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Biotin deficiency
Results: 65

#	Item
51	Microsoft Word - biotinidase Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:35:52 Genetic genealogy Multiple carboxylase deficiency Biotinidase Biotin Rare diseases Newborn screening Biotin deficiency Holocarboxylase synthetase deficiency Health Genetics Biotinidase deficiency
52	IDPH logo final panton 294 Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2010-02-10 11:12:42 Rare diseases Epidemiology Newborn screening Phenylketonuria Medical genetics Biotinidase deficiency Cystic fibrosis Sickle-cell disease Biotin Health Medicine Pediatrics
53	Additional information: WE CAN NOW CHECK YOUR Add to Reading List Source URL: www.ct.gov Language: English - Date: 2007-07-09 15:53:18 Rare diseases Newborn screening Phenylketonuria Biotin Human breast milk Fatty acid metabolism Medium-chain acyl-coenzyme A dehydrogenase deficiency Milk Protein Health Medicine Genetic genealogy
54	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
55	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
56	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
57	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
58	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
59	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
60	Microsoft Word - Biotinidase_Deficiency.doc Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2007-05-01 14:40:55 Biotinidase Genetic genealogy Medical genetics Biotin Biotin deficiency Holocarboxylase synthetase deficiency Genetics Genes Biotinidase deficiency

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