Yamagata T - Search Results

1

Pharmacokinetics of Isoniazid-induced Rhabdomyolysis in a Girl.

Kurane K, Goto M, Sano K, Noguchi K, Tamura D, Yamagata T. Kurane K, et al. Among authors: yamagata t. Intern Med. 2018 Dec 1;57(23):3501-3502. doi: 10.2169/internalmedicine.1341-18. Epub 2018 Jul 6. Intern Med. 2018. PMID: 29984757 Free PMC article. No abstract available.

2

Utility of serum ferritin and lactate dehydrogenase as surrogate markers for steroid therapy for Mycoplasma pneumoniae pneumonia.

Kawamata R, Yokoyama K, Sato M, Goto M, Nozaki Y, Takagi T, Kumagai H, Yamagata T. Kawamata R, et al. Among authors: yamagata t. J Infect Chemother. 2015 Nov;21(11):783-9. doi: 10.1016/j.jiac.2015.07.009. Epub 2015 Aug 19. J Infect Chemother. 2015. PMID: 26298038

3

A patient with Temple syndrome satisfying the clinical diagnostic criteria of Silver-Russell syndrome.

Goto M, Kagami M, Nishimura G, Yamagata T. Goto M, et al. Among authors: yamagata t. Am J Med Genet A. 2016 Sep;170(9):2483-5. doi: 10.1002/ajmg.a.37827. Epub 2016 Jun 30. Am J Med Genet A. 2016. PMID: 27362607 Free PMC article. No abstract available.

4

Role of Class III phosphoinositide 3-kinase in the brain development: possible involvement in specific learning disorders.

Inaguma Y, Matsumoto A, Noda M, Tabata H, Maeda A, Goto M, Usui D, Jimbo EF, Kikkawa K, Ohtsuki M, Momoi MY, Osaka H, Yamagata T, Nagata KI. Inaguma Y, et al. Among authors: yamagata t. J Neurochem. 2016 Oct;139(2):245-255. doi: 10.1111/jnc.13832. Epub 2016 Sep 19. J Neurochem. 2016. PMID: 27607605 Free article.

5

Role of a circadian-relevant gene NR1D1 in brain development: possible involvement in the pathophysiology of autism spectrum disorders.

Goto M, Mizuno M, Matsumoto A, Yang Z, Jimbo EF, Tabata H, Yamagata T, Nagata KI. Goto M, et al. Among authors: yamagata t. Sci Rep. 2017 Mar 6;7:43945. doi: 10.1038/srep43945. Sci Rep. 2017. PMID: 28262759 Free PMC article.

6

Characteristics of headaches in Japanese elementary and junior high school students: A school-based questionnaire survey.

Goto M, Yokoyama K, Nozaki Y, Itoh K, Kawamata R, Matsumoto S, Yamagata T. Goto M, et al. Among authors: yamagata t. Brain Dev. 2017 Oct;39(9):791-798. doi: 10.1016/j.braindev.2017.05.010. Epub 2017 May 31. Brain Dev. 2017. PMID: 28578816

7

The presence of diminished white matter and corpus callosal thinning in a case with a SOX9 mutation.

Matsumoto A, Imagawa E, Miyake N, Ikeda T, Kobayashi M, Goto M, Matsumoto N, Yamagata T, Osaka H. Matsumoto A, et al. Among authors: yamagata t. Brain Dev. 2018 Apr;40(4):325-329. doi: 10.1016/j.braindev.2017.09.002. Epub 2017 Sep 28. Brain Dev. 2018. PMID: 28965976

8

Hypercytokinemia with hemophagocytic syndrome due to human metapneumovirus.

Tamura D, Inoue S, Kawahara Y, Mori M, Yamagata T. Tamura D, et al. Among authors: yamagata t. Pediatr Int. 2018 Oct;60(10):974-976. doi: 10.1111/ped.13665. Pediatr Int. 2018. PMID: 30345702 No abstract available.

9

Involuntary Eye Movements Accompanied by Head Thrusting to View Objects.

Goto M, Makino S, Yamagata T. Goto M, et al. Among authors: yamagata t. Pediatr Neurol. 2019 Apr;93:59-60. doi: 10.1016/j.pediatrneurol.2018.09.014. Epub 2018 Oct 23. Pediatr Neurol. 2019. PMID: 30553551 No abstract available.

10

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: yamagata t. 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

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