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Biotinidase
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#	Item
101	Missouri Guidelines for Newborn Screening Specimens Add to Reading List Source URL: www.health.mo.gov Language: English - Date: 2011-12-05 18:06:12 Inborn errors of carbohydrate metabolism Galactosemia Newborn screening Biotinidase deficiency Neonatal intensive care unit Infant Medicine Health Pediatrics
102	State of Illinois Rod R. Blagojevich, Governor Department of Public Health Eric E. Whitaker, M.D., M.P.H., Director Newborn Metabolic Add to Reading List Source URL: www.idph.state.il.us Language: English - Date: 2007-07-24 10:41:11 Medical genetics Newborn screening Propionic acidemia Fatty-acid metabolism disorder 2-Methylbutyryl-CoA dehydrogenase deficiency Biotinidase deficiency Isovaleric acidemia Medium-chain acyl-coenzyme A dehydrogenase deficiency Methylmalonic acidemia Health Rare diseases Genetic genealogy
103	Newborn Screening for Biotinidase Deficiency Add to Reading List Source URL: www.kdheks.gov Language: English - Date: 2013-09-05 15:51:35 Endocrinology Congenital hypothyroidism Hypothyroidism Thyroid Desiccated thyroid extract Newborn screening Thyroid disease in pregnancy Cretinism Health Thyroid disease Anatomy
104	Newborn Screening for Biotinidase Deficiency Add to Reading List Source URL: www.kdheks.gov Language: English - Date: 2012-02-06 15:23:12 Pediatrics Intersexuality Congenital adrenal hyperplasia Lipoid congenital adrenal hyperplasia 21-Hydroxylase Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency Newborn screening Cytochrome P450 reductase Adrenal gland Adrenal gland disorders Health Medicine
105	Newborn Screening for Biotinidase Deficiency Add to Reading List Source URL: www.kdheks.gov Language: English - Date: 2012-02-06 15:23:13 Medicine Pancreas disorders Channelopathy Cystic fibrosis Sweat test Immunoreactive trypsinogen Mucus Meconium Ivacaftor Health Pediatrics Biology
106	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
107	Microsoft Word - 35 PS 621 et seq _2_.doc Add to Reading List Source URL: genes-r-us.uthscsa.edu Language: English - Date: 2012-07-10 11:10:50 Genetic genealogy Newborn screening Maple syrup urine disease Phenylketonuria Methylmalonic acidemia Propionic acidemia Isovaleric acidemia Galactosemia Biotinidase deficiency Health Medicine Rare diseases
108	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
109	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
110	Microsoft Word - 3MCC.doc Add to Reading List Source URL: www.chfs.ky.gov Language: English - Date: 2014-09-09 15:58:40 3-Methylcrotonyl-CoA carboxylase deficiency Carnitine Rare diseases Amino acid Protein Very long-chain acyl-coenzyme A dehydrogenase deficiency Biotinidase deficiency Health Chemistry Medicine

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