Tsutomu Ogata - Search Results

Year	Number of Results
2002	15
2003	6
2004	14
2005	12
2006	21
2007	8
2008	20
2009	11
2010	15
2011	15
2012	26
2013	29
2014	28
2015	28
2016	32
2017	30
2018	22
2019	15
2020	23
2021	20
2022	25
2023	15
2024	11

1

Case Report: Novel compound heterozygous TPRKB variants cause Galloway-Mowat syndrome.

Hiraide T, Hayashi T, Ito Y, Urushibata R, Uchida H, Kitagata R, Ishigaki H, Ogata T, Saitsu H, Fukuda T. Hiraide T, et al. Among authors: ogata t. Front Pediatr. 2024 Apr 3;12:1360867. doi: 10.3389/fped.2024.1360867. eCollection 2024. Front Pediatr. 2024. PMID: 38628357 Free PMC article.

2

A Case of 17α-hydroxylase/17,20-lyase Deficiency Diagnosed at 45 Years of Age with Hyperaldosteronism.

Ikeya A, Yamashita M, Kakizawa K, Kawauchi Y, Matsushita A, Fujisawa Y, Ogata T, Sasaki S. Ikeya A, et al. Among authors: ogata t. Intern Med. 2024 Apr 9. doi: 10.2169/internalmedicine.3084-23. Online ahead of print. Intern Med. 2024. PMID: 38599871 Free article.

3

Expression levels and DNA methylation profiles of the growth gene SHOX in cartilage tissues and chondrocytes.

Hattori A, Seki A, Inaba N, Nakabayashi K, Takeda K, Tatsusmi K, Naiki Y, Nakamura A, Ishiwata K, Matsumoto K, Nasu M, Okamura K, Michigami T, Katoh-Fukui Y, Umezawa A, Ogata T, Kagami M, Fukami M. Hattori A, et al. Among authors: ogata t. Sci Rep. 2024 Apr 5;14(1):8069. doi: 10.1038/s41598-024-58530-9. Sci Rep. 2024. PMID: 38580675 Free PMC article.

4

Efficacy and safety of GH treatment in Japanese children with short stature due to SHOX deficiency: a randomized phase 3 study.

Ogata T, Fukami M, Tanizawa K, Yamamoto T, Sato Y, Hirai H, Takasao N, Ibaraki R, Noda M. Ogata T, et al. Clin Pediatr Endocrinol. 2024;33(2):43-49. doi: 10.1297/cpe.2023-0070. Epub 2024 Jan 28. Clin Pediatr Endocrinol. 2024. PMID: 38572386 Free PMC article.

5

Diabetes mellitus with severe insulin resistance in a young male patient with a heterozygous pathogenic IRS1 frameshift variant.

Osawa Y, Ichiwata N, Kenmotsu J, Okada T, Masunaga Y, Ogata T, Morioka I, Urakami T. Osawa Y, et al. Among authors: ogata t. Clin Pediatr Endocrinol. 2024;33(2):87-93. doi: 10.1297/cpe.2023-0081. Epub 2024 Feb 23. Clin Pediatr Endocrinol. 2024. PMID: 38572380 Free PMC article.

6

A novel GNAS-Gsα splice donor site variant in a girl with pseudohypoparathyroidism type 1A and her mother with pseudopseudohypoparathyroidism.

Sano S, Iwamoto S, Matsushita R, Masunaga Y, Fujisawa Y, Ogata T. Sano S, et al. Among authors: ogata t. Clin Pediatr Endocrinol. 2024;33(2):66-70. doi: 10.1297/cpe.2023-0065. Epub 2024 Jan 6. Clin Pediatr Endocrinol. 2024. PMID: 38572379 Free PMC article.

7

Assessment of patients' characteristics associated with the efficacy and safety of oral valganciclovir treatment for infants with symptomatic congenital cytomegalovirus disease.

Kakei Y, Morioka I, Imai T, Itohara K, Yano I, Takahashi N, Yoshikawa T, Moriuchi H, Ito Y, Fujioka K, Oka A; Japanese Congenital Cytomegalovirus Study Group. Kakei Y, et al. J Infect Chemother. 2024 Mar 13:S1341-321X(24)00081-3. doi: 10.1016/j.jiac.2024.03.006. Online ahead of print. J Infect Chemother. 2024. PMID: 38484931

8

RNA sequencing and target long-read sequencing reveal an intronic transposon insertion causing aberrant splicing.

Kawakami R, Hiraide T, Watanabe K, Miyamoto S, Hira K, Komatsu K, Ishigaki H, Sakaguchi K, Maekawa M, Yamashita K, Fukuda T, Miyairi I, Ogata T, Saitsu H. Kawakami R, et al. Among authors: ogata t. J Hum Genet. 2024 Feb;69(2):91-99. doi: 10.1038/s10038-023-01211-8. Epub 2023 Dec 15. J Hum Genet. 2024. PMID: 38102195

9

TBX5 pathogenic variant in a patient with congenital heart defect and tracheal stenosis.

Yamoto K, Kato F, Yamoto M, Fukumoto K, Shimizu K, Saitsu H, Ogata T. Yamoto K, et al. Among authors: ogata t. Congenit Anom (Kyoto). 2024 Jan;64(1):23-27. doi: 10.1111/cga.12548. Epub 2023 Dec 7. Congenit Anom (Kyoto). 2024. PMID: 38062907

10

(Epi)genetic and clinical characteristics in 84 patients with pseudohypoparathyroidism type 1B.

Urakawa T, Sano S, Kawashima S, Nakamura A, Shima H, Ohta M, Yamada Y, Nishida A, Narusawa H, Ohtsu Y, Matsubara K, Dateki S, Maruo Y, Fukami M, Ogata T, Kagami M. Urakawa T, et al. Among authors: ogata t. Eur J Endocrinol. 2023 Dec 6;189(6):590-600. doi: 10.1093/ejendo/lvad163. Eur J Endocrinol. 2023. PMID: 38039118

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