Kashimada K - Search Results

1

Two novel HSD3B2 missense mutations with diverse residual enzymatic activities for Δ5-steroids.

Takasawa K, Ono M, Hijikata A, Matsubara Y, Katsumata N, Takagi M, Morio T, Ohara O, Kashimada K, Mizutani S. Takasawa K, et al. Among authors: kashimada k. Clin Endocrinol (Oxf). 2014 Jun;80(6):782-9. doi: 10.1111/cen.12394. Epub 2014 Jan 16. Clin Endocrinol (Oxf). 2014. PMID: 24372086

2

A highly specific heterologous enzyme immunoassay for 5 alpha-androstane-3 alpha, 17 beta-diol 17-glucuronide (androstanediol-17G) and developmental patterns of urinary androstanediol-17G excretions.

Onishi T, Takei H, Kambegawa A, Saisho S, Kashimada K, Koyama S, Mizutani S, Rao PN. Onishi T, et al. Among authors: kashimada k. Steroids. 2002 Mar;67(3-4):175-83. doi: 10.1016/s0039-128x(01)00152-0. Steroids. 2002. PMID: 11856541

3

Defects in growth and bone metabolism in klotho mutant mice are resistant to GH treatment.

Kashimada K, Yamashita T, Tsuji K, Nifuji A, Mizutani S, Nabeshima Y, Noda M. Kashimada K, et al. J Endocrinol. 2002 Sep;174(3):403-10. doi: 10.1677/joe.0.1740403. J Endocrinol. 2002. PMID: 12208660

4

A boy with "transient" growth hormone deficiency in prepubertal stage despite normal growth hormone secretion in childhood and after puberty.

Kashimada K, Onishi T, Ono M, Miyai K, Ohta M, Mizutani S. Kashimada K, et al. Endocr J. 2007 Dec;54(6):1015-9. doi: 10.1507/endocrj.k07-068. Epub 2007 Nov 14. Endocr J. 2007. PMID: 18000342 Free article.

5

Liquid chromatography-tandem mass spectrometric method for determination of salivary 17alpha-hydroxyprogesterone: a noninvasive tool for evaluating efficacy of hormone replacement therapy in congenital adrenal hyperplasia.

Shibayama Y, Higashi T, Shimada K, Kashimada K, Onishi T, Ono M, Miyai K, Mizutani S. Shibayama Y, et al. Among authors: kashimada k. J Chromatogr B Analyt Technol Biomed Life Sci. 2008 May 1;867(1):49-56. doi: 10.1016/j.jchromb.2008.03.009. Epub 2008 Mar 16. J Chromatogr B Analyt Technol Biomed Life Sci. 2008. PMID: 18378505

6

Clinical course of patients with nonclassical 21-hydroxylase deficiency (21-OHD) diagnosed in infancy and childhood.

Kashimada K, Ono M, Onishi T, Koyama S, Toyoura T, Imai K, Saisho S, Mizutani S. Kashimada K, et al. Endocr J. 2008 May;55(2):397-404. doi: 10.1507/endocrj.k07e-057. Epub 2008 Apr 2. Endocr J. 2008. PMID: 18385531 Free article.

7

Two cases of transient pseudohypoaldosteronism due to group B streptococcus pyelonephritis.

Kashimada K, Omori T, Takizawa F, Mizutani S. Kashimada K, et al. Pediatr Nephrol. 2008 Sep;23(9):1569-70. doi: 10.1007/s00467-008-0843-9. Epub 2008 May 15. Pediatr Nephrol. 2008. PMID: 18481108 No abstract available.

8

Two preterm infants with late onset circulatory collapse induced by levothyroxine sodium.

Takizawa F, Kashimada K, Enomoto K, Miyai K, Ono M, Asada G, Shimizu J, Mizutani S. Takizawa F, et al. Among authors: kashimada k. Pediatr Int. 2010 Jun;52(3):e154-7. doi: 10.1111/j.1442-200X.2010.03072.x. Pediatr Int. 2010. PMID: 20723116 No abstract available.

9

Initial high dose hydrocortisone (HDC) treatment for 21-hydroxylase deficiency (21-OHD) does not affect linear growth during the first three years of life.

Takasawa K, Ono M, Miyai K, Matsubara Y, Takizawa F, Onishi T, Kashimada K, Mizutani S. Takasawa K, et al. Among authors: kashimada k. Endocr J. 2012;59(11):1001-6. doi: 10.1507/endocrj.ej12-0036. Epub 2012 Jul 10. Endocr J. 2012. PMID: 22785554 Free article.

10

Longitudinal analysis of growth and body composition of Japanese 21-OHD patients in childhood.

Matsubara Y, Ono M, Miyai K, Takizawa F, Takasawa K, Onishi T, Kashimada K, Mizutani S. Matsubara Y, et al. Among authors: kashimada k. Endocr J. 2013;60(2):149-54. doi: 10.1507/endocrj.ej12-0123. Epub 2012 Sep 28. Endocr J. 2013. PMID: 23018978 Free article.

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