Momoi MY - Search Results

1

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

2

[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.

3

[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.

4

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

5

[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.

6

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.

7

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

8

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

9

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

10

Two new XPD patients compound heterozygous for the same mutation demonstrate diverse clinical features.

Fujimoto M, Leech SN, Theron T, Mori M, Fawcett H, Botta E, Nozaki Y, Yamagata T, Moriwaki S, Stefanini M, Momoi MY, Nakagawa H, Shuster S, Moss C, Lehmann AR. Fujimoto M, et al. Among authors: momoi my. J Invest Dermatol. 2005 Jul;125(1):86-92. doi: 10.1111/j.0022-202X.2005.23745.x. J Invest Dermatol. 2005. PMID: 15982307 Free article.

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