3-Methylcrotonyl-CoA carboxylase deficiency - PDFSEARCH.IO - Document Search Engine

3-Methylcrotonyl-CoA carboxylase deficiency
Results: 66

#	Item
1	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
2	A Guide for Prenatal Educators This booklet is made possible by & Add to Reading List Source URL: spanish.babysfirsttest.org Language: English - Date: 2014-03-24 17:53:47 Pediatrics Rare diseases Inborn errors of carbohydrate metabolism B vitamins Epidemiology Newborn screening Phenylketonuria 3-Methylcrotonyl-CoA carboxylase deficiency Galactosemia Health Medicine Genetic genealogy
3	Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) Add to Reading List Source URL: health.mo.gov Language: English - Date: 2009-02-03 16:52:02 Rare diseases 3-Methylcrotonyl-CoA carboxylase deficiency Newborn screening Methylcrotonyl-CoA carboxylase Biotinidase deficiency Propionic acidemia Health Genetic genealogy Medical genetics
4	Microsoft Word - Organic_Acidemias.doc Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2007-05-01 15:47:00 Genetic genealogy Isovaleric acidemia Propionic acidemia Organic acidemia Newborn screening Methylmalonic acidemia Malonyl-CoA decarboxylase deficiency 3-Methylcrotonyl-CoA carboxylase deficiency Medical genetics Health Rare diseases Medicine
5	(ISOVALERIC ACID CoA DEHYDROGENASE DEFICIENCY; IVA; IVD) Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2007-05-01 10:03:12 Medical genetics Organic acidemia Isovaleric acidemia Propionic acidemia Newborn screening Methylmalonic acidemia Glutaric aciduria type 1 Malonyl-CoA decarboxylase deficiency 3-Methylcrotonyl-CoA carboxylase deficiency Health Rare diseases Genetic genealogy
6	Title 15 - Mississippi Department of Health Add to Reading List Source URL: www.msdh.state.ms.us Language: English - Date: 2014-03-27 09:48:48 Newborn screening Congenital adrenal hyperplasia Galactosemia Phenylketonuria Biotinidase deficiency Congenital hypothyroidism 3-Methylcrotonyl-CoA carboxylase deficiency Inborn error of metabolism 2-Methylbutyryl-CoA dehydrogenase deficiency Health Medicine Pediatrics
7	DRAFT[removed]ARTICLE 2. NEWBORN AND INFANT SCREENING Section R9[removed]. Add to Reading List Source URL: www.azdhs.gov Language: English - Date: 2013-08-21 11:09:22 Medical genetics Newborn screening Methylmalonic acidemia Propionic acidemia Biotinidase deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency Malonyl-CoA decarboxylase deficiency 3-Methylcrotonyl-CoA carboxylase deficiency Isovaleric acidemia Health Rare diseases Genetic genealogy
8	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
9	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
10	DKB6:[TIGRE.TIGRE_WIP.NYREG06]NYREG06_10 Add to Reading List Source URL: docs.dos.ny.gov Language: English - Date: 2012-02-24 17:34:46 Epidemiology Newborn screening Pediatrics Krabbe disease Public library 3-Methylcrotonyl-CoA carboxylase deficiency Health Rare diseases Medicine