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7. Deficiency of laminin alpha 2-chain mRNA in muscle in a patient with merosin-negative congenital muscular dystrophy. Hayashi YK; Koga R; Tsukahara T; Ishii H; Matsuishi T; Yamashita Y; Nonaka I; Arahata K Muscle Nerve; 1995 Sep; 18(9):1027-30. PubMed ID: 7643867 [No Abstract] [Full Text] [Related]
8. [Congenital atonic-sclerotic muscular dystrophy (Ullrich disease)]. Fernández M; Pacheco M; Garaizar C; Prats JM Neurologia; 1991; 6(7):259-62. PubMed ID: 1768446 [TBL] [Abstract][Full Text] [Related]
9. Characteristic clinical findings in some neurogenic myopathies and in some myogenic myopathies causing muscular weakness, hypotonia and atrophy in infancy and early childhood. Gamstorp I Birth Defects Orig Artic Ser; 1971 Feb; 7(2):72-81. PubMed ID: 5173129 [TBL] [Abstract][Full Text] [Related]
11. Congenital muscular dystrophy: a clinico-pathological and follow-up study of 15 patients. Donner M; Rapola J; Somer H Neuropadiatrie; 1975 Aug; 6(3):239-58. PubMed ID: 1242211 [TBL] [Abstract][Full Text] [Related]
12. [Early autism and congenital muscular dystrophy: a clinical case]. Saccomani L; Veneselli E; Di Stefano S; Celle ME; De Negri M Pediatr Med Chir; 1992; 14(2):231-3. PubMed ID: 1508762 [TBL] [Abstract][Full Text] [Related]
18. [2 autopsy cases of congenital muscular dystrophy of Fukuyama type--a typical and an atypical cases]. Koga M; Abe M; Tateishi J; Antoku Y; Iwashita H; Miyoshino S No To Shinkei; 1984 Nov; 36(11):1103-8. PubMed ID: 6525323 [TBL] [Abstract][Full Text] [Related]
19. [On a congenital distal muscular dystrophy with a benign course]. Heyck H; Lüders CJ; Wolter M Nervenarzt; 1968 Dec; 39(12):549-52. PubMed ID: 5733571 [No Abstract] [Full Text] [Related]