Expanding screening for rare metabolic disease in the newborn: An analysis of costs, effect and ethical consequences for decision-making in Finland-Reference-Cited by-同舟云学术

Expanding screening for rare metabolic disease in the newborn: An analysis of costs, effect and ethical consequences for decision-making in Finland

Published:2007-01-02 Issue:8 Volume:94 Page:1126-1136
ISSN:0803-5253
Container-title:Acta Paediatrica
language:en
Short-container-title:

Author:

Autti-Rämö Ilona,Måkelå Marjukka,Sintonen Harri,Koskinen Hanna,Laajalahti Liisa,Halila Ritva,Kååriåinen Helena,Lapatto Risto,Nåntö-salonen Kirsti,Pulkki Kari,Renlund Martin,Salo Matti,Tyni Tiina

Publisher

Wiley

Subject

General Medicine,Pediatrics, Perinatology and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1651-2227.2005.tb02056.x/fullpdf

Reference37 articles.

1. The Influence of phenylalanine intake on the chemistry and behaviour of a phenylketonuric child;Bickel;Acta Paediatr Scand,1954

2. A simple method for detecting phenylketonuria in large populations of newborn infants;Guthrie;Pediatrics,1963

3. Effect of expanded newborn screening for biochemical genetic disorders on child outcomes and parental stress;Waisbren;JAMA,2003

4. Finnish disease heritage I: characteristics, causes, background;Norio;Hum Genet,2003

5. Prevalence of phenylketonuria and some other metabolic disorders among mentally retarded patients in Finland;Palo;Acta Neurol Scand,1967

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