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8. Fukuyama muscular dystrophy associated with lack of C-terminal domain of dystrophin. Tachi N; Chiba S; Matsuo M; Matsumura K; Saito K Pediatr Neurol; 2001 May; 24(5):373-8. PubMed ID: 11516613 [TBL] [Abstract][Full Text] [Related]
9. [A patient of Walker-Warburg syndrome with a haplotype different from that in Fukuyama-type congenital muscular dystrophy]. Sasaki M; Kondo E; Yamashita Y; Toda T; Nonaka I No To Hattatsu; 1999 Sep; 31(5):445-51. PubMed ID: 10487070 [TBL] [Abstract][Full Text] [Related]
10. Laminin alpha 2-chain gene mutations in two siblings presenting with limb-girdle muscular dystrophy. Naom I; D'Alessandro M; Sewry CA; Philpot J; Manzur AY; Dubowitz V; Muntoni F Neuromuscul Disord; 1998 Oct; 8(7):495-501. PubMed ID: 9829280 [TBL] [Abstract][Full Text] [Related]
11. Merosin-positive congenital muscular dystrophy: a large inbred family. Mahjneh I; Bushby K; Anderson L; Muntoni F; Tolvanen-Mahjneh H; Bashir R; Pizzi A; Brockington M; Marconi G Neuropediatrics; 1999 Feb; 30(1):22-8. PubMed ID: 10222457 [TBL] [Abstract][Full Text] [Related]
12. Congenital muscular dystrophy with complete laminin-alpha2-deficiency, cortical dysplasia, and cerebral white-matter changes in children. Tsao CY; Mendell JR; Rusin J; Luquette M J Child Neurol; 1998 Jun; 13(6):253-6. PubMed ID: 9660506 [TBL] [Abstract][Full Text] [Related]
13. Mutations in the laminin alpha2-chain gene in two children with early-onset muscular dystrophy. Naom I; D'alessandro M; Sewry CA; Jardine P; Ferlini A; Moss T; Dubowitz V; Muntoni F Brain; 2000 Jan; 123 ( Pt 1)():31-41. PubMed ID: 10611118 [TBL] [Abstract][Full Text] [Related]
14. The Fukuyama congenital muscular dystrophy story. Toda T; Kobayashi K; Kondo-Iida E; Sasaki J; Nakamura Y Neuromuscul Disord; 2000 Mar; 10(3):153-9. PubMed ID: 10734260 [TBL] [Abstract][Full Text] [Related]
16. Congenital muscular dystrophy with adducted thumbs, ptosis, external ophthalmoplegia, mental retardation and cerebellar hypoplasia: a novel form of CMD. Voit T; Parano E; Straub V; Schröder JM; Schaper J; Pavone P; Falsaperla R; Pavone L; Herrmann R Neuromuscul Disord; 2002 Oct; 12(7-8):623-30. PubMed ID: 12207929 [TBL] [Abstract][Full Text] [Related]
17. Congenital muscular dystrophy syndromes distinguished by alkaline and acid phosphatase, merosin, and dystrophin staining. Connolly AM; Pestronk A; Planer GJ; Yue J; Mehta S; Choksi R Neurology; 1996 Mar; 46(3):810-14. PubMed ID: 8618688 [TBL] [Abstract][Full Text] [Related]
18. Congenital muscular dystrophy with primary laminin alpha2 (merosin) deficiency presenting as inflammatory myopathy. Pegoraro E; Mancias P; Swerdlow SH; Raikow RB; Garcia C; Marks H; Crawford T; Carver V; Di Cianno B; Hoffman EP Ann Neurol; 1996 Nov; 40(5):782-91. PubMed ID: 8957020 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. A new mutation of the fukutin gene in a non-Japanese patient. Silan F; Yoshioka M; Kobayashi K; Simsek E; Tunc M; Alper M; Cam M; Guven A; Fukuda Y; Kinoshita M; Kocabay K; Toda T Ann Neurol; 2003 Mar; 53(3):392-6. PubMed ID: 12601708 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]