Okada S - Search Results

1

Interstitial deletion of 14q, 46, XY, del (14) (q24.3q32.1) associated with status nonepileptic myoclonia and delayed myelination.

Ono J, Kurahashi H, Okinaga T, Mano T, Imai K, Inui K, Okada S. Ono J, et al. Among authors: okada s. J Child Neurol. 1999 Nov;14(11):756-8. doi: 10.1177/088307389901401116. J Child Neurol. 1999. PMID: 10593558 Review.

2

Delayed myelination in a patient with 18q- syndrome.

Ono J, Harada K, Yamamoto T, Onoe S, Okada S. Ono J, et al. Among authors: okada s. Pediatr Neurol. 1994 Jul;11(1):64-7. doi: 10.1016/0887-8994(94)90095-7. Pediatr Neurol. 1994. PMID: 7527214

3

MR findings and neurologic manifestations in Lowe oculocerebrorenal syndrome.

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

4

Band heterotopia or double cortex in a male: bridging structures suggest abnormality of the radial glial guide system.

Ono J, Mano T, Andermann E, Harada K, Sakurai K, Ikeda T, Yoshihara N, Shimizu K, Okada S, Andermann F. Ono J, et al. Among authors: okada s. Neurology. 1997 Jun;48(6):1701-3. doi: 10.1212/wnl.48.6.1701. Neurology. 1997. PMID: 9191790

5

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. Among authors: okada s. Pediatr Neurol. 1999 Jan;20(1):70-2. doi: 10.1016/s0887-8994(98)00099-x. Pediatr Neurol. 1999. PMID: 10029266

6

Evaluation of myelination by means of the T2 value on magnetic resonance imaging.

Ono J, Kodaka R, Imai K, Itagaki Y, Tanaka J, Inui K, Nagai T, Sakurai K, Harada K, Okada S. Ono J, et al. Among authors: okada s. Brain Dev. 1993 Nov-Dec;15(6):433-8. doi: 10.1016/0387-7604(93)90083-k. Brain Dev. 1993. PMID: 8147502

7

Differentiation of dys- and demyelination using diffusional anisotropy.

Ono J, Harada K, Mano T, Sakurai K, Okada S. Ono J, et al. Among authors: okada s. Pediatr Neurol. 1997 Jan;16(1):63-6. doi: 10.1016/s0887-8994(96)00249-4. Pediatr Neurol. 1997. PMID: 9044406

8

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. Among authors: okada s. Clin Genet. 1996 Dec;50(6):474-8. doi: 10.1111/j.1399-0004.1996.tb02715.x. Clin Genet. 1996. PMID: 9147876

9

Regional cortical dysplasia associated with suspected hypomelanosis of Ito.

Ono J, Harada K, Kodaka R, Ishida M, Okada S. Ono J, et al. Among authors: okada s. Pediatr Neurol. 1997 Oct;17(3):252-4. doi: 10.1016/s0887-8994(97)00084-2. Pediatr Neurol. 1997. PMID: 9390703

10

Isolated lissencephaly sequence with balanced chromosome translocation involving 17p13.3.

Honda A, Ono J, Kurahashi H, Mano T, Imai K, Okada S. Honda A, et al. Among authors: okada s. Brain Dev. 1998 Apr;20(3):190-2. doi: 10.1016/s0387-7604(98)00018-7. Brain Dev. 1998. PMID: 9628198

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