Neonatal screening for phenylketonuria and congenital hypothyroidism in Principado de Asturias (Spain) using two types of blood samples-Reference-Cited by-同舟云学术

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Neonatal screening for phenylketonuria and congenital hypothyroidism in Principado de Asturias (Spain) using two types of blood samples

Published:1995-10 Issue:3 Volume:4 Page:131-138
ISSN:0925-6164
Container-title:Screening
language:en
Short-container-title:Screening

Author:

Fernández-Iglesias C.,Flórez I.G.,Rodríguez-González M.C.,Gascón S.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology, and Child Health

Reference18 articles.

1. Neonatal mass screening for metabolic disorders;Bickel;Eur J Pediatr,1981

2. Thyroxine determination in dried blood by radioimmunoassay: a screening method for neonatal hypothyroidism;Dussault,1973

3. Preliminary report on a mass screening program for neonatal hypothyroidism;Dussault;J Pediatr,1975

4. Thyroid development and disorders of thyroid function in the newborn;Fisher;N Engl J Med,1981

5. Blood screening for phenylketonuria;Guthrie;J Am Med Assoc,1961

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Birth prevalence of phenylalanine hydroxylase deficiency: a systematic literature review and meta-analysis;Orphanet Journal of Rare Diseases;2021-06-03

2. Global prevalence of classic phenylketonuria based on Neonatal Screening Program Data: systematic review and meta-analysis;Clinical and Experimental Pediatrics;2020-02-15

3. Settlement;SSRN Electronic Journal;2008

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