240 related articles for article (PubMed ID: 20146070)
1. 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]
2. Rimmed vacuoles in facioscapulohumeral muscular dystrophy: a unique ultrastructural feature.
Neudecker S; Krasnianski M; Bahn E; Zierz S
Acta Neuropathol; 2004 Sep; 108(3):257-9. PubMed ID: 15221332
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. [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]
5. Facioscapulohumeral muscular dystrophy.
Tawil R
Curr Neurol Neurosci Rep; 2004 Jan; 4(1):51-4. PubMed ID: 14683629
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. 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]
9. Muscle MRI findings in facioscapulohumeral muscular dystrophy.
Gerevini S; Scarlato M; Maggi L; Cava M; Caliendo G; Pasanisi B; Falini A; Previtali SC; Morandi L
Eur Radiol; 2016 Mar; 26(3):693-705. PubMed ID: 26115655
[TBL] [Abstract][Full Text] [Related]
10. Facioscapulohumeral muscular dystrophy with EcoRI/BlnI fragment size of more than 32 kb.
Vielhaber S; Jakubiczka S; Schröder JM; Sailer M; Feistner H; Heinze HJ; Wieacker P; Bettecken T
Muscle Nerve; 2002 Apr; 25(4):540-8. PubMed ID: 11932972
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Facioscapulohumeral muscular dystrophy and Charcot-Marie-Tooth neuropathy 1A - evidence for "double trouble" overlapping syndromes.
Schreiber O; Schneiderat P; Kress W; Rautenstrauss B; Senderek J; Schoser B; Walter MC
BMC Med Genet; 2013 Sep; 14():92. PubMed ID: 24041033
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. [Facioscapulohumeral muscular dystrophy. The spectrum of clinical manifestations and molecular genetic changes].
Krasnianski M; Neudecker S; Eger K; Schulte-Mattler W; Zierz S
Nervenarzt; 2003 Feb; 74(2):151-8. PubMed ID: 12596016
[TBL] [Abstract][Full Text] [Related]
15. Isolated facial diplegia and very late-onset myopathy in two siblings: atypical presentations of facioscapulohumeral dystrophy.
Figueroa JJ; Chapin JE
J Neurol; 2010 Mar; 257(3):444-6. PubMed ID: 19826857
[TBL] [Abstract][Full Text] [Related]
16. Facioscapulohumeral muscular dystrophy: hearing loss and other atypical features of patients with large 4q35 deletions.
Trevisan CP; Pastorello E; Tomelleri G; Vercelli L; Bruno C; Scapolan S; Siciliano G; Comacchio F
Eur J Neurol; 2008 Dec; 15(12):1353-8. PubMed ID: 19049553
[TBL] [Abstract][Full Text] [Related]
17. Facioscapulohumeral muscular dystrophy 1 patients participating in the UK FSHD registry can be subdivided into 4 patterns of self-reported symptoms.
Banerji CRS; Cammish P; Evangelista T; Zammit PS; Straub V; Marini-Bettolo C
Neuromuscul Disord; 2020 Apr; 30(4):315-328. PubMed ID: 32327287
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. [Facio-scapula-humeral muscular dystrophy: clinical picture and molecular genetics].
Dorobek M
Neurol Neurochir Pol; 2003; 37(1):151-9. PubMed ID: 12910837
[TBL] [Abstract][Full Text] [Related]
20. Atypical phenotypes in patients with facioscapulohumeral muscular dystrophy 4q35 deletion.
Krasnianski M; Eger K; Neudecker S; Jakubiczka S; Zierz S
Arch Neurol; 2003 Oct; 60(10):1421-5. PubMed ID: 14568813
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]