Fatty-acid metabolism disorder

Results: 210



#Item
11Medical genetics / Fatty-acid metabolism disorder / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Newborn screening / Fatty acid metabolism / Very long-chain acyl-coenzyme A dehydrogenase deficiency / Short-chain acyl-coenzyme A dehydrogenase deficiency / Health / Rare diseases / Genetic genealogy

Microsoft Word - VLCAD.doc

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Source URL: health.mo.gov

Language: English - Date: 2007-09-14 09:09:50
12Fatty-acid metabolism disorder / Newborn screening / Fatty acid metabolism / Short-chain acyl-coenzyme A dehydrogenase deficiency / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Health / Rare diseases / Medicine

Microsoft Word - SCAD.doc

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Source URL: health.mo.gov

Language: English - Date: 2007-09-14 09:00:00
13Genetic genealogy / Glutaric acidemia type 2 / Fatty-acid metabolism disorder / Glutaric aciduria type 1 / Newborn screening / Fatty acid metabolism / Propionic acidemia / Very long-chain acyl-coenzyme A dehydrogenase deficiency / Health / Rare diseases / Medicine

Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD)

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Source URL: health.mo.gov

Language: English - Date: 2009-02-03 16:51:42
14Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Fatty acids / Fatty-acid metabolism disorder / Acute fatty liver of pregnancy / Hepatology / Newborn screening / Fatty acid metabolism / Mitochondrial trifunctional protein / Health / Medicine / Rare diseases

Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD)

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Source URL: health.mo.gov

Language: English - Date: 2009-02-03 16:51:53
15Fatty-acid metabolism disorder / Carnitine-acylcarnitine translocase deficiency / Carnitine / Newborn screening / Health / Rare diseases / Medicine

Carnitine/Acylcarnitine Translocase Deficiency (CACT) A fatty acid oxidation disorder What is it? Carnitine/Acylcarnitine Translocase Deficiency (also known as CACT) is an inherited fatty acid oxidation disorder. Patient

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Source URL: health.mo.gov

Language: English - Date: 2007-09-13 15:09:34
16Medium-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
17Rare diseases / Systemic primary carnitine deficiency / Fatty-acid metabolism disorder / Carnitine / Newborn screening / Fatty acid metabolism / Cud / Carnitine palmitoyltransferase I deficiency / Carnitine-acylcarnitine translocase deficiency / Health / Medicine / Hepatology

Microsoft Word - mso31.doc

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Source URL: health.mo.gov

Language: English - Date: 2006-09-11 10:19:50
18Hepatology / Chemistry / Fatty-acid metabolism disorder / Fatty acids / Fatty acid metabolism / Carnitine O-palmitoyltransferase / Carnitine / Newborn screening / Carnitine palmitoyltransferase II deficiency / Health / Medicine / Rare diseases

Microsoft Word - CPT-11.doc

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Source URL: health.mo.gov

Language: English - Date: 2007-09-13 15:39:40
193-hydroxy-3-methylglutaryl-CoA lyase deficiency / Genetic genealogy / 3-hydroxy-3-methylglutaryl-CoA lyase / Newborn screening / Protein families / Fatty-acid metabolism disorder / HMG-CoA reductase / Health / Rare diseases / Medicine

Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD)

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Source URL: health.mo.gov

Language: English - Date: 2009-02-03 16:51:10
20Fatty-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
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