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42. Lethal congenital muscular dystrophy with cataracts and a minor brain anomaly: new entity or variant of Walker-Warburg syndrome? Wargowski DS; Chitayat D; Tyson RW; Norman MG; Friedman JM Am J Med Genet; 1991 Apr; 39(1):19-24. PubMed ID: 1867258 [TBL] [Abstract][Full Text] [Related]
45. A Fukuyama type of congenital muscular dystrophy associated with atypical gyrate atrophy of the choroid and retina. A case report. Mishima H; Hirata H; Ono H; Choshi K; Nishi Y; Fukuda K Acta Ophthalmol (Copenh); 1985 Apr; 63(2):155-9. PubMed ID: 4003043 [TBL] [Abstract][Full Text] [Related]
46. A case of merosin-negative congenital muscular dystrophy with extensive white matter abnormalities and electroencephalographic changes in a Syrian boy. Al-Ajmi MO; Abdulla JK; Neubauer D J Med Liban; 2001; 49(3):173-8. PubMed ID: 12184464 [TBL] [Abstract][Full Text] [Related]
47. [A case of non-Fukuyama type congenital muscular dystrophy with progression in early adulthood, ocular involvement, and sensorineural deafness]. Yamada H; Komiyama A; Suzuki Y; Misugi N; Hasegawa O Rinsho Shinkeigaku; 1993 Apr; 33(4):405-10. PubMed ID: 8370203 [TBL] [Abstract][Full Text] [Related]
48. Muscle involvement in Walker-Warburg syndrome. Clinicopathologic features of four cases. Lichtig C; Ludatscher RM; Mandel H; Gershoni-Baruch R Am J Clin Pathol; 1993 Nov; 100(5):493-6. PubMed ID: 8249887 [TBL] [Abstract][Full Text] [Related]
49. Congenital muscular dystrophy with short stature, proximal contractures and distal laxity. Mercuri E; Lampe A; Straub V; Yuva Y; Longman C; Wright M; Brown S; Sewry C; Bonnemann C; Kinali M; Brockington M; Hausser I; Hilton Jones D; Voit T; Bushby K; Muntoni F Neuropediatrics; 2004 Aug; 35(4):224-9. PubMed ID: 15328561 [TBL] [Abstract][Full Text] [Related]
50. An autopsy study of a familial oculopharyngeal muscular dystrophy (OPMD) with distal spread and neurogenic involvement. Schmitt HP; Krause KH Muscle Nerve; 1981; 4(4):296-305. PubMed ID: 7254232 [TBL] [Abstract][Full Text] [Related]
51. [Congenital muscular dystrophy: histochemical study of the skeletal muscle in 17 patients]. Oliveira AS; Schmidt B; Ferreira Neto A; Kiyomoto BH; Gabbai AA; Lima JG Arq Neuropsiquiatr; 1991 Jun; 49(2):185-91. PubMed ID: 1810237 [TBL] [Abstract][Full Text] [Related]
52. Congenital muscular dystrophy. A histochemical study with morphometric analysis on biopsied muscles. Kihira S; Nonaka I J Neurol Sci; 1985 Sep; 70(2):139-49. PubMed ID: 4056819 [TBL] [Abstract][Full Text] [Related]
53. [Congenital muscular dystrophy with laminin-a2 deficiency in early infancy: diagnosis and long-term follow-up]. Panteliadis C; Karatza E; Xinias I; Flaris N; Tzitiridou M; Ramantani G Klin Padiatr; 2005; 217(5):281-5. PubMed ID: 16167276 [TBL] [Abstract][Full Text] [Related]
54. [Congenital muscular dystrophy with leukoencephalopathy]. Aver'ianov IuN Zh Nevrol Psikhiatr Im S S Korsakova; 1993; 93(5):27-9. PubMed ID: 8154212 [TBL] [Abstract][Full Text] [Related]
55. Two Dutch siblings with congenital muscular dystrophy (Fukuyama type). Vles JS; de Krom MC; Visser R; Höweler CJ Clin Neurol Neurosurg; 1983; 85(3):175-80. PubMed ID: 6315292 [TBL] [Abstract][Full Text] [Related]
56. Emery-Dreifuss muscular dystrophy. An autopsy case. Hara H; Nagara H; Mawatari S; Kondo A; Sato H J Neurol Sci; 1987 Jun; 79(1-2):23-31. PubMed ID: 3612171 [TBL] [Abstract][Full Text] [Related]
57. Merosin negative congenital muscular dystrophy: a short report. Ralte AM; Sharma MC; Gulati S; Das M; Sarkar C Neurol India; 2003 Sep; 51(3):417-9. PubMed ID: 14652462 [TBL] [Abstract][Full Text] [Related]
58. Abnormality of cerebral gangliosides in Fukuyama type congenital muscular dystrophy. Izumi T; Hara K; Ogawa T; Osawa M; Saito K; Novo ML; Fukuyama Y; Takashima S Brain Dev; 1995; 17(1):33-7. PubMed ID: 7762760 [TBL] [Abstract][Full Text] [Related]
59. Maturational defect of regenerating muscle fibers in cases with Duchenne and congenital muscular dystrophies. Miike T Muscle Nerve; 1983 Oct; 6(8):545-52. PubMed ID: 6196637 [TBL] [Abstract][Full Text] [Related]
60. Severe progressive form of congenital muscular dystrophy with calf pseudohypertrophy, macroglossia and respiratory insufficiency. Quijano-Roy S; Galan L; Ferreiro A; Cheliout-Héraut F; Gray F; Fardeau M; Barois A; Guicheney P; Romero NB; Estournet B Neuromuscul Disord; 2002 Jun; 12(5):466-75. PubMed ID: 12031620 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]