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About 4,918 results

ALLMedicine™ Polycystic Kidney Disease Center

Research & Reviews  1,728 results

Parapelvic Cysts: An Imaging Marker of Kidney Disease Potentially Leading to the Diagno...
https://doi.org/10.1007/s40620-022-01375-0 10.1111/j.1464-410X.2011.10847.x 10.1038/sj.ki.5001784 10.1007/s11255-016-1414-9 10.1148/radiol.2019182646 10.1093/ajcp/8.1.28 10.1016/s0022-5347(17)64914-0 10.1007/BF02388397 10.1053/j.ajkd.2011.12.022 10.1093/ndt/gfx009 10.1186/1757-1626-1-161 10.1093/ckj/sfs189 10.4068/cmj.2019.55.1.65 10.1148/radiol.11111595 10.1148/radiol.2491070783 10.1016/j.jacr.2017.04.028 10.1016/j.juro.2016.09.160 10.1016/j.urology.2005.04.003 10.2214/ajr.169.3.9275902 10.1016/s0022-5347(17)42845-x 10.1016/s0022-5347(17)57588-6 10.7727/wimjopen.2014.220 10.1055/s-0031-1296080 10.1016/0090-4295(76)90192-8 10.1073/pnas.202476899 10.1016/j.pediatrneurol.2013.08.001 10.1371/journal.pone.0180939 10.1007/s40620-020-00714-3 10.1038/s41598-021-02812-z 10.5414/CN110510 10.1002/ccr3.1431 10.1259/bjr.20160632 10.1007/s00261-020-02629-w 10.1007/s40620-019-00663-6 10.1159/000502907 10.1371/journal.pone.0230898 10.3390/ijms22010206.PMID:33379210;PMCID:PMC7794923 10.1038/ki.2008.141 10.1111/j.1523-1755.2004.00846.x 10.29245/2572-9411/2020/2.1195 10.1016/S0022-2275(20)41159-9 10.1016/S0022-2275(20)39163-X 10.1016/j.febslet.2007.03.065 10.1038/nm.2171 10.1007/s40620-021-01062-6 10.1097/01.ju.0000103642.29044.71 10.1186/s12894-015-0042-5 10.1159/000475886 10.1089/end.2011.0559 10.1159/000497313 10.1038/s41598-020-76006-4 10.22037/uj.v16i7.6466 10.1089/end.2009.0326 10.1002/ccr3.1302 10.1177/0300060519855573 10.1159/000488685 10.1089/end.2019.0515 10.1590/S1677-5538.IBJU.2018.0074.PMID:30088721;PMCID:PMC6237515
Journal of Nephrology; Capuano I, Buonanno P et. al.

Jun 25th, 2022 - Simple renal cysts are a common finding during abdominal imaging assessment. The incidence increases with age and it is higher in male gender. Parapelvic cysts are a subset of simple cysts that arise within the renal parenchyma, adjacent to the re...

Changing Health Disparities in Autosomal Dominant Polycystic Kidney Disease (ADPKD).
https://doi.org/10.2215/CJN.05790522
Clinical Journal of the American Society of Nephrology : ... Ruff SF

Jun 21st, 2022 - Changing Health Disparities in Autosomal Dominant Polycystic Kidney Disease (ADPKD).|2022|Ruff SF,|

Health Disparities in Autosomal Dominant Polycystic Kidney Disease (ADPKD) in the Unite...
https://doi.org/10.2215/CJN.00840122
Clinical Journal of the American Society of Nephrology : ... McGill RL, Saunders MR et. al.

Jun 21st, 2022 - Autosomal dominant polycystic kidney disease (ADPKD) occurs at conception and is often diagnosed decades prior to kidney failure. Nephrology care and transplantation access should be independent of race and ethnicity. However, institutional racism...

Research priorities for autosomal dominant polycystic kidney disease: a UK priority set...
https://doi.org/10.1136/bmjopen-2021-055780
BMJ Open; Harris T, Bridges HR et. al.

Jun 16th, 2022 - Autosomal dominant polycystic kidney disease (ADPKD) is the most common inherited kidney condition, accounting for 7%-10% of patients with kidney failure. Fundamental basic science and clinical research on ADPKD is underway worldwide but no one ha...

Evaluating the Safety and effectivenesS in Adult KorEaN Patients Treated With Tolvaptan for Management of Autosomal domInAnt poLycystic Kidney Disease
https://clinicaltrials.gov/ct2/show/NCT03949894

Jun 16th, 2022 - To evaluate the safety and therapeutic effectiveness of tolvaptan when administered to slow the progression of cyst development and renal function insufficiency in adult Korean patients diagnosed with rapidly progressive ADPKD who have chronic kid...

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Guidelines  14 results

A digest from evidence-based Clinical Practice Guideline for Polycystic Kidney Disease ...
https://doi.org/10.1007/s10157-021-02097-6
Clinical and Experimental Nephrology; Nishio S, Tsuchiya K et. al.

Sep 27th, 2021 - A digest from evidence-based Clinical Practice Guideline for Polycystic Kidney Disease 2020.|2021|Nishio S,Tsuchiya K,Nakatani S,Muto S,Mochizuki T,|diagnosis,genetics,therapy,diagnosis,drug therapy,

International consensus statement on the diagnosis and management of autosomal dominant...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7136168
Nature Reviews. Nephrology; Gimpel C, Bergmann C et. al.

May 24th, 2019 - These recommendations were systematically developed on behalf of the Network for Early Onset Cystic Kidney Disease (NEOCYST) by an international group of experts in autosomal dominant polycystic kidney disease (ADPKD) from paediatric and adult nep...

