Naito E - Search Results

1

[Case of methylmalonic acidemia presenting clinically Leigh encephalopathy].

Ito H, Mori K, Ito M, Naito E, Yokota I, Kuroda Y. Ito H, et al. Among authors: naito e. No To Hattatsu. 2004 Jul;36(4):324-9. No To Hattatsu. 2004. PMID: 15272617 Japanese.

2

Serial brain imaging analysis of stroke-like episodes in MELAS.

Ito H, Mori K, Harada M, Minato M, Naito E, Takeuchi M, Kuroda Y, Kagami S. Ito H, et al. Among authors: naito e. Brain Dev. 2008 Aug;30(7):483-8. doi: 10.1016/j.braindev.2008.01.003. Epub 2008 Mar 4. Brain Dev. 2008. PMID: 18289816

3

Transient left temporal lobe lesion in Menkes disease may influence the generation of tonic spasms.

Ito H, Mori K, Sakata M, Naito E, Harada M, Kagami S. Ito H, et al. Among authors: naito e. Brain Dev. 2011 Apr;33(4):345-8. doi: 10.1016/j.braindev.2010.05.009. Epub 2010 Jun 17. Brain Dev. 2011. PMID: 21382542

4

[A case with MELAS associated with epilepsia partialis continua].

Miyazaki M, Saijo T, Mori K, Tayama M, Naito E, Hashimoto T, Kuroda Y, Nonaka I. Miyazaki M, et al. Among authors: naito e. No To Hattatsu. 1991 Jan;23(1):65-70. No To Hattatsu. 1991. PMID: 1899796 Japanese.

5

Effect of sodium dichloroacetate on human pyruvate metabolism.

Naito E, Kuroda Y, Toshima K, Takeda E, Saijo T, Kobashi H, Yokota I, Ito M. Naito E, et al. Brain Dev. 1989;11(3):195-7. doi: 10.1016/s0387-7604(89)80098-1. Brain Dev. 1989. PMID: 2751069

6

[Defects of pyruvate metabolism in cultured lymphoblastoid cells of 20 patients with Leigh syndrome].

Naito E, Ito M, Yokota I, Saijo T, Matsuda J, Osaka H, Kimura S, Kuroda Y. Naito E, et al. No To Hattatsu. 1996 Nov;28(6):495-500. No To Hattatsu. 1996. PMID: 8940876 Japanese.

7

Biochemical and molecular analysis of an X-linked case of Leigh syndrome associated with thiamin-responsive pyruvate dehydrogenase deficiency.

Naito E, Ito M, Yokota I, Saijo T, Matsuda J, Osaka H, Kimura S, Kuroda Y. Naito E, et al. J Inherit Metab Dis. 1997 Aug;20(4):539-48. doi: 10.1023/a:1005305614374. J Inherit Metab Dis. 1997. PMID: 9266390

8

Three novel SURF-1 mutations in Japanese patients with Leigh syndrome.

Ogawa Y, Naito E, Ito M, Yokota I, Saijo T, Shinahara K, Kuroda Y. Ogawa Y, et al. Among authors: naito e. Pediatr Neurol. 2002 Mar;26(3):196-200. doi: 10.1016/s0887-8994(01)00382-4. Pediatr Neurol. 2002. PMID: 11955926

9

Diagnosis and molecular analysis of three male patients with thiamine-responsive pyruvate dehydrogenase complex deficiency.

Naito E, Ito M, Yokota I, Saijo T, Ogawa Y, Kuroda Y. Naito E, et al. J Neurol Sci. 2002 Sep 15;201(1-2):33-7. doi: 10.1016/s0022-510x(02)00187-9. J Neurol Sci. 2002. PMID: 12163191

10

Thiamine-responsive pyruvate dehydrogenase deficiency in two patients caused by a point mutation (F205L and L216F) within the thiamine pyrophosphate binding region.

Naito E, Ito M, Yokota I, Saijo T, Matsuda J, Ogawa Y, Kitamura S, Takada E, Horii Y, Kuroda Y. Naito E, et al. Biochim Biophys Acta. 2002 Oct 9;1588(1):79-84. doi: 10.1016/s0925-4439(02)00142-4. Biochim Biophys Acta. 2002. PMID: 12379317 Free article.

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