Heather Carmichael Olson, PhD epub A Call to Action: Advancing Essential Services and Research on Fetal Alcohol Spectrum Disorders: A Report of the National Task Force on Fetal Alcohol Syndrome and Fetal Alcohol Effect

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A Call to Action: Advancing Essential Services and Research on Fetal Alcohol Spectrum Disorders: A Report of the National Task Force on Fetal Alcohol Syndrome and Fetal Alcohol Effect

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18,9 x 0,6 x 24,6 cm 28 Şubat 2018 ROBERT H BORK 21,6 x 0,2 x 27,9 cm Additional Contributors 30 Ekim 2011 WADE H MCCREE 1 Ocak 2017 28 Ekim 2011 18,9 x 0,3 x 24,6 cm 18,9 x 0,5 x 24,6 cm Mdpi AG 29 Ekim 2011 ERWIN N GRISWOLD 3 Ocak 2017 18,9 x 0,4 x 24,6 cm Kolektif 18,9 x 0,2 x 24,6 cm
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yazar Heather Carmichael Olson, PhD Melinda M. Ohlemiller, BA, MA Mary J. O'Connor, PhD, ABPP Carole W. Brown, EdD Colleen A. Morris, MD Karla Damus, RN, PhD U.S. Department of Health and Human Services
isbn 10 1478281480
isbn 13 978-1478281481
Yayımcı CreateSpace Independent Publishing Platform
Dilim İngilizce
Boyutlar ve boyutlar 21,6 x 0,2 x 27,9 cm
Tarafından yayınlandı A Call to Action: Advancing Essential Services and Research on Fetal Alcohol Spectrum Disorders: A Report of the National Task Force on Fetal Alcohol Syndrome and Fetal Alcohol Effect 20 Temmuz 2012

In 2004, the National Task Force on Fetal Alcohol Syndrome and Fetal Alcohol Effect, coordinated by the Centers for Disease Control and Prevention’s National Center on Birth Defects and Developmental Disabilities, established a working group committed to addressing the needs of individuals living with fetal alcohol spectrum disorders (FASDs) and their families. The culmination of this working group’s discussions and Task Force deliberations is reflected in this Call to Action report. The document highlights ten recommendations to improve and expand efforts regarding early identification, diagnostic services, and quality research on interventions for individuals with FASDs and their families. Additional background information is provided to support these recommendations and to further educate readers on the topic of FASDs, progress to date, and what still needs to be done to support individuals with FASDs. The intent of this report is to guide federal, state and local agencies, researchers and clinicians, family support groups, and other partners on actions needed to advance essential services for individuals with FASDs and their families and to promote continued intervention research efforts.

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