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期刊名:Advances in kidney disease and health

缩写:ADV KIDNEY DIS HEAL

ISSN:2949-8147

e-ISSN:2949-8139

IF/分区:3.1/Q2

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共收录本刊相关文章索引211
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Matthew Gittus,Tess Harris,Albert Cm Ong Matthew Gittus
Autosomal dominant polycystic kidney disease (ADPKD) is the most common inherited kidney disease. It has been associated with a significant physical and psychological burden, leading to a reduced quality of life. The purpose of this literat...
Alan S L Yu,Douglas P Landsittel Alan S L Yu
This article describes the use of prognostic, predictive, and response biomarkers that have been developed for autosomal dominant polycystic kidney disease and their use in clinical care or drug development. We focus on biochemical markers ...
Fouad T Chebib,Ronald D Perrone Fouad T Chebib
Autosomal dominant polycystic kidney disease (ADPKD) is a hereditary disorder characterized by relentless growth of innumerable renal cysts bilaterally, associated with decline in glomerular filtration rate over the course of decades. The b...
Julie Xia Zhou,Vicente E Torres Julie Xia Zhou
Autosomal dominant polycystic kidney disease (ADPKD) is characterized by the formation of numerous kidney cysts which leads to kidney failure. ADPKD is responsible for approximately 10% of patients with kidney failure. Overwhelming evidence...
Angélique Dachy,Liselotte Van Loo,Djalila Mekahli Angélique Dachy
The clinical management of autosomal dominant polycystic kidney disease (ADPKD) in adults has shifted from managing complications to delaying disease progression through newly emerging therapies. Regarding pediatric management of the diseas...
William Ackley,Neera K Dahl,Meyeon Park William Ackley
Autosomal dominant polycystic kidney disease (ADPKD) is the most common genetic kidney disorder and the fourth leading cause of end-stage kidney disease. ADPKD encompasses a wide range of morbidity in addition to chronic kidney disease and ...
Cortney N Steele,Kristen L Nowak Cortney N Steele
Autosomal dominant polycystic kidney disease is a slowly progressive, lifelong disease characterized by continuous development and enlargement of kidney cysts. Thus, nonpharmacological interventions are crucial in disease management and hav...
Jiahe Qiu,Gregory G Germino,Luis F Menezes Jiahe Qiu
Autosomal dominant polycystic kidney disease is the most common inherited cause of end-stage kidney disease worldwide. Most cases result from mutation of either of 2 genes, PKD1 and PKD2, which encode proteins that form a probable receptor/...
Biruh T Workeneh,Priti Meena,Mirjam Christ-Crain et al. Biruh T Workeneh et al.
Hyponatremia is one of the most common problems encountered in clinical practice and one of the least-understood because accurate diagnosis and management require some familiarity with water homeostasis physiology, making the topic seemingl...