[PDF] Top 20 La regulación emocional y el trastorno límite de la personalidad
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Incremental health care resource utilization and expenditures associated with autosomal dominant polycystic kidney disease
... of autosomal recessive PKD or unspecified cystic kidney disease and 61 persons who had no medical claim information, a total of 3,844 individuals remained in the ADPKD ...cardiovascular ... See full document
18
Medical resource utilization and costs associated with autosomal dominant polycystic kidney disease in the USA: a retrospective matched cohort analysis of private insurer data
... sought health care, our analysis shows that a size- able proportion of ADPKD patients seek care early, when signs and symptoms may not have been ...preventative health care before signs ... See full document
5
Modelling the long-term benefits of tolvaptan therapy on renal function decline in autosomal dominant polycystic kidney disease: an exploratory analysis using the ADPKD outcomes model
... was associated with noteworthy delays to ESRD onset among modelled ADPKD cohorts, particularly those with early- stage and rapidly progressing ...providing care to ADPKD patients who progress to ... See full document
13
Temporal and geographical external validation study and extension of the Mayo Clinic prediction model to predict eGFR in the younger population of Swiss ADPKD patients
... affect disease progression [7]; all other therapies target co-morbidities that may contribute to progression but do not affect the underlying disease ...and associated high treatment costs ...of ... See full document
5
<p>Management of Autosomal Dominant Polycystic Kidney Disease (ADPKD) During Pregnancy: Risks and Challenges</p>
... an autosomal dominant condition, meaning the offspring has 50% chance of inheriting a pathogenic variant from an affected ...experienced health professional to assist in decision-making regarding ... See full document
31
Case report: a thiazide diuretic to treat polyuria induced by tolvaptan
... for autosomal dominant polycystic kidney disease (ADPKD), but there are tolerability issues due to aquaretic side- effects such as ... See full document
11
Incidence of post transplant diabetes mellitus in Erbil Teaching Hospital
... Hypertension was found in 25 patients (35.7%) before transplant while 14 patients (20%) developed hypertension after transplant. The cause of renal failure was idiopathic in 63 patients (90%), nephritic syndrome in five ... See full document
6
Autosomal dominant polycystic kidney disease with ectopic unilateral multicystic dysplastic kidney
... sporadic disease condition of abnormal metanephric ...total kidney func- tion of many subjects with MCDK could be well- maintained ...the kidney structure destruc- tion by the continuous cyst growth ... See full document
63
Risk of intracranial hemorrhage associated with autosomal dominant polycystic kidney disease in patients with end stage renal disease
... factors associated with development of ...cerebrovascular disease includ- ing cerebrovascular accident (CVA) and transient ischemic attack (TIA), the risk of ICH among ADPKD patients still remained ... See full document
10
Relationship between sclerostin and cardiovascular calcification in hemodialysis patients: a cross-sectional study
... bone disease in ESRD patient ...is associated with levels of circulating sclerostin and whether valvular calcifica- tion goes along with local sclerostin ... See full document
18
Familial Arachnoid Cysts in Association With Autosomal Dominant Polycystic Kidney Disease
... Arachnoid cysts are extraparenchymal accumula- tions of cerebrospinal fluid covered by a thin mem- brane that is continuous with the normal arachnoid. Although their precise causative mechanisms are un- known, they are ... See full document
17
Genetic mechanisms and signaling pathways in autosomal dominant polycystic kidney disease
... and disease mechanism ADPKD is genetically heterogeneous with two loci identified, PKD1 ...mild disease, and potentially to define trial/treatment populations (21, ... See full document
12
Transcriptome analysis reveals manifold mechanisms of cyst development in ADPKD
... The intracellular NOD-like receptor (NLR) family plays a central role in regulation of the innate immune response. The NLRs NOD1 and NOD2 sense bacterial peptidoglycan fragments and respond by stimulating the activation ... See full document
8
<p>Autosomal dominant polycystic kidney disease: updated perspectives</p>
... cystic disease (class 1) and is strati fi ed into fi ve classes (A, B, C, D, E) based on the growth rates ...progressive disease in the majority of patients with ADPKD, ... See full document
10
STAT5 drives abnormal proliferation in autosomal dominant polycystic kidney disease.
... Autosomal dominant polycystic kidney disease (ADPKD) leads to renal failure. The hallmark of ADPKD is increased epithelial proliferation, which has been proposed to be due to atypical ... See full document
5
Chronic asymptomatic pyuria precedes overt urinary tract infection and deterioration of renal function in autosomal dominant polycystic kidney disease
... Chronic asymptomatic pyuria and overt UTI were also associated with ΔeGFR in the ADPKD patients. The patients in group B exhibited a greater ΔeGFR (-2.7 ± 4.56 vs. -1.17 ± 5.8 ml/min/1.73m 2 per year; P = 0.01) ... See full document
84
Myeloperoxidase-antineutrophil cytoplasmic antibody-associated crescentic glomerulonephritis in autosomal dominant polycystic kidney disease
... In ADPKD patients, the presence of multiple cysts in both kidneys is considered as a contraindication to percutaneous renal biopsy due to the presumed risk of complications and difficulty in obtaining suitable tissue for ... See full document
18
Hyperuricemia and deterioration of renal function in autosomal dominant polycystic kidney disease
... A total of 612 patients were screened at the ADPKD clinic in Seoul National University Hospital. ADPKD was diagnosed according to the unified criteria proposed by Pei et al. [14]. We selected 365 patients aged > 18 ... See full document
21
Urine proteome of autosomal dominant polycystic kidney disease patients
... The proteome of urine collected from 30 ADPKD patients and 30 healthy subjects was compared using a combined IEF-LC-MS-MS/MS relative quantitation of iTRAQ labeled tryptic peptides. From each sample an equal amount of ... See full document
5
Polycystic Kidney Disease:The Cyst-ematic Destruction of Renal Function
... Cyclin-dependent kinases (CDK) are used to regulate the cell cycle, transcription and mRNA processing. However, in PKD the dysregulation of this cell cycle has been thought to be the main reason behind the cystogenesis. ... See full document
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