Ochiai Y - Search Results

1

Further delineation of the behavioral and neurologic features in Costello syndrome.

Kawame H, Matsui M, Kurosawa K, Matsuo M, Masuno M, Ohashi H, Fueki N, Aoyama K, Miyatsuka Y, Suzuki K, Akatsuka A, Ochiai Y, Fukushima Y. Kawame H, et al. Among authors: ochiai y. Am J Med Genet A. 2003 Apr 1;118A(1):8-14. doi: 10.1002/ajmg.a.10236. Am J Med Genet A. 2003. PMID: 12605434

2

Patellar dislocation in Kabuki syndrome.

Kurosawa K, Kawame H, Ochiai Y, Nakashima M, Tohma T, Ohashi H. Kurosawa K, et al. Among authors: ochiai y. Am J Med Genet. 2002 Mar 1;108(2):160-3. doi: 10.1002/ajmg.10247. Am J Med Genet. 2002. PMID: 11857567

3

Epilepsy and neurological findings in 11 individuals with 1p36 deletion syndrome.

Kurosawa K, Kawame H, Okamoto N, Ochiai Y, Akatsuka A, Kobayashi M, Shimohira M, Mizuno S, Wada K, Fukushima Y, Kawawaki H, Yamamoto T, Masuno M, Imaizumi K, Kuroki Y. Kurosawa K, et al. Among authors: ochiai y. Brain Dev. 2005 Aug;27(5):378-82. doi: 10.1016/j.braindev.2005.02.004. Epub 2005 Apr 13. Brain Dev. 2005. PMID: 16023556

4

Self-induced vomiting in X-linked alpha-thalassemia/mental retardation syndrome.

Kurosawa K, Akatsuka A, Ochiai Y, Ikeda J, Maekawa K. Kurosawa K, et al. Among authors: ochiai y. Am J Med Genet. 1996 Jun 14;63(3):505-6. doi: 10.1002/ajmg.1320630304. Am J Med Genet. 1996. PMID: 8967323 No abstract available.

5

A Japanese patient with X-linked alpha-thalassemia/mental retardation syndrome: an additional case report.

Kurosawa K, Asoh M, Akatsuka A, Matsuo T, Ochiai Y, Maekawa K. Kurosawa K, et al. Among authors: ochiai y. Jpn J Hum Genet. 1996 Sep;41(3):329-32. doi: 10.1007/BF01913176. Jpn J Hum Genet. 1996. PMID: 8996969

6

[Clinical spectrum and management of holoprosencephaly].

Kawame H, Kurosawa K, Akatsuka A, Ochiai Y. Kawame H, et al. Among authors: ochiai y. No To Hattatsu. 2000 Jul;32(4):301-6. No To Hattatsu. 2000. PMID: 10916368 Japanese.

7

Polymicrogyria is an uncommon manifestation in 22q11.2 deletion syndrome.

Kawame H, Kurosawa K, Akatsuka A, Ochiai Y, Mizuno K. Kawame H, et al. Among authors: ochiai y. Am J Med Genet. 2000 Sep 4;94(1):77-8. doi: 10.1002/1096-8628(20000904)94:1<77::aid-ajmg16>3.0.co;2-v. Am J Med Genet. 2000. PMID: 10982488 No abstract available.

8

Gonadal sex cord stromal tumor in a patient with Rubinstein-Taybi syndrome.

Kurosawa K, Fukutani K, Masuno M, Kawame H, Ochiai Y. Kurosawa K, et al. Among authors: ochiai y. Pediatr Int. 2002 Jun;44(3):330-2. doi: 10.1046/j.1442-200x.2002.01539.x. Pediatr Int. 2002. PMID: 11982910 No abstract available.

9

Studies on chromosomal anomaly syndrome with epilepsy.

Sugama S, Akatsuka A, Ochiai Y, Tsuzura S, Maekawa K. Sugama S, et al. Among authors: ochiai y. Jpn J Psychiatry Neurol. 1993 Jun;47(2):283-5. doi: 10.1111/j.1440-1819.1993.tb02074.x. Jpn J Psychiatry Neurol. 1993. PMID: 8271565 No abstract available.

10

[Clinical consideration of patients with neonatal bilateral basal ganglia-thalamic lesion due to hypoxic ischemic encephalopathy].

Sugama S, Atsukawa K, Kusano K, Akatsuka A, Ochiai Y, Tsuzura S, Maekawa K. Sugama S, et al. Among authors: ochiai y. No To Hattatsu. 1994 Jul;26(4):295-301. No To Hattatsu. 1994. PMID: 8074889 Japanese.

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