Urinary tract infections in immunocompromised patients with diabetes, chronic kidney disease, and kidney transplant
Context This paper provides a brief overview of urinary tract infections (UTIs) in
immunocompromised patients from the perspective of a practicing urologist. Objective The …
immunocompromised patients from the perspective of a practicing urologist. Objective The …
Inherited renal cystic diseases
B Kim, BF King, TJ Vrtiska, MV Irazabal, VE Torres… - Abdominal …, 2016 - Springer
A number of inherited renal diseases present with renal cysts and often lead to end-stage
renal disease. With recent advances in genetics, increasing number of genes and mutations …
renal disease. With recent advances in genetics, increasing number of genes and mutations …
Diagnostic algorithm in the management of acute febrile abdomen in patients with autosomal dominant polycystic kidney disease
M Neuville, R Hustinx, J Jacques, JM Krzesinski… - PloS one, 2016 - journals.plos.org
Background Acute febrile abdomen represents a diagnostic challenge in patients with
autosomal dominant polycystic kidney disease (ADPKD). Although criteria have been …
autosomal dominant polycystic kidney disease (ADPKD). Although criteria have been …
International multi-specialty Delphi survey: identification of diagnostic criteria for hepatic and renal cyst infection
MA Lantinga, AJM Darding, RGL de Sévaux, A Alam… - Nephron, 2016 - karger.com
Background: Cyst infection is one of the complications of autosomal dominant polycystic
kidney disease and polycystic liver disease. The diagnosis is typically made on a mix of …
kidney disease and polycystic liver disease. The diagnosis is typically made on a mix of …
18F-FDG PET/CT demonstrated renal and hepatic cyst infection in a patient with autosomal dominant polycystic kidney disease
D Albano, G Bosio, F Bertagna - Nuclear Medicine Review, 2016 - journals.viamedica.pl
Infection of renal or hepatic cyst is a serious complication of autosomal dominant polycystic
kidney disease (ADPKD) and early diagnosis is crucial for the correct management. We …
kidney disease (ADPKD) and early diagnosis is crucial for the correct management. We …
Диагностика и лечение больных с поликистозом почек и инфицированными кистами
РН Трушкин, АЕ Лубенников… - … и клиническая урология, 2016 - cyberleninka.ru
Инфицированные кисты у пациентов с поликистозом почек представляется собой
сложную проблему для врачей-урологов, нефрологов, врачей диагностических служб. С …
сложную проблему для врачей-урологов, нефрологов, врачей диагностических служб. С …
[PDF][PDF] La polykystose rénale autosomique dominante: comment et pourquoi identifier les patients «rapidement progresseurs» vers l'insuffisance rénale terminale
A Bodson, P Meunier, JM Krzesinski, F Jouret - Rev Med Liège, 2016 - rmlg.uliege.be
La polykystose rénale autosomique dominante (PKRAD) est une maladie héréditaire
fréquente qui se caractérise par le développement progressif de kystes multiples et …
fréquente qui se caractérise par le développement progressif de kystes multiples et …
Polycystic Kidney Disease
SS Joshi, GP Paner, SS Chang - The Kidney: A Comprehensive Guide to …, 2016 - Springer
Autosomal dominant (ADPKD) and autosomal recessive (ARPKD) polycystic kidney
diseases represent clinically challenging disease states that affect adults and children …
diseases represent clinically challenging disease states that affect adults and children …