[PDF] Top 20 The Association between Autosomal Dominant Polycystic Kidney Disease and Renal Cell Carcinoma
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The Association between Autosomal Dominant Polycystic Kidney Disease and Renal Cell Carcinoma
... 2013 Bilateral Papillary Renal Cell Carcinoma and Angiomyolipoma in the Patients with Autosomal Dominant Polycystic Kidney Disease: Case Report of Two Cases and Literature Review.. 2012 [r] ... See full document
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Percutaneous radiofrequency ablation with contrast enhanced ultrasonography for solitary and sporadic renal cell carcinoma in patients with autosomal dominant polycystic kidney disease
... with renal cell carcinoma (RCC) in autosomal dominant polycystic kidney disease (ADPKD) from January 2009 to December 2014 with a media follow-up of 33 ...and ... See full document
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Familial Arachnoid Cysts in Association With Autosomal Dominant Polycystic Kidney Disease
... ABSTRACT. Autosomal dominant polycystic kidney disease (ADPKD) is a systemic disorder well-known for its association with intracranial ...in association with ...tosomal ... See full document
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Association of plasma somatostatin with disease severity and progression in patients with autosomal dominant polycystic kidney disease
... a kidney disease, specifically ...excretion, disease severity and disease progression in ...balance between plasma SST concen- tration and SST receptor ...δ cell in the pancreas ... See full document
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Autosomal dominant polycystic kidney disease with diffuse proliferative glomerulonephritis an unusual association: a case report and review of the literature
... An open renal biopsy was carried out on our patient. Under low magnification light microscopy, cysts lined by flattened cells were observed. A total of 56 glomeruli were seen with variable mesangial ... See full document
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Autosomal Dominant Polycystic Kidney Disease in the Neonatal Period: Association with a Cerebral Arteriovenous Malformation
... Our two patients definitely had the autosomal dominant PKD: their father has PKD; their kidney biopsies showed cysts of glomeruli and tubuli in cortex and medulla; and the liver biopsy w[r] ... See full document
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Incidental renal cell carcinoma presenting in a renal transplant recipient with autosomal dominant polycystic kidney disease: a case report
... the renal artery has been reported as an effective and less invasive renal contraction therapy for ...enlarged polycystic kidneys has been proposed as an alternative to nephrectomy before ... See full document
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Simultaneous occurrence of renal cell carcinoma and angiomyolipoma in the same kidney
... Renal cell carcinoma (RCC) is a common neoplasm in general ...Clear cell (conventional) type, the most common, accounts for approximately 60% of all renal ...of kidney. Sporadic ... See full document
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Hyperuricemia and deterioration of renal function in autosomal dominant polycystic kidney disease
... explain renal dysfunction by hyperuricemia. First, association be- tween increased sUA level and cardiovascular disease has been reported ...observed between the normouricemic and ... See full document
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Functional polycystin 1 dosage governs autosomal dominant polycystic kidney disease severity
... severe disease in siblings of an early-onset case in families with otherwise typical ...early-onset disease (29, ...of renal disease in a candidate gene association study, while ... See full document
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Polycystic liver disease: an overview of pathogenesis, clinical manifestations and management
... liver disease (PLD) is the result of embryonic ductal plate malformation of the intrahepatic biliary ...isolated polycystic liver disease (PCLD) and autosomal dominant polycystic ... See full document
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Imaging of kidney cysts and cystic kidney diseases in children: an international working group consensus statement
... focal disease (simple and complex kidney cysts), afect a whole kidney (eg, multicystic dysplastic kid- ney or cystic dysplasia), or manifest as bilateral cystic disease (eg, autosomal ... See full document
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A model to predict disease progression in patients with autosomal dominant polycystic kidney disease (ADPKD): the ADPKD Outcomes Model
... and disease progression towards ESRD is heterogeneous and prolonged over several de- cades, the size and length of clinical trials in ADPKD are insufficient to capture the natural history of the disease ... See full document
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Study of Autosomal Dominant Polycystic Kidney Disease Clinical Profile and Family Screening
... expansion of innumerable fluid- filled cysts ranging in equivalent size from a pea to a grapefruit. Cyst arise from the nephron and collecting tubules They are seen with lesser frequency in the liver (approximately 80%). ... See full document
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Acute Effects of Tolvaptan on Renal Hemodynamics in Autosomal Dominant Polycystic Kidney Disease —A Randomized, Cross Over, Double Blind, Placebo Controlled Study of Renal Plasma Flow and Glomerular Filtration Rate
... of renal autoregulation on change in GFR and RPF is well known from previous studies during alteration in blood pressure ...disagreements between the studies could be due to difference in the method of ... See full document
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Safety and tolerability of autologous bone marrow mesenchymal stromal cells in ADPKD patients
... the disease gene to their ...external renal complications due to PKD prior to ...external renal complications from PKD during the 12 months of ...had autosomal dominant ... See full document
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Autosomal dominant tubulointerstitial kidney disease-UMOD is the most frequent non polycystic genetic kidney disease
... Autosomal dominant tubulointerstitial kidney disease (ADTKD) is a rare genetic kidney ...associated kidney disease (UAKD), ADTKD-UMOD is characterised by early onset ... See full document
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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
... period between the TEMPO trials and a paucity of TKV data in REPRISE; despite this, predictions generated by the ADPKD remained consistent with observed ...greater renal benefits among patients with ... See full document
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A Prospective Study on Clinical Profile of Autosomal Dominant Polycystic Kidney Disease (ADPKD) in Jammu for a Period of 1 Year
... sugar, renal function tests—serum urea, serum creatinine, serum electrolytes (Na + , K + ), liver function tests—serum bili- rubin, SGOT, SGPT, serum alkaline phosphatase, serum proteins, serum albumin, complete ... See full document
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Urinary exosomal expression of activator of G protein signaling 3 in polycystic kidney disease
... ADPKD: autosomal dominant polycystic kidney disease; RTECs: renal tubular epithelial cells; CRIPS: consortium for radiologic imaging studies of polycystic kidney ... See full document
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