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Metabolism: Clinical and Experimental|April 29, 2010
Novel intronic CYP21A2 mutation in a Japanese patient with classic salt-wasting steroid 21-hydroxylase deficiencyNoriyuki Katsumata, Takashi Shinagawa, Reiko Horikawa, et al.
Metabolism: Clinical and Experimental|October 2, 2009
Novel CYP17A1 mutation in a Japanese patient with combined 17alpha-hydroxylase/17,20-lyase deficiencyNoriyuki Katsumata, Eishin Ogawa, Ikuma Fujiwara, et al.
Pediatric Endocrinology Reviews : PER|January 22, 2013
Neonatal screening for congenital adrenal hyperplasia in JapanToshihiro Tajima, Kaori Fujikura, Masaru Fukushi, et al.
Pediatric Research|June 23, 2009
Elevated free thyroxine levels detected by a neonatal screening systemToshihiro Tajima, Wakako Jo, Kaori Fujikura, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|May 3, 2014
Central Congenital Hypothyroidism Detected by Neonatal Screening in Sapporo, Japan (2000-2004): It's Prevalence and Clinical CharacteristicsFumie Fujiwara, Kaori Fujikura, Koji Okuhara, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|May 3, 2014
Results from 28 years of newborn screening for congenital adrenal hyperplasia in sapporoShuntaro Morikawa, Akie Nakamura, Kaori Fujikura, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|February 10, 2023
Guidelines for Newborn Screening of Congenital Hypothyroidism (2021 Revision)Keisuke Nagasaki, Kanshi Minamitani, Akie Nakamura, et al.
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