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Propionic acid
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#	Item
71	Parent Fact Sheet DISORDER Methylmalonic Acidemia Mutase Deficiency (MUT) CAUSE MMA stands for "methylmalonic acidemia". It is one type of organic acid disorder. People with MMA have Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-08 18:18:59 Genetic genealogy Methylmalonic acidemia Vitamin B12 Acidosis Methylmalonic acid Protein Propionic acidemia Glutaric aciduria type 1 Health Medicine Rare diseases
72	Microsoft Word[removed]Condition list.doc Add to Reading List Source URL: www.ndhealth.gov Language: English - Date: 2012-08-28 15:52:15 Medical genetics Hyperammonemia Glutaric aciduria type 1 Isovaleric acidemia Medium-chain acyl-coenzyme A dehydrogenase deficiency Methylmalonic acidemia Propionic acidemia Fatty-acid metabolism disorder Carnitine-acylcarnitine translocase deficiency Health Rare diseases Genetic genealogy
73	SACHDNC Recommended Uniform Screening Panel1 Add to Reading List Source URL: www.hrsa.gov Language: English - Date: 2013-05-02 18:14:46 Newborn screening Methylmalonic acidemia Isovaleric acidemia Propionic acidemia Fatty-acid metabolism disorder Glutaric aciduria type 1 Glutaric acidemia type 2 Carnitine-acylcarnitine translocase deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Medicine
74	(ISOVALERIC ACID CoA DEHYDROGENASE DEFICIENCY; IVA; IVD) Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2007-05-01 10:03:12 Medical genetics Organic acidemia Isovaleric acidemia Propionic acidemia Newborn screening Methylmalonic acidemia Glutaric aciduria type 1 Malonyl-CoA decarboxylase deficiency 3-Methylcrotonyl-CoA carboxylase deficiency Health Rare diseases Genetic genealogy
75	Microsoft Word - Amino_Acidemias.doc Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2007-05-01 14:35:52 Medical genetics Maple syrup urine disease Glycine encephalopathy Newborn screening Phenylketonuria Amino acid Phenylalanine Organic acidemia Propionic acidemia Health Rare diseases Genetic genealogy
76	Acute management of propionic acidemia Add to Reading List Source URL: www.oaanews.org Language: English - Date: 2012-01-04 11:28:34 Hyperammonemia Glycogen storage disease type I Acidosis Propionic acidemia Newborn screening Metabolic acidosis Arterial blood gas Dialysis Acid–base homeostasis Medicine Health Rare diseases
77	Visio-C3[removed] edits.vsd Add to Reading List Source URL: www.ncbi.nlm.nih.gov Language: English Coenzymes Nutrition Methylmalonic acidemia Propionic acidemia Vitamin B12 Methylmalonyl-CoA mutase Propionyl-CoA carboxylase Methylmalonyl-CoA Methylmalonic acid Chemistry Health Rare diseases
78	American College of Medical Genetics ACT SHEET Add to Reading List Source URL: www.ncbi.nlm.nih.gov Language: English Methylmalonic acidemia Newborn screening Methylmalonic acid Propionic acidemia Methylmalonyl-CoA mutase Hyperammonemia Vitamin B12 Medical genetics Propionyl-CoA Medicine Health Rare diseases
79	ARTICLE IN PRESS Molecular Genetics and Metabolism xxx[removed]xxx–xxx Add to Reading List Source URL: www.oaanews.org Language: English - Date: 2011-08-22 14:10:55 Genetic genealogy Hepatology Fatty acids Metabolism Quaternary ammonium compounds Carnitine Propionic acidemia Fatty-acid metabolism disorder Inborn error of lipid metabolism Health Medicine Rare diseases
80	Organic Acidurias A guide for patients, parents and families Jane Gick Add to Reading List Source URL: www.e-imd.org Language: English - Date: 2012-05-31 08:37:37 Medical genetics Isovaleric acidemia Propionic acidemia Organic acidemia Methylmalonic acidemia Urea cycle disorder Amino acid Protein Metabolism Health Rare diseases Genetic genealogy

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