Imamine H - Search Results

1

Pulmonary hypertension with bronchopulmonary dysplasia: Aichi cohort study.

Kawai Y, Hayakawa M, Tanaka T, Yamada Y, Nakayama A, Kato Y, Kouwaki M, Kato T, Tanaka R, Muramatsu K, Hayashi S, Yamamoto H, Takemoto K, Ieda K, Nagaya Y, Honda S, Shinohara O, Funato Y, Kokubo M, Imamine H, Miyata M. Kawai Y, et al. Among authors: imamine h. Pediatr Int. 2022 Jan;64(1):e15271. doi: 10.1111/ped.15271. Pediatr Int. 2022. PMID: 35972055

2

The Tei index permits evaluation of cardiopulmonary function during inhaled nitric oxide therapy in the hypoxic newborn piglet.

Sugiura T, Suzuki S, Hussein MH, Kato T, Okubo Y, Imamine H, Sugiura T, Togari H. Sugiura T, et al. Among authors: imamine h. Biol Neonate. 2004;86(3):176-82. doi: 10.1159/000079424. Epub 2004 Jun 29. Biol Neonate. 2004. PMID: 15237241

3

Prevalence of SEN virus among children in Japan.

Sugiura T, Goto K, Imamine H, Ando T, Ban K, Sugiyama K, Togari H. Sugiura T, et al. Among authors: imamine h. Virus Res. 2004 Mar 15;100(2):223-8. doi: 10.1016/j.virusres.2003.12.028. Virus Res. 2004. PMID: 15019240

4

Possible relationship between elevated plasma ACTH and tall stature in familial glucocorticoid deficiency.

Imamine H, Mizuno H, Sugiyama Y, Ohro Y, Sugiura T, Togari H. Imamine H, et al. Tohoku J Exp Med. 2005 Feb;205(2):123-31. doi: 10.1620/tjem.205.123. Tohoku J Exp Med. 2005. PMID: 15673970 Free article.

5

Clinical significance of heterozygous carriers associated with compensated hypothyroidism in R450H, a common inactivating mutation of the thyrotropin receptor gene in Japanese.

Kanda K, Mizuno H, Sugiyama Y, Imamine H, Togari H, Onigata K. Kanda K, et al. Among authors: imamine h. Endocrine. 2006 Dec;30(3):383-8. doi: 10.1007/s12020-006-0018-z. Endocrine. 2006. PMID: 17526952

6

Clinical characteristics of eight patients with congenital nephrogenic diabetes insipidus.

Mizuno H, Sugiyama Y, Ohro Y, Imamine H, Kobayashi M, Sasaki S, Uchida S, Togari H. Mizuno H, et al. Among authors: imamine h. Endocrine. 2004 Jun;24(1):55-9. doi: 10.1385/ENDO:24:1:055. Endocrine. 2004. PMID: 15249704

7

Longitudinal evaluation of patients with a homozygous R450H mutation of the TSH receptor gene.

Mizuno H, Kanda K, Sugiyama Y, Imamine H, Ito T, Kato I, Togari H, Kamoda T, Onigata K. Mizuno H, et al. Among authors: imamine h. Horm Res. 2009;71(6):318-23. doi: 10.1159/000223415. Epub 2009 Jun 6. Horm Res. 2009. PMID: 19506388

8

Severity of virilization of external genitalia in Japanese patients with salt-wasting 21-hydroxylase deficiency.

Sugiyama Y, Mizuno H, Hayashi Y, Imamine H, Ito T, Kato I, Yamamoto-Tomita M, Aoyama M, Asai K, Togari H. Sugiyama Y, et al. Among authors: imamine h. Tohoku J Exp Med. 2008 Aug;215(4):341-8. doi: 10.1620/tjem.215.341. Tohoku J Exp Med. 2008. PMID: 18679008 Free article.

9

A Case of a Preterm Infant with 21-Hydroxylase Deficiency: Implications of the Biochemical Diagnosis with Urinary Pregnanetriolone by Gas Chromatography/Mass Spectrometry in Selected Ion Monitoring (GCMS-SIM).

Hamajima T, Ohki S, Imamine H, Mizuno H, Homma K, Hasegawa T. Hamajima T, et al. Among authors: imamine h. Clin Pediatr Endocrinol. 2004;13(1):65-70. doi: 10.1297/cpe.13.65. Epub 2004 Jul 7. Clin Pediatr Endocrinol. 2004. PMID: 24790300 Free PMC article.

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