Iwasaki N - Search Results

1

The evaluation of autonomic nervous function in a patient with hereditary sensory and autonomic neuropathy type IV with novel mutations of the TRKA gene.

Ohto T, Iwasaki N, Fujiwara J, Ohkoshi N, Kimura S, Kawade K, Tanaka R, Matsui A. Ohto T, et al. Among authors: iwasaki n. Neuropediatrics. 2004 Oct;35(5):274-8. doi: 10.1055/s-2004-821254. Neuropediatrics. 2004. PMID: 15534759

2

A pediatric case of critical illness polyneuropathy: clinical and pathological findings.

Ohto T, Iwasaki N, Ohkoshi N, Aoki T, Ichinohe M, Tanaka R, Moriyama N, Ieshima A, Kuwajima K, Matsui A. Ohto T, et al. Among authors: iwasaki n. Brain Dev. 2005 Oct;27(7):535-8. doi: 10.1016/j.braindev.2004.12.007. Epub 2005 Apr 11. Brain Dev. 2005. PMID: 16198212

3

Mutation analysis of the leucine-rich, glioma inactivated 1 gene (LGI1) in Japanese febrile seizure patients.

Nakayama J, Hamano K, Iwasaki N, Ohta M, Nakahara S, Matsui A, Arinami T. Nakayama J, et al. Among authors: iwasaki n. Neuropediatrics. 2003 Jun;34(5):234-6. doi: 10.1055/s-2003-43255. Neuropediatrics. 2003. PMID: 14598228

4

[A case of infantile epileptic apnea with congenital brain anomaly].

Ohto T, Iwasaki N, Takahashi M, Tanaka R, Hamano K, Matsui A. Ohto T, et al. Among authors: iwasaki n. No To Hattatsu. 2003 Nov;35(6):511-4. No To Hattatsu. 2003. PMID: 14631748 Japanese.

5

Life-threatening vocal cord paralysis in a patient with group A xeroderma pigmentosum.

Ohto T, Iwasaki N, Okubo H, Shin K, Matsui A. Ohto T, et al. Among authors: iwasaki n. Pediatr Neurol. 2004 Mar;30(3):222-4. doi: 10.1016/j.pediatrneurol.2003.09.009. Pediatr Neurol. 2004. PMID: 15033209

6

Evaluation of hippocampal infolding using magnetic resonance imaging.

Okada Y, Kato T, Iwai K, Iwasaki N, Ohto T, Matsui A. Okada Y, et al. Among authors: iwasaki n. Neuroreport. 2003 Jul 18;14(10):1405-9. doi: 10.1097/01.wnr.0000078381.40088.d0. Neuroreport. 2003. PMID: 12876483

7

Significant evidence for linkage of febrile seizures to chromosome 5q14-q15.

Nakayama J, Hamano K, Iwasaki N, Nakahara S, Horigome Y, Saitoh H, Aoki T, Maki T, Kikuchi M, Migita T, Ohto T, Yokouchi Y, Tanaka R, Hasegawa M, Matsui A, Hamaguchi H, Arinami T. Nakayama J, et al. Among authors: iwasaki n. Hum Mol Genet. 2000 Jan 1;9(1):87-91. doi: 10.1093/hmg/9.1.87. Hum Mol Genet. 2000. PMID: 10587582

8

Abnormal brain MRI signal in 18q-syndrome not due to dysmyelination.

Tanaka R, Iwasaki N, Hayashi M, Nakayama J, Ohto T, Takahashi M, Numano T, Homma K, Hamano K, Sumazaki R. Tanaka R, et al. Among authors: iwasaki n. Brain Dev. 2012 Mar;34(3):234-7. doi: 10.1016/j.braindev.2011.05.008. Epub 2011 Jun 12. Brain Dev. 2012. PMID: 21669507

9

Monozygotic twins with de novo ZIC2 gene mutations discordant for the type of holoprosencephaly.

Nakayama J, Kinugasa H, Ohto T, Tanaka R, Nakayama T, Noguchi E, Arinami T, Iwasaki N. Nakayama J, et al. Among authors: iwasaki n. Neurology. 2016 Apr 12;86(15):1456-1458. doi: 10.1212/WNL.0000000000002567. Epub 2016 Mar 9. Neurology. 2016. PMID: 26962069 No abstract available.

10

A quantitative study of the progress of myelination in the rat central nervous system, using the immunohistochemical method for proteolipid protein.

Hamano K, Takeya T, Iwasaki N, Nakayama J, Ohto T, Okada Y. Hamano K, et al. Among authors: iwasaki n. Brain Res Dev Brain Res. 1998 Jun 15;108(1-2):287-93. doi: 10.1016/s0165-3806(98)00063-7. Brain Res Dev Brain Res. 1998. PMID: 9693804

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