154 related articles for article (PubMed ID: 12398841)
1. 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]
2. 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]
3. 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]
4. [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]
5. 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]
6. [Scapulo-peroneal weakness with tardive symptoms of facio-scapulo-humeral muscular dystrophy, connected to 4q35 chromosomal deletion].
Zeevaert B; Sadzot B; Deprez M; Wang FC
Rev Neurol (Paris); 2002 Dec; 158(12 Pt 1):1210-3. PubMed ID: 12690743
[TBL] [Abstract][Full Text] [Related]
7. [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]
8. 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]
9. [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]
10. Facioscapulohumeral muscular dystrophy.
Tawil R
Curr Neurol Neurosci Rep; 2004 Jan; 4(1):51-4. PubMed ID: 14683629
[TBL] [Abstract][Full Text] [Related]
11. Extension of the clinical range of facioscapulohumeral dystrophy: report of six cases.
van der Kooi AJ; Visser MC; Rosenberg N; van den Berg-Vos R; Wokke JH; Bakker E; de Visser M
J Neurol Neurosurg Psychiatry; 2000 Jul; 69(1):114-6. PubMed ID: 10864616
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Facioscapulohumeral (FSHD1) and other forms of muscular dystrophy in the same family: is there more in muscular dystrophy than meets the eye?
Tonini MM; Passos-Bueno MR; Cerqueira A; Pavanello R; Vainzof M; Dubowitz V; Zatz M
Neuromuscul Disord; 2002 Aug; 12(6):554-7. PubMed ID: 12117479
[TBL] [Abstract][Full Text] [Related]
14. [First facioscapulohumeral muscular dystrophy prenatal diagnosis in a Bulgarian family].
Buzhkov BTs; Vŭzharova R; Dimitrova V; Dimova I; Tŭrnev I; van der Wielen M; van der Maarel S; Bakker B
Akush Ginekol (Sofiia); 2005; 44(2):30-3. PubMed ID: 15853025
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. FSH dystrophy 4q35 deletion in patients presenting with facial-sparing scapular myopathy.
Felice KJ; North WA; Moore SA; Mathews KD
Neurology; 2000 May; 54(10):1927-31. PubMed ID: 10822431
[TBL] [Abstract][Full Text] [Related]
17. [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]
18. 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]
19. 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]
20. Teaching NeuroImages: Hemiatrophy as a clinical presentation in facioscapulohumeral muscular dystrophy.
Sugie K; Hayashi YK; Kin T; Goto K; Nishino I; Ueno S
Neurology; 2009 Aug; 73(5):e24. PubMed ID: 19652136
[No Abstract] [Full Text] [Related]
[Next] [New Search]