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1 ith PHPT, of whom 265 (8%) were symptomatic (nephrolithiasis).
2 al insights to stop the growing incidence of nephrolithiasis.
3 re previously reported to be associated with nephrolithiasis.
4 TRPV5 channel activity and protects against nephrolithiasis.
5 is inappropriate in patients with recurrent nephrolithiasis.
6 eceptor (VDR) in target tissues; and calcium nephrolithiasis.
7 itical for understanding the pathogenesis of nephrolithiasis.
8 Hypercalciuria is a major risk factor for nephrolithiasis.
9 id peroxidation during hyperoxaluria-induced nephrolithiasis.
10 hyperoxaluria and idiopathic calcium oxalate nephrolithiasis.
11 ic metabolic acidosis, nephrocalcinosis, and nephrolithiasis.
12 ces, paraesthesias, hyperbilirubinaemia, and nephrolithiasis.
13 n and improved accuracy in the evaluation of nephrolithiasis.
14 with HIV infection, has been associated with nephrolithiasis.
15 provide a suitable model of human hereditary nephrolithiasis.
16 cidence of hyperoxaluria and calcium oxalate nephrolithiasis.
17 se stone recurrence in patients with calcium nephrolithiasis.
18 es have been associated with a lower risk of nephrolithiasis.
19 st 2 L of urine per day to prevent recurrent nephrolithiasis.
20 ted sequelae, including nephrocalcinosis and nephrolithiasis.
21 rt an adverse effect of high temperatures on nephrolithiasis.
22 ed claudin-14 associated with hypercalciuric nephrolithiasis.
23 risk of radiation exposure to patients with nephrolithiasis.
24 scribes a 60-year-old patient with bilateral nephrolithiasis.
25 roxaluria or even idiopathic calcium oxalate nephrolithiasis.
26 promising adjuncts for preventing recurrent nephrolithiasis.
27 lly considered a poor experimental model for nephrolithiasis.
28 variant(s) are candidate risk modifiers for nephrolithiasis.
29 Sixty-one percent had nephrolithiasis.
30 alate increases the risk for calcium oxalate nephrolithiasis.
31 e dietary oxalate as a major risk factor for nephrolithiasis.
32 e 2 diabetes at increased risk for uric acid nephrolithiasis.
33 ons as causing a recessive Mendelian form of nephrolithiasis.
34 cal prevention, and surgical intervention of nephrolithiasis.
35 contribute to the hypercalciuria and calcium nephrolithiasis.
36 conducted of 45,619 men without a history of nephrolithiasis.
37 ke seems to increase the risk of symptomatic nephrolithiasis.
38 ally invasive techniques in the treatment of nephrolithiasis.
39 stinuria is the commonest inherited cause of nephrolithiasis (~1% in adults; ~6% in children) and is
40 red with the high-dose scan were as follows: nephrolithiasis, 91%; ureterolithiasis, 94%; obstruction
42 ntribute to the recent increase in pediatric nephrolithiasis, a definite underlying cause remains elu
43 ue from normal rats and rats developing CaOx nephrolithiasis after challenge with ethylene glycol.
44 n mRNA expression in rat kidneys during CaOx nephrolithiasis after challenge with ethylene glycol.
45 luoroscopy used during surgical treatment of nephrolithiasis also contributes to patient radiation ex
46 yndrome have resulted in increasing rates of nephrolithiasis among women, decreasing the male-to-fema
54 The increased oxalate excretion can cause nephrolithiasis and nephrocalci-nosis and can, in some c
55 est that knowledge of the molecular cause of nephrolithiasis and nephrocalcinosis may have practical
57 nced CT (5-mm section width, no overlap) for nephrolithiasis and other causes of twinkling artifact.
58 between the induction of hyperoxaluria/CaOx nephrolithiasis and the expression of the bikunin gene i
60 ydrate, the most common solid phase in human nephrolithiasis, and also inhibits the nucleation, growt
64 cribing further uses of alpha-antagonists in nephrolithiasis, and reporting improvements in extracorp
65 have been described as being associated with nephrolithiasis, and these mutations explain about 15% o
70 dney stone cases, suggesting that additional nephrolithiasis-associated genes remain to be discovered
71 o establish the relationship between calcium nephrolithiasis, bone densitometry scoring, and bone min
72 's disease, also known as X-linked recessive nephrolithiasis, but the effects of diuretics on calcium
73 h ambient temperatures are a risk factor for nephrolithiasis, but the precise relationship between te
75 ncrease of 1.6-2.2 million lifetime cases of nephrolithiasis by 2050, representing up to a 30% increa
76 rted that Uromodulin (UMOD) protects against nephrolithiasis by upregulating the renal calcium channe
77 t in the denosumab to teriparatide group had nephrolithiasis, classified as being possibly related to
80 ques and the renal papillae in patients with nephrolithiasis, detailing genetic discoveries related t
82 ant advances have been made in understanding nephrolithiasis from single gene defects, the understand
84 ient population is all adults with recurrent nephrolithiasis (>/=1 prior kidney stone episode).
85 (n=12), patients (n=12) with hypercalciuric nephrolithiasis had significantly decreased levels of ur
88 in adults, the trends occurring in pediatric nephrolithiasis have not been studied rigorously, which
92 citrate, or allopurinol to prevent recurrent nephrolithiasis in patients with active disease in which
94 relation between oxalate intake and incident nephrolithiasis in the Health Professionals Follow-up St
100 linicians look for the underlying causes for nephrolithiasis is imperative to direct management.
101 e disease, the best management for recurrent nephrolithiasis is likely a combination of surgical and
106 Xp11.22, are associated with hypercalciuric nephrolithiasis (kidney stones) in the Northern European
107 terized by hypercalciuria, nephrocalcinosis, nephrolithiasis, low molecular weight proteinuria, Fanco
108 ldren and 166 adults) from 268 families with nephrolithiasis (n=256) or isolated nephrocalcinosis (n=
110 ninvasive first-line therapy for millions of nephrolithiasis patients, has not improved substantially
116 l imaging method for patients with suspected nephrolithiasis should be computed tomography (CT) or ul
120 nce is raised by factors unique to pediatric nephrolithiasis that could expose an affected child to m
121 a change in the current trends of pediatric nephrolithiasis that is characterized by a significant i
122 opportunities to learn more about pediatric nephrolithiasis, thereby fueling the much-needed researc
123 inkling artifact is commonly associated with nephrolithiasis, this finding is relatively insensitive
124 d to the emergency department with suspected nephrolithiasis to undergo initial diagnostic ultrasonog
125 ing dysfunction, flank pain, abdominal pain, nephrolithiasis, urinary tract infection and decreased b
126 is review describes the relationship between nephrolithiasis, vascular disease and metabolic syndrome
128 ditional genes whose mutations are linked to nephrolithiasis, we performed targeted next-generation s
129 ups; no cases of hypercalcemia and 1 case of nephrolithiasis were reported in the placebo group.
131 scribed for patients with idiopathic calcium nephrolithiasis, who account for > 80% of new diagnoses
132 .S. population living in high-risk zones for nephrolithiasis will grow from 40% in 2000 to 56% by 205
133 e cost increase associated with this rise in nephrolithiasis would be $0.9-1.3 billion annually (year
134 ithiasis (Dent's disease, X-linked recessive nephrolithiasis (XRN), and X-linked recessive hypophosph
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