Eto Y - Search Results

1

Constitutionally tall stature with morphological abnormality of the pituitary gland.

Miyata I, Yoshikawa H, Eto Y. Miyata I, et al. Among authors: eto y. Endocr J. 2004 Apr;51(2):189-95. doi: 10.1507/endocrj.51.189. Endocr J. 2004. PMID: 15118269 Free article.

2

Successful intrauterine therapy for fetal goitrous hypothyroidism during late gestation.

Miyata I, Abe-Gotyo N, Tajima A, Yoshikawa H, Teramoto S, Seo M, Kanno K, Sugiura K, Tanaka T, Eto Y. Miyata I, et al. Among authors: eto y. Endocr J. 2007 Dec;54(5):813-7. doi: 10.1507/endocrj.k07-047. Epub 2007 Oct 3. Endocr J. 2007. PMID: 17917306 Free article.

3

Lymphocytic hypophysitis with central diabetes insipidus and subsequent hypopituitarism masking a suprasellar germinoma in a 13-year-old girl.

Mikami-Terao Y, Akiyama M, Yanagisawa T, Takahashi-Fujigasaki J, Yokoi K, Fukuoka K, Sakuma M, Miyata I, Fujisawa K, Oi S, Eto Y. Mikami-Terao Y, et al. Among authors: eto y. Childs Nerv Syst. 2006 Oct;22(10):1338-43. doi: 10.1007/s00381-006-0078-7. Epub 2006 Mar 25. Childs Nerv Syst. 2006. PMID: 16565852

4

Identification and functional analysis of the novel S179R POU1F1 mutation associated with combined pituitary hormone deficiency.

Miyata I, Vallette-Kasic S, Saveanu A, Takeuchi M, Yoshikawa H, Tajima A, Tojo K, Reynaud R, Gueydan M, Enjalbert A, Tajima N, Eto Y, Brue T. Miyata I, et al. Among authors: eto y. J Clin Endocrinol Metab. 2006 Dec;91(12):4981-7. doi: 10.1210/jc.2005-2289. Epub 2006 Sep 12. J Clin Endocrinol Metab. 2006. PMID: 16968807

5

Serum glucagon-like peptide-2 levels in neonates: comparison between extremely low-birthweight infants and normal-term infants.

Yoshikawa H, Miyata I, Eto Y. Yoshikawa H, et al. Among authors: eto y. Pediatr Int. 2006 Oct;48(5):464-9. doi: 10.1111/j.1442-200X.2006.02255.x. Pediatr Int. 2006. PMID: 16970784

6

Right testicular necrosis and left vanishing testis in a neonate.

Miyata I, Yoshikawa H, Ikemoto M, Eto Y. Miyata I, et al. Among authors: eto y. J Pediatr Endocrinol Metab. 2007 Mar;20(3):449-54. doi: 10.1515/jpem.2007.20.3.449. J Pediatr Endocrinol Metab. 2007. PMID: 17451086

7

A Neonatal Case of Autosomal Dominant Hypoparathyroidism without Mutation of the CASR Gene.

Miyata I, Yoshikawa H, Kurokawa N, Kanno K, Hayashi Y, Eto Y. Miyata I, et al. Among authors: eto y. Clin Pediatr Endocrinol. 2008;17(1):17-22. doi: 10.1297/cpe.17.17. Epub 2008 Feb 14. Clin Pediatr Endocrinol. 2008. PMID: 24790357 Free PMC article.

8

11-year-old boy with sarcoidosis and generalized brawny induration of muscle.

Akiyama M, Wada Y, Ando K, Miyata I, Usui N, Tanaka H, Inoue K, Eto Y. Akiyama M, et al. Among authors: eto y. Pediatr Int. 2002 Feb;44(1):93-7. doi: 10.1046/j.1442-200x.2002.01489.x. Pediatr Int. 2002. PMID: 11982881 No abstract available.

9

A novel mutation of the arginine vasopressin receptor 2 gene in a patient with congenital nephrogenic diabetes insipidus.

Tajima A, Miyata I, Katayama A, Toyoda S, Eto Y. Tajima A, et al. Among authors: eto y. Clin Pediatr Endocrinol. 2005;14(1):27-33. doi: 10.1297/cpe.14.27. Epub 2005 Feb 14. Clin Pediatr Endocrinol. 2005. PMID: 24790307 Free PMC article.

10

In vitro and pathological investigations of MODY5 with the R276X-HNF1beta (TCF2) mutation.

Fujimoto K, Sasaki T, Hiki Y, Nemoto M, Utsunomiya Y, Yokoo T, Nakai N, Ohashi T, Hosoya T, Eto Y, Tajima N. Fujimoto K, et al. Among authors: eto y. Endocr J. 2007 Dec;54(5):757-64. doi: 10.1507/endocrj.k07-051. Epub 2007 Sep 18. Endocr J. 2007. PMID: 17878605 Free article.

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