Watanabe S - Search Results

1

[Case of infantile autism with pediatric Wernicke's encephalopathy due to severe eating disorder].

Watanabe S, Yamakura S, Hirano K, Okumura Y, Aiba H. Watanabe S, et al. No To Hattatsu. 2009 Jan;41(1):43-6. No To Hattatsu. 2009. PMID: 19172816 Japanese.

2

[Effect of tacrolimus in a case of autoimmune encephalitis].

Hirano K, Aiba H, Yano M, Watanabe S, Okumura Y, Takahashi Y. Hirano K, et al. Among authors: watanabe s. No To Hattatsu. 2007 Nov;39(6):436-9. No To Hattatsu. 2007. PMID: 18027565 Japanese.

3

[Studies on bone mineral status with bone quantitative ultrasonography in severely handicapped school children--correlations with gross motor function and dietary status].

Watanabe S, Inakazu E, Yano M, Endo Y, Okumura Y, Hirano K, Aiba H. Watanabe S, et al. No To Hattatsu. 2012 Jul;44(4):327-32. No To Hattatsu. 2012. PMID: 22844766 Japanese.

4

[A case of acute encephalitis with refractory repetitive partial seizures successfully controlled by very-high-dose phenobarbital therapy found in a boy].

Watanabe S, Okumura Y, Aiba H. Watanabe S, et al. No To Hattatsu. 2014 Nov;46(6):443-6. No To Hattatsu. 2014. PMID: 25558588 Japanese.

5

Coexistence of a CAV3 mutation and a DMD deletion in a family with complex muscular diseases.

Hiraide T, Ogata T, Watanabe S, Nakashima M, Fukuda T, Saitsu H. Hiraide T, et al. Among authors: watanabe s. Brain Dev. 2019 May;41(5):474-479. doi: 10.1016/j.braindev.2019.01.005. Epub 2019 Feb 2. Brain Dev. 2019. PMID: 30723005

6

POLR3A variants in striatal involvement without diffuse hypomyelination.

Hiraide T, Kubota K, Kono Y, Watanabe S, Matsubayashi T, Nakashima M, Kaname T, Fukao T, Shimozawa N, Ogata T, Saitsu H. Hiraide T, et al. Among authors: watanabe s. Brain Dev. 2020 Apr;42(4):363-368. doi: 10.1016/j.braindev.2019.12.012. Epub 2020 Jan 10. Brain Dev. 2020. PMID: 31932101

7

A de novo TOP2B variant associated with global developmental delay and autism spectrum disorder.

Hiraide T, Watanabe S, Matsubayashi T, Yanagi K, Nakashima M, Ogata T, Saitsu H. Hiraide T, et al. Among authors: watanabe s. Mol Genet Genomic Med. 2020 Mar;8(3):e1145. doi: 10.1002/mgg3.1145. Epub 2020 Jan 17. Mol Genet Genomic Med. 2020. PMID: 31953910 Free PMC article.

8

Clinical and molecular genetic characterization of two siblings with trisomy 2p24.3-pter and monosomy 5p14.3-pter.

Fukushi D, Kurosawa K, Suzuki Y, Suzuki K, Yamada K, Watanabe S, Yokochi K, Wakamatsu N. Fukushi D, et al. Among authors: watanabe s. Am J Med Genet A. 2017 Aug;173(8):2201-2209. doi: 10.1002/ajmg.a.38313. Epub 2017 Jun 9. Am J Med Genet A. 2017. PMID: 28599099

9

De novo heterozygous variants in KIF5B cause kyphomelic dysplasia.

Itai T, Wang Z, Nishimura G, Ohashi H, Guo L, Wakano Y, Sugiura T, Hayakawa H, Okada M, Saisu T, Kitta A, Doi H, Kurosawa K, Hotta Y, Hosono K, Sato M, Shimizu K, Takikawa K, Watanabe S, Ikeda N, Suzuki M, Fujita A, Uchiyama Y, Tsuchida N, Miyatake S, Miyake N, Matsumoto N, Ikegawa S. Itai T, et al. Among authors: watanabe s. Clin Genet. 2022 Jul;102(1):3-11. doi: 10.1111/cge.14133. Epub 2022 Apr 5. Clin Genet. 2022. PMID: 35342932

10

Multielement-Doped Tungstic Acids via Submerged Photosynthesis for Enhanced All-Solar Photoelectrochemical Responses.

Lin HI, Jeem M, Zhang L, Watanabe S. Lin HI, et al. Among authors: watanabe s. ACS Appl Mater Interfaces. 2025 Jan 14. doi: 10.1021/acsami.4c19279. Online ahead of print. ACS Appl Mater Interfaces. 2025. PMID: 39810514

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