Tay-Sachs Disease Learning Center On Healthline.com Central Pontine Myelinolysis, GALT Deficiency, Gaucher's Disease, Hepatic Encephalopathy, Homocystinuria, Kernicterus, Leigh's Disease, LeschNyhan Syndrome, Menkes' Syndrome, Reye http://www.healthline.com/channel/tay-sachs-disease.html
GALT Deficiency GALT deficiency Lack of the enzyme called GALT (galactose1-phosphate uridyl transferase) which causes the genetic metabolic disease galactosemia, one of the diseases in many http://health-search.closerlooksearch.com/health-topics/G/Gammaglobulin.html
GALT Deficiency Causes UDP-hexose Deficit In Human Galactosemic Abstract. Previously we reported that stable transfection of human UDPglucose pyrophosphorylase (hUGP2) rescued galactose-1-phosphate uridyltransferase (GALT http://glycob.oxfordjournals.org/content/13/4/285.abstract
GALT Deficiency Treatment, Cure Prevention, GALT Deficiency Offers complete guide on GALT Deficiency Treatment and Prevention. Also offers a list of Causes and Symptoms of GALT Deficiency, its Diagnosis and related Products to Cure it. http://www.getsmartinfo.com/health-conditions-g-1/galt-deficiency.php
Galt Deficiency This is PremierDoctors's supplementary directory of commonly searched topics. If you can't find what you're looking for, click here to visit our Home Page. http://www.premierdoctors.com/go/GALT-Deficiency.html
GALT Deficiency Causes UDP-hexose Deficit In Human Galactosemic Authors K. Lai, S. D. Langley, F. W. Khwaja, E. W. Schmitt, L. J. Elsas. Citations 4 The following links allow you to view and download full papers. These links are http://academic.research.microsoft.com/Paper/6556258.aspx?viewType=1
GFMN Homepage You've found us! We are a group of families from Minnesota and surrounding states living with Galactosemia. We were founded in 1998, for the purpose of sharing information about http://www.galactosemia-mn.com/
GANES Hello, and welcome to the GANES website! My name is Angie Forsyth, and I am the founder and current president of GANES the Galactosemia Association of the North Eastern States. http://galactosemia.com/
Galactose-1-Phosphate Uridyltransferase Deficiency (Galactosemia Individuals with GALT deficiency manifest abnormal galactose tolerance. Frequency United States. Incidence is approximately 1 case per 40,00060,000 persons. 3 http://emedicine.medscape.com/article/944069-overview
NEWBORN SCREENING Disorder Name Galactosemia Acronym GALT deficiency. What is galactosemia? What causes galactosemia? If galactosemia is not treated, what problems occur? http://www.newbornscreening.info/Parents/otherdisorders/Galactosemia.html
Galactosemia This page includes the following topics and synonyms Galactosemia, GALT Deficiency. http://www.fpnotebook.com/Endo/Metabolism/Glctsm.htm
Galactosemia Galactosemia is a genetic disorder that is characterized by the patient’s inability to metabolize sugar (galactose) into glucose. Glucose is readily usable by the body but http://www.rare-disorders.com/galactosemia.html
Citations Of GALT Deficiency Causes UDP-hexose Deficit In Human The spectrum of all glycan structures — the glycome — is immense. In humans, its size is orders of magnitude greater than the number of proteins that are encoded by the http://academic.research.microsoft.com/Detail.aspx?entitytype=1&searchtype=5
Newborn Screening Case Management This handbook is meant to give you the basic information that will help you understand how to care for your child with galactosemia. http://www.dshs.state.tx.us/newborn/handbook.shtm
Classical And Duarte Galactosemia Newborn Screening, Biochemical Newborn screening for galactosemia is routine in 50 US states, but detects many newborns with partial galactose1-phosphate uridyltransferase (GALT) deficiency (less than 10% http://www.ashg.org/genetics/abstracts/abs06/f1393.htm
