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Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|November 6, 2018
Health problems of adolescent and adult patients with 21-hydroxylase deficiencyToshihiro TajimaInternational Journal of Neonatal Screening|January 25, 2022
Newborn Screening in Japan-2021Toshihiro TajimaClinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|August 5, 2022
Genetic causes of central precocious pubertyToshihiro TajimaClinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|January 8, 2025
Newborn screening for congenital adrenal hyperplasia: Utility of liquid chromatography with tandem mass spectrometry as a secondary testToshihiro TajimaPediatric Nephrology (Berlin, Germany)|February 18, 2005
Renal cysts and nephrocalcinosis in a patient with Bartter syndrome type IIIToru Watanabe, Toshihiro TajimaPediatric Research|April 9, 2005
Molecular basis of adrenal insufficiencyKenji Fujieda, Toshihiro TajimaClinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|May 3, 2014
Prenatal diagnosis and treatment of steroid 21-hydroxylase deficiencyToshihiro Tajima, Kenji FujiedaClinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|February 12, 2016
Neonatal mass screening for 21-hydroxylase deficiencyToshihiro Tajima, Masaru FukushiPediatric Nephrology (Berlin, Germany)|October 31, 2003
Two heterozygous mutations of CLDN16 in a Japanese patient with FHHNCToshihiro Tajima, Jun Nakae, Kenji FujiedaClinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|August 31, 2013
Molecular and Clinical Findings in Patients with LHX4 and OTX2 MutationsToshihiro Tajima, Katsura Ishizu, Akie NakamuraPageof 15