<--- Back to Details
First PageDocument Content
Biology / Maple syrup urine disease / Branched-chain alpha-keto acid dehydrogenase complex / Inborn error of metabolism / Newborn screening / Branched-chain amino acid / Dihydrolipoamide dehydrogenase / Propionic acidemia / Methylmalonic acidemia / Health / Rare diseases / Medicine
Date: 2007-06-25 16:37:12
Biology
Maple syrup urine disease
Branched-chain alpha-keto acid dehydrogenase complex
Inborn error of metabolism
Newborn screening
Branched-chain amino acid
Dihydrolipoamide dehydrogenase
Propionic acidemia
Methylmalonic acidemia
Health
Rare diseases
Medicine

Microsoft Word - msud_ref

Add to Reading List

Source URL: www.idph.state.ia.us

Download Document from Source Website

File Size: 33,33 KB

Share Document on Facebook

Similar Documents

Newborn screening / Isovaleric acidemia / Methylmalonic acidemia / Acyl CoA dehydrogenase / Biotinidase deficiency / Galactosemia / Methylmalonic acid / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Guthrie test / Health / Rare diseases / Medicine

Newborn Screening Year in Review 86,586 For Babies Born in 2013 Bloodspot Samples Received Initial

DocID: 14zTU - View Document

Newborn screening / Isovaleric acidemia / Galactosemia / Methylmalonic acidemia / Propionic acidemia / Malonyl-CoA decarboxylase deficiency / Inborn error of metabolism / Argininosuccinic aciduria / Organic acidemia / Health / Rare diseases / Medicine

TIMELINESS OF NEWBORN SCREENING – DACHDNC LABORATORY STANDARDS AND PROCEDURES SUBCOMMITTEE DRAFT FINDINGS AND PROPOSED RECOMMENDATIONS Kellie Kelm, PhD

DocID: 12v8A - View Document

Medical genetics / Newborn screening / Isovaleric acidemia / Propionic acidemia / Methylmalonic acidemia / Fatty-acid metabolism disorder / Very long-chain acyl-coenzyme A dehydrogenase deficiency / Galactosemia / Malonyl-CoA decarboxylase deficiency / Health / Rare diseases / Genetic genealogy

Timeliness of Newborn Screening – DACHDNC’s laboratory standards and procedures subcommittee draft findings

DocID: 12jOC - View Document

Newborn screening / Isovaleric acidemia / Methylmalonic acidemia / Acyl CoA dehydrogenase / Biotinidase deficiency / Galactosemia / Methylmalonic acid / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Guthrie test / Health / Rare diseases / Medicine

Newborn Screening Year in Review 86,586 For Babies Born in 2013 Bloodspot Samples Received Initial

DocID: 11G3r - View Document

Pediatrics / Epidemiology / Newborn screening / Mental retardation / Medical tests / Screening / Methylmalonic acidemia / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Isovaleric acidemia / Health / Medicine / Rare diseases

Microsoft Word - Newborn Screening framework_FINAL.doc

DocID: U9E1 - View Document