Clinical practice guideline monitoring children and young people with, or at risk of de...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6489289
BMC Nephrology; Dudley J, Winyard P et. al.

May 2nd, 2019 - Autosomal Dominant Polycystic Kidney Disease (ADPKD) is thought to affect about 1 in 1000 people in the UK. ADPKD causes a progressive decline in kidney function, with kidney failure tending to occur in middle age. Children and young people with A...

Evidence-based clinical practice guidelines for polycystic kidney disease 2014.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4956721
Clinical and Experimental Nephrology; Horie S, Mochizuki T et. al.

Apr 21st, 2016 - Evidence-based clinical practice guidelines for polycystic kidney disease 2014.|2016|Horie S,Mochizuki T,Muto S,Hanaoka K,Fukushima Y,|diagnosis,epidemiology,therapy,diagnosis,epidemiology,genetics,therapy,

KHA-CARI Autosomal Dominant Polycystic Kidney Disease Guideline: Diet and Lifestyle Man...
https://doi.org/10.1016/j.semnephrol.2015.10.008
Seminars in Nephrology; Campbell KL, Rangan GK et. al.

Jan 1st, 2016 - KHA-CARI Autosomal Dominant Polycystic Kidney Disease Guideline: Diet and Lifestyle Management.|2016|Campbell KL,Rangan GK,Lopez-Vargas P,Tong A,|administration & dosage,administration & dosage,physiology,complications,physiopathology,therapy,admi...

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Drugs  4 results see all →

Clinicaltrials.gov  126 results

Evaluating the Safety and effectivenesS in Adult KorEaN Patients Treated With Tolvaptan for Management of Autosomal domInAnt poLycystic Kidney Disease
https://clinicaltrials.gov/ct2/show/NCT03949894

Jun 16th, 2022 - To evaluate the safety and therapeutic effectiveness of tolvaptan when administered to slow the progression of cyst development and renal function insufficiency in adult Korean patients diagnosed with rapidly progressive ADPKD who have chronic kid...

Safety of Lixivaptan in Subjects Previously Treated With Tolvaptan for Autosomal Dominant Polycystic Kidney Disease
https://clinicaltrials.gov/ct2/show/NCT04152837

Jun 9th, 2022 - This is a Phase 3, open-label, repeat-dose study designed to assess liver safety, non-liver safety, and efficacy in subjects who previously experienced liver chemistry test abnormalities while treated with tolvaptan and were permanently discontinu...

Efficacy and Safety of Lixivaptan in the Treatment of Autosomal Dominant Polycystic Kidney Disease
https://clinicaltrials.gov/ct2/show/NCT04064346

Jun 8th, 2022 - Part 1: Approximately 2500 participants with ADPKD will be screened in order to qualify the 1350 individuals who will then be randomized to receive lixivaptan or placebo. Each participant has a 2/3 chance of receiving lixivaptan and a 1/3 chance o...

Effect of Beetroot Juice on Reducing Hypertension in Autosomal Dominant Polycystic Kidney Disease
https://clinicaltrials.gov/ct2/show/NCT05401409

Jun 2nd, 2022 - People with autosomal dominant polycystic kidney disease (ADPKD) develop high blood pressure and kidney disease. Previous studies have shown that a commonly occurring chemical, nitric oxide (NO), is reduced in ADPKD, and may contribute, in part, t...

Study of the Efficacy and Safety of Tesevatinib in Subjects With ADPKD
https://clinicaltrials.gov/ct2/show/NCT03203642

Jun 1st, 2022 - Safety and efficacy of 50mg tesevatinib in comparison to placebo in patients with autosomal dominant polycystic kidney disease (ADPKD) will be assessed. The primary purpose of this study is focused on evaluating the change from baseline in height-...

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News  75 results

Stroke Study Reveals a High Frequency of Mendelian Disorders
https://www.medscape.com/viewarticle/976120

Jun 23rd, 2022 - The study covered in this summary was published in medrxiv.org as a preprint and has not yet been peer reviewed. Key Takeaways Exome sequencing (ES) is useful in evaluating stroke patients, particularly younger patients less than 1 year old. Due t...

Mayo Classification by Ultrasound Useful in Predicting Rapid Progression of Rare Kidney Disease
https://www.medscape.com/viewarticle/966321

Jan 11th, 2022 - NEW YORK (Reuters Health) - The Mayo classification (MC) of autosomal dominant polycystic kidney disease (ADPKD) based on ultrasound rather than magnetic resonance imaging (MRI) findings performs well, especially at the extremes of the MC (classes...

Kidney Donors Reveal What It's Like to Match for Surgery
https://www.medscape.com/viewarticle/962376

Nov 5th, 2021 - From the time they were young, Amy DeAngelis and her younger sister Laura Johnson knew that Laura would need a new kidney someday. A condition called polycystic kidney disease runs in their family, and eventually the affected organs fail. Amy had ...

Fast Five Quiz: Autosomal Dominant Polycystic Kidney Disease (ADPKD)
https://www.medscape.com/viewarticle/954016

Aug 6th, 2021 - Autosomal-dominant polycystic kidney disease (ADPKD) is the most common hereditary renal disease and the fourth leading cause of end-stage renal disease worldwide. As many as 12 million people are affected by ADPKD, which stems primarily from muta...

Fast Five Quiz: Autosomal Dominant Polycystic Kidney Disease Presentation and Diagnosis
https://www.medscape.com/viewarticle/950557

Jun 29th, 2021 - Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disease worldwide. It is characterized by progressive development of renal cysts, hypertension, and destruction of the kidney parenchyma. Most patients with ...

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Patient Education  20 results see all →