Sawada H - Search Results

1

Molecular and clinical features of K_ATP -channel neonatal diabetes mellitus in Japan.

Hashimoto Y, Dateki S, Hirose M, Satomura K, Sawada H, Mizuno H, Sugihara S, Maruyama K, Urakami T, Sugawara H, Shirai K, Yorifuji T. Hashimoto Y, et al. Among authors: sawada h. Pediatr Diabetes. 2017 Nov;18(7):532-539. doi: 10.1111/pedi.12447. Epub 2016 Sep 29. Pediatr Diabetes. 2017. PMID: 27681997

2

Clinical characteristics of septo-optic dysplasia accompanied by congenital central hypothyroidism in Japan.

Nagasaki K, Kubota T, Kobayashi H, Sawada H, Numakura C, Harada S, Takasawa K, Minamitani K, Ishii T, Okada S, Kamasaki H, Sugihara S, Adachi M, Tajima T. Nagasaki K, et al. Among authors: sawada h. Clin Pediatr Endocrinol. 2017;26(4):207-213. doi: 10.1297/cpe.26.207. Epub 2017 Sep 28. Clin Pediatr Endocrinol. 2017. PMID: 29026269 Free PMC article.

3

A hot-spot mutation in CDC42 (p.Tyr64Cys) and novel phenotypes in the third patient with Takenouchi-Kosaki syndrome.

Motokawa M, Watanabe S, Nakatomi A, Kondoh T, Matsumoto T, Morifuji K, Sawada H, Nishimura T, Nunoi H, Yoshiura KI, Moriuchi H, Dateki S. Motokawa M, et al. Among authors: sawada h. J Hum Genet. 2018 Mar;63(3):387-390. doi: 10.1038/s10038-017-0396-5. Epub 2018 Jan 15. J Hum Genet. 2018. PMID: 29335451 Free article.

4

Incidence and Characteristics of Adrenal Crisis in Children Younger than 7 Years with 21-Hydroxylase Deficiency: A Nationwide Survey in Japan.

Ishii T, Adachi M, Takasawa K, Okada S, Kamasaki H, Kubota T, Kobayashi H, Sawada H, Nagasaki K, Numakura C, Harada S, Minamitani K, Sugihara S, Tajima T. Ishii T, et al. Among authors: sawada h. Horm Res Paediatr. 2018;89(3):166-171. doi: 10.1159/000486393. Epub 2018 Feb 16. Horm Res Paediatr. 2018. PMID: 29455197

5

Levothyroxine Dosage as Predictor of Permanent and Transient Congenital Hypothyroidism: A Multicenter Retrospective Study in Japan.

Itonaga T, Higuchi S, Shimura K, Nagasaki K, Satoh M, Takubo N, Takahashi I, Sawada H, Hasegawa Y. Itonaga T, et al. Among authors: sawada h. Horm Res Paediatr. 2019;92(1):45-51. doi: 10.1159/000502418. Epub 2019 Sep 25. Horm Res Paediatr. 2019. PMID: 31553976 Clinical Trial.

6

A novel mutation of the PHKA2 gene in a patient with X-linked liver glycogenosis type 1.

Hidaka F, Sawada H, Matsuyama M, Nunoi H. Hidaka F, et al. Among authors: sawada h. Pediatr Int. 2005 Dec;47(6):687-90. doi: 10.1111/j.1442-200x.2005.02131.x. Pediatr Int. 2005. PMID: 16354226 No abstract available.

7

Nephrotic syndrome complicated by idiopathic central diabetes insipidus.

Konomoto T, Tanaka E, Imamura H, Orita M, Sawada H, Nunoi H. Konomoto T, et al. Among authors: sawada h. Pediatr Nephrol. 2014 May;29(5):927-30. doi: 10.1007/s00467-013-2728-9. Epub 2014 Jan 10. Pediatr Nephrol. 2014. PMID: 24408226

8

Osteogenesis imperfecta complicated with renal hypoplasia leads to chronic kidney disease.

Konomoto T, Kurogi J, Sawada H, Hisano S, Nunoi H. Konomoto T, et al. Among authors: sawada h. Pediatr Int. 2017 Mar;59(3):369-370. doi: 10.1111/ped.13221. Pediatr Int. 2017. PMID: 28317307 No abstract available.

9

A novel variant of IGSF1 in siblings with congenital central hypothyroidism whose diagnosis was prompted by school health checkups.

Yamamura Y, Fukami M, Matsuyama M, Sawada H. Yamamura Y, et al. Among authors: sawada h. Clin Pediatr Endocrinol. 2024;33(1):17-22. doi: 10.1297/cpe.2023-0046. Epub 2023 Nov 3. Clin Pediatr Endocrinol. 2024. PMID: 38299175 Free PMC article.

10

Living donor liver transplantation from a heterozygous parent for classical maple syrup urine disease.

Kadohisa M, Matsumoto S, Sawada H, Honda M, Murokawa T, Hayashida S, Ohya Y, Lee KJ, Yamamoto H, Mitsubuchi H, Endo F, Inomata Y. Kadohisa M, et al. Among authors: sawada h. Pediatr Transplant. 2015 May;19(3):E66-9. doi: 10.1111/petr.12447. Epub 2015 Feb 23. Pediatr Transplant. 2015. PMID: 25708273

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