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Biotinidase
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161	Microsoft Word - 3MCC.doc Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-09 04:53:48 3-Methylcrotonyl-CoA carboxylase deficiency Carnitine Rare diseases Amino acid Protein Very long-chain acyl-coenzyme A dehydrogenase deficiency Biotinidase deficiency Health Chemistry Medicine
162	PARENT FACT SHEET DISORDER Biotinidase Deficiency (BIO) CAUSE BIO affects the way a person’s body uses the vitamin, biotin. Biotin is an important vitamin that Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-09 04:53:44 B vitamins Genes Biotin Cofactors Biotin deficiency Vitamin Genetics Nutrition Chemistry
163	PARENT FACT SHEET DISORDER Multiple carboxylase deficiency (MCD) CAUSE MCD occurs when an enzyme called “holocarboxylase synthetase” (HCS) is either missing or not working Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-09 06:52:19 Biology Genes Biotin Cofactors Holocarboxylase synthetase Vitamin Multiple carboxylase deficiency Biotin deficiency Biotinidase deficiency Genetics Nutrition B vitamins
164	Disease Name Biotinidase Deficiency Alternate name(s) Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-08 19:47:02 Medical genetics Genes Multiple carboxylase deficiency B vitamins Biotinidase Biotin Biotin deficiency Holocarboxylase synthetase deficiency Genetics Biotinidase deficiency Genetic genealogy
165	Rhode Island screens babies for 28 health conditions and hearing loss. The conditions are grouped in the categories explained below, and a list of all the conditions is on the other side of this card. Early detection and Add to Reading List Source URL: www.health.ri.gov Language: English - Date: 2014-06-27 15:48:15 Medical genetics Newborn screening Methylmalonic acidemia Propionic acidemia Isovaleric acidemia Glutaric aciduria type 1 Biotinidase deficiency 3-Methylcrotonyl-CoA carboxylase deficiency Biotin Health Rare diseases Genetic genealogy
166	english one simple step.pmd Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2009-09-24 13:46:08 Pediatrics Rare diseases Epidemiology Newborn screening Medical genetics Phenylketonuria Biotinidase deficiency Cystic fibrosis Biotin Health Medicine Biology
167	Inside: Continuing Medical Education for U.S. Physicians and Nurses April 13, [removed]Vol[removed]No. RR-3 Recommendations and Add to Reading List Source URL: www.cdc.gov Language: English - Date: 2001-08-06 09:59:11 Chemistry Newborn screening Phenylketonuria Tandem mass spectrometry Fatty-acid metabolism disorder Medium-chain acyl-coenzyme A dehydrogenase deficiency Isovaleric acidemia Carnitine Biotinidase deficiency Health Rare diseases Medicine
168	PDF Document Add to Reading List Source URL: www.state.tn.us Language: English - Date: 2013-01-02 12:32:31 Newborn screening Phenylketonuria Galactosemia Congenital adrenal hyperplasia Congenital hypothyroidism Biotinidase deficiency Inborn error of metabolism Genetic testing PKU Health Medicine Pediatrics
169	Biotinidase Deficiency Jewell C. Ward, MD, Ph D, Chief, Division of Medical Genetics Department of Pediatrics University of Tennessee-Memphis 711 Jefferson, CDD, Room 522 Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2007-05-01 10:01:52 Biotinidase deficiency Genes Biotinidase Biocytin Biotin Newborn screening Medical genetics Biotin deficiency Holocarboxylase synthetase deficiency Medicine Health Genetics
170	Phenylketonuria, Hypothyroidism and Other Metabolic/Genetic Defects Add to Reading List Source URL: tn.gov Language: English - Date: 2013-01-02 12:32:31 Newborn screening Phenylketonuria Galactosemia Congenital adrenal hyperplasia Congenital hypothyroidism Biotinidase deficiency Inborn error of metabolism Genetic testing PKU Health Medicine Pediatrics

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