Nagahara K - Search Results

1

Genetic Analysis of Japanese Children Clinically Diagnosed with Familial Hypercholesterolemia.

Nagahara K, Nishibukuro T, Ogiwara Y, Ikegawa K, Tada H, Yamagishi M, Kawashiri MA, Ochi A, Toyoda J, Nakano Y, Adachi M, Mizuno K, Hasegawa Y, Dobashi K. Nagahara K, et al. J Atheroscler Thromb. 2022 May 1;29(5):667-677. doi: 10.5551/jat.62807. Epub 2021 May 20. J Atheroscler Thromb. 2022. PMID: 34011801 Free PMC article.

2

Cord serum adiponectin is positively related to postnatal body mass index gain.

Nakano Y, Itabashi K, Nagahara K, Sakurai M, Aizawa M, Dobashi K, Mizuno K, Tanaka D. Nakano Y, et al. Among authors: nagahara k. Pediatr Int. 2012 Feb;54(1):76-80. doi: 10.1111/j.1442-200X.2011.03521.x. Pediatr Int. 2012. PMID: 22115040

3

Feeding choice has a gender-associated effect on infant growth.

Nagahara K, Dobashi K, Itabashi K. Nagahara K, et al. Pediatr Int. 2013 Aug;55(4):481-7. doi: 10.1111/ped.12123. Pediatr Int. 2013. PMID: 23659739

4

AICAR Attenuates TNFα-Induced Inappropriate Secretion of Monocyte Chemoattractant Protein-1 and Adiponectin in 3T3-L1 Adipocytes.

Nagahara K, Dobashi K, Ishikawa T, Nakano Y, Abe Y, Tanaka D, Itabashi K. Nagahara K, et al. J Atheroscler Thromb. 2016 Dec 1;23(12):1345-1354. doi: 10.5551/jat.34835. Epub 2016 May 11. J Atheroscler Thromb. 2016. PMID: 27170207 Free PMC article.

5

Evaluation of Hip/Height^P Ratio as an Index for Adiposity and Metabolic Complications in Obese Children: Comparison with Waist-related Indices.

Dobashi K, Takahashi K, Nagahara K, Tanaka D, Itabashi K. Dobashi K, et al. Among authors: nagahara k. J Atheroscler Thromb. 2017 Jan 1;24(1):47-54. doi: 10.5551/jat.35311. Epub 2016 Jun 8. J Atheroscler Thromb. 2017. PMID: 27298049 Free PMC article.

6

Evaluation of Phosphorylated Urinary Na-Cl Cotransporter Is Potentially Useful in a Patient With Pseudohypoaldosteronism Type II due to Mutation in CUL3.

Nagahara K, Abe Y, Hojo A, Dobashi K, Chiga M, Isobe K, Uchida S, Itabashi K. Nagahara K, et al. Glob Pediatr Health. 2014 Sep 26;1:2333794X14552899. doi: 10.1177/2333794X14552899. eCollection 2014. Glob Pediatr Health. 2014. PMID: 27335910 Free PMC article. No abstract available.

7

A Japanese familial case of hypochondroplasia with a novel mutation in FGFR3.

Nagahara K, Harada Y, Futami T, Takagi M, Nishimura G, Hasegawa Y. Nagahara K, et al. Clin Pediatr Endocrinol. 2016 Jul;25(3):103-6. doi: 10.1297/cpe.25.103. Epub 2016 Jul 20. Clin Pediatr Endocrinol. 2016. PMID: 27507911 Free PMC article. No abstract available.

8

A novel de novo germline mutation Glu40Lys in AKT3 causes megalencephaly with growth hormone deficiency.

Takagi M, Dobashi K, Nagahara K, Kato M, Nishimura G, Fukuzawa R, Narumi S, Hasegawa T. Takagi M, et al. Among authors: nagahara k. Am J Med Genet A. 2017 Apr;173(4):1071-1076. doi: 10.1002/ajmg.a.38099. Epub 2017 Feb 12. Am J Med Genet A. 2017. PMID: 28190287

9

Diagnosis of congenital hyperinsulinism: Biochemical profiles during hypoglycemia.

Sakakibara A, Hashimoto Y, Kawakita R, Hosokawa Y, Nagahara K, Hasegawa Y, Hoshino S, Nagasaka H, Yorifuji T. Sakakibara A, et al. Among authors: nagahara k. Pediatr Diabetes. 2018 Mar;19(2):259-264. doi: 10.1111/pedi.12548. Epub 2017 Jun 9. Pediatr Diabetes. 2018. PMID: 28597971

10

A Japanese boy with fructose-1,6-bisphosphatase deficiency who had a novel FBP1 mutation (p.Phe90Val).

Nagahara K, Ariyasu D, Igaki J, Hasegawa Y, Hasegawa Y. Nagahara K, et al. Clin Pediatr Endocrinol. 2017;26(4):275-278. doi: 10.1297/cpe.26.275. Epub 2017 Sep 28. Clin Pediatr Endocrinol. 2017. PMID: 29026278 Free PMC article. No abstract available.

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