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Biotinidase
Results: 180

#	Item
111	Newborn Screening for Biotinidase Deficiency Add to Reading List Source URL: www.kdheks.gov Language: English - Date: 2012-02-06 15:23:17 Medicine Food and drink Galactose-1-phosphate uridylyltransferase deficiency Galactosemic cataract Inborn errors of carbohydrate metabolism Health Galactosemia
112	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
113	TSH: Abnormal or Borderline Disorder Group Result Value Interpretation Add to Reading List Source URL: azdhs.gov Language: English - Date: 2013-01-02 12:41:10 Adrenal gland disorders Rare diseases Intersexuality Biotinidase Genes Congenital adrenal hyperplasia Galactosemia Fatty-acid metabolism disorder Cystic fibrosis Health Medicine Pediatrics
114	OFFICE OF NEWBORN SCREENING 2008 CONFIRMED CASE REPORT PRIMARY PANEL OF 28 BLOODSPOT DISORDERS DISORDER ANALYTE Add to Reading List Source URL: azdhs.gov Language: English - Date: 2012-04-12 12:46:54 Medical genetics Newborn screening Propionic acidemia Methylmalonic acidemia Isovaleric acidemia Biotinidase deficiency Glutaric aciduria type 1 Medium-chain acyl-coenzyme A dehydrogenase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
115	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
116	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 13:46:16 Genes Pediatrics Genodermatoses Holocarboxylase synthetase deficiency Newborn screening Biotinidase deficiency Biotin Thiolase Holocarboxylase synthetase Health Genetics Chemistry
117	2011 Newborn Screening data as of August 2012.xlsx Add to Reading List Source URL: azdhs.gov Language: English - Date: 2012-09-04 18:41:39 Medical genetics Newborn screening Propionic acidemia Methylmalonic acidemia Isovaleric acidemia Glutaric aciduria type 1 Medium-chain acyl-coenzyme A dehydrogenase deficiency Biotinidase deficiency Maple syrup urine disease Health Rare diseases Genetic genealogy
118	2009 Summary including hearing.xlsx Add to Reading List Source URL: azdhs.gov Language: English - Date: 2012-04-12 12:46:56 Medical genetics Propionic acidemia Isovaleric acidemia Methylmalonic acidemia Biotinidase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Thiolase Multiple carboxylase deficiency Thalassemia Health Rare diseases Genetic genealogy
119	Agency of Human Services Division of Maternal and Child Health Children with Special Health Needs Vermont Newborn Screening Program REFUSAL TO CONSENT to REPEAT NEWBORN SCREENING Add to Reading List Source URL: healthvermont.gov Language: English - Date: 2011-07-21 16:18:35 Genetic genealogy Newborn screening Propionic acidemia Methylmalonic acidemia Isovaleric acidemia Maple syrup urine disease Glutaric aciduria type 1 Biotinidase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Medicine
120	Agency of Human Services Division of Maternal and Child Health Children with Special Health Needs Vermont Newborn Screening Program REFUSAL TO CONSENT to REPEAT NEWBORN SCREENING Add to Reading List Source URL: www.healthvermont.gov Language: English - Date: 2011-07-21 16:18:35 Genetic genealogy Newborn screening Propionic acidemia Methylmalonic acidemia Isovaleric acidemia Maple syrup urine disease Glutaric aciduria type 1 Biotinidase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Medicine