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Hans H Goebel

Showing results (51-60 of 89) with videos related to

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Neuromuscular Disorders : NMD|December 24, 2016
20th Anniversary Meeting of the Meryon Society Worcester College, OxfordAlan E H Emery, Marcia Emery, Michael Swash, et al.
Acta Neuropathologica|March 11, 2005
The enlarging spectrum of desminopathies: new morphological findings, eastward geographic spread, novel exon 3 desmin mutationAlexandra Vrabie, Lev G Goldfarb, Alexey Shatunov, et al.
Brain Pathology (Zurich, Switzerland)|March 5, 2004
July 2003: 62-year-old female with progressive muscular weaknessAntje Bornemann, Jürgen Bohl, Hans-Michael Schneider, et al.
American Journal of Medical Genetics|October 12, 2002
Late infantile neuronal ceroid lipofuscinosis: quantitative description of the clinical course in patients with CLN2 mutationsRobert Steinfeld, Peter Heim, Henning von Gregory, et al.
Seminars in Pediatric Neurology|July 3, 2018
The Curse of Apneic SpellsJosefine Radke, Mona Dreesmann, Michael Radke, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 6, 2002
Neuronal loss and brain atrophy in mice lacking cathepsins B and LUte Felbor, Benedikt Kessler, Walther Mothes, et al.
Brain Pathology (Zurich, Switzerland)|February 28, 2024
Meeting report of the 20th International Congress of Neuropathology (ICN) 2023 in BerlinHans H Goebel, Arend Koch, Helena Radbruch, et al.
Neuromuscular Disorders : NMD|October 27, 2021
Congenital myopathy and epidermolysis bullosa due to PLEC variantMaggie C Walter, Peter Reilich, Sabine Krause, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 8, 2005
Camptocormia associated with focal myositis in multiple-system atrophyNico J Diederich, Hans H Goebel, Georges Dooms, et al.
Neuromuscular Disorders : NMD|December 12, 2001
Mutations in the beta-tropomyosin (TPM2) gene--a rare cause of nemaline myopathyKati Donner, Miina Ollikainen, Maaret Ridanpää, et al.
Pageof 9

Showing results (51-60 of 89) with videos related to

Sort By:
Pageof 9
Neuromuscular Disorders : NMD|December 24, 2016
20th Anniversary Meeting of the Meryon Society Worcester College, OxfordAlan E H Emery, Marcia Emery, Michael Swash, et al.
Acta Neuropathologica|March 11, 2005
The enlarging spectrum of desminopathies: new morphological findings, eastward geographic spread, novel exon 3 desmin mutationAlexandra Vrabie, Lev G Goldfarb, Alexey Shatunov, et al.
Brain Pathology (Zurich, Switzerland)|March 5, 2004
July 2003: 62-year-old female with progressive muscular weaknessAntje Bornemann, Jürgen Bohl, Hans-Michael Schneider, et al.
American Journal of Medical Genetics|October 12, 2002
Late infantile neuronal ceroid lipofuscinosis: quantitative description of the clinical course in patients with CLN2 mutationsRobert Steinfeld, Peter Heim, Henning von Gregory, et al.
Seminars in Pediatric Neurology|July 3, 2018
The Curse of Apneic SpellsJosefine Radke, Mona Dreesmann, Michael Radke, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 6, 2002
Neuronal loss and brain atrophy in mice lacking cathepsins B and LUte Felbor, Benedikt Kessler, Walther Mothes, et al.
Brain Pathology (Zurich, Switzerland)|February 28, 2024
Meeting report of the 20th International Congress of Neuropathology (ICN) 2023 in BerlinHans H Goebel, Arend Koch, Helena Radbruch, et al.
Neuromuscular Disorders : NMD|October 27, 2021
Congenital myopathy and epidermolysis bullosa due to PLEC variantMaggie C Walter, Peter Reilich, Sabine Krause, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 8, 2005
Camptocormia associated with focal myositis in multiple-system atrophyNico J Diederich, Hans H Goebel, Georges Dooms, et al.
Neuromuscular Disorders : NMD|December 12, 2001
Mutations in the beta-tropomyosin (TPM2) gene--a rare cause of nemaline myopathyKati Donner, Miina Ollikainen, Maaret Ridanpää, et al.
Pageof 9