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Inborn errors of carbohydrate metabolism
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61	Nebraska WIC Formulary - Product Reference Guide Infant Formula BOOST® KID ESSENTIALS - Nestle Description Add to Reading List Source URL: dhhs.ne.gov Language: English - Date: 2014-10-27 16:52:57 Food science Soy products Milk Food allergies Inborn errors of carbohydrate metabolism Infant formula Lactose intolerance Milk allergy Amino acid-based formula Food and drink Health Medicine
62	Your Baby and Newborn Screening The State of Tennessee Newborn Screening Program Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2014-06-12 11:50:16 Rare diseases Epidemiology Newborn screening Inborn errors of carbohydrate metabolism Galactosemia Phenylketonuria Biotinidase deficiency Cystic fibrosis Sickle-cell disease Health Medicine Pediatrics
63	V. Failure to Thrive Congenital Heart Disease and Renal Disease Infants with Malabsorption Add to Reading List Source URL: www.maine.gov Language: English - Date: 2014-10-02 08:03:48 Soy products Infant feeding Food science Milk Inborn errors of carbohydrate metabolism Infant formula Boost Enfamil Milk substitute Food and drink Nutrition Health
64	Galactosemia Carmen Lozzio, MD University of Tennessee Developmental and Genetics Center Knoxville, Tennessee Outcome without screening: Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2006-10-30 12:05:26 Galactosemia Biology Galactose-1-phosphate uridylyltransferase deficiency Galactose—1-phosphate uridylyltransferase Galactosemic cataract Galactokinase Galactitol Galactose Newborn screening Inborn errors of carbohydrate metabolism Health Medicine
65	Galactosemia What is galactosemia? Galactosemia is an inherited condition that affects the way a person’s body breaks down galactose. When a person eats or drinks a product that contains lactose or milk sugar (e.g., da Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2007-05-01 14:49:16 Biology Galactosemia Galactose-1-phosphate uridylyltransferase deficiency Galactosemic cataract Galactose—1-phosphate uridylyltransferase Inborn errors of carbohydrate metabolism Medicine Health
66	TDH Division of Laboratory Services Directory of Services Revised[removed]Newborn Screening Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2013-08-26 11:01:32 Hematology Inborn errors of carbohydrate metabolism Transfusion medicine Pediatrics Epidemiology Newborn screening Galactosemia Biotinidase deficiency Phenylketonuria Medicine Health Biology
67	[removed]March 2005 COMMENTS ON EC Working document: Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2012-03-20 14:21:20 Infant feeding Breastfeeding Milk Breast milk Inborn errors of carbohydrate metabolism Infant formula Human breast milk Infant Milk substitute Nutrition Food and drink Biology
68	Table of Contents Contents Page What is SCADD? ......................................... 1-5 Add to Reading List Source URL: www.cdph.ca.gov Language: English - Date: 2014-10-06 16:45:49 Epidemiology Newborn screening Pediatrics Weakness Fatty-acid metabolism disorder Inborn errors of carbohydrate metabolism Very long-chain acyl-coenzyme A dehydrogenase deficiency Galactosemia Health Medicine Rare diseases
69	Parents’ Guide to Galactosemia Part 2: Your Child Six Months and Older To Parents This booklet was written for parents of children with Add to Reading List Source URL: www.cdph.ca.gov Language: English - Date: 2014-10-06 16:45:51 Health Galactosemia Galactose-1-phosphate uridylyltransferase deficiency Galactose—1-phosphate uridylyltransferase Inborn errors of carbohydrate metabolism Food and drink Biology
70	ARTICLE The angiotensin-converting enzyme insertion/deletion polymorphism modifies the clinical outcome in patients with Pompe disease Paola de Filippi, PhD1, Sabrina Ravaglia, MD, PhD2, Bruno Bembi, MD3, Alfredo Costa, Add to Reading List Source URL: www.nature.com Language: English - Date: 2012-01-04 14:12:58 Genetic genealogy Rare diseases Hepatology Genetics Glycogen storage disease type II Glycogen storage disease type V Lysosomal storage disease Genotype Acid alpha-glucosidase Health Inborn errors of carbohydrate metabolism Medicine

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