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Journal Abstract Search
68 related items for PubMed ID: 943262
1. [Atypical facioscapulohumeral muscular dystrophy associated with congenital facial diplegia noted during infancy]. Miyazaki M, Tawara S, Terao A, Araki S, Shirabe T. Rinsho Shinkeigaku; 1976 Jan; 16(1):32-8. PubMed ID: 943262 [No Abstract] [Full Text] [Related]
13. De novo facioscapulohumeral muscular dystrophy defined by DNA probe p13E-11 (D4F104S1). Jardine PE, Koch MC, Lunt PW, Maynard J, Bathke KD, Harper PS, Upadhyaya M. Arch Dis Child; 1994 Sep; 71(3):221-7. PubMed ID: 7979495 [Abstract] [Full Text] [Related]
14. Electromyographic study on congenital facial diplegia. Sumitsuji N, Tanaka M, Yuasa R. Electromyography; 1970 Sep; 10(4):399-414. PubMed ID: 5521840 [No Abstract] [Full Text] [Related]
16. Atypical facet of Möbius syndrome: association with facioscapulohumeral muscular dystrophy. Kolski HK, Leonard NJ, Lemmers RJ, Bamforth JS. Muscle Nerve; 2008 Apr; 37(4):526-9. PubMed ID: 18059038 [Abstract] [Full Text] [Related]
17. Permanent paralysis of the atrium in a patient with facioscapulohumeral muscular dystrophy. Baldwin BJ, Talley RC, Johnson C, Nutter DO. Am J Cardiol; 1973 May; 31(5):649-53. PubMed ID: 4698137 [No Abstract] [Full Text] [Related]