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Myhre syndrome: Age-dependent progressive phenotype.
Nomura R, Miyai K, Nishimura G, Kashimada K, Morio T. Nomura R, et al. Among authors: kashimada k. Pediatr Int. 2017 Nov;59(11):1205-1206. doi: 10.1111/ped.13413. Pediatr Int. 2017. PMID: 29359479 No abstract available.
RMRP mutations in Japanese patients with cartilage-hair hypoplasia.
Nakashima E, Mabuchi A, Kashimada K, Onishi T, Zhang J, Ohashi H, Nishimura G, Ikegawa S. Nakashima E, et al. Among authors: kashimada k. Am J Med Genet A. 2003 Dec 15;123A(3):253-6. doi: 10.1002/ajmg.a.20281. Am J Med Genet A. 2003. PMID: 14608646
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
114 results