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         Galt Deficiency:     more detail

21. 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

22. 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

23. 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

24. 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

25. Galactosemia - Wikipedia, The Free Encyclopedia
Essential fructosuria Fructose intolerance. galactose / galactosemia GALK deficiency GALT deficiency / GALE deficiency
http://en.wikipedia.org/wiki/Galactosemia

26. 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

27. 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

28. 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/

29. 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/

30. 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

31. 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

32. Galactosemia
This page includes the following topics and synonyms Galactosemia, GALT Deficiency.
http://www.fpnotebook.com/Endo/Metabolism/Glctsm.htm

33. Parents Of Galactosemic Children, Inc.
Information about galctosemia and a resource for families living with galactosemia.
http://www.galactosemia.org/

34. 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

35. 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

36. Galactosemia GeneReviews NCBI Bookshelf
Classic Galactosemia, GALT Deficiency, Galactose1-Phosphate Uridyltransferase Deficiency. Includes Variant Galactosemias
http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=galactosemia

37. 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

38. OMIM 230400
database omim entry 230400 linkdb 230400 mim entry 230400 title 230400 galactosemia ;;galactose1-phosphate uridylyltransferase deficiency;; galt deficiency
http://www.genome.jp/dbget-bin/www_bget?omim 230400

39. GalactoseProduction And Disposal In Patients With GALT Deficiency
Does the GAR in infants and children with galactosemia show a developmental pattern that may be linked to the growth rate?
http://www.galactosemia.com/resources/berry-talk.pdf

40. 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

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