Osawa M - Search Results

1

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. Kobayashi K, et al. Among authors: osawa m. Nature. 1998 Jul 23;394(6691):388-92. doi: 10.1038/28653. Nature. 1998. PMID: 9690476

2

Linkage-disequilibrium mapping narrows the Fukuyama-type congenital muscular dystrophy (FCMD) candidate region to <100 kb.

Toda T, Miyake M, Kobayashi K, Mizuno K, Saito K, Osawa M, Nakamura Y, Kanazawa I, Nakagome Y, Tokunaga K, Nakahori Y. Toda T, et al. Among authors: osawa m. Am J Hum Genet. 1996 Dec;59(6):1313-20. Am J Hum Genet. 1996. PMID: 8940277 Free PMC article.

3

Prenatal diagnosis of Fukuyama type congenital muscular dystrophy by polymorphism analysis.

Kondo E, Saito K, Toda T, Osawa M, Yamamoto T, Kobayashi M, Fukuyama Y. Kondo E, et al. Among authors: osawa m. Am J Med Genet. 1996 Dec 11;66(2):169-74. doi: 10.1002/(SICI)1096-8628(19961211)66:2<169::AID-AJMG8>3.0.CO;2-M. Am J Med Genet. 1996. PMID: 8958324

4

Molecular genetic evidence of clinical heterogeneity in Fukuyama-type congenital muscular dystrophy.

Kondo-Iida E, Saito K, Tanaka H, Tsuji S, Ishihara T, Osawa M, Fukuyama Y, Toda T. Kondo-Iida E, et al. Among authors: osawa m. Hum Genet. 1997 Apr;99(4):427-32. doi: 10.1007/s004390050384. Hum Genet. 1997. PMID: 9099829

5

Polymorphism analysis of Fukuyama type congenital muscular dystrophy (FCMD) siblings with different phenotypes.

Kondo-Iida E, Saito K, Osawa M, Ishihara T, Toda T, Fukuyama Y. Kondo-Iida E, et al. Among authors: osawa m. Brain Dev. 1997 Apr;19(3):181-6. doi: 10.1016/s0387-7604(96)00556-6. Brain Dev. 1997. PMID: 9134189

6

Prenatal diagnosis of Fukuyama type congenital muscular dystrophy in eight Japanese families by haplotype analysis using new markers closest to the gene.

Saito K, Kondo-Iida E, Kawakita Y, Juan D, Ikeya K, Osawa M, Fukuyama Y, Toda T, Nakabayashi M, Yamamoto T, Kobayashi M. Saito K, et al. Among authors: osawa m. Am J Med Genet. 1998 May 26;77(4):310-6. Am J Med Genet. 1998. PMID: 9600742

7

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. Kondo-Iida E, et al. Among authors: osawa m. Hum Mol Genet. 1999 Nov;8(12):2303-9. doi: 10.1093/hmg/8.12.2303. Hum Mol Genet. 1999. PMID: 10545611

8

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. Saito K, et al. Among authors: osawa m. Am J Med Genet. 2000 May 29;92(3):184-90. doi: 10.1002/(sici)1096-8628(20000529)92:3<184::aid-ajmg5>3.0.co;2-n. Am J Med Genet. 2000. PMID: 10817652

9

Pial-glial barrier abnormalities in fetuses with Fukuyama congenital muscular dystrophy.

Yamamoto T, Toyoda C, Kobayashi M, Kondo E, Saito K, Osawa M. Yamamoto T, et al. Among authors: osawa m. Brain Dev. 1997 Jan;19(1):35-42. doi: 10.1016/s0387-7604(96)00056-3. Brain Dev. 1997. PMID: 9071488

10

Early ultrastructural changes in the central nervous system in Fukuyama congenital muscular dystrophy.

Yamamoto T, Shibata N, Kanazawa M, Kobayashi M, Komori T, Kondo E, Saito K, Osawa M. Yamamoto T, et al. Among authors: osawa m. Ultrastruct Pathol. 1997 Jul-Aug;21(4):355-60. doi: 10.3109/01913129709021933. Ultrastruct Pathol. 1997. PMID: 9206000

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