Momoi MY - Search Results

1

Mutation analysis of methyl-CpG binding protein family genes in autistic patients.

Li H, Yamagata T, Mori M, Yasuhara A, Momoi MY. Li H, et al. Among authors: momoi my. Brain Dev. 2005 Aug;27(5):321-5. doi: 10.1016/j.braindev.2004.08.003. Brain Dev. 2005. PMID: 15967618

2

Association of autism in two patients with hereditary multiple exostoses caused by novel deletion mutations of EXT1.

Li H, Yamagata T, Mori M, Momoi MY. Li H, et al. Among authors: momoi my. J Hum Genet. 2002;47(5):262-5. doi: 10.1007/s100380200036. J Hum Genet. 2002. PMID: 12032595

3

Dichloroacetate treatment for mitochondrial cytopathy: long-term effects in MELAS.

Mori M, Yamagata T, Goto T, Saito S, Momoi MY. Mori M, et al. Among authors: momoi my. Brain Dev. 2004 Oct;26(7):453-8. doi: 10.1016/j.braindev.2003.12.009. Brain Dev. 2004. PMID: 15351081 Clinical Trial.

4

RSK2 gene mutations in Coffin-Lowry syndrome with drop episodes.

Nakamura M, Yamagata T, Mori M, Momoi MY. Nakamura M, et al. Among authors: momoi my. Brain Dev. 2005 Mar;27(2):114-7. doi: 10.1016/j.braindev.2004.02.015. Brain Dev. 2005. PMID: 15668050

5

Absence of causative mutations and presence of autism-related allele in FOXP2 in Japanese autistic patients.

Li H, Yamagata T, Mori M, Momoi MY. Li H, et al. Among authors: momoi my. Brain Dev. 2005 Apr;27(3):207-10. doi: 10.1016/j.braindev.2004.06.002. Brain Dev. 2005. PMID: 15737702

6

Expression analysis and mutation detection of DLX5 and DLX6 in autism.

Nakashima N, Yamagata T, Mori M, Kuwajima M, Suwa K, Momoi MY. Nakashima N, et al. Among authors: momoi my. Brain Dev. 2010 Feb;32(2):98-104. doi: 10.1016/j.braindev.2008.12.021. Epub 2009 Feb 4. Brain Dev. 2010. PMID: 19195802

7

[A case of bilateral striatal necrosis associated with vesicular skin eruption].

Saitoh M, Yamagata T, Mizuguchi M, Momoi MY. Saitoh M, et al. Among authors: momoi my. No To Hattatsu. 2003 Nov;35(6):515-20. No To Hattatsu. 2003. PMID: 14631749 Review. Japanese.

8

[Magnetic resonance findings in a case of Gradenigo syndrome: widespread inflammation involving the paranasal sinuses and middle ear].

Yozu A, Suwa K, Mori M, Yamagata T, Mizuguchi M, Momoi MY. Yozu A, et al. Among authors: momoi my. No To Hattatsu. 2004 Jul;36(4):334-8. No To Hattatsu. 2004. PMID: 15272619 Japanese.

9

Early-onset ataxia with oculomotor apraxia with a novel APTX mutation.

Ito A, Yamagata T, Mori M, Momoi MY. Ito A, et al. Among authors: momoi my. Pediatr Neurol. 2005 Jul;33(1):53-6. doi: 10.1016/j.pediatrneurol.2005.01.012. Pediatr Neurol. 2005. PMID: 15876520

10

[Pediatric neurology practice after adolescence].

Momoi MY, Mori M. Momoi MY, et al. No To Hattatsu. 2005 May;37(3):208-13. No To Hattatsu. 2005. PMID: 15915735 Japanese.

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