Results 171 to 180 of about 86,962 (305)

No sex difference in mutations rates of Duchenne muscular dystrophy. [PDF]

, 1980
N. Yasuda, K Kondo
openalex   +1 more source

Gel Electrophoretic Detection of Black Market ACE‐031

Drug Testing and Analysis, Volume 17, Issue 10, Page 1934-1946, October 2025.
This article presents a study on black market ACE‐031 products and their detection by gel‐electrophoresis and Western blotting. Of the 14 tested products, only 12 contained an ACVR2B‐immunoreactive protein. However, mass spectrometry revealed that the products did not contain the ACVR2B‐Fc fusion protein ACE‐031 but instead the full‐length human ...
Christian Reichel, Thomas Filip, Günter Gmeiner, Mario Thevis   +3 more
wiley   +1 more source

The Values and Preferences of People Living With Motor Neurone Disease (MND): A Systematic Review Protocol

Clinical and Public Health Guidelines, Volume 2, Issue 4, October 2025.
ABSTRACT Objective To systematically review the values and preferences of people with lived experience of motor neurone disease (MND), including those living with MND, caregivers and genetic carriers, regarding their health‐related outcomes. Introduction MND is a devastating neurodegenerative disease that significantly impacts those living with the ...
Timothy Hugh Barker, Grace Holland, Camille Schubert, Danielle Pollock, Cindy Stern, Nipun Shrestha, Wojtek Wiercioch, Samer Karam, Steve Vucic, Jay Beasley‐Hall, Lynne Giles, Tracy Merlin, Zachary Munn   +12 more
wiley   +1 more source

Isoenzyme distribution of creatine kinase and lactate dehydrogenase in serum and skeletal muscle in Duchenne muscular dystrophy, collagen disease, and other muscular disorders.

, 1978
Walid G. Yasmineh, G. A. Ibrahim, M Abbasnezhad, E A Awad   +3 more
openalex   +1 more source

Oxygen treatment of sleep hypoxaemia in Duchenne muscular dystrophy. [PDF]

, 1989
Phil E M Smith, R. H. T. Edwards, Peter Calverley   +2 more
openalex   +1 more source

MyomiRs Expression in Limb Girdle Muscular Dystrophy

IUBMB Life, Volume 77, Issue 10, October 2025.
ABSTRACT This manuscript is a comprehensive review focused on the role of microRNAs (miRs)—short RNA molecules—in Limb Girdle Muscular Dystrophy (LGMD). LGMD encompasses various and heterogeneous rare genetic neuromuscular diseases, characterized by the progressive wasting and deterioration of muscle fibers, predominantly affecting the pelvic and ...
G. Breveglieri, M. T. Altieri, M. T. Rodia, R. Costa, F. Frabetti, G. Cenacchi, G. Sabbioni, M. Borgatti   +7 more
wiley   +1 more source

The application of linkage analysis to genetic counselling in families with Duchenne or Becker muscular dystrophy. [PDF]

, 1987
Shirley Hodgson, A.P. Walker, C Cole, K Hart, Lynn Johnson, J Z Heckmatt, Victor Dubowitz, Martin Bobrow   +7 more
openalex   +1 more source

Immunoproteasome Inhibition Positively Impacts the Gut‐Muscle Axis in Duchenne Muscular Dystrophy

Journal of Cachexia, Sarcopenia and Muscle, Volume 16, Issue 5, October 2025.
ABSTRACT Background Duchenne Muscular Dystrophy (DMD) features immune‐muscle crosstalk, where muscle fibre degeneration enhances pro‐inflammatory macrophage infiltration, worsening inflammation and impairing regeneration. Methods We investigated the impact of immunoproteasome (IP) inhibition on the gut‐muscle axis in mdx mice, a well‐established model ...
Andrea Farini, Francesco Strati, Monica Molinaro, Debora Mostosi, Sabrina Saccone, Luana Tripodi, Jacopo Troisi, Annamaria Landolfi, Chiara Amoroso, Barbara Cassani, Aitor Blanco‐Míguez, Emma Leonetti, Davide Bazzani, Mattia Bolzan, Francesco Fortunato, Flavio Caprioli, Federica Facciotti, Yvan Torrente   +17 more
wiley   +1 more source

Association of Diaphragm Involvement Assessed by Ultrasound With Disease Severity in Facioscapulohumeral Muscular Dystrophy

Journal of Cachexia, Sarcopenia and Muscle, Volume 16, Issue 5, October 2025.
ABSTRACT Background Respiratory involvement is a comorbidity that should not be overlooked in clinical practice in facioscapulohumeral muscular dystrophy type 1 (FSHD1), with a reported association for severe disease outcomes such as wheelchair dependency.
Xiang Xu, Fuze Zheng, Xin Lin, Liangliang Qiu, Long Chen, Jing Xu, Li Kang, Jie Chen, Liulei Wu, Ying Zheng, Minghui Zeng, Xiaodan Lin, Qifang He, Li Chen, Feng Lin, Ning Wang, Minting Lin, Guorong Lyu, Zhiqiang Wang   +18 more
wiley   +1 more source

Burden of Duchenne muscular dystrophy in Australia: a scoping review. [PDF]

BMJ Neurol Open
Lee E, Choi S, Kim H.
europepmc   +1 more source