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Items: 17

1.

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.

Clin Pediatr Endocrinol. 2017;26(4):275-278. doi: 10.1297/cpe.26.275. Epub 2017 Sep 28. No abstract available.

2.

Endoplasmic Reticulum (ER) Stress and Endocrine Disorders.

Ariyasu D, Yoshida H, Hasegawa Y.

Int J Mol Sci. 2017 Feb 11;18(2). pii: E382. doi: 10.3390/ijms18020382. Review.

3.

Gradually increasing ethinyl estradiol for Turner syndrome may produce good final height but not ideal BMD.

Hasegawa Y, Ariyasu D, Izawa M, Igaki-Miyamoto J, Fukuma M, Hatano M, Yagi H, Goto M.

Endocr J. 2017 Feb 27;64(2):221-227. doi: 10.1507/endocrj.EJ16-0170. Epub 2016 Dec 2.

4.

A case of transient neonatal diabetes due to a novel mutation in ABCC8.

Takagi M, Takeda R, Yagi H, Ariyasu D, Fukuzawa R, Hasegawa T.

Clin Pediatr Endocrinol. 2016 Oct;25(4):139-141. Epub 2016 Oct 18. No abstract available.

5.

Early-onset urological disorders due to Wolfram syndrome: A case of neonatal onset.

Fukuma M, Ariyasu D, Hatano M, Yagi H, Hasegawa Y.

Clin Pediatr Endocrinol. 2016 Apr;25(2):67-9. doi: 10.1297/cpe.25.67. Epub 2016 Apr 28. No abstract available.

6.

Hypophosphatemic rickets developed after treatment with etidronate disodium in a patient with generalized arterial calcification in infancy.

Miyai K, Ariyasu D, Numakura C, Yoneda K, Nakazato H, Hasegawa Y.

Bone Rep. 2015 Sep 9;3:57-60. doi: 10.1016/j.bonr.2015.09.001. eCollection 2015 Dec.

7.

Endoplasmic reticulum stress and apoptosis contribute to the pathogenesis of dominantly inherited isolated GH deficiency due to GH1 gene splice site mutations.

Ariyasu D, Yoshida H, Yamada M, Hasegawa Y.

Endocrinology. 2013 Sep;154(9):3228-39. doi: 10.1210/en.2013-1249. Epub 2013 Jun 4.

PMID:
23736291
8.

Microduplication of Xq24 and Hartsfield syndrome with holoprosencephaly, ectrodactyly, and clefting.

Takenouchi T, Okuno H, Kosaki R, Ariyasu D, Torii C, Momoshima S, Harada N, Yoshihashi H, Takahashi T, Awazu M, Kosaki K.

Am J Med Genet A. 2012 Oct;158A(10):2537-41. doi: 10.1002/ajmg.a.35465. Epub 2012 Aug 10.

PMID:
22887648
9.

High iFGF23 level despite hypophosphatemia is one of the clinical indicators to make diagnosis of XLH.

Igaki JM, Yamada M, Yamazaki Y, Koto S, Izawa M, Ariyasu D, Suzuki E, Hasegawa H, Hasegawa Y.

Endocr J. 2011;58(8):647-55. Epub 2011 May 19.

10.

Serum FSH level below 10 mIU/mL at twelve years old is an index of spontaneous and cyclical menstruation in Turner syndrome.

Aso K, Koto S, Higuchi A, Ariyasu D, Izawa M, Miyamoto Igaki J, Hasegawa Y.

Endocr J. 2010;57(10):909-13. Epub 2010 Aug 24.

11.

Three children with plastic bronchitis associated with 2009 H1N1 influenza virus infection.

Terano C, Miura M, Fukuzawa R, Saito Y, Arai H, Sasaki M, Ariyasu D, Hasegawa Y.

Pediatr Infect Dis J. 2011 Jan;30(1):80-2. doi: 10.1097/INF.0b013e3181f10fff.

PMID:
20686435
12.

Patients with Hypophosphatemic Osteomalacia Need Continuous Treatment during Adulthood.

Suzuki E, Yamada M, Ariyasu D, Izawa M, Miyamoto J, Koto S, Hasegawa Y.

Clin Pediatr Endocrinol. 2009;18(1):29-33. doi: 10.1297/cpe.18.29. Epub 2009 Feb 19.

13.

The Range of 2.2-3.3 mg/gCr of Pregnanetriol in the First Morning Urine Sample as an Index of Optimal Control in CYP21 Deficiency.

Izawa M, Aso K, Higuchi A, Ariyasu D, Hasegawa Y.

Clin Pediatr Endocrinol. 2008;17(3):75-80. doi: 10.1297/cpe.17.75. Epub 2008 Aug 8.

14.

Pregnanetriol in the Range of 1.2-2.1 mg/m(2)/day as an Index of Optimal Control in CYP21A2 Deficiency.

Izawa M, Aso K, Higuchi A, Ariyasu D, Hasegawa Y.

Clin Pediatr Endocrinol. 2007;16(2):45-52. doi: 10.1297/cpe.16.45. Epub 2007 May 17.

15.

WT1 intron 9 splice acceptor site mutation in a 46,XY male with focal segmental glomerulosclerosis.

Kanemoto K, Ishikura K, Ariyasu D, Hamasaki Y, Hataya H, Hasegawa Y, Ikeda M.

Pediatr Nephrol. 2007 Mar;22(3):454-8. Epub 2006 Oct 24.

PMID:
17061122
16.

Genetic and enzymatic analysis for two Japanese patients with idiopathic infantile arterial calcification.

Numakura C, Yamada M, Ariyasu D, Maesaka A, Kobayashi H, Nishimura G, Ikeda M, Hasegawa Y.

J Bone Miner Metab. 2006;24(1):48-52.

PMID:
16369898
17.

Cryptococcal meningitis in an immunocompetent child.

Shinjoh M, Miyairi I, Sakurai M, Takahashi M, Ariyasu D, Nakayama T, Tokumura M, Yamashita R, Sunakawa K, Takahashi T.

Eur J Pediatr. 2005 Sep;164(9):596-7. Epub 2005 Jun 15. No abstract available.

PMID:
15959803

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