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.
199 related articles for article (PubMed ID: 18834683)
1. Phenotypic spectrum of Fukutinopathy: most severe phenotype of Fukutinopathy. Yoshioka M Brain Dev; 2009 Jun; 31(6):419-22. PubMed ID: 18834683 [TBL] [Abstract][Full Text] [Related]
2. Genetic identity of Fukuyama-type congenital muscular dystrophy and Walker-Warburg syndrome. Toda T; Yoshioka M; Nakahori Y; Kanazawa I; Nakamura Y; Nakagome Y Ann Neurol; 1995 Jan; 37(1):99-101. PubMed ID: 7818265 [TBL] [Abstract][Full Text] [Related]
3. [Fukuyama-type congenital muscular dystrophy]. Toda T Rinsho Shinkeigaku; 2000 Dec; 40(12):1297-9. PubMed ID: 11464484 [TBL] [Abstract][Full Text] [Related]
4. Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome. Beltrán-Valero de Bernabé D; Currier S; Steinbrecher A; Celli J; van Beusekom E; van der Zwaag B; Kayserili H; Merlini L; Chitayat D; Dobyns WB; Cormand B; Lehesjoki AE; Cruces J; Voit T; Walsh CA; van Bokhoven H; Brunner HG Am J Hum Genet; 2002 Nov; 71(5):1033-43. PubMed ID: 12369018 [TBL] [Abstract][Full Text] [Related]
5. Novel mutations and genotype-phenotype relationships in 107 families with Fukuyama-type congenital muscular dystrophy (FCMD). Kondo-Iida E; Kobayashi K; Watanabe M; Sasaki J; Kumagai T; Koide H; Saito K; Osawa M; Nakamura Y; Toda T Hum Mol Genet; 1999 Nov; 8(12):2303-9. PubMed ID: 10545611 [TBL] [Abstract][Full Text] [Related]
6. An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy. Kobayashi K; Nakahori Y; Miyake M; Matsumura K; Kondo-Iida E; Nomura Y; Segawa M; Yoshioka M; Saito K; Osawa M; Hamano K; Sakakihara Y; Nonaka I; Nakagome Y; Kanazawa I; Nakamura Y; Tokunaga K; Toda T Nature; 1998 Jul; 394(6691):388-92. PubMed ID: 9690476 [TBL] [Abstract][Full Text] [Related]
7. [Recent progress, genetic diagnosis and its problem on congenital muscular dystrophies (Fukuyama and non-Fukuyama types)]. Toda T Rinsho Shinkeigaku; 1995 Dec; 35(12):1419-21. PubMed ID: 8752416 [TBL] [Abstract][Full Text] [Related]
8. Worldwide distribution and broader clinical spectrum of muscle-eye-brain disease. Taniguchi K; Kobayashi K; Saito K; Yamanouchi H; Ohnuma A; Hayashi YK; Manya H; Jin DK; Lee M; Parano E; Falsaperla R; Pavone P; Van Coster R; Talim B; Steinbrecher A; Straub V; Nishino I; Topaloglu H; Voit T; Endo T; Toda T Hum Mol Genet; 2003 Mar; 12(5):527-34. PubMed ID: 12588800 [TBL] [Abstract][Full Text] [Related]
9. Diagnostic criteria for Walker-Warburg syndrome. Dobyns WB; Pagon RA; Armstrong D; Curry CJ; Greenberg F; Grix A; Holmes LB; Laxova R; Michels VV; Robinow M Am J Med Genet; 1989 Feb; 32(2):195-210. PubMed ID: 2494887 [TBL] [Abstract][Full Text] [Related]
10. Clinical and genetic distinction between Walker-Warburg syndrome and muscle-eye-brain disease. Cormand B; Pihko H; Bayés M; Valanne L; Santavuori P; Talim B; Gershoni-Baruch R; Ahmad A; van Bokhoven H; Brunner HG; Voit T; Topaloglu H; Dobyns WB; Lehesjoki AE Neurology; 2001 Apr; 56(8):1059-69. PubMed ID: 11320179 [TBL] [Abstract][Full Text] [Related]
11. Cobblestone lissencephaly with normal eyes and muscle. Dobyns WB; Patton MA; Stratton RF; Mastrobattista JM; Blanton SH; Northrup H Neuropediatrics; 1996 Apr; 27(2):70-5. PubMed ID: 8737821 [TBL] [Abstract][Full Text] [Related]
12. [Analysis of genotype and phenotype in fukuyama congenital muscular dystrophy]. Wang Z; Kayoko S; Makiko O Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2000 Oct; 17(5):305-8. PubMed ID: 11024205 [TBL] [Abstract][Full Text] [Related]
13. Haplotype-phenotype correlation in Fukuyama congenital muscular dystrophy. Saito K; Osawa M; Wang ZP; Ikeya K; Fukuyama Y; Kondo-Iida E; Toda T; Ohashi H; Kurosawa K; Wakai S; Kaneko K Am J Med Genet; 2000 May; 92(3):184-90. PubMed ID: 10817652 [TBL] [Abstract][Full Text] [Related]
14. Clinical spectrum and genetic studies of Fukuyama congenital muscular dystrophy. Yoshioka M; Kuroki S Am J Med Genet; 1994 Nov; 53(3):245-50. PubMed ID: 7856660 [TBL] [Abstract][Full Text] [Related]
15. Broader clinical spectrum of Fukuyama-type congenital muscular dystrophy manifested by haplotype analysis. Yoshioka M; Toda T; Kuroki S; Hamano K J Child Neurol; 1999 Nov; 14(11):711-5. PubMed ID: 10593547 [TBL] [Abstract][Full Text] [Related]
16. Walker-Warburg syndrome with microtia and absent auditory canals. Gershoni-Baruch R; Mandel H; Miller B; Sujov P; Braun J Am J Med Genet; 1990 Sep; 37(1):87-91. PubMed ID: 2240049 [TBL] [Abstract][Full Text] [Related]
17. Fukutin protein is expressed in neurons of the normal developing human brain but is reduced in Fukuyama-type congenital muscular dystrophy brain. Saito Y; Mizuguchi M; Oka A; Takashima S Ann Neurol; 2000 Jun; 47(6):756-64. PubMed ID: 10852541 [TBL] [Abstract][Full Text] [Related]
18. Fukuyama-type congenital muscular dystrophy: the first human disease to be caused by an ancient retrotransposal integration. Toda T; Kobayashi K J Mol Med (Berl); 1999 Dec; 77(12):816-23. PubMed ID: 10682317 [TBL] [Abstract][Full Text] [Related]
19. Muscle-eye-brain disease: a neuropathological study. Haltia M; Leivo I; Somer H; Pihko H; Paetau A; Kivelä T; Tarkkanen A; Tomé F; Engvall E; Santavuori P Ann Neurol; 1997 Feb; 41(2):173-80. PubMed ID: 9029066 [TBL] [Abstract][Full Text] [Related]
20. Fukuyama-type congenital muscular dystrophy and the Walker-Warburg syndrome. Kimura S; Sasaki Y; Kobayashi T; Ohtsuki N; Tanaka Y; Hara M; Miyake S; Yamada M; Iwamoto H; Misugi N Brain Dev; 1993; 15(3):182-91. PubMed ID: 8214343 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]