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Biotin deficiency
Results: 65

#	Item
1	Chart of Metabolic Disorders Screened Table of Disorders Screened by Program Condition Incidence Add to Reading List Source URL: health.hawaii.gov Language: English - Date: 2015-02-26 15:37:45 Rare diseases Fatty-acid metabolism disorder Very long-chain acyl-coenzyme A dehydrogenase deficiency Glutaric aciduria type 1 Carnitine Biotinidase deficiency Biotin Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency Health Genetic genealogy Medical genetics
2	American College of Medical Genetics ACT SHEET Newborn Screening ACT Sheet Add to Reading List Source URL: www.babysfirsttest.org Language: English - Date: 2012-11-09 11:16:32 Genodermatoses Holocarboxylase synthetase deficiency Multiple carboxylase deficiency 3-Methylcrotonyl-CoA carboxylase deficiency Newborn screening Biotinidase deficiency 3-hydroxy-3-methylglutaryl-CoA lyase deficiency Biotin Medical genetics Medicine Health Pediatrics
3	Microsoft Word - Biotinidase_Deficiency_fact_sheet_for_web_2003_doc.doc Add to Reading List Source URL: health.mo.gov Language: English - Date: 2009-04-15 07:49:08 Biotinidase deficiency Biotinidase Biotin Genetic disorder Medical genetics Biotin deficiency Holocarboxylase synthetase deficiency Medicine Genetics Health
4	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
5	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
6	Microsoft PowerPoint - #1Therrell Secretary's Advisory Committee[removed]pps Add to Reading List Source URL: www.hrsa.gov Language: English - Date: 2014-12-04 01:13:28 Medicine Epidemiology Newborn screening Pediatrics Biotinidase deficiency Biotinidase Biotin Phenylketonuria Maple syrup urine disease Health Rare diseases Chemistry
7	Parents‛ Guide To BD Biotinidase Deficiency California Department of Public Health Add to Reading List Source URL: www.cdph.ca.gov Language: English - Date: 2014-10-06 16:45:50 Genetics Genes Biotinidase deficiency Biotinidase Biotin Newborn screening Vitamin Biotin deficiency Holocarboxylase synthetase deficiency B vitamins Health Nutrition
8	Mitochondrial Carbonic Anhydrase VA Deficiency Resulting from CA5A Alterations Presents with Hyperammonemia in Early Childhood Add to Reading List Source URL: www.tidebc.org Language: English - Date: 2014-02-13 12:45:25 Enzymes Carbonic anhydrase Carbonic anhydrase inhibitors Hyperammonemia Propionyl-CoA carboxylase Pyruvate carboxylase Biotin Medium-chain acyl-coenzyme A dehydrogenase deficiency Acetazolamide Chemistry Medicine Health
9	Beginning with specimens tested on November 30, 1998, the Newborn Screening Program (NBS) will be implementing significant changes in the way in which we report results Add to Reading List Source URL: www.cdph.ca.gov Language: English - Date: 2013-01-26 23:54:01 Medicine Biotinidase Newborn screening Biotin Biotin deficiency 3-Methylcrotonyl-CoA carboxylase deficiency Health Genetics Biotinidase deficiency
10	Biotinidase Deficiency (BlOT) (metabolic condition: organic acid disorder) Also known as: • BTD deficiency How is BlOT treated? Add to Reading List Source URL: www.albertahealthservices.ca Language: English - Date: 2013-09-16 18:30:59 B vitamins Biotinidase deficiency Genes Biotinidase Biotin Multiple carboxylase deficiency Medical genetics 3-Methylcrotonyl-CoA carboxylase deficiency Holocarboxylase synthetase deficiency Medicine Genetics Health