Muramatsu K - Search Results

1

Adeno-associated virus vector-based gene therapies for pediatric diseases.

Muramatsu K, Muramatsu SI. Muramatsu K, et al. Among authors: muramatsu si. Pediatr Neonatol. 2023 Feb;64 Suppl 1:S3-S9. doi: 10.1016/j.pedneo.2022.09.004. Epub 2022 Sep 30. Pediatr Neonatol. 2023. PMID: 36266189 Free article. Review.

2

Gene Therapy in a Mouse Model of Niemann-Pick Disease Type C1.

Kurokawa Y, Osaka H, Kouga T, Jimbo E, Muramatsu K, Nakamura S, Takayanagi Y, Onaka T, Muramatsu SI, Yamagata T. Kurokawa Y, et al. Among authors: muramatsu k, muramatsu si. Hum Gene Ther. 2021 Jun;32(11-12):589-598. doi: 10.1089/hum.2020.175. Epub 2021 Feb 22. Hum Gene Ther. 2021. PMID: 33256498 Free PMC article.

3

WDR45 variants cause ferrous iron loss due to impaired ferritinophagy associated with nuclear receptor coactivator 4 and WD repeat domain phosphoinositide interacting protein 4 reduction.

Tsukida K, Muramatsu SI, Osaka H, Yamagata T, Muramatsu K. Tsukida K, et al. Among authors: muramatsu k, muramatsu si. Brain Commun. 2022 Nov 23;4(6):fcac304. doi: 10.1093/braincomms/fcac304. eCollection 2022. Brain Commun. 2022. PMID: 36751498 Free PMC article.

4

Therapeutic strategy for Fabry disease by intravenous administration of adeno-associated virus 2 or 9 in α-galactosidase A-deficient mice.

Hayashi Y, Sehara Y, Watano R, Ohba K, Takayanagi Y, Muramatsu K, Sakiyama Y, Mizukami H. Hayashi Y, et al. Among authors: muramatsu k. J Gene Med. 2023 Dec;25(12):e3560. doi: 10.1002/jgm.3560. Epub 2023 Jun 30. J Gene Med. 2023. PMID: 37392007

5

Neurodevelopmental outcome and respiratory management of congenital central hypoventilation syndrome: a retrospective study.

Ogata T, Muramatsu K, Miyana K, Ozawa H, Iwasaki M, Arakawa H. Ogata T, et al. Among authors: muramatsu k. BMC Pediatr. 2020 Jul 13;20(1):342. doi: 10.1186/s12887-020-02239-x. BMC Pediatr. 2020. PMID: 32660452 Free PMC article.

6

Rapid progression of a walking disability in a 5-year-old boy with a CLN6 mutation.

Matsumoto A, Nagashima M, Iwama K, Mizuguchi T, Makino S, Ikeda T, Muramatsu K, Matsumoto N, Yamagata T, Osaka H. Matsumoto A, et al. Among authors: muramatsu k. Brain Dev. 2019 Sep;41(8):726-730. doi: 10.1016/j.braindev.2019.04.009. Epub 2019 Apr 24. Brain Dev. 2019. PMID: 31029456

7

MELAS syndrome with m.4450 G > A mutation in mitochondrial tRNA^Met gene.

Kuwajima M, Goto M, Kurane K, Shimbo H, Omika N, Jimbo EF, Muramatsu K, Tajika M, Shimura M, Murayama K, Kurosawa K, Yamagata T, Osaka H. Kuwajima M, et al. Among authors: muramatsu k. Brain Dev. 2019 May;41(5):465-469. doi: 10.1016/j.braindev.2019.01.006. Epub 2019 Feb 7. Brain Dev. 2019. PMID: 30739820

8

Praxis-induced reflex seizures in two Japanese cases with ring chromosome 20 syndrome.

Yamagishi H, Goto M, Osaka H, Kuwajima M, Muramatsu K, Yamagata T. Yamagishi H, et al. Among authors: muramatsu k. Epileptic Disord. 2020 Apr 1;22(2):214-218. doi: 10.1684/epd.2020.1146. Epileptic Disord. 2020. PMID: 32301722

9

Gallbladder cancer with ascites in a child with metachromatic leukodystrophy.

Koshu K, Ikeda T, Tamura D, Muramatsu K, Osaka H, Ono S, Adachi K, Nanba E, Nakajima T, Yamagata T. Koshu K, et al. Among authors: muramatsu k. Brain Dev. 2021 Jan;43(1):140-143. doi: 10.1016/j.braindev.2020.08.002. Epub 2020 Aug 24. Brain Dev. 2021. PMID: 32855001

10

Forced normalization of Lennox-Gastaut syndrome using lacosamide: A case report.

Ono-Takiguchi Y, Muramatsu K, Koshu K, Yamagata T. Ono-Takiguchi Y, et al. Among authors: muramatsu k. Brain Dev. 2021 Oct;43(9):963-966. doi: 10.1016/j.braindev.2021.05.006. Epub 2021 May 26. Brain Dev. 2021. PMID: 34049745

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