Momoi MY - Search Results

1

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

2

Non-invasive screening of fragile X syndrome A using urine and hair roots.

Suwa K, Momoi MY. Suwa K, et al. Among authors: momoi my. Brain Dev. 2004 Sep;26(6):380-3. doi: 10.1016/j.braindev.2003.11.002. Brain Dev. 2004. PMID: 15275700

3

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

4

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

5

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

6

Late-onset Leigh syndrome with myoclonic epilepsy with ragged-red fibers.

Monden Y, Mori M, Kuwajima M, Goto T, Yamagata T, Momoi MY. Monden Y, et al. Among authors: momoi my. Brain Dev. 2013 Jun;35(6):582-5. doi: 10.1016/j.braindev.2012.08.006. Epub 2012 Sep 13. Brain Dev. 2013. PMID: 22981260

7

[NARP].

Yamagata T, Momoi MY. Yamagata T, et al. Among authors: momoi my. Nihon Rinsho. 2002 Apr;60 Suppl 4:298-301. Nihon Rinsho. 2002. PMID: 12013870 Review. Japanese. No abstract available.

8

[Pure mitochondrial myopathy].

Mori M, Momoi MY. Mori M, et al. Among authors: momoi my. Nihon Rinsho. 2002 Apr;60 Suppl 4:302-5. Nihon Rinsho. 2002. PMID: 12013872 Review. Japanese. No abstract available.

9

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

10

[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.

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