scholarly journals Improving participation by Aboriginal children in blood lead screening services in Broken Hill, NSW

2012 ◽  
Vol 23 (12) ◽  
pp. 234 ◽  
Author(s):  
Susan L. Thomas ◽  
Frances Boreland ◽  
David M. Lyle
2008 ◽  
Vol 19 (10) ◽  
pp. 180 ◽  
Author(s):  
Katina Kardamanidis ◽  
David M. Lyle ◽  
Frances Boreland

2004 ◽  
Vol 119 (2) ◽  
pp. 141-143 ◽  
Author(s):  
Embry M. Howell ◽  
Loretta Russette

PEDIATRICS ◽  
1994 ◽  
Vol 93 (2) ◽  
pp. 201-204
Author(s):  
Birt Harvey

In October 1991, the Centers for Disease Control and Prevention (CDC) recommended blood lead (BPb) screening for virtually all 1-year-old children and, preferably, for all 2-year-old children as well.1 In April 1993, the US Department of Health and Human Services distributed guidelines recommending that all newborns, regardless of race or ethnicity, be screened for sickle cell anemia.2 In June 1993, the National Institutes of Health issued a consensus conference recommendation that all infants be tested for hearing impairment within the first 3 months of life, preferably before newborns leave the hospital.3 In each instance, these screening recommendations were developed because a group of experts, after identifying a child health problem within its area of interest, believed that universal screening was indicated.


1995 ◽  
Vol 41 (3) ◽  
pp. 469-470 ◽  
Author(s):  
K Verebey ◽  
J F Rosen ◽  
D J Schonfeld ◽  
D Carriero ◽  
Y M Eng ◽  
...  

2005 ◽  
Vol 44 (7) ◽  
pp. 569-574 ◽  
Author(s):  
Arthur N. Feinberg ◽  
C. Kim Cummings

2007 ◽  
Vol 41 (7) ◽  
pp. 57
Author(s):  
Michele G. Sullivan

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