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Biotin deficiency
Results: 65

#	Item
31	Minnesota Department of Health[removed]POSITIVE NEWBORN SCREEN Add to Reading List Source URL: www.health.state.mn.us Language: English - Date: 2014-04-04 11:40:16 Medicine Biotinidase Biotin Newborn screening Multiple carboxylase deficiency Biotin deficiency Health Genetics Biotinidase deficiency
32	2012 Minnesota Department of Health POSITIVE NEWBORN SCREEN Add to Reading List Source URL: www.health.state.mn.us Language: English - Date: 2014-04-04 11:40:08 Medicine Biotinidase Newborn screening Biotin Multiple carboxylase deficiency Biotin deficiency Health Genetics Biotinidase deficiency
33	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.tn.gov 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
34	Microsoft Word - Biotinidase_Deficiency.doc Add to Reading List Source URL: health.tn.gov Language: English - Date: 2007-05-01 14:40:55 Biotinidase Genetic genealogy Medical genetics Biotin Biotin deficiency Holocarboxylase synthetase deficiency Genetics Genes Biotinidase deficiency
35	Newborn Screening for Biotinidase Deficiency Add to Reading List Source URL: www.kdheks.gov Language: English - Date: 2012-02-06 15:23:10 Medicine Biotinidase Rare diseases Biotin Newborn screening Biotin deficiency 3-Methylcrotonyl-CoA carboxylase deficiency Health Genetics Biotinidase deficiency
36	Disease Name Biotinidase Deficiency Alternate name(s) Add to Reading List Source URL: www.chfs.ky.gov Language: English - Date: 2014-09-12 05:36:15 Medical genetics Genes Multiple carboxylase deficiency B vitamins Biotinidase Biotin Biotin deficiency Holocarboxylase synthetase deficiency Genetics Biotinidase deficiency Genetic genealogy
37	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: www.chfs.ky.gov Language: English - Date: 2014-09-11 16:38:28 Biology Genes Biotin Cofactors Holocarboxylase synthetase Vitamin Multiple carboxylase deficiency Biotin deficiency Biotinidase deficiency Genetics Nutrition B vitamins
38	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: www.chfs.ky.gov Language: English - Date: 2014-09-11 06:35:25 B vitamins Genes Biotin Cofactors Biotin deficiency Vitamin Genetics Nutrition Chemistry
39	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: 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
40	American College of Medical Genetics ACT SHEET Newborn Screening ACT Sheet Add to Reading List Source URL: www.babysfirsttest.org Language: English - Date: 2013-01-09 13:27:59 Genes Pediatrics Genodermatoses Holocarboxylase synthetase deficiency Newborn screening Biotinidase deficiency Biotin Thiolase Holocarboxylase synthetase Health Genetics Chemistry

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