Ono J - Search Results

1

Analysis of all exons of TSC1 and TSC2 genes for germline mutations in Japanese patients with tuberous sclerosis: report of 10 mutations.

Yamashita Y, Ono J, Okada S, Wataya-Kaneda M, Yoshikawa K, Nishizawa M, Hirayama Y, Kobayashi E, Seyama K, Hino O. Yamashita Y, et al. Among authors: ono j. Am J Med Genet. 2000 Jan 17;90(2):123-6. Am J Med Genet. 2000. PMID: 10607950

2

Alteration of the LIS1 gene in Japanese patients with isolated lissencephaly sequence or Miller-Dieker syndrome.

Sakamoto M, Ono J, Okada S, Masuno M, Nakamura Y, Kurahashi H. Sakamoto M, et al. Among authors: ono j. Hum Genet. 1998 Nov;103(5):586-9. doi: 10.1007/s004390050873. Hum Genet. 1998. PMID: 9860301

3

Genetic alteration of the DCX gene in Japanese patients with subcortical laminar heterotopia or isolated lissencephaly sequence.

Sakamoto M, Ono J, Okada S, Nakamura Y, Kurahashi H. Sakamoto M, et al. Among authors: ono j. J Hum Genet. 2000;45(3):167-70. doi: 10.1007/s100380050204. J Hum Genet. 2000. PMID: 10807542

4

Mutational analysis of MECP2 in Japanese patients with atypical Rett syndrome.

Inui K, Akagi M, Ono J, Tsukamoto H, Shimono K, Mano T, Imai K, Yamada M, Muramatsu T, Sakai N, Okada S. Inui K, et al. Among authors: ono j. Brain Dev. 2001 Jul;23(4):212-5. doi: 10.1016/s0387-7604(01)00197-8. Brain Dev. 2001. PMID: 11376998

5

Partial deletion of the long arm of chromosome 11: ten Japanese children.

Ono J, Hasegawa T, Sugama S, Sagehashi N, Hase Y, Oku K, Endo Y, Ohdo S, Ishikiriyama S, Tsukamoto H, Okada S. Ono J, et al. Clin Genet. 1996 Dec;50(6):474-8. doi: 10.1111/j.1399-0004.1996.tb02715.x. Clin Genet. 1996. PMID: 9147876

6

Molecular cloning of the chromosomal breakpoint in the LIS1 gene of a patient with isolated lissencephaly and balanced t(8;17).

Kurahashi H, Sakamoto M, Ono J, Honda A, Okada S, Nakamura Y. Kurahashi H, et al. Among authors: ono j. Hum Genet. 1998 Aug;103(2):189-92. doi: 10.1007/s004390050805. Hum Genet. 1998. PMID: 9760204

7

Treatment Outcome of Carotid Stenting and CEA in the Same Period.

Kobayashi E, Uchino Y, Ono J, Yamaura A. Kobayashi E, et al. Among authors: ono j. Interv Neuroradiol. 2004 Mar 30;10 Suppl 1(Suppl 1):93-6. doi: 10.1177/15910199040100S114. Epub 2008 Jun 9. Interv Neuroradiol. 2004. PMID: 20587280 Free PMC article.

8

Central nervous system abnormalities in chromosome deletion at 11q23.

Ono J, Harada K, Hasegawa T, Sakurai K, Kodaka R, Tanabe Y, Tanaka J, Igarashi T, Nagai T, Okada S. Ono J, et al. Clin Genet. 1994 Jun;45(6):325-9. doi: 10.1111/j.1399-0004.1994.tb04042.x. Clin Genet. 1994. PMID: 7523004

9

MR findings and neurologic manifestations in Lowe oculocerebrorenal syndrome.

Ono J, Harada K, Mano T, Yamamoto T, Okada S. Ono J, et al. Pediatr Neurol. 1996 Feb;14(2):162-4. doi: 10.1016/0887-8994(96)83274-7. Pediatr Neurol. 1996. PMID: 8703232

10

Ring chromosome 14 complicated with complex partial seizures and hypoplastic corpus callosum.

Ono J, Nishiike K, Imai K, Otani K, Okada S. Ono J, et al. Pediatr Neurol. 1999 Jan;20(1):70-2. doi: 10.1016/s0887-8994(98)00099-x. Pediatr Neurol. 1999. PMID: 10029266

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