Wada H - Search Results

1

Amino-terminal deletion of 53% of dystrophin results in an intermediate Duchenne-Becker muscular dystrophy phenotype.

Takeshima Y, Nishio H, Narita N, Wada H, Ishikawa Y, Ishikawa Y, Minami R, Nakamura H, Matsuo M. Takeshima Y, et al. Among authors: wada h. Neurology. 1994 Sep;44(9):1648-51. doi: 10.1212/wnl.44.9.1648. Neurology. 1994. PMID: 7936290

2

Decreased expression of full-length mRNA for cBCD541 does not correlate with spinal muscular atrophy phenotype severity.

Nishio H, Ishikawa Y, Lee MJ, Fujii M, Kanda F, Jinnai K, Takahashi K, Takeshima Y, Wada H, Takada S, Nakamura H, Matsuo M, Sumino K. Nishio H, et al. Among authors: wada h. Neurology. 1997 May;48(5):1266-70. doi: 10.1212/wnl.48.5.1266. Neurology. 1997. PMID: 9153454

3

High incidence of a survival motor neuron gene/cBCD541 gene ratio of 2 in Japanese parents of spinal muscular atrophy patients: a characteristic background of spinal muscular atrophy in Japan?

Nishio H, Ishikawa Y, Lee MJ, Takeshima Y, Wada H, Takada S, Nakamura H, Matsuo M, Sumino K. Nishio H, et al. Among authors: wada h. J Neurol. 1999 Jan;246(1):48-52. doi: 10.1007/s004150050305. J Neurol. 1999. PMID: 9987714

4

Complete skipping of exon 66 due to novel mutations of the dystrophin gene was identified in two Japanese families of Duchenne muscular dystrophy with severe mental retardation.

Wibawa T, Takeshima Y, Mitsuyoshi I, Wada H, Surono A, Nakamura H, Matsuo M. Wibawa T, et al. Among authors: wada h. Brain Dev. 2000 Mar;22(2):107-12. doi: 10.1016/s0387-7604(99)00126-6. Brain Dev. 2000. PMID: 10722962

5

Oligonucleotides against a splicing enhancer sequence led to dystrophin production in muscle cells from a Duchenne muscular dystrophy patient.

Takeshima Y, Wada H, Yagi M, Ishikawa Y, Ishikawa Y, Minami R, Nakamura H, Matsuo M. Takeshima Y, et al. Among authors: wada h. Brain Dev. 2001 Dec;23(8):788-90. doi: 10.1016/s0387-7604(01)00326-6. Brain Dev. 2001. PMID: 11720794 No abstract available.

6

Analysis of dystrophin mRNA from skeletal muscle but not from lymphocytes led to identification of a novel nonsense mutation in a carrier of Duchenne muscular dystrophy.

Ito T, Takeshima Y, Yagi M, Kamei S, Wada H, Nakamura H, Matsuo M. Ito T, et al. Among authors: wada h. J Neurol. 2003 May;250(5):581-7. doi: 10.1007/s00415-003-1040-1. J Neurol. 2003. PMID: 12736738

7

A novel point mutation (G-1 to T) in a 5' splice donor site of intron 13 of the dystrophin gene results in exon skipping and is responsible for Becker muscular dystrophy.

Hagiwara Y, Nishio H, Kitoh Y, Takeshima Y, Narita N, Wada H, Yokoyama M, Nakamura H, Matsuo M. Hagiwara Y, et al. Among authors: wada h. Am J Hum Genet. 1994 Jan;54(1):53-61. Am J Hum Genet. 1994. PMID: 8279470 Free PMC article.

8

Cardiac involvement in a family with Becker muscular dystrophy.

Yu Y, Yamabe H, Fujita H, Inoue T, Yokota Y, Nishio H, Wada H, Matsuo M, Yokoyama M. Yu Y, et al. Among authors: wada h. Intern Med. 1995 Sep;34(9):919-23. doi: 10.2169/internalmedicine.34.919. Intern Med. 1995. PMID: 8580570 Free article.

9

Hybrid survival motor neuron genes in Japanese patients with spinal muscular atrophy.

Nishio H, Horikawa H, Yakura H, Sugie K, Nakamuro T, Koterazawa K, Ishikawa Y, Lee MJ, Wada H, Takeshima Y, Matsuo M, Sumino K. Nishio H, et al. Among authors: wada h. Acta Neurol Scand. 1999 Jun;99(6):374-80. doi: 10.1111/j.1600-0404.1999.tb07367.x. Acta Neurol Scand. 1999. PMID: 10577272

10

Glucose, free fatty acid and ketone body metabolism in Duchenne muscular dystrophy.

Nishio H, Wada H, Matsuo T, Horikawa H, Takahashi K, Nakajima T, Matsuo M, Nakamura H. Nishio H, et al. Among authors: wada h. Brain Dev. 1990;12(4):390-402. doi: 10.1016/s0387-7604(12)80071-4. Brain Dev. 1990. PMID: 2240459

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