Walter, et al.
Neuromuscular Disorders : NMD|July 24, 2007
Late onset Pompe disease: clinical and neurophysiological spectrum of 38 patients including long-term follow-up in 18 patientsWolfgang Müller-Felber, Rita Horvath, Klaus Gempel, et al.
Neuromuscular Disorders : NMD|May 30, 2006
Novel splice site mutation in the caveolin-3 gene leading to autosomal recessive limb girdle muscular dystrophyJuliane S Müller, Henriett Piko, Benedikt G H Schoser, et al.
Clinical Genetics|October 10, 2018
MPV17 mutations in juvenile- and adult-onset axonal sensorimotor polyneuropathyMatthias Baumann, Herbert Schreiber, Beate Schlotter-Weigel, et al.
Acta Neuropathologica|September 19, 2025
Complement profiling of sural nerves in chronic-inflammatory demyelinating polyneuropathyFrauke Stascheit, Andreas Roos, Christina B Schroeter, et al.
Pageof 3