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1 mice, a hereditary disorder characterized by progressive renal failure.
2 roscopic haematuria, glomerulonephritis, and progressive renal failure.
3  causes luminal cecal fluid accumulation and progressive renal failure.
4 merular and tubulointerstitial fibrosis, and progressive renal failure.
5 S disease are at risk for the development of progressive renal failure.
6  develop precocious hyperuricemia, gout, and progressive renal failure.
7 ephrotoxic effects, which frequently lead to progressive renal failure.
8 ed by extensive formation of renal cysts and progressive renal failure.
9 cumented in the remnant kidney (RK) model of progressive renal failure.
10 alpha3.alpha4.alpha5 network, which leads to progressive renal failure.
11 fections are common; 30% of patients develop progressive renal failure.
12 Jewish origin, the nephropathy develops into progressive renal failure.
13 anding of the mechanisms of hypertension and progressive renal failure.
14 entify the inherited factors contributing to progressive renal failure.
15 ease, a common inherited disease that causes progressive renal failure.
16 bulointerstitial fibrosis, inflammation, and progressive renal failure.
17 est results were normal, but she had rapidly progressive renal failure.
18 ury, which may be relevant to development of progressive renal failure.
19                                              Progressive renal failure affects the structure and acti
20 ons (irbesartan, amlodipine, and placebo) on progressive renal failure and all-cause mortality were a
21 r that has a complex phenotype that includes progressive renal failure and blindness.
22 ephritis (PICGN) is a major cause of rapidly progressive renal failure and is commonly linked to ANCA
23 (CNS), a rare entity, is known to present as progressive renal failure and its leading presentation w
24  typically in the clinical setting of fever, progressive renal failure and nephromegaly, strongly sup
25  useful target in the therapeutic control of progressive renal failure and other pathological process
26  filtered protein is a proposed mechanism of progressive renal failure associated with glomerular dis
27 iduals with JS have retinal dystrophy and/or progressive renal failure characterized by nephronophthi
28 d complement activation, tubular damage, and progressive renal failure despite the presence of abunda
29 irus long terminal repeat (MMTV LTR) undergo progressive renal failure due to abnormal kidney develop
30 nherited disease characterized by hematuria, progressive renal failure, hearing loss, and ocular abno
31                              Some aspects of progressive renal failure, however, cause changes in pla
32 es the development of glomerulosclerosis and progressive renal failure in a diverse range of kidney d
33 r outlet obstruction are a frequent cause of progressive renal failure in children.
34 ated CD2-associated protein (CD2AP) leads to progressive renal failure in mice and humans.
35 embrane (GBM), the kidney ultrafilter, cause progressive renal failure in millions of people worldwid
36  underlying proximal tubular dysfunction and progressive renal failure in nephropathic cystinosis are
37 scular hypertension, but it can also lead to progressive renal failure (ischemic nephropathy) caused
38  the poorly recognized inheritance of slowly progressive renal failure leading to ESRD in later life.
39 al delirium in 2; postinterventional stroke, progressive renal failure, progressive heart failure, or
40 generalized proximal tubular dysfunction and progressive renal failure, remain largely unknown.
41 interaction of more than two loci to produce progressive renal failure, suggesting that the genetic d
42    Haemolytic uraemic syndrome is a triad of progressive renal failure, thrombocytopenia and haemolyt
43 and quickly leads to marked inflammation and progressive renal failure, with features relevant to hum