Neonatal screening and a new cause of congenital central hypothyroidism
Author:
Affiliation:
1. Department of Pediatrics, Hokkaido University School of Medicine, Sapporo, Japan.
Publisher
Korean Society of Pediatric Endocrinology
Subject
Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology and Child Health
Link
http://e-apem.org/upload/pdf/apem-19-117.pdf
Reference31 articles.
1. Newborn screening strategies for congenital hypothyroidism: an update
2. Approach to the Diagnosis and Treatment of Neonatal Hypothyroidism
3. Clinical Effectiveness and Cost-Effectiveness of the Use of the Thyroxine/Thyroxine-Binding Globulin Ratio to Detect Congenital Hypothyroidism of Thyroidal and Central Origin in a Neonatal Screening Program
4. Central Congenital Hypothyroidism Detected by Neonatal Screening in Sapporo, Japan (2000-2004): It's Prevalence and Clinical Characteristics
5. Elevated Free Thyroxine Levels Detected by a Neonatal Screening System
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3. Genetic Basis of Congenital Central Hypothyroidism in Children: Expanding the Mutational Spectrum of POU1F1 and ATP6V0A4;International Journal of General Medicine;2023-08
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