Imataka G - Search Results

1

Lipid Peroxidation via Regulating the Metabolism of Docosahexaenoic Acid and Arachidonic Acid in Autistic Behavioral Symptoms.

Yui K, Imataka G, Shiohama T. Yui K, et al. Among authors: imataka g. Curr Issues Mol Biol. 2023 Nov 15;45(11):9149-9164. doi: 10.3390/cimb45110574. Curr Issues Mol Biol. 2023. PMID: 37998751 Free PMC article.

2

Inflammatory changes in infantile-onset LMNA-associated myopathy.

Komaki H, Hayashi YK, Tsuburaya R, Sugie K, Kato M, Nagai T, Imataka G, Suzuki S, Saitoh S, Asahina N, Honke K, Higuchi Y, Sakuma H, Saito Y, Nakagawa E, Sugai K, Sasaki M, Nonaka I, Nishino I. Komaki H, et al. Among authors: imataka g. Neuromuscul Disord. 2011 Aug;21(8):563-8. doi: 10.1016/j.nmd.2011.04.010. Epub 2011 May 31. Neuromuscul Disord. 2011. PMID: 21632249

3

Partial trisomy 3p and monosomy 5p diagnosed by spectral karyotyping (SKY).

Imataka G, Tsuboi T, Kuribayashi R, Miyamoto K, Ichikawa G, Suzumura H, Arisaka O. Imataka G, et al. Genet Couns. 2013;24(4):445-8. Genet Couns. 2013. PMID: 24551991 No abstract available.

4

Trisomy 11/22 diagnosed by spectral karyotyping (SKY).

Imataka G, Takaya Y, Hagisawa S, Yamanouchi H, Eguchi M. Imataka G, et al. Genet Couns. 2004;15(3):391-4. Genet Couns. 2004. PMID: 15517836 No abstract available.

5

GM2 gangliosidosis AB variant: clinical and biochemical studies of a Japanese patient.

Sakuraba H, Itoh K, Shimmoto M, Utsumi K, Kase R, Hashimoto Y, Ozawa T, Ohwada Y, Imataka G, Eguchi M, Furukawa T, Schepers U, Sandhoff K. Sakuraba H, et al. Among authors: imataka g. Neurology. 1999 Jan 15;52(2):372-7. doi: 10.1212/wnl.52.2.372. Neurology. 1999. PMID: 9932959

6

Transient ischaemic attack in a case of a morbidly obese girl associated with metabolic syndrome.

Imataka G, Ichikawa G, Shimura N, Arisaka O. Imataka G, et al. Acta Paediatr. 2012 Nov;101(11):e483-4. doi: 10.1111/j.1651-2227.2012.02816.x. Epub 2012 Sep 7. Acta Paediatr. 2012. PMID: 22928482 No abstract available.

7

Monosomy 5p and partial trisomy 8q due to maternal balanced translocation.

Imataka G, Arisaka O. Imataka G, et al. Genet Couns. 2013;24(4):435-7. Genet Couns. 2013. PMID: 24551988 No abstract available.

8

[Case of theophylline-induced seizures successfully treated with mild hypothermic therapy and methylpredonisolone pulse therapy].

Miyamoto K, Mitsui M, Katashio H, Wake K, Imataka G, Yamnouchi H, Eguchi M. Miyamoto K, et al. Among authors: imataka g. No To Hattatsu. 2006 May;38(3):219-20. No To Hattatsu. 2006. PMID: 16715938 Japanese. No abstract available.

9

Acute encephalopathy in children with Dravet syndrome.

Okumura A, Uematsu M, Imataka G, Tanaka M, Okanishi T, Kubota T, Sudo A, Tohyama J, Tsuji M, Ohmori I, Naiki M, Hiraiwa-Sofue A, Sato H, Saitoh S, Shimizu T. Okumura A, et al. Among authors: imataka g. Epilepsia. 2012 Jan;53(1):79-86. doi: 10.1111/j.1528-1167.2011.03311.x. Epub 2011 Nov 16. Epilepsia. 2012. PMID: 22092154 Free article.

10

The spectrum of ZEB2 mutations causing the Mowat-Wilson syndrome in Japanese populations.

Yamada Y, Nomura N, Yamada K, Matsuo M, Suzuki Y, Sameshima K, Kimura R, Yamamoto Y, Fukushi D, Fukuhara Y, Ishihara N, Nishi E, Imataka G, Suzumura H, Hamano S, Shimizu K, Iwakoshi M, Ohama K, Ohta A, Wakamoto H, Kajita M, Miura K, Yokochi K, Kosaki K, Kuroda T, Kosaki R, Hiraki Y, Saito K, Mizuno S, Kurosawa K, Okamoto N, Wakamatsu N. Yamada Y, et al. Among authors: imataka g. Am J Med Genet A. 2014 Aug;164A(8):1899-908. doi: 10.1002/ajmg.a.36551. Epub 2014 Apr 8. Am J Med Genet A. 2014. PMID: 24715670

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