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.
6. [Progress in researches on the molecular genetics of facioscapulohumeral muscular dystrophy]. Su Q; Zhang C Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Oct; 18(5):398-401. PubMed ID: 11592052 [TBL] [Abstract][Full Text] [Related]
7. Typical facioscapulohumeral dystrophy phenotype in patients without FSHD 4q35 deletion. Krasnianski M; Neudecker S; Eger K; Jakubiczka S; Zierz S J Neurol; 2003 Sep; 250(9):1084-7. PubMed ID: 14504970 [TBL] [Abstract][Full Text] [Related]
8. Rapid and accurate diagnosis of facioscapulohumeral muscular dystrophy. Goto K; Nishino I; Hayashi YK Neuromuscul Disord; 2006 Apr; 16(4):256-61. PubMed ID: 16545566 [TBL] [Abstract][Full Text] [Related]
9. A case of fascioscapulohumeral muscular dystrophy misdiagnosed as Becker's muscular dystrophy for 20 years. Ramos VF; Thaisetthawatkul P Age Ageing; 2012 Mar; 41(2):273-4. PubMed ID: 21795275 [TBL] [Abstract][Full Text] [Related]
10. [The genetic basis of muscle disease]. Bindoff L; Gilhus NE Tidsskr Nor Laegeforen; 2003 Sep; 123(18):2588-92. PubMed ID: 14714051 [TBL] [Abstract][Full Text] [Related]
11. Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy. Osborne RJ; Welle S; Venance SL; Thornton CA; Tawil R Neurology; 2007 Feb; 68(8):569-77. PubMed ID: 17151338 [TBL] [Abstract][Full Text] [Related]
12. Atypical facet of Möbius syndrome: association with facioscapulohumeral muscular dystrophy. Kolski HK; Leonard NJ; Lemmers RJ; Bamforth JS Muscle Nerve; 2008 Apr; 37(4):526-9. PubMed ID: 18059038 [TBL] [Abstract][Full Text] [Related]
13. Diagnostic challenges in facioscapulohumeral muscular dystrophy. Sacconi S; Salviati L; Bourget I; Figarella D; Péréon Y; Lemmers R; van der Maarel S; Desnuelle C Neurology; 2006 Oct; 67(8):1464-6. PubMed ID: 17060574 [TBL] [Abstract][Full Text] [Related]
15. Becker's muscular dystrophy aggravating facioscapulohumeral muscular dystrophy--double trouble as an explanation for an atypical phenotype. Rudnik-Schöneborn S; Weis J; Kress W; Häusler M; Zerres K Neuromuscul Disord; 2008 Nov; 18(11):881-5. PubMed ID: 18684626 [TBL] [Abstract][Full Text] [Related]
16. Prenatal diagnosis for facioscapulohumeral muscular dystrophy (FSHD). Upadhyaya M; MacDonald M; Ravine D Prenat Diagn; 1999 Oct; 19(10):959-65. PubMed ID: 10521823 [TBL] [Abstract][Full Text] [Related]
17. Asymptomatic elevation of serum creatine kinase leading to the diagnosis of 4q35 facioscapulohumeral muscular dystrophy. Zouvelou V; Manta P; Kalfakis N; Evdokimidis I; Vassilopoulos D J Clin Neurosci; 2009 Sep; 16(9):1218-9. PubMed ID: 19502063 [TBL] [Abstract][Full Text] [Related]
18. Isolation and characterization of mesoangioblasts from facioscapulohumeral muscular dystrophy muscle biopsies. Morosetti R; Mirabella M; Gliubizzi C; Broccolini A; Sancricca C; Pescatori M; Gidaro T; Tasca G; Frusciante R; Tonali PA; Cossu G; Ricci E Stem Cells; 2007 Dec; 25(12):3173-82. PubMed ID: 17761758 [TBL] [Abstract][Full Text] [Related]
19. A severe case of facioscapulohumeral muscular dystrophy (FSHD) with some uncommon clinical features and a short 4q35 fragment. Dorobek M; Kabzińska D Eur J Paediatr Neurol; 2004; 8(6):313-6. PubMed ID: 15542386 [TBL] [Abstract][Full Text] [Related]
20. [Gene diagnosis of facioscapulohumeral muscular dystrophy]. Zeng Y; Zhang C; Su Q Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Jun; 18(3):213-5. PubMed ID: 11402453 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]