171 related articles for article (PubMed ID: 16901430)
21. 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]
22. Facio-scapulo-humeral muscular dystrophy with early joint contractures and rigid spine.
Papadopoulos C; Zouvelou V; Papadimas GK
Acta Myol; 2019 Mar; 38(1):25-28. PubMed ID: 31309179
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. Facioscapulohumeral muscular dystrophy: a multicenter study on hearing function.
Trevisan CP; Pastorello E; Ermani M; Angelini C; Tomelleri G; Tonin P; Mongini T; Palmucci L; Galluzzi G; Tupler RG; Marioni G; Rimini A
Audiol Neurootol; 2008; 13(1):1-6. PubMed ID: 17715463
[TBL] [Abstract][Full Text] [Related]
25. Early onset as a marker for disease severity in facioscapulohumeral muscular dystrophy.
Goselink RJM; Mul K; van Kernebeek CR; Lemmers RJLF; van der Maarel SM; Schreuder THA; Erasmus CE; Padberg GW; Statland JM; Voermans NC; van Engelen BGM
Neurology; 2019 Jan; 92(4):e378-e385. PubMed ID: 30568007
[TBL] [Abstract][Full Text] [Related]
26. [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]
27. Association of schizophrenia and mental retardation with facio-scapulohumeral muscular dystrophy.
Sharma S; Namrata S
Neurol India; 2004 Mar; 52(1):104-5. PubMed ID: 15069253
[TBL] [Abstract][Full Text] [Related]
28. [Clinical phenotype and genotype of early-onset facioscapulohumeral muscular dystrophy type 1].
Chen XY; Chang XZ; Fu XN; Ge L; Fan YB; Liu JY; Wang ZQ; Zhang W; Xiong H
Zhonghua Er Ke Za Zhi; 2020 May; 58(5):408-412. PubMed ID: 32392958
[No Abstract] [Full Text] [Related]
29. Facioscapulohumeral muscular dystrophy presenting with isolated axial myopathy and bent spine syndrome.
Kottlors M; Kress W; Meng G; Glocker FX
Muscle Nerve; 2010 Aug; 42(2):273-5. PubMed ID: 20658601
[TBL] [Abstract][Full Text] [Related]
30. [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]
31. Phenotype of combined Duchenne and facioscapulohumeral muscular dystrophy.
Korngut L; Siu VM; Venance SL; Levin S; Ray P; Lemmers RJ; Keith J; Campbell C
Neuromuscul Disord; 2008 Jul; 18(7):579-82. PubMed ID: 18586493
[TBL] [Abstract][Full Text] [Related]
32. [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]
33. 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]
34. Respiratory muscle dysfunction in facioscapulohumeral muscular dystrophy.
Santos DB; Boussaid G; Stojkovic T; Orlikowski D; Letilly N; Behin A; Butel S; Lofaso F; Prigent H
Neuromuscul Disord; 2015 Aug; 25(8):632-9. PubMed ID: 26023000
[TBL] [Abstract][Full Text] [Related]
35. [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]
36. Clinical features of facioscapulohumeral muscular dystrophy 1 in childhood.
Steel D; Main M; Manzur A; Muntoni F; Munot P
Dev Med Child Neurol; 2019 Aug; 61(8):964-971. PubMed ID: 30663041
[TBL] [Abstract][Full Text] [Related]
37. A severe case of facioscapulohumeral muscular dystrophy (FSHD) with some uncommon clinical features and a short 4q35 fragment.
Dorobek M; Kabzińska D
Eur J Paediatr Neurol; 2004; 8(6):313-6. PubMed ID: 15542386
[TBL] [Abstract][Full Text] [Related]
38. Facioscapulohumeral Dystrophy in Childhood: A Nationwide Natural History Study.
Goselink RJM; Schreuder THA; van Alfen N; de Groot IJM; Jansen M; Lemmers RJLF; van der Vliet PJ; van der Stoep N; Theelen T; Voermans NC; van der Maarel SM; van Engelen BGM; Erasmus CE
Ann Neurol; 2018 Nov; 84(5):627-637. PubMed ID: 30179273
[TBL] [Abstract][Full Text] [Related]
39. An unusual family with Leber's hereditary optic neuropathy and facioscapulohumeral muscular dystrophy.
Chuenkongkaew WL; Lertrit P; Limwongse C; Nilanont Y; Boonyapisit K; Sangruchi T; Chirapapaisan N; Suphavilai R
Eur J Neurol; 2005 May; 12(5):388-91. PubMed ID: 15804271
[TBL] [Abstract][Full Text] [Related]
40. Facioscapulohumeral muscular dystrophy and limb-girdle muscular dystrophy: "double trouble" overlapping syndrome?
Simeoni S; Russo V; Gigli GL; Scalise A
J Neurol Sci; 2015 Jan; 348(1-2):292-3. PubMed ID: 25528007
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]