Newborn Screening Follow-Up Within the Lifespan Context. Michigan's Experience

American Journal of Preventive Medicine

Volumn 38, Issue 4 SUPPL., 2010, Pages

  Grigorescu, Violanda ^a   Kleyn, Mary J ^a   Korzeniewski, Steven J ^a   Young, William I ^a   Whitten Shurney, Wanda ^b  

^a MICHIGAN DEPARTMENT OF COMMUNITY HEALTH   (United States)

^b CHILDREN'S HOSPITAL OF MICHIGAN   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COMORBIDITY; FOLLOW UP; HEALTH CARE COST; HEALTH CARE POLICY; HEALTH CARE UTILIZATION; HEALTH PROGRAM; HEALTH SURVEY; HUMAN; LIFESPAN; NEWBORN SCREENING; OUTCOME ASSESSMENT; REVIEW; SICKLE CELL ANEMIA; STATISTICAL MODEL; UNITED STATES;

ANEMIA, SICKLE CELL; GENETIC TESTING; HETEROZYGOTE DETECTION; HUMANS; INFANT, NEWBORN; MICHIGAN; NEONATAL SCREENING; POPULATION SURVEILLANCE; PUBLIC HEALTH INFORMATICS;

EID: 77949429435     PISSN: 07493797     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.amepre.2010.01.002     Document Type: Review

References (5)

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3. Platt O.S., Brambilla D.J., Rosse W.F., et al. Mortality in sickle cell disease: life expectancy and risk factors for early death. NEJM 330 (1994) 1639-1644
4. Grosse S.D., Boulet S.L., Amendah D.D., and Oyeku S.O. Administrative data sets and health services research on hemoglobinopathies: a review of the literature. Am J Prev Med 38 4S (2010) S557-S567
5. Korzeniewski S.J., Grigorescu V., Copeland G., et al. Methodological innovations in data gathering: newborn screening linkage with live births records, Michigan, 1/2007-3/2008. Matern Child Health J (2009 April 8) [Epub ahead of print]