183 related articles for article (PubMed ID: 26005816)
1. [Facioscapulohumeral muscular dystrophy: Report of seven patients].
Cea G; Jiménez D
Rev Med Chil; 2015 Mar; 143(3):304-9. PubMed ID: 26005816
[TBL] [Abstract][Full Text] [Related]
2. Facioscapulohumeral dystrophy presenting as infantile facial diplegia and late-onset limb-girdle myopathy in members of the same family.
Felice KJ; Jones JM; Conway SR
Muscle Nerve; 2005 Sep; 32(3):368-72. PubMed ID: 15880682
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Early-onset facioscapulohumeral muscular dystrophy type 1 with some atypical features.
Dorobek M; van der Maarel SM; Lemmers RJ; Ryniewicz B; Kabzińska D; Frants RR; Gawel M; Walecki J; Hausmanowa-Petrusewicz I
J Child Neurol; 2015 Apr; 30(5):580-7. PubMed ID: 24717985
[TBL] [Abstract][Full Text] [Related]
5. Facioscapulohumeral muscular dystrophy presenting with hypertrophic cardiomyopathy: a case study.
Tsuji M; Kinoshita M; Imai Y; Kawamoto M; Kohara N
Neuromuscul Disord; 2009 Feb; 19(2):140-2. PubMed ID: 19147353
[TBL] [Abstract][Full Text] [Related]
6. [Clinical and genetic characteristics of facioscapulohumeral muscular dystrophy Landuzi-Dezherina type 1].
Dadali EL; Sharkova IV; Zernov NV; Rudenskaya GE; Skoblov MY
Zh Nevrol Psikhiatr Im S S Korsakova; 2017; 117(11):122-128. PubMed ID: 29265097
[TBL] [Abstract][Full Text] [Related]
7. Facioscapulohumeral dystrophy.
Kissel JT
Semin Neurol; 1999; 19(1):35-43. PubMed ID: 10711987
[TBL] [Abstract][Full Text] [Related]
8. Facioscapulohumeral muscular dystrophy presenting isolated monomelic lower limb atrophy. Report of two patients with and without 4q35 rearrangement.
Uncini A; Galluzzi G; Di Muzio A; De Angelis MV; Ricci E; Scoppetta C; Servidei S
Neuromuscul Disord; 2002 Nov; 12(9):874-7. PubMed ID: 12398841
[TBL] [Abstract][Full Text] [Related]
9. [Facioscapulohumeral muscular dystrophy. Clinical picture, atypical forms, diagnostics, genetics].
Jordan B; Müller-Reible C; Zierz S
Nervenarzt; 2011 Jun; 82(6):712-22. PubMed ID: 21567298
[TBL] [Abstract][Full Text] [Related]
10. [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]
11. Genotype-phenotype study in an FSHD family with a proximal deletion encompassing p13E-11 and D4Z4.
Deak KL; Lemmers RJ; Stajich JM; Klooster R; Tawil R; Frants RR; Speer MC; van der Maarel SM; Gilbert JR
Neurology; 2007 Feb; 68(8):578-82. PubMed ID: 17229919
[TBL] [Abstract][Full Text] [Related]
12. Focal and other unusual presentations of facioscapulohumeral muscular dystrophy.
Hassan A; Jones LK; Milone M; Kumar N
Muscle Nerve; 2012 Sep; 46(3):421-5. PubMed ID: 22907234
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Clinical and genetic features of patients with facial-sparing facioscapulohumeral muscular dystrophy.
He JJ; Lin XD; Lin F; Xu GR; Xu LQ; Hu W; Wang DN; Lin HX; Lin MT; Wang N; Wang ZQ
Eur J Neurol; 2018 Feb; 25(2):356-364. PubMed ID: 29112784
[TBL] [Abstract][Full Text] [Related]
15. Correlation between muscle involvement, phenotype and D4Z4 fragment size in facioscapulohumeral muscular dystrophy.
Wang CH; Leung M; Liang WC; Hsieh TJ; Chen TH; Jong YJ
Neuromuscul Disord; 2012 Apr; 22(4):331-8. PubMed ID: 22153988
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Early onset facioscapulohumeral muscular dystrophy - Long-term follow-up of a patient with total facial diplegia.
Rudnik-Schöneborn S; Huemer M; Weis J; Sauer E; Meng G
Neuromuscul Disord; 2019 Dec; 29(12):973-976. PubMed ID: 31708336
[TBL] [Abstract][Full Text] [Related]
18. [Facioscapulohumeral muscular dystrophy].
Wilbers J; Frants RR; van Engelen BG; Padberg GW; van der Maarel SM
Ned Tijdschr Tandheelkd; 2010 Jan; 117(1):11-4. PubMed ID: 20180344
[TBL] [Abstract][Full Text] [Related]
19. FSHD-like patients without 4q35 deletion.
Yamanaka G; Goto K; Ishihara T; Oya Y; Miyajima T; Hoshika A; Nishino I; Hayashi YK
J Neurol Sci; 2004 Apr; 219(1-2):89-93. PubMed ID: 15050443
[TBL] [Abstract][Full Text] [Related]
20. Severe phenotype in infantile facioscapulohumeral muscular dystrophy.
Klinge L; Eagle M; Haggerty ID; Roberts CE; Straub V; Bushby KM
Neuromuscul Disord; 2006 Oct; 16(9-10):553-8. PubMed ID: 16934468
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]