Search Results - "Spuler, Simone"

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.

Myopathy causing camptocormia in idiopathic Parkinson's disease: A multidisciplinary approach.

Authors: Spuler, Simone Krug, Henriette Klein, Christine et al.

Source: Movement Disorders. Apr2010, Vol. 25 Issue 5, p552-559. 8p.

Dysferlin-deficient muscular dystrophy features amyloidosis.

Authors: Spuler, Simone Carl, Miriam Zabojszcza, Joanna et al.

Source: Annals of Neurology. Mar2008, Vol. 63 Issue 3, p323-328. 6p.

Identification of prognostic biomarkers in a large cohort of patients with LGMD R2.

Authors: Bolano-Diaz, Carla F. Verdu-Diaz, Jose Hao, Dan et al.

Source: Journal of Neurology. Jun2026, Vol. 273 Issue 6, p1-13. 13p.

A newLMNAmutation causing limb girdle muscular dystrophy 1B.

Authors: Spuler, Simone Geier, Christian Osterzie, Karl Josef et al.

Source: Journal of Neurology. May2005, Vol. 252 Issue 5, p621-623. 3p.

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.

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.

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.

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.

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.

Nonexcitable muscle membrane predicts intensive care unit-acquired paresis in mechanically ventilated, sedated patients.

Authors: Weber-Carstens, Steffen Koch, Susanne Spuler, Simone et al.

Source: Critical Care Medicine. Sep2009, Vol. 37 Issue 9, p2632-2637. 6p. 3 Charts, 1 Graph.

Cardiac and pulmonary findings in dysferlinopathy: A 3‐year, longitudinal study.

Authors: Moore, Ursula Fernandez‐Torron, Roberto Jacobs, Marni et al.

Source: Muscle & Nerve. May2022, Vol. 65 Issue 5, p531-540. 10p.

Progressive myocardial injury in myotonic dystrophy type II and facioscapulohumeral muscular dystrophy 1: a cardiovascular magnetic resonance follow-up study.

Authors: Blaszczyk, Edyta Lim, Carolin Kellman, Peter et al.

Source: Journal of Cardiovascular Magnetic Resonance (Elsevier B.V. ). 11/8/2021, Vol. 23 Issue 1, p1-16. 16p.

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.

Dysferlin-Peptides Reallocate Mutated Dysferlin Thereby Restoring Function.

Authors: Schoewel, Verena Marg, Andreas Kunz, Severine et al.

Source: PLoS ONE. Nov2012, Vol. 7 Issue 11, Special section p1-11. 11p.

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.