Newborn screening for galactosaemia-Reference-Cited by-同舟云学术

Newborn screening for galactosaemia

Published:2016-07-03 Issue: Volume: Page:
ISSN:1465-1858
Container-title:Cochrane Database of Systematic Reviews
language:en
Short-container-title:

Author:

Lak Rohollah¹,Yazdizadeh Bahareh²,Davari Majid³,Nouhi Mojtaba⁴,Kelishadi Roya⁵

Affiliation:

1. Tehran University of Medical Sciences; Department of Public Health; Tehran Iran

2. Tehran University of Medical Sciences; Knowledge Utilization Research Center; 1547 North Karegar St, Enghelab Ave Tehran Iran

3. Faculty of Pharmacy, Tehran University of Medical Sciences; Department of Pharmacoeconomics and Pharmaceutical Administration; Tehran Iran

4. Iran University of Medical Sciences; Health Management and Economics Research Center; ValiAsr St Vanak Square Tehran Iran 1996713883

5. Isfahan University of Medical Sciences; Child Growth and Development Research Center, Research Institute for Primordial Prevention of Non-Communicable Diseases; Hezar Jerib Ave Isfahan Iran

Publisher

Wiley

Subject

Pharmacology (medical)

Reference16 articles.

1. Research for newborn screening: Developing a national framework;Botkin;Pediatrics,2005

2. Novel GALT variations and mutation spectrum in the Korean population with decreased galactose-1-phosphate uridyltransferase activity;Choi;BMC Medical Genetics,2014

3. Fridovich-Keil JL Walter JH Galactosemia The Online Metabolic & Molecular Bases of Inherited Disease. http://www.ommbid.com/ 2008 1 20

4. The clinical and molecular spectrum of galactosaemia in patients from the Cape Town region of South Africa;Henderson;BMC Pediatrics,2002

5. Measuring inconsistency in meta-analyses;Higgins;BMJ,2003

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