Numata-Uematsu Y - Search Results

1

Genomic analysis identifies masqueraders of full-term cerebral palsy.

Takezawa Y, Kikuchi A, Haginoya K, Niihori T, Numata-Uematsu Y, Inui T, Yamamura-Suzuki S, Miyabayashi T, Anzai M, Suzuki-Muromoto S, Okubo Y, Endo W, Togashi N, Kobayashi Y, Onuma A, Funayama R, Shirota M, Nakayama K, Aoki Y, Kure S. Takezawa Y, et al. Ann Clin Transl Neurol. 2018 Mar 26;5(5):538-551. doi: 10.1002/acn3.551. eCollection 2018 May. Ann Clin Transl Neurol. 2018. PMID: 29761117 Free PMC article.

2

Acute encephalitis with refractory, repetitive partial seizures: Pathological findings and a new therapeutic approach using tacrolimus.

Sato Y, Numata-Uematsu Y, Uematsu M, Kikuchi A, Nakayama T, Kakisaka Y, Kobayashi T, Hino-Fukuyo N, Suzuki H, Takahashi Y, Saito Y, Tanuma N, Hayashi M, Iwasaki M, Haginoya K, Kure S. Sato Y, et al. Brain Dev. 2016 Sep;38(8):772-6. doi: 10.1016/j.braindev.2016.02.006. Epub 2016 Feb 20. Brain Dev. 2016. PMID: 26906012

3

Reversible brain atrophy in glutaric aciduria type 1.

Numata-Uematsu Y, Sakamoto O, Kakisaka Y, Okubo Y, Oikawa Y, Arai-Ichinoi N, Kure S, Uematsu M. Numata-Uematsu Y, et al. Brain Dev. 2017 Jun;39(6):532-535. doi: 10.1016/j.braindev.2017.01.003. Epub 2017 Jan 29. Brain Dev. 2017. PMID: 28143689

4

Initial vasodilatation in a child with reversible cerebral vasoconstriction syndrome.

Oikawa Y, Okubo Y, Numata-Uematsu Y, Aihara Y, Kitamura T, Takayanagi M, Takahashi Y, Kure S, Uematsu M. Oikawa Y, et al. J Clin Neurosci. 2017 May;39:108-110. doi: 10.1016/j.jocn.2017.01.010. Epub 2017 Feb 10. J Clin Neurosci. 2017. PMID: 28209305

5

Novel biallelic mutations in the PNPT1 gene encoding a mitochondrial-RNA-import protein PNPase cause delayed myelination.

Sato R, Arai-Ichinoi N, Kikuchi A, Matsuhashi T, Numata-Uematsu Y, Uematsu M, Fujii Y, Murayama K, Ohtake A, Abe T, Kure S. Sato R, et al. Clin Genet. 2018 Feb;93(2):242-247. doi: 10.1111/cge.13068. Epub 2017 Oct 4. Clin Genet. 2018. PMID: 28594066

6

Rett-like features and cortical visual impairment in a Japanese patient with HECW2 mutation.

Nakamura H, Uematsu M, Numata-Uematsu Y, Abe Y, Endo W, Kikuchi A, Takezawa Y, Funayama R, Shirota M, Nakayama K, Niihori T, Aoki Y, Haginoya K, Kure S. Nakamura H, et al. Brain Dev. 2018 May;40(5):410-414. doi: 10.1016/j.braindev.2017.12.015. Epub 2018 Feb 1. Brain Dev. 2018. PMID: 29395664

7

Attachment Disorder and Early Media Exposure: Neurobehavioral symptoms mimicking autism spectrum disorder.

Numata-Uematsu Y, Yokoyama H, Sato H, Endo W, Uematsu M, Nara C, Kure S. Numata-Uematsu Y, et al. J Med Invest. 2018;65(3.4):280-282. doi: 10.2152/jmi.65.280. J Med Invest. 2018. PMID: 30282873 Free article.

8

Behavioral problems and family distress in tuberous sclerosis complex.

Uematsu M, Numata-Uematsu Y, Aihara Y, Kobayashi T, Fujikawa M, Togashi N, Shiihara T, Ohashi K, Hattori A, Saitoh S, Kure S. Uematsu M, et al. Epilepsy Behav. 2020 Oct;111:107321. doi: 10.1016/j.yebeh.2020.107321. Epub 2020 Jul 19. Epilepsy Behav. 2020. PMID: 32698109

9

Gingival Pigmentation in a Boy.

Nakagawa T, Wada Y, Miura A, Numata-Uematsu Y, Niizuma H, Kure S. Nakagawa T, et al. J Pediatr. 2021 Jul;234:274-275. doi: 10.1016/j.jpeds.2021.03.052. Epub 2021 Mar 29. J Pediatr. 2021. PMID: 33794216 No abstract available.

10

Leigh syndrome-like MRI changes in a patient with biallelic HPDL variants treated with ketogenic diet.

Numata-Uematsu Y, Uematsu M, Yamamoto T, Saitsu H, Katata Y, Oikawa Y, Saijyo N, Inui T, Murayama K, Ohtake A, Osaka H, Takanashi JI, Kure S, Inoue K. Numata-Uematsu Y, et al. Mol Genet Metab Rep. 2021 Sep 4;29:100800. doi: 10.1016/j.ymgmr.2021.100800. eCollection 2021 Dec. Mol Genet Metab Rep. 2021. PMID: 34522618 Free PMC article.

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