These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
2. Early-onset benign autosomal-dominant limb-girdle myopathy with contractures (Bethlem myopathy). Tachi N; Tachi M; Sasaki K; Imamura S Pediatr Neurol; 1989; 5(4):232-6. PubMed ID: 2803379 [TBL] [Abstract][Full Text] [Related]
3. [Early-onset benign autosomal dominant limb-girdle myopathy with contractures (Bethlem myopathy) in a Japanese family]. Sasabe F; Takase Y; Fukusako T; Yamamoto K; Morimatsu M Rinsho Shinkeigaku; 1992 Feb; 32(2):138-42. PubMed ID: 1611771 [TBL] [Abstract][Full Text] [Related]
4. A Danish family with limb-girdle muscular dystrophy with autosomal dominant inheritance. Nielsen JF; Jakobsen J Neuromuscul Disord; 1994 Mar; 4(2):139-42. PubMed ID: 8012194 [TBL] [Abstract][Full Text] [Related]
5. Bethlem myopathy: early-onset benign autosomal dominant myopathy with contractures. Description of two new families. Merlini L; Morandi L; Granata C; Ballestrazzi A Neuromuscul Disord; 1994; 4(5-6):503-11. PubMed ID: 7881296 [TBL] [Abstract][Full Text] [Related]
6. Novel mutations in collagen VI genes: expansion of the Bethlem myopathy phenotype. Scacheri PC; Gillanders EM; Subramony SH; Vedanarayanan V; Crowe CA; Thakore N; Bingler M; Hoffman EP Neurology; 2002 Feb; 58(4):593-602. PubMed ID: 11865138 [TBL] [Abstract][Full Text] [Related]
7. Early-onset benign limb-girdle myopathy with contractures and facial involvement affecting a father and daughter. Malandrini A; Scarpini C; Fabrizi GM; Parrotta E; Salvadori C; Guazzi GC J Neurol Sci; 1995 Oct; 132(2):195-200. PubMed ID: 8543948 [TBL] [Abstract][Full Text] [Related]
8. [A family of autosomal dominant facio-limb-girdle muscular dystrophy]. Takao S; Kira J; Kohtake N; Yoshimura T; Goto I Fukuoka Igaku Zasshi; 1996 Dec; 87(12):278-82. PubMed ID: 9011111 [TBL] [Abstract][Full Text] [Related]
9. Bethlem myopathy: a series of 16 patients and description of seven new associated mutations. Panadés-de Oliveira L; Rodríguez-López C; Cantero Montenegro D; Marcos Toledano MDM; Fernández-Marmiesse A; Esteban Pérez J; Hernández Lain A; Domínguez-González C J Neurol; 2019 Apr; 266(4):934-941. PubMed ID: 30706156 [TBL] [Abstract][Full Text] [Related]
10. Bethlem myopathy in a Taiwanese family. Lien LM; Yang CC; Chen WH; Chiu HC J Formos Med Assoc; 2001 Jun; 100(6):416-9. PubMed ID: 11480253 [TBL] [Abstract][Full Text] [Related]
11. DNAJB6 myopathy: a vacuolar myopathy with childhood onset. Suarez-Cedeno G; Winder T; Milone M Muscle Nerve; 2014 Apr; 49(4):607-10. PubMed ID: 24170373 [TBL] [Abstract][Full Text] [Related]
12. [A pedigree of autosomal dominant limb-girdle myopathy with rimmed vacuole formation]. Kishibayashi J; Sunohara N; Saito Y Rinsho Shinkeigaku; 1997 Jul; 37(7):603-10. PubMed ID: 9396357 [TBL] [Abstract][Full Text] [Related]
13. Muscle MRI in Ullrich congenital muscular dystrophy and Bethlem myopathy. Mercuri E; Lampe A; Allsop J; Knight R; Pane M; Kinali M; Bonnemann C; Flanigan K; Lapini I; Bushby K; Pepe G; Muntoni F Neuromuscul Disord; 2005 Apr; 15(4):303-10. PubMed ID: 15792870 [TBL] [Abstract][Full Text] [Related]
14. Respiratory muscle involvement in Bethlem myopathy. Haq RU; Speer MC; Chu ML; Tandan R Neurology; 1999 Jan; 52(1):174-6. PubMed ID: 9921869 [TBL] [Abstract][Full Text] [Related]