ライフサイエンスコーパス: primary hyperoxaluria

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1 rocalcinosis in oxalate nephropathy, such as primary hyperoxaluria.

2 Primary hyperoxaluria 1 (PH1; Online Mendelian Inheritan

3 is a potential drug target for treatment of primary hyperoxaluria, a genetic disorder where overprod

4 fined despite their clinical significance in primary hyperoxaluria and idiopathic calcium oxalate nep

5 nding the molecular aspect and management of primary hyperoxalurias as well as nephropathic cystinosi

6 Primary hyperoxaluria is a rare autosomal recessive meta

7 Primary hyperoxaluria (PH) is a rare autosomal recessive

8 sferase (AGT), the metabolic error in type 1 primary hyperoxaluria (PH1).

9 the enzymatic defect responsible for type 1 primary hyperoxaluria (PH1).

10 Primary Hyperoxaluria Type 1 (PH1) is a rare autosomal r

11 Primary hyperoxaluria type 1 (PH1) is an inborn error of

12 Primary hyperoxaluria type 1 (PH1) is caused by defects

13 Primary hyperoxaluria type 1 (PH1), an inherited rare di

14 ially lethal hereditary kidney stone disease primary hyperoxaluria type 1 (PH1).

15 ccumulation of intracellular oxalate and the primary hyperoxaluria type 1 (PH1).

16 editary calcium oxalate kidney stone disease primary hyperoxaluria type 1 (PH1).

17 ecreasing glycolate and glyoxylate levels in primary hyperoxaluria type 1 patients who have the inabi

18 In a mouse model of primary hyperoxaluria type 1, rectal administration of O

19 cy of this enzyme is the underlying cause of primary hyperoxaluria type 2 (PH2) and leads to increase

20 atment for end-stage renal disease caused by primary hyperoxaluria type I (PH1).

21 phosphate (PLP)-dependent enzymes, including primary hyperoxaluria type I (PH1).

22 Primary hyperoxaluria type I is a severe kidney stone di

23 f which results in the kidney stone disease, primary hyperoxaluria type I, identifying mutations that

24 nine:glyoxylate aminotransferase, mutated in primary hyperoxaluria type I.

25 Primary hyperoxaluria type II (PH2) is a rare monogenic

26 Primary hyperoxaluria type-1 (PH1) is an autosomal reces

27 haperones) may be effective for treatment of primary hyperoxaluria, we propose that the methods descr

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