HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Sandra Supraha Goreta Selected Research

Congenital disorder of glycosylation type 1C

1/2011Employment of single-strand conformation polymorphism analysis in screening for α-1,3 glucosyltransferase gene mutation A333V in Croatian population.

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown:


Sandra Supraha Goreta Research Topics

Disease

1Congenital Disorders of Glycosylation
01/2012
1Congenital, Hereditary, and Neonatal Diseases and Abnormalities (Congenital Disorders)
01/2012
1Congenital disorder of glycosylation type 1C
01/2011
1Gilbert Disease
01/2008
1Hyperbilirubinemia
01/2008

Drug/Important Bio-Agent (IBA)

3EnzymesIBA
01/2012 - 01/2011
1LipidsIBA
01/2011
1Glucose (Dextrose)FDA LinkGeneric
01/2011
1GlucosyltransferasesIBA
01/2011
1OligosaccharidesIBA
01/2011
1Uridine Diphosphate (UDP)IBA
01/2008