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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.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|November 24, 2015
Guidelines for Mass Screening of Congenital Hypothyroidism (2014 revision), , , et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|November 24, 2015
Guidelines for diagnosis and treatment of 21-hydroxylase deficiency (2014 revision), , , et al.
Molecular Genetics and Metabolism|July 18, 2013
Newborn screening and diagnosis of mucopolysaccharidosesShunji Tomatsu, Tadashi Fujii, Masaru Fukushi, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|August 5, 2022
Clinical guidelines for the diagnosis and treatment of 21-hydroxylase deficiency (2021 revision)Tomohiro Ishii, Kenichi Kashimada, Naoko Amano, et al.
Journal of Inherited Metabolic Disease|January 29, 2010
Validation of keratan sulfate level in mucopolysaccharidosis type IVA by liquid chromatography-tandem mass spectrometryShunji Tomatsu, Adriana M Montaño, Toshihiro Oguma, et al.
Journal of Inherited Metabolic Disease|February 18, 2010
Dermatan sulfate and heparan sulfate as a biomarker for mucopolysaccharidosis IShunji Tomatsu, Adriana M Montaño, Toshihiro Oguma, et al.
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