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42. Facioscapulohumeral muscular dystrophy with chromosome 9p deletion. Ueyama H; Kumamoto T; Mita S; Kimura E; Nakagawa M; Uchino M; Ando M Neurology; 1996 Feb; 46(2):566-9. PubMed ID: 8614537 [TBL] [Abstract][Full Text] [Related]
43. A study of Duchenne's muscular dystrophy in females. A clinical, biochemical, pathological and chromosomal study of two families. Reddy MV; Prabhakar V; Sadasivan G; Ebenezer LN Neurol India; 1968; 16(2):41-5. PubMed ID: 5682570 [No Abstract] [Full Text] [Related]
44. [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]
45. Estimate of severe autosomal recessive limb-girdle muscular dystrophy (LGMD2C, LGMD2D) among sporadic muscular dystrophy males: a study of 415 familes. Stec I; Kress W; Meng G; Müller B; Müller CR; Grimm T J Med Genet; 1995 Dec; 32(12):930-3. PubMed ID: 8825917 [TBL] [Abstract][Full Text] [Related]
46. A late autosomal dominant form of limb-girdle muscular dystrophy. A clinical, genetic, and morphological study. De Coster W; De Reuck J; Thiery E Eur Neurol; 1974; 12(3):159-72. PubMed ID: 4426323 [No Abstract] [Full Text] [Related]
47. De novo DNA rearrangement in atypical facioscapulohumeral muscular dystrophy. Jardine P; Jones M; Tyfield L; Upadhyaya M; Lunt P Clin Genet; 1993 Sep; 44(3):167. PubMed ID: 8275579 [No Abstract] [Full Text] [Related]
48. Early muscular dystrophy: differential patterns of weakness in duchenne, limb-girdle and facioscapulohumeral types. Chyatte SB; Vignos PJ; Watkins M Arch Phys Med Rehabil; 1966 Aug; 47(8):499-503. PubMed ID: 5914825 [No Abstract] [Full Text] [Related]
49. [Duchenne's muscular dystrophy in a girl with 45,X/46,XX chromosomal mosaicism]. Aver'ianov IuN; Bogomazov EA; Logunova LV Zh Nevropatol Psikhiatr Im S S Korsakova; 1977; 77(10):1449-52. PubMed ID: 930487 [TBL] [Abstract][Full Text] [Related]
50. [Association of dystrophinopathy with facial-scapular-humeral dystrophy in the same family]. Serrano PJ; García Pérez A; Vilches RM; Mínguez A; Hernández Ramos FJ Rev Neurol; 1995; 23(120):301-3. PubMed ID: 7497180 [TBL] [Abstract][Full Text] [Related]
51. [Biochemical, histological and clinical findings in a four-year-old female carrier of benign X-linked muscular dystrophy (Becker type)]. Moser H Humangenetik; 1971; 11(4):328-35. PubMed ID: 5576061 [No Abstract] [Full Text] [Related]
52. Muscular dystrophy contrasted with denervation: different mechanisms underlying spontaneous fibrillations. Desmedt JE Electroencephalogr Clin Neurophysiol Suppl; 1978; (34):531-46. PubMed ID: 108083 [TBL] [Abstract][Full Text] [Related]
53. The genetics of muscular dystrophies. Harper PS Prog Med Genet; 1985; 6():53-90. PubMed ID: 3915367 [No Abstract] [Full Text] [Related]
54. Oculopharyngeal muscular dystrophy treated by inferior constrictor myotomy. Montgomery WW; Lynch JP Trans Am Acad Ophthalmol Otolaryngol; 1971; 75(5):986-93. PubMed ID: 5097831 [No Abstract] [Full Text] [Related]
55. A workshop on facioscapulohumeral (Landouzy-Déjérine) disease, Manchester, 16 to 17 November 1988. Lunt PW J Med Genet; 1989 Aug; 26(8):535-7. PubMed ID: 2671375 [No Abstract] [Full Text] [Related]
56. Correction of myopathic face associated with myotonic muscular dystrophy. A case report. Kamiishi H; Ohtsuka H; Shioya N J Maxillofac Surg; 1977 Feb; 5(1):48-54. PubMed ID: 265351 [TBL] [Abstract][Full Text] [Related]
57. [Differential diagnosis of a benign course of muscular dystrophy using molecular genetic methods]. Wagner M; Diedrich U; Pozsàr C; Becker PE; Reiss J Nervenarzt; 1990 Apr; 61(4):244-7. PubMed ID: 2352571 [No Abstract] [Full Text] [Related]