DPKD

(redirected from Dominant Polycystic Kidney Disease)
AcronymDefinition
DPKDData Plane Development Kit (packet processing; Linux Foundation)
DPKDDominant Polycystic Kidney Disease
DPKDDistributed and Parallel Knowledge Discovery (data mining)
References in periodicals archive ?
Gene expression in early and progression phases of autosomal dominant polycystic kidney disease. BMC Res Notes 2008 Dec;1:131.
Computed tomography (CT) abnormalities leading to CT-initiated exclusion from kidney donation in 81 patients n Collecting system 41 Renal calculi 39 Ureteropelvic junction obstruction 2 due to crossing vessels Renal vasculature 29 Supernumerary arteries and/or early 20 arterial branching Renal arterial aneurysms 2 Renal vein anomalies 2 Atherosclerotic plaque at the renal arterial ostium 1 Duplicated IVC 1 Fibromuscular dysplasia 1 Polyarteritis nodosa 1 Renal arterio-venous malformation 1 Renal parenchyma 9 Autosomal dominant polycystic kidney disease 3 Renal cell carcinoma 2 Renal scarring 2 Complex renal cyst 1 Segmental renal infarction 1 Extra-renal 2 Pulmonary nodule 2 Katerina Mastrocostas (1); Christina M.
Meijer et al., "Renal replacement therapy for autosomal dominant polycystic kidney disease (ADPKD) in Europe: prevalence and survival-an analysis of data from the ERA-EDTA registry," Nephrology Dialysis Transplantation, vol.
Abbreviations ADPKD: Autosomal dominant polycystic kidney disease ADPLD: Autosomal dominant polycystic liver disease CLF: Chronic liver failure HA: Hepatic artery IVC: Inferior vena cava MELD: Model for end stage liver disease OLT: Orthotopic liver transplant PLD: Polycystic liver disease PV: Portal vein RHV: Right hepatic vein.
Autosomal dominant polycystic kidney disease (ADPKD) is the most common life-threatening monogenic disease.
Prenatal diagnosis of autosomal dominant polycystic kidney disease (PKD 1) presenting in utero and prognosis for very early onset disease.
Comparison of volume-reductive therapies for massive polycystic liver disease in autosomal dominant polycystic kidney disease. Hepatol Res 2016;46:183-91.
Autosomal dominant polycystic kidney disease (ADPKD) is characterized by the progressive development of multiple renal cysts that destroy the renal parenchyma.
Strandgaard, "Improved prognosis in patients with autosomal dominant polycystic kidney disease in Denmark," Clinical Journal of the American Society of Nephrology, vol.
Autosomal dominant polycystic kidney disease (ADPKD) is characterised by the progressive development and enlargement of kidney cysts throughout the renal tissue, which leads to increases in renal volume and ultimately renal failure.
(1) Genetic syndromes and collagen vascular diseases are another potential source of multiple aneurysms in children, and include entities such as Marfan syndrome, Ehlers-Danlos syndrome, Loeys-Dietz syndrome, thoracic aortic aneurysm and dissection (TAAD), as well as Turner syndrome, neurofibromatosis, and autosomal dominant polycystic kidney disease (ADPKD).
* Qualification of Biomarker--Total Kidney Volume in Studies for Treatment of Autosomal Dominant Polycystic Kidney Disease, Draft Guidance, August 2015 (4)
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