Results 101 to 110 of about 466,013 (152)

Correction to: Validation of a novel western blot assay to monitor patterns and levels of alpha dystroglycan in skeletal muscle of patients with limb girdle muscular dystrophies. [PDF]

J Muscle Res Cell Motil
Rajasingham T, Rodriguez HM, Betz A, Sproule DM, Sinha U.   +4 more
europepmc   +1 more source

Robust genotyping tool for autosomal recessive type of limb-girdle muscular dystrophies. [PDF]

BMC Musculoskelet Disord, 2016
Inashkina I, Jankevics E, Stavusis J, Vasiljeva I, Viksne K, Micule I, Strautmanis J, Naudina MS, Cimbalistiene L, Kucinskas V, Krumina A, Utkus A, Burnyte B, Matuleviciene A, Lace B.   +14 more
europepmc   +1 more source

The Classification, Natural History and Treatment of the Limb Girdle Muscular Dystrophies. [PDF]

J Neuromuscul Dis, 2015
Murphy AP, Straub V.
europepmc   +1 more source

Autosomal dominant and recessive limb-girdle muscular dystrophies : clinical, genetic relative frequency in a large Italian population

, 2007
A. Prelle, M. Moggio, F. Magri, N. Bresolin, M. G. D'Angelo, C. Lamperti, G.P. Comi, R. Cagliani, C. Zecca, F. Fortunato, S. Ghezzi, S. Lucchiari, R. Del Bo, M. Mora, M. Guglieri, L. Morandi, S. Salani   +16 more
core   +2 more sources

Validation of a novel western blot assay to monitor patterns and levels of alpha dystroglycan in skeletal muscle of patients with limb girdle muscular dystrophies. [PDF]

J Muscle Res Cell Motil
Rajasingham T, Rodriguez HM, Betz A, Sproule DM, Sinha U.   +4 more
europepmc   +1 more source

Autosomal recessive limb-girdle muscular dystrophies in the Czech Republic. [PDF]

BMC Neurol, 2014
Stehlíková K, Skálová D, Zídková J, Mrázová L, Vondráček P, Mazanec R, Voháňka S, Haberlová J, Hermanová M, Zámečník J, Souček O, Ošlejšková H, Dvořáčková N, Solařová P, Fajkusová L.   +14 more
europepmc   +1 more source

Anesthetic Management of a 33-Year-Old Female With Limb-Girdle Muscular Dystrophy Undergoing Laparoscopic Cholecystectomy: A Case Report. [PDF]

Cureus
Gargori N, Alboloshi AA, Nawawi A, Farsi S.   +3 more
europepmc   +1 more source

LGMD R18 Mimicking Wilson Disease: 6-Year Longitudinal Muscle MRI Evolution and Clinical Insights into <i>TRAPPC11</i> Mutation. [PDF]

Diagnostics (Basel)
Chou YT, Chou HP, Chen YW.
europepmc   +1 more source

Report on the 7th Ottawa International Conference on Neuromuscular Disease & Biology - September 11-13, 2025, Ottawa, Canada. [PDF]

J Neuromuscul Dis
Warman-Chardon J, Jasmin BJ, Kothary R, Parks RJ.   +3 more
europepmc   +1 more source