Ideguchi H - Search Results

1

Diagnosing nocturnal frontal lobe epilepsy: a case study of two children.

Tomonoh Y, Yasumoto S, Ihara Y, Fujita T, Nakamura N, Ninomiya S, Kodama R, Ideguchi H, Inoue T, Mitsudome A, Hirose S. Tomonoh Y, et al. Among authors: ideguchi h. Seizure. 2011 Sep;20(7):583-5. doi: 10.1016/j.seizure.2011.03.004. Epub 2011 Apr 21. Seizure. 2011. PMID: 21511499 Free article.

2

Early onset and focal spike discharges as indicators of poor prognosis for myoclonic-astatic epilepsy.

Inoue T, Ihara Y, Tomonoh Y, Nakamura N, Ninomiya S, Fujita T, Ideguchi H, Yasumoto S, Zhang B, Hirose S. Inoue T, et al. Among authors: ideguchi h. Brain Dev. 2014 Aug;36(7):613-9. doi: 10.1016/j.braindev.2013.08.009. Epub 2013 Sep 19. Brain Dev. 2014. PMID: 24055341

3

Coffin-Siris syndrome with bilateral macular dysplasia caused by a novel exonic deletion in ARID1B.

Fujita T, Ihara Y, Hayashi H, Ishii A, Ideguchi H, Inoue T, Imaizumi T, Yamamoto T, Hirose S. Fujita T, et al. Among authors: ideguchi h. Congenit Anom (Kyoto). 2020 Nov;60(6):189-193. doi: 10.1111/cga.12383. Epub 2020 Jul 30. Congenit Anom (Kyoto). 2020. PMID: 32618029

4

A Pancreatic Solid Pseudo-Papillary Tumor Detected After Abdominal Injury.

Ishii A, Yoshimura K, Ideguchi H, Hirose S. Ishii A, et al. Among authors: ideguchi h. Gastroenterology Res. 2013 Apr;6(2):67-70. doi: 10.4021/gr534e. Epub 2013 May 3. Gastroenterology Res. 2013. PMID: 27785229 Free PMC article.

5

Reduced PLP1 expression in induced pluripotent stem cells derived from a Pelizaeus-Merzbacher disease patient with a partial PLP1 duplication.

Shimojima K, Inoue T, Imai Y, Arai Y, Komoike Y, Sugawara M, Fujita T, Ideguchi H, Yasumoto S, Kanno H, Hirose S, Yamamoto T. Shimojima K, et al. Among authors: ideguchi h. J Hum Genet. 2012 Sep;57(9):580-6. doi: 10.1038/jhg.2012.71. Epub 2012 Jun 14. J Hum Genet. 2012. PMID: 22695888

6

Genome sequencing and RNA-seq analyses of mitochondrial complex I deficiency revealed Alu insertion-mediated deletion in NDUFV2.

Kishita Y, Shimura M, Kohda M, Fushimi T, Nitta KR, Yatsuka Y, Hirose S, Ideguchi H, Ohtake A, Murayama K, Okazaki Y. Kishita Y, et al. Among authors: ideguchi h. Hum Mutat. 2021 Nov;42(11):1422-1428. doi: 10.1002/humu.24274. Epub 2021 Sep 2. Hum Mutat. 2021. PMID: 34405929

7

A case of X-linked alpha-thalassemia/mental retardation syndrome: analysis of hemoglobin by an automated glycated hemoglobin analyzer.

Kuno T, Ideguchi H, Yoshida N, Masuyama T, Ohta M, Nishimura S, Tasaki H, Miyazaki S, Hara H, Matsumoto K. Kuno T, et al. Among authors: ideguchi h. Acta Paediatr Jpn. 1997 Oct;39(5):615-8. doi: 10.1111/j.1442-200x.1997.tb03651.x. Acta Paediatr Jpn. 1997. PMID: 9363663

8

[Genetic screening for alpha-thalassemia deletional determinants by GapPCR method].

Katol J, Takao M, Ideguchi H, Sawada H, Kawashima H, Ono J. Katol J, et al. Among authors: ideguchi h. Rinsho Byori. 2006 Nov;54(11):1095-100. Rinsho Byori. 2006. PMID: 17240829 Japanese.

9

A diabetic patient in whom Hb Weesp was incidentally detected when her HbA1c level was measured.

Hatayama T, Umeda F, Yamauchi T, Ideguchi H. Hatayama T, et al. Among authors: ideguchi h. Diabetol Int. 2019 Jul 5;10(4):300-302. doi: 10.1007/s13340-019-00402-z. eCollection 2019 Oct. Diabetol Int. 2019. PMID: 31592030 Free PMC article.

10

[Diagnosis and gene analysis of congenital hemolytic anemia].

Ideguchi H. Ideguchi H. Rinsho Byori. 2006 Jun;54(6):593-600. Rinsho Byori. 2006. PMID: 16872009 Japanese.

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