Zobrazeno 1 - 10
of 207
pro vyhledávání: '"muscular disease"'
Autor:
David Troxell
Publikováno v:
Journal of Mechanical Ventilation, Vol 5, Iss 2, Pp 69-79 (2024)
Noninvasive ventilation (NIV) has rapidly expanded as the principle respiratory support strategy in a variety of disease states ultimately resulting in respiratory insufficiency including COPD, overlap syndrome (COPD + comingled sleep disordered brea
Externí odkaz:
https://doaj.org/article/d1c25879f4a449f3ba89c5f1f1338a17
Publikováno v:
Veterinary Sciences, Vol 11, Iss 11, p 556 (2024)
Diseases of the musculature can be caused, for example, by alimentary or traumatic issues. In three bald eagles with painful lameness and/or a reduced range of the hip joint, a muscular disease was diagnosed via radiographic examination. The eagles w
Externí odkaz:
https://doaj.org/article/c6c5f8ffdd01486cb658fa420b2ba62e
Autor:
Deenen, Johanna C.W. a, b, Horlings, Corinne G.C. c, Voermans, Nicol C. a, ⁎, van Doorn, Pieter A. d, Faber, Catharina G. e, van der Kooi, Anneke J. f, Kuks, Jan B.M. g, Notermans, Nicolette C. h, Visser, Leo H. i, Broekgaarden, Ria H.A. j, Horemans, Anja M.C. j, Verschuuren, Jan J.G.M. k, Verbeek, André L.M. b, 1, van Engelen, Baziel G.M. a, 1
Publikováno v:
In Neuromuscular Disorders September 2024 42:27-35
Akademický článek
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Autor:
Jane N. T. Sattoe, Sander R. Hilberink
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
IntroductionAging with a childhood-onset disability, such as cerebral palsy (CP), spina bifida (SB), and muscular diseases (MD), comes along with significant impairments and comorbidities. Despite the increasing evidence an overall picture is lacking
Externí odkaz:
https://doaj.org/article/bf0c203497a94670acbdbe678fe2e8dd
Autor:
Keisuke Watanuki, Hiroshi Koga
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
IntroductionAnti-3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMGCR) myopathy is a recently recognized pathology, but appears less common in children and the characteristics of pediatric cases remain unclear.Case reportWe report a pediatric case
Externí odkaz:
https://doaj.org/article/001088acd1e94182be2845596ad1e4e2
Publikováno v:
Neurological Research and Practice, Vol 4, Iss 1, Pp 1-32 (2022)
Abstract Background Major efforts have been made in the last decade to develop and improve therapies for proximal spinal muscular atrophy (SMA). The introduction of Nusinersen/Spinraza™ as an antisense oligonucleotide therapy, Onasemnogene abeparvo
Externí odkaz:
https://doaj.org/article/aacdb715c31044bfbb97d4bce198a0c4
Autor:
Marlena Rohm, Leon Volke, Lara Schlaffke, Robert Rehmann, Nicolina Südkamp, Andreas Roos, Anne Schänzer, Andreas Hentschel, Matthias Vorgerd
Publikováno v:
Cells, Vol 12, Iss 12, p 1602 (2023)
Pompe disease is a rare genetic metabolic disorder caused by mutations in acid-alpha glucoside (GAA) leading to pathological lysosomal glycogen accumulation associated with skeletal muscle weakness, respiratory difficulties and cardiomyopathy, depend
Externí odkaz:
https://doaj.org/article/7a6e8d90f5014814bf8c059a78c72fa0
Publikováno v:
Iranian Journal of Toxicology, Vol 14, Iss 4, Pp 245-252 (2020)
Background: Statins frequently cause myopathy especially in combination with fibrates, and physical activity is considered a trigger for the muscle disorder. Elevated plasma levels of creatine kinase (CK), lactate dehydrogenase (LDH) and aldolase, ar
Externí odkaz:
https://doaj.org/article/1f2b2fde9a9d407db4d76c4004de1c96
Akademický článek
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