These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
107 related articles for article (PubMed ID: 1332322)
21. 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]
24. [Landouzy-Dejerine syndrome. Evolution of the concept of facio-scapulo-humeral amyotrophia]. Schmitt J; Barrucand D; Schmidt C Rev Neurol (Paris); 1977 Apr; 133(4):279-82. PubMed ID: 929032 [TBL] [Abstract][Full Text] [Related]
25. [A familial form of progressive muscular dystrophy with multiple contractures of the major joints]. Iadgarov IS; Badalian LO; Temin PA; Arkhipov BA; Bulaeva NV; Amanova ZA Zh Nevropatol Psikhiatr Im S S Korsakova; 1991; 91(9):89-93. PubMed ID: 1664624 [TBL] [Abstract][Full Text] [Related]
26. [Malate dehydrogenase activity in children with myopathy]. Gil'manov VKh Zh Nevropatol Psikhiatr Im S S Korsakova; 1973; 73(6):829-31. PubMed ID: 4753593 [No Abstract] [Full Text] [Related]
27. [Myopathy (terminology, clinical picture, and diagnosis)]. Kazakov VM; Kovalenko TM; Demin EV; Sedletskiĭ IuI; Mikhaĭlov EP Zh Nevropatol Psikhiatr Im S S Korsakova; 1978; 78(4):481-8. PubMed ID: 654722 [TBL] [Abstract][Full Text] [Related]
29. Facioscapulohumeral dystrophy associated with hearing loss and Coats syndrome. Taylor DA; Carroll JE; Smith ME; Johnson MO; Johnston GP; Brooke MH Ann Neurol; 1982 Oct; 12(4):395-8. PubMed ID: 7149664 [No Abstract] [Full Text] [Related]
30. [Identification of primary and secondary forms of progressive muscular dystrophy, from data of clinico-genetic and biochemical studies]. Bondarenko ES; Tamarkina AD; Zakoshchikova LV Vestn Akad Med Nauk SSSR; 1973; 28(7):38-44. PubMed ID: 4786657 [No Abstract] [Full Text] [Related]
32. Emery-dreifuss humeroperoneal muscular dystrophy: an x-linked myopathy with unusual contractures and bradycardia. Hopkins LC; Jackson JA; Elsas LJ Ann Neurol; 1981 Sep; 10(3):230-7. PubMed ID: 7294729 [TBL] [Abstract][Full Text] [Related]
33. Prosthetic treatment of a patient with facioscapulohumeral muscular dystrophy: a clinical report. Güler AU; Ceylan G; Ozkoç O; Aydiin M; Cengiz N J Prosthet Dent; 2003 Oct; 90(4):321-4. PubMed ID: 14564285 [TBL] [Abstract][Full Text] [Related]
34. Inflammatory facioscapulohumeral muscular dystrophy and Coats syndrome. Wulff JD; Lin JT; Kepes JJ Ann Neurol; 1982 Oct; 12(4):398-401. PubMed ID: 7149665 [No Abstract] [Full Text] [Related]
35. [A 34-year-old woman with delayed motor milestones, high arched palate, and proximal muscle weakness]. Yamamoto T; Kitada T; Hirasawa E; Mori H; Mizuno Y No To Shinkei; 1996 Jul; 48(7):677-84. PubMed ID: 8753005 [TBL] [Abstract][Full Text] [Related]
37. [Pathogenesis of creatinuria and aminoaciduria in neuromuscular diseases]. Il'ina NA; Poliakova NF; Khokhlov AP Zh Nevropatol Psikhiatr Im S S Korsakova; 1977; 77(7):1025-8. PubMed ID: 197760 [TBL] [Abstract][Full Text] [Related]