Refine search

Search Disease/ Diagnostics

show results
Refine your search

Search term:

<< < Results 21 - 27 of 27
EC Number
Disease
PubMed ID
Title of Publication
Category
Confidence Level
Hyperoxaluria, Primary
Folding Defects Leading to Primary Hyperoxaluria.
ongoing research
therapeutic application
unassigned
1
1
0
Hyperoxaluria, Primary
Nine novel HOGA1 gene mutations identified in primary hyperoxaluria type 3 and distinct clinical and biochemical characteristics in Chinese children.
causal interaction
ongoing research
therapeutic application
unassigned
2
2
1
0
Hyperoxaluria, Primary
Mutation Hot Spot Region in the HOGA1 Gene Associated with Primary Hyperoxaluria Type 3 in the Chinese Population.
unassigned
0
Hyperoxaluria, Primary
Regulation of human 4-hydroxy-2-oxoglutarate aldolase by pyruvate and ?-ketoglutarate: implications for primary hyperoxaluria type-3.
diagnostic usage
ongoing research
unassigned
2
3
0
Hyperoxaluria, Primary
[Genetic aspects of primary hyperoxaluria: epidemiology, ethiology, pathogenesis, and clinical signs of the disorder].
diagnostic usage
unassigned
1
0
Urolithiasis
Primary hyperoxaluria type III gene HOGA1 (formerly DHDPSL) as a possible risk factor for idiopathic calcium oxalate urolithiasis.
diagnostic usage
unassigned
3
0
Urolithiasis
Re: primary hyperoxaluria type III gene HOGA1 (formerly DHDPSL) as a possible risk factor for idiopathic calcium oxalate urolithiasis.
diagnostic usage
therapeutic application
unassigned
3
1
0
<< < Results 21 - 27 of 27