Neonatal screening of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: Lille experience 1980–1996
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference34 articles.
1. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency: newborn screening and its relationship to the diagnosis and treatment of the disorder;Pang;Screening,1993
2. Microfilter paper method for 17-alpha-hydroxyprogesterone radioimmunoassay: its application for rapid screening for congenital adrenal hyperplasia;Pang;J Clin Endocrinol Metab,1977
3. A pilot newborn screening for congenital adrenal hyperplasia in Alaska;Pang;J Clin Endocrinol Metab,1982
4. Worldwide experience in newborn screening for classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency;Pang;Pediatrics,1988
5. Newborn screening, prenatal diagnosis and prenatal treatment of congenital adrenal hyperplasia du to 21-hydroxylase deficiency;Pang;Trends Endocrinol Metab,1990
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1. Assessment of the Degree of Clinical Suspicion of 21-Hydroxylase Deficiency Prior to the Newborn Screening Result;Hormone and Metabolic Research;2023-06-16
2. Анализ распространенности и заболеваемости надпочечниковой недостаточностью в мире;Ateroscleroz;2023-01-20
3. Neonatal screening for congenital adrenal hyperplasia in Southern Brazil: a population based study with 108,409 infants;BMC Pediatrics;2017-01-17
4. Genetic Disorders of the Adrenal Gland;Emery and Rimoin's Principles and Practice of Medical Genetics;2013
5. Cortisol assay in dried blood spots to reduce false positive rate in congenital adrenal hyperplasia screening;Clinica Chimica Acta;2012-08
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