142 related articles for article (PubMed ID: 17715463)
21. Hearing loss in facioscapulohumeral muscular dystrophy.
Brouwer OF; Padberg GW; Ruys CJ; Brand R; de Laat JA; Grote JJ
Neurology; 1991 Dec; 41(12):1878-81. PubMed ID: 1745341
[TBL] [Abstract][Full Text] [Related]
22. Molecular genetics of facioscapulohumeral muscular dystrophy (FSHD).
Fisher J; Upadhyaya M
Neuromuscul Disord; 1997 Jan; 7(1):55-62. PubMed ID: 9132141
[TBL] [Abstract][Full Text] [Related]
23. [Genetic investigations in facioscapulohumeral muscular dystrophy: a preliminary report].
Dorobek M; Kabzińska D; Ryniewicz B; Fidziańska-Dolot A; Hausmanowa-Petrusewicz I
Neurol Neurochir Pol; 2004; 38(2):83-8. PubMed ID: 15307599
[TBL] [Abstract][Full Text] [Related]
24. Facioscapulohumeral muscular dystrophy presenting with unusual phenotypes and atypical morphological features of vacuolar myopathy.
Reilich P; Schramm N; Schoser B; Schneiderat P; Strigl-Pill N; Müller-Höcker J; Kress W; Ferbert A; Rudnik-Schöneborn S; Noth J; Lochmüller H; Weis J; Walter MC
J Neurol; 2010 Jul; 257(7):1108-18. PubMed ID: 20146070
[TBL] [Abstract][Full Text] [Related]
25. [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]
26. Clinical and genetic analysis of Korean patients with facioscapulohumeral muscular dystrophy.
Ki CS; Lee ST; Kim KS; Kim JW; Hong YH; Sung JJ; Park KS; Lee KW
J Korean Med Sci; 2008 Dec; 23(6):959-63. PubMed ID: 19119436
[TBL] [Abstract][Full Text] [Related]
27. [Gene diagnosis of facioscapulohumeral muscular dystrophy].
Zhang JL; Shen DG; Zhou PK; Liu JW; Jia N; Liu H; Wang HB; Yang SX; Frants RR
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Jun; 20(3):232-4. PubMed ID: 12778451
[TBL] [Abstract][Full Text] [Related]
28. Large scale genotype-phenotype analyses indicate that novel prognostic tools are required for families with facioscapulohumeral muscular dystrophy.
Ricci G; Scionti I; Sera F; Govi M; D'Amico R; Frambolli I; Mele F; Filosto M; Vercelli L; Ruggiero L; Berardinelli A; Angelini C; Antonini G; Bucci E; Cao M; Daolio J; Di Muzio A; Di Leo R; Galluzzi G; Iannaccone E; Maggi L; Maruotti V; Moggio M; Mongini T; Morandi L; Nikolic A; Pastorello E; Ricci E; Rodolico C; Santoro L; Servida M; Siciliano G; Tomelleri G; Tupler R
Brain; 2013 Nov; 136(Pt 11):3408-17. PubMed ID: 24030947
[TBL] [Abstract][Full Text] [Related]
29. Unusual clinical presentations in patients harboring the facioscapulohumeral dystrophy 4q35 deletion.
Felice KJ; Moore SA
Muscle Nerve; 2001 Mar; 24(3):352-6. PubMed ID: 11353419
[TBL] [Abstract][Full Text] [Related]
30. Facioscapulohumeral muscular dystrophy: new insights from compound heterozygotes and implication for prenatal genetic counselling.
Scionti I; Fabbri G; Fiorillo C; Ricci G; Greco F; D'Amico R; Termanini A; Vercelli L; Tomelleri G; Cao M; Santoro L; Percesepe A; Tupler R
J Med Genet; 2012 Mar; 49(3):171-8. PubMed ID: 22217918
[TBL] [Abstract][Full Text] [Related]
31. An inherited 4q35-EcoRI-DNA-fragment of 35 kb in a family with a sporadic case of facioscapulohumeral muscular dystrophy (FSHD).
Busse K; Köhler J; Stegmann K; Pongratz D; Koch MC; Schreiber H
Neuromuscul Disord; 2000 Mar; 10(3):178-81. PubMed ID: 10734264
[TBL] [Abstract][Full Text] [Related]
32. Tongue atrophy in facioscapulohumeral muscular dystrophy.
Yamanaka G; Goto K; Matsumura T; Funakoshi M; Komori T; Hayashi YK; Arahata K
Neurology; 2001 Aug; 57(4):733-5. PubMed ID: 11524495
[TBL] [Abstract][Full Text] [Related]
33. Cochlear Dysfunction Is a Frequent Feature of Facioscapulohumeral Muscular Dystrophy Type 1 (FSHD1).
Frezza E; Fuccillo E; Petrucci A; Greco G; Nucera G; Bruno E; Giardina E; Tupler R; Di Mauro R; Di Girolamo S; Massa R
Otol Neurotol; 2021 Jan; 42(1):18-23. PubMed ID: 32976345
[TBL] [Abstract][Full Text] [Related]
34. Facioscapulohumeral muscular dystrophy: clinical diversity and genetic abnormalities in Japanese patients.
Nakagawa M; Matsuzaki T; Higuchi I; Fukunaga H; Inui T; Nagamitsu S; Yamada H; Arimura K; Osame M
Intern Med; 1997 May; 36(5):333-9. PubMed ID: 9213170
[TBL] [Abstract][Full Text] [Related]
35. Molecular diagnosis of facioscapulohumeral muscular dystrophy.
Upadhyaya M; Cooper DN
Expert Rev Mol Diagn; 2002 Mar; 2(2):160-71. PubMed ID: 11962336
[TBL] [Abstract][Full Text] [Related]
36. [Mechanism of translocation between chromosomes 4q and 10q in facioscapulohumeral muscular dystrophy].
Wang N; Wu ZY; Wang CD; Wang ZQ; Lin MT; Fang L; Murong SX
Zhonghua Yi Xue Za Zhi; 2003 Apr; 83(8):650-3. PubMed ID: 12887821
[TBL] [Abstract][Full Text] [Related]
37. Phenotypic-genotypic correlation will assist genetic counseling in 4q35-facioscapulohumeral muscular dystrophy.
Lunt PW; Jardine PE; Koch M; Maynard J; Osborn M; Williams M; Harper PS; Upadhyaya M
Muscle Nerve Suppl; 1995; (2):S103-9. PubMed ID: 23573595
[TBL] [Abstract][Full Text] [Related]
38. Facioscapulohumeral muscular dystrophy. Phenotype-genotype correlation in patients with borderline D4Z4 repeat numbers.
Butz M; Koch MC; Müller-Felber W; Lemmers RJ; van der Maarel SM; Schreiber H
J Neurol; 2003 Aug; 250(8):932-7. PubMed ID: 12928911
[TBL] [Abstract][Full Text] [Related]
39. 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]
40. Facioscapulohumeral dystrophy in children: design of a prospective, observational study on natural history, predictors and clinical impact (iFocus FSHD).
Goselink RJ; Schreuder TH; Mul K; Voermans NC; Pelsma M; de Groot IJ; van Alfen N; Franck B; Theelen T; Lemmers RJ; Mah JK; van der Maarel SM; van Engelen BG; Erasmus CE
BMC Neurol; 2016 Aug; 16():138. PubMed ID: 27530735
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]