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Neuropathology and Applied Neurobiology
|
January 12, 2023
Molecular mechanisms in chloroquine-exposed muscle cells elucidated by combined proteomic and microscopic studies
Vietxuan Phan, Denisa Hathazi, Corinna Preuße, et al.
Emergency Medicine International
|
April 3, 2024
A Single High-Sensitivity Cardiac Troponin T Strategy for Ruling Out Myocardial Infarction
Patrik Gilje, Moman A Mohammad, Andreas Roos, et al.
Orphanet Journal of Rare Diseases
|
February 10, 2021
Protein signature of human skin fibroblasts allows the study of the molecular etiology of rare neurological diseases
Andreas Hentschel, Artur Czech, Ute Münchberg, et al.
International Journal of Molecular Sciences
|
December 20, 2018
Neuromuscular Junction Changes in a Mouse Model of Charcot-Marie-Tooth Disease Type 4C
Silvia Cipriani, Vietxuan Phan, Jean-Jacques Médard, et al.
American Journal of Medical Genetics. Part A
|
October 31, 2009
Pure distal trisomy 2q: a rare chromosomal abnormality with recognizable phenotype
Miriam Elbracht, Andreas Roos, Nadine Schönherr, et al.
Cells
|
June 28, 2023
Dysregulation of Metabolism and Proteostasis in Skeletal Muscle of a Presymptomatic Pompe Mouse Model
Marlena Rohm, Leon Volke, Lara Schlaffke, et al.
Journal of Neuromuscular Diseases
|
March 4, 2025
Glycogenosis type XI, a rare association between muscle and skin manifestations - the contribution of proteomics for the understanding of the underlying myopathology
Andreas Hentschel, Emmanuelle Lacene, Guy Brochier, et al.
Journal of Neurochemistry
|
May 11, 2018
FYCO1 mediates clearance of α-synuclein aggregates through a Rab7-dependent mechanism
Theodora Saridaki, Markus Nippold, Elisabeth Dinter, et al.
Genes & Diseases
|
September 26, 2022
ANO5-related muscle diseases: From clinics and genetics to pathology and research strategies
Jon Christiansen, Anne-Katrin Güttsches, Ulrike Schara-Schmidt, et al.
The Lancet. Neurology
|
May 30, 2020
Advances in the diagnosis of inherited neuromuscular diseases and implications for therapy development
Rachel Thompson, Sally Spendiff, Andreas Roos, et al.
Page
of 21
Search research articles
Search
Showing results (51-60 of 209) with videos related to
Sort By:
Page
of 21
Neuropathology and Applied Neurobiology
|
January 12, 2023
Molecular mechanisms in chloroquine-exposed muscle cells elucidated by combined proteomic and microscopic studies
Vietxuan Phan, Denisa Hathazi, Corinna Preuße, et al.
Emergency Medicine International
|
April 3, 2024
A Single High-Sensitivity Cardiac Troponin T Strategy for Ruling Out Myocardial Infarction
Patrik Gilje, Moman A Mohammad, Andreas Roos, et al.
Orphanet Journal of Rare Diseases
|
February 10, 2021
Protein signature of human skin fibroblasts allows the study of the molecular etiology of rare neurological diseases
Andreas Hentschel, Artur Czech, Ute Münchberg, et al.
International Journal of Molecular Sciences
|
December 20, 2018
Neuromuscular Junction Changes in a Mouse Model of Charcot-Marie-Tooth Disease Type 4C
Silvia Cipriani, Vietxuan Phan, Jean-Jacques Médard, et al.
American Journal of Medical Genetics. Part A
|
October 31, 2009
Pure distal trisomy 2q: a rare chromosomal abnormality with recognizable phenotype
Miriam Elbracht, Andreas Roos, Nadine Schönherr, et al.
Cells
|
June 28, 2023
Dysregulation of Metabolism and Proteostasis in Skeletal Muscle of a Presymptomatic Pompe Mouse Model
Marlena Rohm, Leon Volke, Lara Schlaffke, et al.
Journal of Neuromuscular Diseases
|
March 4, 2025
Glycogenosis type XI, a rare association between muscle and skin manifestations - the contribution of proteomics for the understanding of the underlying myopathology
Andreas Hentschel, Emmanuelle Lacene, Guy Brochier, et al.
Journal of Neurochemistry
|
May 11, 2018
FYCO1 mediates clearance of α-synuclein aggregates through a Rab7-dependent mechanism
Theodora Saridaki, Markus Nippold, Elisabeth Dinter, et al.
Genes & Diseases
|
September 26, 2022
ANO5-related muscle diseases: From clinics and genetics to pathology and research strategies
Jon Christiansen, Anne-Katrin Güttsches, Ulrike Schara-Schmidt, et al.
The Lancet. Neurology
|
May 30, 2020
Advances in the diagnosis of inherited neuromuscular diseases and implications for therapy development
Rachel Thompson, Sally Spendiff, Andreas Roos, et al.
Page
of 21