Biotinidase

Results: 180



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61Spreadsheet / Biotinidase / Lua / Software / Computing / BTD

PDF Document

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Source URL: www.pragma-ade.com

Language: English - Date: 2013-03-22 13:41:16
62Pediatrics / 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: umanitoba.ca

Language: English - Date: 2014-11-21 14:14:10
63Rare diseases / Fatty-acid metabolism disorder / Glutaric aciduria type 1 / Very long-chain acyl-coenzyme A dehydrogenase deficiency / Carnitine / Biotinidase deficiency / Biotin / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Health / Medicine / Genetic genealogy

Microsoft Word - Chart_of_Table_of_Metabolic_Disorders_rev.doc

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Source URL: health.hawaii.gov

Language: English - Date: 2013-05-30 20:03:03
64Rare diseases / Medical genetics / Adrenal gland disorders / Epidemiology / Newborn screening / Phenylketonuria / Biotinidase deficiency / PKU / Genetic disorder / Health / Medicine / Pediatrics

Article Title: Genetic Implications of Newborn Screening Author: Andrea Amalfitano D.O., Ph.D1* 1

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Source URL: amdapompe.ehclients.com

Language: English - Date: 2012-01-17 11:45:12
65Rare diseases / Mental retardation / Epidemiology / Newborn screening / Inborn errors of carbohydrate metabolism / Phenylketonuria / Galactosemia / Urea cycle disorder / Biotinidase deficiency / Health / Medicine / Pediatrics

Newborn screening could save your Y ‘

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Source URL: health.hawaii.gov

Language: English - Date: 2013-04-30 19:27:38
66Rare diseases / 3-Methylcrotonyl-CoA carboxylase deficiency / Newborn screening / Biotinidase deficiency / Biotin deficiency / Health / Genetic genealogy / Medical genetics

NEWBORN SCREENING FACT SHEET 3MCC Deficiency (3-Methylcrotonyl CoA Carboxylase Deficiency) 3MCC deficiency can cause episodes of illness called metabolic crises. Some of the first symptoms of a metabolic crisis are:

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Source URL: www.ndhealth.gov

Language: English - Date: 2009-02-19 11:31:55
67Rare diseases / Epidemiology / Newborn screening / Pediatrics / Fatty-acid metabolism disorder / Inborn errors of carbohydrate metabolism / Screening / Biotinidase deficiency / Phenylketonuria / Health / Medicine / Genetic genealogy

NEWBORN SCREENING FACT SHEET SCADD (Short Chain Acyl-CoA Dehydrogenese Deficiency) What is it? SCADD stands for short chain acyl-CoA dehydrogenase deficiency. It is one type of

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Source URL: www.ndhealth.gov

Language: English - Date: 2009-02-20 12:54:56
68Mental retardation / Epidemiology / Newborn screening / Inborn errors of carbohydrate metabolism / Galactosemia / Phenylketonuria / Biotinidase deficiency / Screening / Infant / Health / Medicine / Pediatrics

A BABY’S FIRST STEP IN LIFE A NEWBORN SCREENING GUIDE FOR PARENTS Illinois Department of Public Health WHY DOES MY BABY NEED NEWBORN SCREENING? Most babies born in the United States are healthy, but there are some babi

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Source URL: www.idph.state.il.us

Language: English - Date: 2014-04-07 12:39:22
69Medicine / Chemistry / Biotin / Newborn screening / Biotin deficiency / Health / Biotinidase deficiency / Biotinidase

NEWBORN SCREENING FACT SHEET Biotinidase Deficiency What is it? Biotinidase deficiency is a condition that causes the body to have trouble using biotin, an important vitamin the body needs. Biotin is

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Source URL: www.ndhealth.gov

Language: English - Date: 2009-02-19 11:32:01
70Pediatrics / Genetics / Epidemiology / Newborn screening / Galactosemia / Laboratory techniques / Biotinidase deficiency / Biotinidase / Assay / Health / Inborn errors of carbohydrate metabolism / Chemistry

MICHIGAN DEPARTMENT OF COMMUNITY HEALTH BUREAU OF LABORATORIES Newborn Screening – Enzyme Disorders Rev. Date[removed]

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Source URL: www.michigan.gov

Language: English - Date: 2013-03-15 16:13:48
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