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.
23. [The first Japanese case of autosomal dominant Emery-Dreifuss muscular dystrophy with a novel mutation in the lamin A/C gene]. Onishi Y; Higuchi J; Ogawa T; Namekawa A; Hayashi H; Odakura H; Goto K; Hayashi YK Rinsho Shinkeigaku; 2002 Feb; 42(2):140-4. PubMed ID: 12424964 [TBL] [Abstract][Full Text] [Related]
24. [A case of scapuloperoneal dystrophy having "cartwheel fibers" (author's transl)]. Fukunaga H; Osame M; Nakashima H; Imaguma M; Igata A Rinsho Shinkeigaku; 1978 Sep; 18(9):532-8. PubMed ID: 709973 [No Abstract] [Full Text] [Related]
25. Lamin A N-terminal phosphorylation is associated with myoblast activation: impairment in Emery-Dreifuss muscular dystrophy. Cenni V; Sabatelli P; Mattioli E; Marmiroli S; Capanni C; Ognibene A; Squarzoni S; Maraldi NM; Bonne G; Columbaro M; Merlini L; Lattanzi G J Med Genet; 2005 Mar; 42(3):214-20. PubMed ID: 15744034 [TBL] [Abstract][Full Text] [Related]
26. A family of Emery-Dreifuss muscular dystrophy with extreme difference in severity. Higuchi Y; Hongou M; Ozawa K; Kokawa H; Masaki M Pediatr Neurol; 2005 May; 32(5):358-60. PubMed ID: 15866440 [TBL] [Abstract][Full Text] [Related]
27. Genetic pattern of 3 cases of Emery-Dreifuss muscular dystrophy in a family. Yazdanpanah P; Javan A; Nadimi B; Shirazi HR East Mediterr Health J; 2007; 13(1):201-5. PubMed ID: 17546924 [No Abstract] [Full Text] [Related]