Biotinidase

Results: 180



#Item
131Medical 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

2011 Newborn Screening data as of August 2012.xlsx

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Source URL: www.azdhs.gov

Language: English - Date: 2012-09-04 18:41:39
132Newborn screening / Congenital hearing loss / Galactosemia / Screening / Cystic fibrosis / Congenital hypothyroidism / Phenylketonuria / Biotinidase deficiency / Infant / Health / Medicine / Pediatrics

2007 Executive Summary.pub

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Source URL: dhhs.ne.gov

Language: English - Date: 2014-08-22 13:53:14
133Rare diseases / Epidemiology / Newborn screening / Inborn errors of carbohydrate metabolism / Association of Public Health Laboratories / Screening / Galactosemia / Phenylketonuria / Biotinidase deficiency / Health / Medicine / Pediatrics

NEWBORN SCREENING IN NEBRASKA Newborn Screening for Metabolic & Inherited Disorders and Early Hearing Detection &

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Source URL: dhhs.ne.gov

Language: English - Date: 2014-08-22 13:53:14
134Medical 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

2009 Summary including hearing.xlsx

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Source URL: www.azdhs.gov

Language: English - Date: 2012-04-12 12:46:56
135Medical 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

OFFICE OF NEWBORN SCREENING 2008 CONFIRMED CASE REPORT PRIMARY PANEL OF 28 BLOODSPOT DISORDERS DISORDER ANALYTE

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Source URL: www.azdhs.gov

Language: English - Date: 2012-04-12 12:46:54
136Newborn screening / Phenylketonuria / Biotinidase deficiency / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Biotin / Galactosemia / Congenital hypothyroidism / Guthrie test / Congenital adrenal hyperplasia / Health / Medicine / Pediatrics

PDF Document

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Source URL: www.ok.gov

Language: English - Date: 2012-11-29 10:48:21
137Pediatrics / Newborn screening / Methylmalonic acidemia / Glutaric aciduria type 1 / Biotinidase deficiency / Isovaleric acidemia / Inborn error of metabolism / Galactosemia / Congenital hypothyroidism / Health / Medicine / Rare diseases

AN ACT RELATING TO HEALTH CARE; AMENDING A SECTION OF THE PUBLIC HEALTH ACT TO REQUIRE TESTING FOR CRITICAL CONGENITAL HEART DISEASE IN NEWBORN INFANTS. BE IT ENACTED BY THE LEGISLATURE OF THE STATE OF NEW MEXICO:

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Source URL: www.nmlegis.gov

Language: English - Date: 2014-03-03 18:02:18
138Pediatrics / Epidemiology / Newborn screening / Mental retardation / Metabolism / Very long-chain acyl-coenzyme A dehydrogenase deficiency / Isovaleric acidemia / Methylmalonic acidemia / Biotinidase deficiency / Health / Medicine / Rare diseases

Health Cadham Provincial Laboratory Provincial Programs and Services P.O. Box 8450

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Source URL: www.gov.mb.ca

Language: English - Date: 2012-05-08 12:28:03
139Rare diseases / Epidemiology / Newborn screening / Inborn errors of carbohydrate metabolism / Adrenal gland disorders / Screening / Biotinidase deficiency / Maternal and Child Health Bureau / Galactosemia / Health / Medicine / Pediatrics

NEWBORN SCREENING IN NEBRASKA Newborn Screening for Metabolic and Inherited Disorders AND Newborn Hearing Screening

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Source URL: dhhs.ne.gov

Language: English - Date: 2014-08-22 10:53:04
140Pediatrics / Epidemiology / Newborn screening / Inborn errors of carbohydrate metabolism / Cystic fibrosis / Biotinidase deficiency / Methylmalonic acidemia / Propionic acidemia / Isovaleric acidemia / Health / Medicine / Rare diseases

NEWBORN SCREENING IN NEBRASKA Newborn Bloodspot Screening for Metabolic & Inherited Disorders and Early Hearing Detection &

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Source URL: dhhs.ne.gov

Language: English - Date: 2014-08-22 16:52:20
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