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Matthias Vorgerd

Showing results (91-100 of 140) with videos related to

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Human Mutation|May 12, 2017
The novel αB-crystallin (CRYAB) mutation p.D109G causes restrictive cardiomyopathyAndreas Brodehl, Anna Gaertner-Rommel, Bärbel Klauke, et al.
Muscle & Nerve|July 13, 2020
Diffusion tensor imaging reveals changes in non-fat infiltrated muscles in late onset Pompe diseaseRobert Rehmann, Martijn Froeling, Marlena Rohm, et al.
Viruses|January 21, 2023
Seroprevalence of Binding and Neutralizing Antibodies against 39 Human Adenovirus Types in Patients with Neuromuscular DisordersPatrick Julian Klann, Xiaoyan Wang, Anna Elfert, et al.
Journal of Cellular and Molecular Medicine|April 23, 2024
Proteomic studies in VWA1-related neuromyopathy allowed new pathophysiological insights and the definition of blood biomarkersMohammed Athamneh, Nassam Daya, Andreas Hentschel, et al.
Cells|January 11, 2024
Synaptopodin-2 Isoforms Have Specific Binding Partners and Display Distinct, Muscle Cell Type-Specific Expression PatternsKeerthika Lohanadan, Marvin Assent, Anja Linnemann, et al.
Biomedicines|October 27, 2022
FYCO1 Increase and Effect of Arimoclomol-Treatment in Human <i>VCP</i>-PathologyAnne-Katrin Guettsches, Nancy Meyer, René P Zahedi, et al.
Scientific Reports|December 21, 2023
Muscle diffusion MRI reveals autophagic buildup in a mouse model for Pompe diseaseMarlena Rohm, Gabriele Russo, Xavier Helluy, et al.
Biological Chemistry|April 22, 2005
Limb girdle muscular dystrophy in a sibling pair with a homozygous Ser606Leu mutation in the alternatively spliced IS2 region of calpain 3Dieter E Jenne, Rudi A Kley, Matthias Vorgerd, et al.
Neuropathology and Applied Neurobiology|September 30, 2022
Target formation in muscle fibres indicates reinnervation - A proteomic study in muscle samples from peripheral neuropathiesKarsten Krause, Britta Eggers, Julian Uszkoreit, et al.
Journal of Neurology|December 16, 2003
Variable reduction of caveolin-3 in patients with LGMD2B/MMMaggie C Walter, Christian Braun, Matthias Vorgerd, et al.
Pageof 14

Showing results (91-100 of 140) with videos related to

Sort By:
Pageof 14
Human Mutation|May 12, 2017
The novel αB-crystallin (CRYAB) mutation p.D109G causes restrictive cardiomyopathyAndreas Brodehl, Anna Gaertner-Rommel, Bärbel Klauke, et al.
Muscle & Nerve|July 13, 2020
Diffusion tensor imaging reveals changes in non-fat infiltrated muscles in late onset Pompe diseaseRobert Rehmann, Martijn Froeling, Marlena Rohm, et al.
Viruses|January 21, 2023
Seroprevalence of Binding and Neutralizing Antibodies against 39 Human Adenovirus Types in Patients with Neuromuscular DisordersPatrick Julian Klann, Xiaoyan Wang, Anna Elfert, et al.
Journal of Cellular and Molecular Medicine|April 23, 2024
Proteomic studies in VWA1-related neuromyopathy allowed new pathophysiological insights and the definition of blood biomarkersMohammed Athamneh, Nassam Daya, Andreas Hentschel, et al.
Cells|January 11, 2024
Synaptopodin-2 Isoforms Have Specific Binding Partners and Display Distinct, Muscle Cell Type-Specific Expression PatternsKeerthika Lohanadan, Marvin Assent, Anja Linnemann, et al.
Biomedicines|October 27, 2022
FYCO1 Increase and Effect of Arimoclomol-Treatment in Human <i>VCP</i>-PathologyAnne-Katrin Guettsches, Nancy Meyer, René P Zahedi, et al.
Scientific Reports|December 21, 2023
Muscle diffusion MRI reveals autophagic buildup in a mouse model for Pompe diseaseMarlena Rohm, Gabriele Russo, Xavier Helluy, et al.
Biological Chemistry|April 22, 2005
Limb girdle muscular dystrophy in a sibling pair with a homozygous Ser606Leu mutation in the alternatively spliced IS2 region of calpain 3Dieter E Jenne, Rudi A Kley, Matthias Vorgerd, et al.
Neuropathology and Applied Neurobiology|September 30, 2022
Target formation in muscle fibres indicates reinnervation - A proteomic study in muscle samples from peripheral neuropathiesKarsten Krause, Britta Eggers, Julian Uszkoreit, et al.
Journal of Neurology|December 16, 2003
Variable reduction of caveolin-3 in patients with LGMD2B/MMMaggie C Walter, Christian Braun, Matthias Vorgerd, et al.
Pageof 14