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Gilbert Wunderlich

Showing results (1-10 of 54) with videos related to

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Neurological Research and Practice|September 27, 2023
Reply to: Camptocormia due to myotinilopathy, Parkinson's disease, or both?Jan Niklas Petry-Schmelzer, Gilbert Wunderlich
Movement Disorders : Official Journal of the Movement Disorder Society|May 19, 2022
Expanded Genetic Spectrum and Variable Disease Onset in AOPEP-Associated DystoniaBenita Menden, Alexander Gutschalk, Gilbert Wunderlich, et al.
Neurological Research and Practice|December 16, 2020
Diagnosis of peripheral neuropathyHelmar C Lehmann, Gilbert Wunderlich, Gereon R Fink, et al.
Practical Neurology|July 30, 2022
Persistent hypokalaemia and intermittent muscle weaknessMonika Rabenstein, Angela Abicht, Anna Brunn, et al.
Deutsche Medizinische Wochenschrift (1946)|July 4, 2017
[30-year-old Patient with suspected Marfan Syndrome and Progressive Gait disturbance]Maryam Balke, Helmar C Lehmann, Gereon R Fink, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 23, 2003
Secondary progressive chronic manganism associated with markedly decreased striatal D2 receptor densityKirn R Kessler, Gilbert Wunderlich, Harald Hefter, et al.
Der Nervenarzt|March 26, 2021
[Neuromuscular complications of SARS-CoV-2 infections-Part 1: peripheral nerves]Helmar C Lehmann, Benedikt Schoser, Gilbert Wunderlich, et al.
Frontiers in Neurology|March 13, 2020
The Maximum Bite Force for Treatment Evaluation in Severely Affected Adult SMA Patients-Protocol for a Longitudinal StudyTeresa Kruse, Helmar C Lehmann, Bert Braumann, et al.
Acta Neurologica Belgica|July 16, 2018
Late onset necrotizing autoimmune myopathy 1 year after cessation of statin treatmentMaryam Balke, Anna Brunn, Kristl G Claeys, et al.
Journal of the Neurological Sciences|July 18, 2016
Oligosymptomatic adrenomyeloneuropathy due to a novel mutation in the ABCD1 start codonVeronika Dunkl, Isabella Rau, Gilbert Wunderlich, et al.
Pageof 6

Showing results (1-10 of 54) with videos related to

Sort By:
Pageof 6
Neurological Research and Practice|September 27, 2023
Reply to: Camptocormia due to myotinilopathy, Parkinson's disease, or both?Jan Niklas Petry-Schmelzer, Gilbert Wunderlich
Movement Disorders : Official Journal of the Movement Disorder Society|May 19, 2022
Expanded Genetic Spectrum and Variable Disease Onset in AOPEP-Associated DystoniaBenita Menden, Alexander Gutschalk, Gilbert Wunderlich, et al.
Neurological Research and Practice|December 16, 2020
Diagnosis of peripheral neuropathyHelmar C Lehmann, Gilbert Wunderlich, Gereon R Fink, et al.
Practical Neurology|July 30, 2022
Persistent hypokalaemia and intermittent muscle weaknessMonika Rabenstein, Angela Abicht, Anna Brunn, et al.
Deutsche Medizinische Wochenschrift (1946)|July 4, 2017
[30-year-old Patient with suspected Marfan Syndrome and Progressive Gait disturbance]Maryam Balke, Helmar C Lehmann, Gereon R Fink, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 23, 2003
Secondary progressive chronic manganism associated with markedly decreased striatal D2 receptor densityKirn R Kessler, Gilbert Wunderlich, Harald Hefter, et al.
Der Nervenarzt|March 26, 2021
[Neuromuscular complications of SARS-CoV-2 infections-Part 1: peripheral nerves]Helmar C Lehmann, Benedikt Schoser, Gilbert Wunderlich, et al.
Frontiers in Neurology|March 13, 2020
The Maximum Bite Force for Treatment Evaluation in Severely Affected Adult SMA Patients-Protocol for a Longitudinal StudyTeresa Kruse, Helmar C Lehmann, Bert Braumann, et al.
Acta Neurologica Belgica|July 16, 2018
Late onset necrotizing autoimmune myopathy 1 year after cessation of statin treatmentMaryam Balke, Anna Brunn, Kristl G Claeys, et al.
Journal of the Neurological Sciences|July 18, 2016
Oligosymptomatic adrenomyeloneuropathy due to a novel mutation in the ABCD1 start codonVeronika Dunkl, Isabella Rau, Gilbert Wunderlich, et al.
Pageof 6