Organic acidemia - PDFSEARCH.IO - Document Search Engine

Organic acidemia
Results: 73

#	Item
41	Microsoft Word - Amino_Acidemias.doc Add to Reading List Source URL: health.tn.gov 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
42	(ISOVALERIC ACID CoA DEHYDROGENASE DEFICIENCY; IVA; IVD) Add to Reading List Source URL: health.tn.gov 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
43	Genetics Newborn Screening Program Add to Reading List Source URL: www.ct.gov Language: English - Date: 2007-07-09 15:52:59 Branched-chain amino acids Biology Malonyl-CoA decarboxylase deficiency Electron-transferring-flavoprotein dehydrogenase Newborn screening Isoleucine Organic acidemia Acyl CoA dehydrogenase ETFA Health Rare diseases Chemistry
44	Volume 6, Issue 3 October 2011 State of Tennessee Add to Reading List Source URL: health.tn.gov Language: English - Date: 2011-10-04 10:57:09 Health sciences Pediatrics Epidemiology Newborn screening Medical specialties Amino acid Organic acidemia Maple syrup urine disease Carnitine Health Medicine Rare diseases
45	Amino Acid Disorders Information for Parents  Overview Amino acid disorders are a group of rare, inherited conditions that affect infants from birth. They are caused by enzymes that do not work properly. Protein is ma Add to Reading List Source URL: www.kdheks.gov Language: English - Date: 2013-09-05 15:51:35 Genetic genealogy Newborn screening Phenylketonuria Maple syrup urine disease Amino acid Protein 3-Methylcrotonyl-CoA carboxylase deficiency Organic acidemia Health Medicine Rare diseases
46	Parent Fact Sheet Disorder Propionic Acidemia (PA) Cause Propionic Acidemia (PA) is one type of organic acid disorder. People with PA have problems breaking down and using certain amino acids from the foods they eat. PA Add to Reading List Source URL: www.chfs.ky.gov Language: English - Date: 2014-09-09 15:31:13 Genetic genealogy Propionic acidemia Carnitine Acidosis Maple syrup urine disease Methylmalonic acidemia Health Rare diseases Medicine
47	NEW Nutricia Metabolics_Logo CMYK Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2014-07-13 19:05:53 Pediatrics Epidemiology Newborn screening Medical genetics Inborn error of metabolism Methylmalonic acidemia Urea cycle disorder Isovaleric acidemia Organic acidemia Health Medicine Rare diseases
48	NEW Nutricia Metabolics_Logo CMYK Add to Reading List Source URL: www.oaanews.org Language: English - Date: 2014-07-13 16:04:14 Pediatrics Epidemiology Newborn screening Medical genetics Inborn error of metabolism Methylmalonic acidemia Urea cycle disorder Isovaleric acidemia Organic acidemia Health Medicine Rare diseases
49	Microsoft PowerPoint - November LP SC presentation [Read-Only] [Compatibility Mode] Add to Reading List Source URL: southeastgenetics.org Language: English - Date: 2010-11-30 18:27:12 Biology Pediatrics Metabolism Dicarboxylic acids GA1 Inborn error of metabolism Organic acidemia Dystonia Hypotonia Health Medicine Glutaric aciduria type 1
50	Parent Fact Sheet DISORDER Methylmalonic Acidemia (Cbl A, B) CAUSE MMA stands for "methylmalonic acidemia". It is one type of organic acid disorder. People with MMA have problems Add to Reading List Source URL: www.chfs.ky.gov Language: English - Date: 2014-09-11 01:32:54 Genetic genealogy Vitamin B12 Methylmalonic acidemia Methylmalonic acid Acidosis Protein Propionic acidemia Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Medicine Rare diseases