Medium-chain acyl-coenzyme A dehydrogenase deficiency

Results: 161



#Item
21Medium-chain acyl-coenzyme A dehydrogenase deficiency / Fatty-acid metabolism disorder / Newborn screening / Medical genetics / Fatty acid metabolism / Very long-chain acyl-coenzyme A dehydrogenase deficiency / Malonyl-CoA decarboxylase deficiency / Medicine / Health / Rare diseases

Microsoft Word - MCAD.doc

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Source URL: health.mo.gov

Language: English - Date: 2007-09-14 07:57:54
22Fatty-acid metabolism disorder / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Carnitine-acylcarnitine translocase deficiency / Short-chain acyl-coenzyme A dehydrogenase deficiency / Fatty acid metabolism / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Mitochondrial trifunctional protein deficiency / Newborn screening / Lipid / Health / Medicine / Rare diseases

Microsoft Word - FAOD.doc

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Source URL: health.state.tn.us

Language: English - Date: 2007-05-01 14:47:24
23Hepatology / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Fatty-acid metabolism disorder / Hypoglycemia / Blood sugar / Very long-chain acyl-coenzyme A dehydrogenase deficiency / Carnitine-acylcarnitine translocase deficiency / Health / Medicine / Diabetes

Table of Contents Contents Page What is MCADD? ........................................ 1-5

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Source URL: www.cdph.ca.gov

Language: English - Date: 2014-10-06 16:45:48
24Medical genetics / Newborn screening / Methylmalonic acidemia / Propionic acidemia / Biotinidase deficiency / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Malonyl-CoA decarboxylase deficiency / 3-Methylcrotonyl-CoA carboxylase deficiency / Isovaleric acidemia / Health / Rare diseases / Genetic genealogy

DRAFT[removed]ARTICLE 2. NEWBORN AND INFANT SCREENING Section R9[removed].

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Source URL: www.azdhs.gov

Language: English - Date: 2013-08-21 11:09:22
25Medical genetics / Newborn screening / Methylmalonic acidemia / Glutaric aciduria type 1 / Galactosemia / Methylmalonyl-CoA mutase deficiency / Phenylketonuria / Isovaleric acidemia / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Health / Rare diseases / Genetic genealogy

METABOLIC/SICKLE CELL SCREENING GUIDELINES As mandated by KRS[removed], Newborn Screening tests include:

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Source URL: www.chfs.ky.gov

Language: English - Date: 2014-12-04 13:18:40
26Newborn screening / Pediatrics / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Inborn errors of carbohydrate metabolism / Hypotonia / Health / Medicine / Epidemiology

Adaptive Turnaround Documents, Newborn Screening and the Medical Home

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Source URL: www.hrsa.gov

Language: English - Date: 2014-12-04 01:13:15
27Genetic genealogy / Newborn screening / Methylmalonic acidemia / Isovaleric acidemia / Fatty-acid metabolism disorder / Hyperammonemia / 3-Methylglutaconic aciduria / Glutaric aciduria type 1 / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Health / Medicine / Rare diseases

Microsoft Word[removed]sheet 1.doc

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Source URL: www.cdph.ca.gov

Language: English - Date: 2013-09-30 16:56:07
28Rare diseases / Medical genetics / Epidemiology / Newborn screening / Inborn error of metabolism / Screening / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Genetic counseling / Guthrie test / Medicine / Health / Pediatrics

Public Comments to the Advisory Committee on Heritable Disorders and Genetic Diseases in Newborns and Children

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Source URL: www.hrsa.gov

Language: English - Date: 2014-12-04 01:13:29
29Enzymes / Carbonic anhydrase / Carbonic anhydrase inhibitors / Hyperammonemia / Propionyl-CoA carboxylase / Pyruvate carboxylase / Biotin / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Acetazolamide / Chemistry / Medicine / Health

Mitochondrial Carbonic Anhydrase VA Deficiency Resulting from CA5A Alterations Presents with Hyperammonemia in Early Childhood

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Source URL: www.tidebc.org

Language: English - Date: 2014-02-13 12:45:25
30Fatty acids / Metabolism / Pediatrics / Inborn error of lipid metabolism / Rare diseases / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Very long-chain acyl-coenzyme A dehydrogenase deficiency / Newborn screening / Carnitine / Health / Medicine / Biology

Death Caused by Perioperative Fasting and Sedation in a Child with Unrecognized VLCAD Charles R. Roe, MD, Hobart E. Wiltse, MD, PhD Lawrence Sweetman, PhD, and Linda L Alvarado, BS Abstract An adopted[removed]year-old girl

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Source URL: www.fodsupport.org

Language: English - Date: 2012-05-31 13:41:07
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