Sawada H - Search Results

1

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

2

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.

3

Central effects of calcitonin receptor-stimulating peptide-1 on energy homeostasis in rats.

Sawada H, Yamaguchi H, Shimbara T, Toshinai K, Mondal MS, Date Y, Murakami N, Katafuchi T, Minamino N, Nunoi H, Nakazato M. Sawada H, et al. Endocrinology. 2006 Apr;147(4):2043-50. doi: 10.1210/en.2005-1226. Epub 2006 Jan 12. Endocrinology. 2006. PMID: 16410305

4

Infantile Cases of Sitosterolaemia with Novel Mutations in the ABCG5 Gene: Extreme Hypercholesterolaemia is Exacerbated by Breastfeeding.

Tada H, Kawashiri MA, Takata M, Matsunami K, Imamura A, Matsuyama M, Sawada H, Nunoi H, Konno T, Hayashi K, Nohara A, Inazu A, Kobayashi J, Mabuchi H, Yamagishi M. Tada H, et al. Among authors: sawada h. JIMD Rep. 2015;21:115-22. doi: 10.1007/8904_2014_404. Epub 2015 Feb 10. JIMD Rep. 2015. PMID: 25665839 Free PMC article.

5

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.

6

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.

7

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

8

Development of a novel ultrasensitive enzyme immunoassay for human glutamic acid decarboxylase 65 antibody.

Numata S, Katakami H, Inoue S, Sawada H, Hashida S. Numata S, et al. Among authors: sawada h. Ann Clin Biochem. 2016 Jul;53(Pt 4):495-503. doi: 10.1177/0004563215609639. Epub 2015 Sep 17. Ann Clin Biochem. 2016. PMID: 26384362

9

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.

10

An autopsy case of an adult woman with Rapid-Onset Obesity with Hypoventilation, Hypothalamic, Autonomic Dysregulation, and Neuroendocrine Tumors (ROHHAD(NET)) syndrome developing nonalcoholic steatohepatitis and hepatocellular carcinoma: A case report.

Hasuike S, Ozono Y, Uchida K, Ogawa S, Tamura H, Uchiyama N, Hatada H, Komaki Y, Nakamura K, Iwakiri H, Sueta M, Nagata K, Nishimura T, Matsuyama M, Sawada H, Oguri T, Sato Y, Kawakami H. Hasuike S, et al. Among authors: sawada h. Medicine (Baltimore). 2024 May 31;103(22):e38383. doi: 10.1097/MD.0000000000038383. Medicine (Baltimore). 2024. PMID: 39259089 Free PMC article.

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