154 related articles for article (PubMed ID: 10864616)
1. 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]
2. 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]
3. [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]
4. 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]
5. [Clinical and genetical features of Japanese early-onset facioscapulohumeral muscular dystrophy].
Yamanaka G; Goto K; Hayashi YK; Miyajima T; Hoshika A; Arahata K
No To Hattatsu; 2002 Jul; 34(4):318-24. PubMed ID: 12134683
[TBL] [Abstract][Full Text] [Related]
6. 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]
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. [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]
9. [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]
10. 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]
11. Compound heterozygosity in a South African patient with facioscapulohumeral muscular dystrophy.
Olckers A; van der Merwe A; Wayne Towers G; Retief CF; Honey E; Schutte CM
Neuromuscul Disord; 2012 Aug; 22(8):728-34. PubMed ID: 22652079
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Early onset facioscapulohumeral muscular dystrophy.
Brouwer OF; Padberg GW; Bakker E; Wijmenga C; Frants RR
Muscle Nerve Suppl; 1995; (2):S67-72. PubMed ID: 23573589
[TBL] [Abstract][Full Text] [Related]
14. Familial facioscapulohumeral muscular dystrophy: phenotypic diversity and genetic abnormality.
Nakagawa M; Higuchi I; Yoshidome H; Isashiki Y; Ohkubo R; Kaseda S; Iwaki H; Fukunaga H; Osame M
Acta Neurol Scand; 1996; 93(2-3):189-92. PubMed ID: 8741141
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. [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]
17. 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]
18. Phenotypic Variability Among Patients With D4Z4 Reduced Allele Facioscapulohumeral Muscular Dystrophy.
Ruggiero L; Mele F; Manganelli F; Bruzzese D; Ricci G; Vercelli L; Govi M; Vallarola A; Tripodi S; Villa L; Di Muzio A; Scarlato M; Bucci E; Antonini G; Maggi L; Rodolico C; Tomelleri G; Filosto M; Previtali S; Angelini C; Berardinelli A; Pegoraro E; Moggio M; Mongini T; Siciliano G; Santoro L; Tupler R
JAMA Netw Open; 2020 May; 3(5):e204040. PubMed ID: 32356886
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. [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]
[Next] [New Search]
