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.
126 related articles for article (PubMed ID: 1664615)
21. The myogenic scapulo-peroneal syndrome. Muscular dystrophy in the K. kindred: clinical study and genetics. Kazakov VM; Bogorodinsky DK; Skorometz AA Clin Genet; 1976 Jul; 10(1):41-50. PubMed ID: 949863 [TBL] [Abstract][Full Text] [Related]
22. [A case of centronuclear myopathy in adults with facio-scapulo-peroneal topography]. Serratrice G; Pellissier JF; Bes A; Arne-Bes MC Rev Neurol (Paris); 1987; 143(10):693-7. PubMed ID: 3423586 [TBL] [Abstract][Full Text] [Related]
23. Myogenic scapuloperoneal syndrome - muscular dystrophy in the K. kindred. Reexamination of the K. family described for the first time by Oransky in 1927. Kazakov VM; Bogorodinsky DK; Skorometz AA Eur Neurol; 1975; 13(4):350-9. PubMed ID: 1149755 [TBL] [Abstract][Full Text] [Related]
24. [Clinical and genetic aspects of progressive muscular dystrophy. Genetic and clinical forms of myopathy; clinical, anatomical, and EMG study]. Voiculescu V; Pruskauer-Apostol B; Mărcuţiu V; Alecu C; Stănescu A Neurol Psihiatr Neurochir; 1973; 18(4):347-58. PubMed ID: 4752178 [No Abstract] [Full Text] [Related]
25. [Emery-Dreifuss muscular dystrophy--reported a family with 5 cases]. Luo D Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1991 Dec; 24(6):330-1, 382. PubMed ID: 1800056 [TBL] [Abstract][Full Text] [Related]
26. The differential diagnosis of the myogenic (facio)-scapulo-peroneal syndrome. Ricker K; Mertens HG Eur Neurol; 1968; 1(5):275-307. PubMed ID: 5696602 [No Abstract] [Full Text] [Related]
27. 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]
28. [A family of scapula-back type of x-linked recessive muscular dystrophy]. Ji XW Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1989 Jun; 22(3):136-8, 190. PubMed ID: 2591265 [TBL] [Abstract][Full Text] [Related]
29. Correction of facial-skeletal deformities in two patients with facio-scapulo-humeral muscular dystrophy. Goldberg MH; McNeish L; Clarizzio L J Oral Maxillofac Surg; 1989 Sep; 47(9):996-9. PubMed ID: 2527295 [TBL] [Abstract][Full Text] [Related]
30. Distal muscular dystrophy with autosomal recessive inheritance. Scoppetta C; Vaccario ML; Casali C; Di Trapani G; Mennuni G Muscle Nerve; 1984; 7(6):478-81. PubMed ID: 6543900 [TBL] [Abstract][Full Text] [Related]
31. 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]
32. Limb-girdle muscular dystrophy: clinical manifestations and detection of preclinical disease. Jackson CE; Strehler DA Pediatrics; 1968 Feb; 41(2):495-502. PubMed ID: 5637795 [No Abstract] [Full Text] [Related]
38. [Association of sporadic limb-girdle muscular dystrophy and autonomous thyroid nodule in 3 Germans]. Di Lorenzo L; Lupoli G; Cosentini E; Rippa PG; Lombardi G Minerva Endocrinol; 1991; 16(3):147-51. PubMed ID: 1806812 [TBL] [Abstract][Full Text] [Related]
39. Coats' disease and muscular dystrophy. Small RG Trans Am Acad Ophthalmol Otolaryngol; 1968; 72(2):225-31. PubMed ID: 5659903 [No Abstract] [Full Text] [Related]
40. New type of X-linked progressive muscular dystrophy involving shoulder girdle and back. Ji XW; Tan J; Chen XY; Yi SX; Liang H Am J Med Genet; 1990 Oct; 37(2):209-12. PubMed ID: 2248287 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]