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.
3. Congenital muscular dystrophy with eye and brain involvement. The Turkish experience in two cases. Topaloğlu H; Cila A; Taşdemir AH; Saatçi I Brain Dev; 1995; 17(4):271-5. PubMed ID: 7503390 [TBL] [Abstract][Full Text] [Related]
4. Ocular manifestations in Fukuyama type congenital muscular dystrophy. Yoshioka M; Kuroki S; Kondo T Brain Dev; 1990; 12(4):423-6. PubMed ID: 2240463 [TBL] [Abstract][Full Text] [Related]
5. Neuropathological findings in muscle-eye-brain disease (MEB-D). Neuropathological delineation of MEB-D from congenital muscular dystrophy of the Fukuyama type. Leyten QH; Renkawek K; Renier WO; Gabreëls FJ; Mooy CM; ter Laak HJ; Mullaart RA Acta Neuropathol; 1991; 83(1):55-60. PubMed ID: 1792864 [TBL] [Abstract][Full Text] [Related]
15. Involvement of the central nervous system in congenital muscular dystrophies. Egger J; Kendall BE; Erdohazi M; Lake BD; Wilson J; Brett EM Dev Med Child Neurol; 1983 Feb; 25(1):32-42. PubMed ID: 6832496 [TBL] [Abstract][Full Text] [Related]
16. [Western type cerebro-muscular dystrophy and congenital merosin deficiency muscular dystrophy: two terms for the same disorder]. Castro-Gago M; Novo-Rodríguez MI; Pintos-Martínez E; Alonso-Martín A; Morales-Redondo R; Eirís-Puñal J Rev Neurol; 1998 Sep; 27(157):459-62. PubMed ID: 9774819 [TBL] [Abstract][Full Text] [Related]
17. New FKRP mutations causing congenital muscular dystrophy associated with mental retardation and central nervous system abnormalities. Identification of a founder mutation in Tunisian families. Louhichi N; Triki C; Quijano-Roy S; Richard P; Makri S; Méziou M; Estournet B; Mrad S; Romero NB; Ayadi H; Guicheney P; Fakhfakh F Neurogenetics; 2004 Feb; 5(1):27-34. PubMed ID: 14652796 [TBL] [Abstract][Full Text] [Related]
18. Expression profiling of muscles from Fukuyama-type congenital muscular dystrophy and laminin-alpha 2 deficient congenital muscular dystrophy; is congenital muscular dystrophy a primary fibrotic disease? Taniguchi M; Kurahashi H; Noguchi S; Sese J; Okinaga T; Tsukahara T; Guicheney P; Ozono K; Nishino I; Morishita S; Toda T Biochem Biophys Res Commun; 2006 Apr; 342(2):489-502. PubMed ID: 16487936 [TBL] [Abstract][Full Text] [Related]