Saitoh S - Search Results

1

MERRF/MELAS overlap syndrome: a double pathogenic mutation in mitochondrial tRNA genes.

Nakamura M, Yabe I, Sudo A, Hosoki K, Yaguchi H, Saitoh S, Sasaki H. Nakamura M, et al. Among authors: saitoh s. J Med Genet. 2010 Oct;47(10):659-64. doi: 10.1136/jmg.2009.072058. Epub 2010 Jul 7. J Med Genet. 2010. PMID: 20610441 Free article.

2

Array comparative genomic hybridization analysis revealed four genomic prognostic biomarkers for primary gastric cancers.

Tomioka N, Morita K, Kobayashi N, Tada M, Itoh T, Saitoh S, Kondo M, Takahashi N, Kataoka A, Nakanishi K, Takahashi M, Kamiyama T, Ozaki M, Hirano T, Todo S. Tomioka N, et al. Among authors: saitoh s. Cancer Genet Cytogenet. 2010 Aug;201(1):6-14. doi: 10.1016/j.cancergencyto.2010.04.017. Cancer Genet Cytogenet. 2010. PMID: 20633762

3

Molecular genetic analysis of 30 families with Joubert syndrome.

Suzuki T, Miyake N, Tsurusaki Y, Okamoto N, Alkindy A, Inaba A, Sato M, Ito S, Muramatsu K, Kimura S, Ieda D, Saitoh S, Hiyane M, Suzumura H, Yagyu K, Shiraishi H, Nakajima M, Fueki N, Habata Y, Ueda Y, Komatsu Y, Yan K, Shimoda K, Shitara Y, Mizuno S, Ichinomiya K, Sameshima K, Tsuyusaki Y, Kurosawa K, Sakai Y, Haginoya K, Kobayashi Y, Yoshizawa C, Hisano M, Nakashima M, Saitsu H, Takeda S, Matsumoto N. Suzuki T, et al. Among authors: saitoh s. Clin Genet. 2016 Dec;90(6):526-535. doi: 10.1111/cge.12836. Epub 2016 Sep 26. Clin Genet. 2016. PMID: 27434533

4

[Angelman syndrome].

Saitoh S. Saitoh S. Ryoikibetsu Shokogun Shirizu. 2001;(33):193-5. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11462396 Review. Japanese. No abstract available.

5

Phenotypic variability in a family with a mitochondrial DNA T8993C mutation.

Suzuki Y, Wada T, Sakai T, Ishikawa Y, Minami R, Tachi N, Saitoh S. Suzuki Y, et al. Among authors: saitoh s. Pediatr Neurol. 1998 Oct;19(4):283-6. doi: 10.1016/s0887-8994(98)00070-8. Pediatr Neurol. 1998. PMID: 9830999

6

Effects of dichloroacetate in three patients with MELAS.

Saitoh S, Momoi MY, Yamagata T, Mori Y, Imai M. Saitoh S, et al. Neurology. 1998 Feb;50(2):531-4. doi: 10.1212/wnl.50.2.531. Neurology. 1998. PMID: 9484392 Clinical Trial.

7

Cortical reflex myoclonus associated with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS): a case report.

Saitoh S, Kohsaka S, Mizukami S, Kajii N. Saitoh S, et al. Brain Dev. 1992 Jul;14(4):260-3. doi: 10.1016/s0387-7604(12)80244-0. Brain Dev. 1992. PMID: 1443410

8

Successful cochlear implantation in a patient with mitochondrial hearing loss and m.625G>A transition.

Sudo A, Takeichi N, Hosoki K, Saitoh S. Sudo A, et al. Among authors: saitoh s. J Laryngol Otol. 2011 Dec;125(12):1282-5. doi: 10.1017/S0022215111002453. Epub 2011 Sep 14. J Laryngol Otol. 2011. PMID: 21914246

9

Single-cell analysis of mitochondrial DNA in patients and a carrier of the tRNA(Leu)(UUR) gene mutation.

Saitoh S, Momoi MY, Yamagata T, Nakauchi H, Nihei K, Fujii M. Saitoh S, et al. J Inherit Metab Dis. 1999 Jun;22(5):608-14. doi: 10.1023/a:1005569711521. J Inherit Metab Dis. 1999. PMID: 10399093

10

[Marshall syndrome].

Saitoh S. Saitoh S. Ryoikibetsu Shokogun Shirizu. 2000;(30 Pt 5):209-10. Ryoikibetsu Shokogun Shirizu. 2000. PMID: 11057199 Review. Japanese. No abstract available.

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