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Rare diseases / Medical genetics / Epidemiology / Newborn screening / Mental retardation / Neonatal heel prick / Phenylketonuria / Galactosemia / Congenital hypothyroidism / Health / Medicine / Pediatrics


A Compendium of Resources on Newborn Screening Policy and System Development Including references from "Serving the Family From Birth to the Medical Home- Recommendations from the Newborn Screening Task Force"
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Document Date: 2010-02-08 15:08:00

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City

Washington DC / Springfield / Rockville / New York / Washington / DC / Atlanta / /

Company

Oregon Public Health Laboratory / State Laboratory / Bain / Oxford University Press / Neometrics Inc. / Wilson / Lenton S / Hershey / Berenbaum SA / National Academy Press / Wisconsin Medical Journal / Forsberg SA. / Motulsky AG / New Zealand Medical Journal / Ades AE / /

Continent

North America / /

Country

Puerto Rico / Netherlands / Canada / Australia / United Kingdom / Taiwan / United States / U.S. Virgin Islands / /

Currency

USD / /

Facility

State Laboratory of Hygiene / Armed Forces Institute of Pathology / University of Wisconsin / laboratory Institutional Review Board / /

IndustryTerm

multi-disorder systems / telephone survey / clinical assessment protocol / information technology / genetic services / newborn screening protocol / healthcare providers / tier protocol / routine information systems / newborn screening follow-up services / on-line information / Potential solutions / collection site / carrier detection / carrier screening / on-line computer system / overall management / appropriate tool / /

MedicalCondition

central hypothyroidism / inherited metabolic disease / Congenital Adrenal Hyperplasia / HIV / individual disorders / permanent primary hypothyroidism / selected metabolic diseases / clearly defined diseases / MCAD deficiency / Galactosemia / hereditary disorders / Disorder / such relatively rare diseases / Phenylketonuria / metabolic disorders / illness / hypoglycemia / adrenal insufficiency / homocystinuria / least thirty different disorders / hereditary metabolic disorders / mental retardation / genetic disease / classic congenital adrenal hyperplasia / metabolic diseases / hypothyroidism / Tay-Sachs disease / congenital disorders / galactosemia and congenital hypothyroidism / metabolic acidosis / metabolic and endocrine disorders / adrenogenital syndrome / genetic diseases / lower disease / childhood disease / diseases / dehydrogenase deficiency / PKU / inborn errors of metabolism / deficiency / biochemically well-defined disorder / disorders / muscular dystrophy / specific congenital and inherited disorders / individual diseases / fatty acid oxidation disorders / each disorder / commonly encountered disorders / congenital and inherited disorders / Cystic Fibrosis / MS / phenylketonuria screening / Hemoglobinopathies / phenylketonuria and congenital hypothyroidism / endocrine disorders / sickle cell disorders / metabolic and endocrine diseases / inherited metabolic disorders / congenital diseases / Disease / Congenital Hypothyroidism / Medium Chain Co-A Dehydrogenase Deficiency / sickle cell disease / genetic and metabolic disorders / Biotinidase Deficiency / metabolic disease / primary hypothyroidism / maple syrup urine disease / /

MedicalTreatment

counseling / drug therapy / /

Organization

World Health Organization / Dutch Pediatric Surveillance Unit / National Institutes of Health / Fetus and Newborn Committee / Illinois Department of Public Health / Formosan Medical Association / Council of Regional Networks for Genetic Services / Arizona Department of Health Services / Armed Forces Institute of Pathology / Oxford University / Department of Health / NHS / Council of Regional Networks / Paediatric Society of New Zealand / Newborn Screening Task Force / Medical Association / Yale / Committee on Genetics / Subcommittee on Screening GABBDI / Wisconsin Division of Health / Ad Hoc Committee Task Force on Neonatal / Health Services Administration / Division of Public Health / National Academy of Sciences / National Screening Committee / Task Force on Genetic Testing / office of Women / U.S.Public Health Service / Cystic Fibrosis Foundation / American Academy of Pediatrics / U.S. military / University of Wisconsin / Council on Regional Networks for Genetic Services / /

Person

Arch Dis / Arch Pediatr Adolesc Med / J. Jones / Walker J. Jones / G. Hanson K. Annable / Genetic / Bailey L. Leslie / Kwon C. Farrell / S. Audit / J. Jones R. Smith / Clin Pediatr / Pract / Wolff J. Litsheim / /

Position

Prime Minister / physician / model for population screening. / King / pilot / advocate for children and families / national leader / counselor / Fernhoff PM / nurse / pediatrician / Newborn Screening General / practicing pediatrician / /

ProgrammingLanguage

L / /

ProvinceOrState

Michigan / Oklahoma / California / Georgia / Arizona / Texas / Wisconsin / Illinois / Oregon / Victoria / Tennessee / Iowa / /

PublishedMedium

Archives of Pediatrics & Adolescent Medicine / Medical Journal / /

Region

northern Taiwan / North East Thames / /

Technology

two tier protocol / information technology / diagnostic tests / genotyping / human genome / genotype / transplantation / newborn screening protocol / clinical assessment protocol / /

SocialTag