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Cystathionine beta synthase
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#	Item
1	PDF Document Add to Reading List Source URL: www.pbs.gov.au Language: English - Date: 2015-03-23 21:11:42 Homocysteine Trimethylglycine Cofactors Vitamin B12 Methionine Folic acid Cystathionine beta synthase Chemistry Homocystinuria Quaternary ammonium compounds
2	Microsoft PowerPoint - 3 dick Deth Methylation Panel.ppt Add to Reading List Source URL: www.autismeval.com Language: English - Date: 2006-06-25 15:37:03 Proteinogenic amino acids Vitamin B12 Cofactors Methionine Glutathione S-Adenosyl methionine Homocysteine Cysteine Cystathionine beta synthase Chemistry Thiols Glucogenic amino acids
3	Viktor Kožich Henk Blom Stefan Kölker Marike Groenendijk Outline Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2014-12-08 11:13:53 Homocysteine Coenzymes Methylenetetrahydrofolate reductase Cystathionine beta synthase Methionine S-Adenosyl methionine S-Adenosyl-L-homocysteine Chemistry Homocystinuria Vitamin B12
4	Homocystinuria What is homocystinuria? Homocystinuria is an inherited condition that affects the way a person’s body uses a part of food called methionine (a precursor to homocystine). A person with homocystinuria cann Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2007-05-01 14:53:38 Homocystinuria Rare diseases Cystathionine beta synthase Homocysteine Recessive Methionine Cystinuria Phenylketonuria Newborn screening Medicine Health Genetic genealogy
5	Homocystinuria Homocystinuria is an autosomal recessive disorder of methionine metabolism. The most common cause of homocystinuria is a deficiency of the amino acid cystathionine B-synthase. Due to this deficiency, eleva Add to Reading List Source URL: www.maine.gov Language: English - Date: 2011-11-10 05:38:06 Homocystinuria Homocysteine Marfan syndrome Methionine Cystathionine beta synthase Cystinuria Newborn screening Hypermethioninemia Health Chemistry Genetic genealogy
6	Overview of Newborn Screening for Homocystinuria – For Parents What is newborn screening? What are the symptoms of homocystinuria? Before babies go home from the nursery, they Add to Reading List Source URL: www.in.gov Language: English - Date: 2014-10-23 17:39:46 Homocystinuria Cystathionine beta synthase Newborn screening Arachnodactyly Cystinuria Methionine Low-protein diet Health Medicine Chemistry
7	Homocystinuria What is homocystinuria? Homocystinuria is an inherited condition that affects the way a person’s body uses a part of food called methionine (a precursor to homocystine). A person with homocystinuria cann Add to Reading List Source URL: health.tn.gov Language: English - Date: 2007-05-01 14:53:38 Homocystinuria Rare diseases Cystathionine beta synthase Homocysteine Recessive Methionine Cystinuria Phenylketonuria Newborn screening Medicine Health Genetic genealogy
8	PARENT FACT SHEET DISORDER Homocystinuria (HCY) CAUSE HCY occurs when an enzyme called “cystathionine beta-synthase” (CBS) is either missing or not working Add to Reading List Source URL: www.chfs.ky.gov Language: English - Date: 2014-09-12 00:15:54 B vitamins Homocystinuria Zwitterions Vitamin B12 Methionine Homocysteine Vitamin B6 Amino acid Folic acid Chemistry Nutrition Cofactors
9	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 15:50:02 Newborn screening Pediatrics Medical terms Homocystinuria Homocysteine Maternal and Child Health Bureau Medical guideline Cystathionine beta synthase Hypermethioninemia Health Medicine Epidemiology
10	PARENT FACT SHEET DISORDER Homocystinuria (HCY) CAUSE HCY occurs when an enzyme called “cystathionine beta-synthase” (CBS) is either missing or not working Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-09 04:53:45 B vitamins Homocystinuria Zwitterions Vitamin B12 Methionine Homocysteine Vitamin B6 Amino acid Folic acid Chemistry Nutrition Cofactors

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