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253 related items for PubMed ID: 37974208
1. Clinical features, imaging findings and molecular data of limb-girdle muscular dystrophies in a cohort of Chinese patients. Lin F, Yang K, Lin X, Jin M, Chen L, Zheng FZ, Qiu LL, Ye ZX, Chen HZ, Lin MT, Wang N, Wang ZQ. Orphanet J Rare Dis; 2023 Nov 16; 18(1):356. PubMed ID: 37974208 [Abstract] [Full Text] [Related]
5. Clinical and genetic characterization of limb girdle muscular dystrophy R7 telethonin-related patients from three unrelated Chinese families. Chen H, Xu G, Lin F, Jin M, Cai N, Qiu L, Ye Z, Wang L, Lin M, Wang N. Neuromuscul Disord; 2020 Feb 16; 30(2):137-143. PubMed ID: 32005491 [Abstract] [Full Text] [Related]
6. Unique Clinical, Radiological and Histopathological Characteristics of a Southeast Asian Cohort of Patients with Limb-Girdle Muscular Dystrophy 2G/LGMD-R7-Telethonin-Related. Chen Z, Saini M, Koh JS, Prasad K, Koh SH, Tay KSS, Lee M, Tan YJ, Ng ASL, Tay SKH, Tan KB, Tandon A, Tan JMM, Chai JYH. J Neuromuscul Dis; 2023 Feb 16; 10(1):91-106. PubMed ID: 36463458 [Abstract] [Full Text] [Related]
11. Reliability and accuracy of skeletal muscle imaging in limb-girdle muscular dystrophies. ten Dam L, van der Kooi AJ, van Wattingen M, de Haan RJ, de Visser M. Neurology; 2012 Oct 16; 79(16):1716-23. PubMed ID: 23035061 [Abstract] [Full Text] [Related]
12. Seven autosomal recessive limb-girdle muscular dystrophies in the Brazilian population: from LGMD2A to LGMD2G. Passos-Bueno MR, Vainzof M, Moreira ES, Zatz M. Am J Med Genet; 1999 Feb 19; 82(5):392-8. PubMed ID: 10069710 [Abstract] [Full Text] [Related]