Mizuno T - Search Results

1

Infantile-onset spinocerebellar ataxia type 5 associated with a novel SPTBN2 mutation: A case report.

Mizuno T, Kashimada A, Nomura T, Moriyama K, Yokoyama H, Hasegawa S, Takagi M, Mizutani S. Mizuno T, et al. Brain Dev. 2019 Aug;41(7):630-633. doi: 10.1016/j.braindev.2019.03.002. Epub 2019 Mar 18. Brain Dev. 2019. PMID: 30898343

2

A case of congenital axonal neuropathy associated with West syndrome.

Mizuno T, Sasaki M, Komaki H, Sakuma H, Saito Y, Nakagawa E, Sugai K, Saito Y, Nonaka I, Sawaishi Y. Mizuno T, et al. Brain Dev. 2011 Sep;33(8):692-6. doi: 10.1016/j.braindev.2010.11.009. Epub 2011 Jan 5. Brain Dev. 2011. PMID: 21211919

3

Genetic analysis of undiagnosed ataxia-telangiectasia-like disorders.

Kashimada A, Hasegawa S, Nomura T, Shiraku H, Moriyama K, Suzuki T, Nakajima K, Mizuno T, Imai K, Sugawara Y, Morio T, Kumada S, Takagi M. Kashimada A, et al. Among authors: mizuno t. Brain Dev. 2019 Feb;41(2):150-157. doi: 10.1016/j.braindev.2018.09.007. Epub 2018 Oct 6. Brain Dev. 2019. PMID: 30301590

4

Long-Term Evaluation of Low-Dose Betamethasone for Ataxia Telangiectasia.

Hasegawa S, Kumada S, Tanuma N, Tsuji-Hosokawa A, Kashimada A, Mizuno T, Moriyama K, Sugawara Y, Shirai I, Miyata Y, Nishida H, Mashimo H, Hasegawa T, Hosokawa T, Hisakawa H, Uematsu M, Fujine A, Miyata R, Sakuma H, Kashimada K, Imai K, Morio T, Hayashi M, Mizutani S, Takagi M. Hasegawa S, et al. Among authors: mizuno t. Pediatr Neurol. 2019 Nov;100:60-66. doi: 10.1016/j.pediatrneurol.2019.05.006. Epub 2019 May 13. Pediatr Neurol. 2019. PMID: 31272782 Clinical Trial.

5

Cerebrospinal fluid abnormalities in developmental and epileptic encephalopathy with a de novo CDK19 variant.

Sugawara Y, Mizuno T, Moriyama K, Ishiwata H, Kato M, Nakashima M, Mizuguchi T, Matsumoto N. Sugawara Y, et al. Among authors: mizuno t. Neurol Genet. 2020 Oct 8;6(6):e527. doi: 10.1212/NXG.0000000000000527. eCollection 2020 Dec. Neurol Genet. 2020. PMID: 33134521 Free PMC article. No abstract available.

6

Clinical variations of epileptic syndrome associated with PACS2 variant.

Mizuno T, Miyata R, Hojo A, Tamura Y, Nakashima M, Mizuguchi T, Matsumoto N, Kato M. Mizuno T, et al. Brain Dev. 2021 Feb;43(2):343-347. doi: 10.1016/j.braindev.2020.10.006. Epub 2020 Nov 23. Brain Dev. 2021. PMID: 33243487

7

Two case reports of KBG syndrome with Dandy-Walker variant.

Tago T, Suzuki T, Kashimada A, Takagi M, Mizuno T. Tago T, et al. Among authors: mizuno t. Pediatr Int. 2021 Dec;63(12):1530-1532. doi: 10.1111/ped.14648. Epub 2021 Aug 21. Pediatr Int. 2021. PMID: 34418234 No abstract available.

8

Moriyama K, Mizuno T, Suzuki T, Inaji M, Maehara T, Fujita A, Kato M, Matsumoto N. Moriyama K, et al. Among authors: mizuno t. Brain Dev. 2023 Jan;45(1):77-81. doi: 10.1016/j.braindev.2022.08.009. Epub 2022 Sep 14. Brain Dev. 2023. PMID: 36114075

9

A p.Arg499His mutation in SPAST is associated with infantile-onset complicated spastic paraplegia: a case report and review of the literature.

Nan H, Shiraku H, Mizuno T, Takiyama Y. Nan H, et al. Among authors: mizuno t. BMC Neurol. 2021 Nov 9;21(1):439. doi: 10.1186/s12883-021-02478-0. BMC Neurol. 2021. PMID: 34753439 Free PMC article. Review.

10

[A case of neurocutaneous melanosis associated with focal cortical dysplasia].

Mizuno T, Nakagawa E, Saito Y, Komaki H, Sugai K, Sasaki M, Otsuki T, Hasegawa T, Yamanouchi H, Kuramochi A. Mizuno T, et al. No To Hattatsu. 2011 Jul;43(4):300-3. No To Hattatsu. 2011. PMID: 21800695 Japanese.

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