Itoh M - Search Results

1

PKD1-Associated Arachnoid Cysts in Autosomal Dominant Polycystic Kidney Disease.

Shigemori K, Higashihara E, Itoh M, Yoshida H, Yamamoto K, Nutahara K, Shiokawa Y, Kaname S, Tambo M, Yamaguchi T, Taguchi S, Yoshioka T, Yokoyama K, Fukuhara H. Shigemori K, et al. Among authors: itoh m. J Stroke Cerebrovasc Dis. 2021 Sep;30(9):105943. doi: 10.1016/j.jstrokecerebrovasdis.2021.105943. Epub 2021 Jun 25. J Stroke Cerebrovasc Dis. 2021. PMID: 34175641 Free article.

2

Long-Term Outcomes of Longitudinal Efficacy Study With Tolvaptan in ADPKD.

Higashihara E, Nutahara K, Itoh M, Okegawa T, Tambo M, Yamaguchi T, Nakamura Y, Taguchi S, Kaname S, Yokoyama K, Yoshioka T, Fukuhara H. Higashihara E, et al. Among authors: itoh m. Kidney Int Rep. 2021 Dec 8;7(2):270-281. doi: 10.1016/j.ekir.2021.11.034. eCollection 2022 Feb. Kidney Int Rep. 2021. PMID: 35155866 Free PMC article.

3

Structural and functional changes in the brains of patients with Rett syndrome: A multimodal MRI study.

Takeguchi R, Kuroda M, Tanaka R, Suzuki N, Akaba Y, Tsujimura K, Itoh M, Takahashi S. Takeguchi R, et al. Among authors: itoh m. J Neurol Sci. 2022 Oct 15;441:120381. doi: 10.1016/j.jns.2022.120381. Epub 2022 Aug 18. J Neurol Sci. 2022. PMID: 36027642

4

Two Siblings Showing a Mild Phenotype of Joubert Syndrome with a Specific CEP290 Variant.

Uda D, Kondo H, Tanda K, Kizaki Z, Nishida M, Dai H, Itoh M. Uda D, et al. Among authors: itoh m. Neuropediatrics. 2023 Jun;54(3):217-221. doi: 10.1055/a-1865-6890. Epub 2022 May 31. Neuropediatrics. 2023. PMID: 35642300

5

Long-Surviving Adult Siblings With Joubert Syndrome Harboring a Novel Compound Heterozygous CPLANE1 Variant.

Matoba K, Chihara N, Satake W, Tokuoka H, Otsuka Y, Ueda T, Sekiguchi K, Itoh M, Matsumoto R. Matoba K, et al. Among authors: itoh m. Neurol Genet. 2022 Sep 26;8(5):e200031. doi: 10.1212/NXG.0000000000200031. eCollection 2022 Oct. Neurol Genet. 2022. PMID: 36176335 Free PMC article.

6

Reply to the letter: "nationwide survey of Arima syndrome: revised diagnostic criteria from epidemiological analysis".

Itoh M, Iwasaki Y, Hayashi M, Arima M. Itoh M, et al. Brain Dev. 2014 Jan;36(1):89. doi: 10.1016/j.braindev.2013.08.012. Epub 2013 Sep 21. Brain Dev. 2014. PMID: 24063856 No abstract available.

7

Two siblings with cortical dysplasia: Clinico-electroencephalographic features.

Fukasawa T, Kubota T, Negoro T, Maruyama S, Honda R, Saito Y, Itoh M, Kakita A, Sugai K, Otsuki T, Kato M, Natsume J, Watanabe K. Fukasawa T, et al. Among authors: itoh m. Pediatr Int. 2015 Jun;57(3):472-5. doi: 10.1111/ped.12509. Epub 2015 May 27. Pediatr Int. 2015. PMID: 26012518

8

MeCP2_e2 partially compensates for lack of MeCP2_e1: A male case of Rett syndrome.

Takeguchi R, Takahashi S, Kuroda M, Tanaka R, Suzuki N, Tomonoh Y, Ihara Y, Sugiyama N, Itoh M. Takeguchi R, et al. Among authors: itoh m. Mol Genet Genomic Med. 2020 Feb;8(2):e1088. doi: 10.1002/mgg3.1088. Epub 2019 Dec 9. Mol Genet Genomic Med. 2020. PMID: 31816669 Free PMC article.

9

An 11-month-old boy with intractable epilepsy from birth.

Itoh M. Itoh M. Neuropathology. 2009 Apr;29(2):196-9. doi: 10.1111/j.1440-1789.2008.00982.x. Epub 2008 Nov 19. Neuropathology. 2009. PMID: 19019176 No abstract available.

10

Three human ARX mutations cause the lissencephaly-like and mental retardation with epilepsy-like pleiotropic phenotypes in mice.

Kitamura K, Itou Y, Yanazawa M, Ohsawa M, Suzuki-Migishima R, Umeki Y, Hohjoh H, Yanagawa Y, Shinba T, Itoh M, Nakamura K, Goto Y. Kitamura K, et al. Among authors: itoh m. Hum Mol Genet. 2009 Oct 1;18(19):3708-24. doi: 10.1093/hmg/ddp318. Epub 2009 Jul 15. Hum Mol Genet. 2009. PMID: 19605412

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