adenine has been researched along with Hyperoxaluria, Primary in 1 studies
Hyperoxaluria, Primary: A genetic disorder characterized by excretion of large amounts of OXALATES in urine; NEPHROLITHIASIS; NEPHROCALCINOSIS; early onset of RENAL FAILURE; and often a generalized deposit of CALCIUM OXALATE. There are subtypes classified by the enzyme defects in glyoxylate metabolism.
Excerpt | Relevance | Reference |
---|---|---|
"All three patients progressed to ESRD, within 1 month following renal biopsy in two and after 9 months in one." | 1.36 | Crystalline nephropathy due to 2,8-dihydroxyadeninuria: an under-recognized cause of irreversible renal failure. ( Boelkins, M; Broviac, J; Cornell, LD; Fidler, ME; Milliner, DS; Nasr, SH; Sethi, S, 2010) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Nasr, SH | 1 |
Sethi, S | 1 |
Cornell, LD | 1 |
Milliner, DS | 1 |
Boelkins, M | 1 |
Broviac, J | 1 |
Fidler, ME | 1 |
1 other study available for adenine and Hyperoxaluria, Primary
Article | Year |
---|---|
Crystalline nephropathy due to 2,8-dihydroxyadeninuria: an under-recognized cause of irreversible renal failure.
Topics: Adenine; Adenine Phosphoribosyltransferase; Adult; Allopurinol; Crystallization; Diagnosis, Differen | 2010 |