Zobrazeno 1 - 10
of 4 952
pro vyhledávání: '"mitochondrial myopathy"'
Autor:
Gao, Xinming1,2, Feng, Binbin1, Du, Chen1, Hou, Congcong1, Jin, Shan1, Tang, Daojun1 tangdaojun@nbu.edu.cn, Zhu, Junquan1 zhujunquan@nbu.edu.cn
Publikováno v:
Journal of Oceanology & Limnology. Jan2024, Vol. 42 Issue 1, p187-200. 14p.
Autor:
Makayla S. Lancaster, Paul Hafen, Andrew S. Law, Catalina Matias, Timothy Meyer, Kathryn Fischer, Marcus Miller, Chunhai Hao, Patrick Gillespie, David McKinzie, Jeffrey J. Brault, Brett H. Graham
Publikováno v:
Journal of Cachexia, Sarcopenia and Muscle, Vol 15, Iss 6, Pp 2729-2742 (2024)
ABSTRACT Background Pathogenic variants in subunits of succinyl‐CoA synthetase (SCS) are associated with mitochondrial encephalomyopathy in humans. SCS catalyses the conversion of succinyl‐CoA to succinate coupled with substrate‐level phosphory
Externí odkaz:
https://doaj.org/article/f835c87ece14456ebee3a61b1dc5674f
Autor:
Meagan S. Kingren, Alexander R. Keeble, Alyson M. Galvan-Lara, Jodi M. Ogle, Zoltán Ungvári, Daret K. St Clair, Timothy A. Butterfield, Allison M. Owen, Christopher S. Fry, Samir P. Patel, Hiroshi Saito
Publikováno v:
Molecular Medicine, Vol 30, Iss 1, Pp 1-17 (2024)
Abstract Background Sepsis, mainly caused by bacterial infections, is the leading cause of in-patient hospitalizations. After discharge, most sepsis survivors suffer from long-term medical complications, particularly chronic skeletal muscle weakness.
Externí odkaz:
https://doaj.org/article/2a5851bddea14470973d44fc590c574b
Publikováno v:
Disability & Rehabilitation; May2024, Vol. 46 Issue 10, p2138-2144, 7p
Autor:
Zweers, Heidi E.E. a, b, ⁎, Kroesen, Sophie H. c, Beerlink, Gijsje a, b, Buit, Elke b, d, Gerrits, Karlijn a, b, Dorhout, Astrid a, b, van Wegberg, Annemiek M.J. a, b, Janssen, Mirian C.H. b, d, Wortmann, Saskia B. b, e, Timmers, Silvie f, Saris, Christiaan G.J. b, g
Publikováno v:
In Molecular Genetics and Metabolism December 2024 143(4)
Publikováno v:
JIMD Reports, Vol 65, Iss 2, Pp 102-109 (2024)
Abstract Ferredoxin‐2 (FDX2) is an electron transport protein required for iron–sulfur clusters biosynthesis. Pathogenic variants in FDX2 have been associated with autosomal recessive FDX2‐related disorder characterized by mitochondrial myopath
Externí odkaz:
https://doaj.org/article/58f5ede61b154c5a8b176c8c42ec6992
Autor:
Khosa, Shaweta1, Khanlou, Negar2 nkhanlou@mednet.ucla.edu, Khosa, Gurveer S.3, Mishra, Shri K.4
Publikováno v:
Neuropathology. Dec2018, Vol. 38 Issue 6, p646-652. 7p.
Autor:
Zhou, Ying1 (AUTHOR), Yi, Jianhua2 (AUTHOR), Liu, Li3 (AUTHOR), Wang, Xiaoping4 (AUTHOR), Dong, Liang1 (AUTHOR), Du, Ailian4 (AUTHOR) lotusdu@126.com
Publikováno v:
International Journal of Neuroscience. Mar2018, Vol. 128 Issue 3, p231-236. 6p.
Publikováno v:
Frontiers in Aging Neuroscience; 2024, p1-13, 13p
Autor:
Gülden Diniz, Önder Yavaşcan, Ümit Başak Şarkış, Zübeyde Yıldırım, Caner Alparslan, Can Öztürk, Afig Berdeli
Publikováno v:
Journal of Behçet Uz Children's Hospital, Vol 13, Iss 3, Pp 198-202 (2023)
Inflammatory myopathies are autoimmune disorders rarely seen in childhood. Normally high-dose corticosteroid is the current treatment for inflammatory myopathies. For a specific subgroup of patients with inflammatory myopathy with cytochrome oxidase
Externí odkaz:
https://doaj.org/article/cd356d91f39e42a7ba960b068e3f6765