298 related articles for article (PubMed ID: 6568938)
21. An autopsy study of a familial oculopharyngeal muscular dystrophy (OPMD) with distal spread and neurogenic involvement.
Schmitt HP; Krause KH
Muscle Nerve; 1981; 4(4):296-305. PubMed ID: 7254232
[TBL] [Abstract][Full Text] [Related]
22. Muscular dystrophy with separate clinical phenotypes in a large family.
Udd B; Kääriänen H; Somer H
Muscle Nerve; 1991 Nov; 14(11):1050-8. PubMed ID: 1745277
[TBL] [Abstract][Full Text] [Related]
23. Emery-Dreifuss muscular dystrophy with unusual features.
Deymeer F; Oge AE; Bayindir C; Kaymaz C; Nişanci Y; Adalet K; Yates JR; Ozdemir C
Muscle Nerve; 1993 Dec; 16(12):1359-65. PubMed ID: 8232393
[TBL] [Abstract][Full Text] [Related]
24. [Scapuloperoneal syndrome].
Uyama E
Ryoikibetsu Shokogun Shirizu; 2001; (36):462-6. PubMed ID: 11596438
[No Abstract] [Full Text] [Related]
25. [Diagnosis of a myopathic disease in adult].
Eymard B
Rev Prat; 2008 Dec; 58(20):2229-43. PubMed ID: 19209654
[TBL] [Abstract][Full Text] [Related]
26. Familial scapuloperoneal myopathy and mitochondrial DNA defect.
Pál E; Bedekovics T; Gáti I
Eur Neurol; 1999; 42(4):211-6. PubMed ID: 10567817
[TBL] [Abstract][Full Text] [Related]
27. A novel autosomal dominant distal myopathy with early respiratory failure: clinico-pathologic characteristics and exclusion of linkage to candidate genetic loci.
Chinnery PF; Johnson MA; Walls TJ; Gibson GJ; Fawcett PR; Jamieson S; Fulthorpe JJ; Cullen M; Hudgson P; Bushby KM
Ann Neurol; 2001 Apr; 49(4):443-52. PubMed ID: 11310621
[TBL] [Abstract][Full Text] [Related]
28. Autosomal dominant congenital fibre type disproportion: a clinicopathological and imaging study of a large family.
Sobrido MJ; Fernández JM; Fontoira E; Pérez-Sousa C; Cabello A; Castro M; Teijeira S; Alvarez S; Mederer S; Rivas E; Seijo-Martínez M; Navarro C
Brain; 2005 Jul; 128(Pt 7):1716-27. PubMed ID: 15857933
[TBL] [Abstract][Full Text] [Related]
29. [Articulation disorder as the initial manifestation of facioscapulohumeral muscular dystrophy in childhood].
Lischka A; Grisold W; Weninger M; Toifl K; Tatzer E
Klin Padiatr; 1986; 198(2):119-21. PubMed ID: 3702273
[TBL] [Abstract][Full Text] [Related]
30. [Abnormal head drooping in facioscapulohumeral muscular dystrophy].
Ichikawa Y; Yamada H; Motoyoshi Y; Shimizu T; Kawai M
Rinsho Shinkeigaku; 1996 Mar; 36(3):503-6. PubMed ID: 8741360
[TBL] [Abstract][Full Text] [Related]
31. Sporadic distal myopathy with early adult onset.
Miller RG; Blank NK; Layzer RB
Ann Neurol; 1979 Mar; 5(3):220-7. PubMed ID: 443754
[TBL] [Abstract][Full Text] [Related]
32. [The first Japanese case of autosomal dominant Emery-Dreifuss muscular dystrophy with a novel mutation in the lamin A/C gene].
Onishi Y; Higuchi J; Ogawa T; Namekawa A; Hayashi H; Odakura H; Goto K; Hayashi YK
Rinsho Shinkeigaku; 2002 Feb; 42(2):140-4. PubMed ID: 12424964
[TBL] [Abstract][Full Text] [Related]
33. Facioscapulohumeral muscular dystrophy: the choice of a biopsy site.
Bodensteiner JB; Schochet SS
Muscle Nerve; 1986; 9(6):544-7. PubMed ID: 3736585
[TBL] [Abstract][Full Text] [Related]
34. Autosomal recessive distal muscular dystrophy: a comparative study with distal myopathy with rimmed vacuole formation.
Nonaka I; Sunohara N; Satoyoshi E; Terasawa K; Yonemoto K
Ann Neurol; 1985 Jan; 17(1):51-9. PubMed ID: 3985587
[TBL] [Abstract][Full Text] [Related]
35. [Facioscapulohumeral neuromuscular syndromes--problems of differential and early diagnosis and genetic counseling].
Bachmann H; Ziegan J; Steinbicker V; von Rohden L; Wagner A
Psychiatr Neurol Med Psychol (Leipz); 1989 Oct; 41(10):586-95. PubMed ID: 2608758
[TBL] [Abstract][Full Text] [Related]
36. [The dystrophic type of scapuloperoneal syndrome].
Steidl L; Urbánek K
Cesk Neurol; 1973 May; 36(3):147-50. PubMed ID: 4704112
[No Abstract] [Full Text] [Related]
37. Emery-Dreifuss muscular dystrophy and other related disorders.
Emery AE
Br Med Bull; 1989 Jul; 45(3):772-87. PubMed ID: 2688828
[TBL] [Abstract][Full Text] [Related]
38. Congenital muscular dystrophy with rigid spine syndrome: a clinical, pathological, radiological, and genetic study.
Flanigan KM; Kerr L; Bromberg MB; Leonard C; Tsuruda J; Zhang P; Gonzalez-Gomez I; Cohn R; Campbell KP; Leppert M
Ann Neurol; 2000 Feb; 47(2):152-61. PubMed ID: 10665485
[TBL] [Abstract][Full Text] [Related]
39. [Familial scapuloperoneal-type myopathy associated with a marked elevation of serum creatine kinase and hepatomegaly].
Maruoka A; Ideguchi H; Nawata H; Goto I; Ibayashi H
Rinsho Shinkeigaku; 1989 Mar; 29(3):325-31. PubMed ID: 2752661
[TBL] [Abstract][Full Text] [Related]
40. [Late scapuloperoneal form of progressive muscular dystrophy].
Stamatoiu I; Florea G; Vasilescu C
Neurol Psihiatr Neurochir; 1965; 10(1):21-7. PubMed ID: 5827299
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]