Search Results - "Spuler, Simone"

"Who Am I to Judge These Things": Intersectional Dimensions of Self-Silencing of People with a Neuromuscular Disease in a Clinical Trial.

Authors: Cuijpers, Floor Muntinga, Maaike Bakker, Minne et al.

Source: IJFAB: International Journal of Feminist Approaches to Bioethics. Fall2022, Vol. 15 Issue 2, p51-75. 25p.

Undetected Neuromuscular Disease in Patients after Heart Transplantation.

Authors: Bekele, Biniam Melese Gazzerro, Elisabetta Schoenrath, Felix et al.

Source: International Journal of Molecular Sciences. Jul2024, Vol. 25 Issue 14, p7819. 17p.

Delay in diagnosis of muscle disorders depends on the subspecialty of the initially consulted physician.

Authors: Spuler, Simone Stroux, Andrea Kuschel, Franziska et al.

Source: BMC Health Services Research. 2011, Vol. 11 Issue 1, p91-95. 5p.

Disintegration of the NuRD Complex in Primary Human Muscle Stem Cells in Critical Illness Myopathy.

Authors: Schneider, Joanna Sundaravinayagam, Devakumar Blume, Alexander et al.

Source: International Journal of Molecular Sciences. Feb2023, Vol. 24 Issue 3, p2772. 17p.

LMNA Co-Regulated Gene Expression as a Suitable Readout after Precise Gene Correction.

Authors: Wang, Haicui Krause, Anne Escobar, Helena et al.

Source: International Journal of Molecular Sciences. Dec2022, Vol. 23 Issue 24, p15525. 13p.

Frizzled related protein deficiency impairs muscle strength, gait and calpain 3 levels.

Authors: Casas-Fraile, Leire Cornelis, Frederique M. Costamagna, Domiziana et al.

Source: Orphanet Journal of Rare Diseases. 5/24/2020, Vol. 15 Issue 1, p1-18. 18p.

Statin-induced myopathic changes in primary human muscle cells and reversal by a prostaglandin F2 alpha analogue.

Authors: Grunwald, Stefanie Anke Popp, Oliver Haafke, Stefanie et al.

Source: Scientific Reports. 2/7/2020, Vol. 10 Issue 1, p1-13. 13p.

Myofibrillar protein synthesis rates are increased in chronically exercised skeletal muscle despite decreased anabolic signaling.

Authors: Langer, Henning T. West, Daniel Senden, Joan et al.

Source: Scientific Reports. 5/9/2022, Vol. 12 Issue 1, p1-11. 11p.

MyoMiner: explore gene co-expression in normal and pathological muscle.

Authors: Malatras, Apostolos Michalopoulos, Ioannis Duguez, Stéphanie et al.

Source: BMC Medical Genomics. 5/11/2020, Vol. 13 Issue 1, p1-16. 16p.

Nerve damage induced skeletal muscle atrophy is associated with increased accumulation of intramuscular glucose and polyol pathway intermediates.

Authors: Langer, Henning Tim Afzal, Shoaib Kempa, Stefan et al.

Source: Scientific Reports. 2/5/2020, Vol. 10 Issue 1, p1-10. 10p.

Statins Aggravate the Risk of Insulin Resistance in Human Muscle.

Authors: Grunwald, Stefanie A. Haafke, Stefanie Grieben, Ulrike et al.

Source: International Journal of Molecular Sciences. Feb2022, Vol. 23 Issue 4, p2398. 1p.

Inflammation-Induced Acute Phase Response in Skeletal Muscle and Critical Illness Myopathy.

Authors: Langhans, Claudia Weber-Carstens, Steffen Schmidt, Franziska et al.

Source: PLoS ONE. Mar2014, Vol. 9 Issue 3, p1-11. 11p.

Altered Expression of Cyclin A 1 In Muscle of Patients with Facioscapulohumeral Muscle Dystrophy (FSHD-1).

Authors: Pakula, Anna Schneider, Joanna Janke, Jürgen et al.

Source: PLoS ONE. Sep2013, Vol. 8 Issue 9, p1-9. 9p.

Linking cytoarchitecture to metabolism: sarcolemma-associated plectin affects glucose uptake by destabilizing microtubule networks in mdx myofibers.

Authors: Raith, Marianne Valencia, Rocio G. Fischer, Irmgard et al.

Source: Skeletal Muscle. 2013, Vol. 3 Issue 1, p1-14. 14p. 1 Diagram, 4 Graphs.

Sarcolemmal Repair Is a Slow Process and Includes EHD2.

Authors: Marg, Andreas Schoewel, Verena Timmel, Tobias et al.

Source: Traffic. Sep2012, Vol. 13 Issue 9, p1286-1294. 9p. 5 Color Photographs, 1 Graph.

Skeletal Muscle 11beta-HSD1 Controls Glucocorticoid- Induced Proteolysis and Expression of E3 Ubiquitin Ligases Atrogin-1 and MuRF-1.

Authors: Biedasek, Katrin Andres, Janin Mai, Knut et al.

Source: PLoS ONE. 2011, Vol. 6 Issue 1, p1-6. 6p.

Fatal Cardiac Arrhythmia and Long-QT Syndrome in a New Form of Congenital Generalized Lipodystrophy with Muscle Rippling (CGL4) Due to PTRF-CAVIN Mutations.

Authors: Rajab, Anna Straub, Volker McCann, Liza J. et al.

Source: PLoS Genetics. Mar2010, Vol. 6 Issue 3, p1-10. 10p. 4 Color Photographs, 1 Black and White Photograph, 1 Diagram, 1 Graph.

Tissue Engineering for the Diaphragm and its Various Therapeutic Possibilities – A Systematic Review.

Authors: Boehm, Agnes K. Hillebrandt, Karl H. Dziodzio, Tomasz et al.

Source: Advanced therapeutics Aug2022; Vol. 5 (8).

Journal Info: Publisher: Wiley-Blackwell ISSN: 2366-3987

"suMus," a novel digital system for arm movement metrics and muscle energy expenditure.

Authors: Gerhalter T Müller C Maron E et al.

Source: Frontiers in physiology [Front Physiol] 2023 Jan 26; Vol. 14, pp. 1057592. Date of Electronic Publication: 2023 Jan 26 (Print Publication: 2023).

Publication Type: Journal Article

Journal Info: Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101549006 Publication Model: eCollection Cited Medium: Print ISSN: 1664-042X (Print) Linking ISSN: 1664042X NLM ISO Abbreviation: Front Physiol Subsets: PubMed not MEDLINE

LONG-TERM RECOVERY IN CRITICAL ILLNESS MYOPATHY IS COMPLETE, CONTRARY TO POLYNEUROPATHY.

Authors: KOCH, SUSANNE WOLLERSHEIM, TOBIAS BIERBRAUER, JEFFREY et al.

Source: Muscle & nerve 2014 Supplement; Vol. 50.

Journal Info: Publisher: Wiley-Blackwell ISSN: 0148-639X