Results 11 to 20 of about 12,370 (174)

Acute Kidney Injury in ADPKD Patients with Pneumonia [PDF]

open access: yesInternational Journal of Nephrology, 2011
Background. In animal models, polycystic kidneys are susceptible to acute kidney injury (AKI). We examined the occurrence of AKI in a cohort of autosomal dominant polycystic kidney disease (ADPKD) and non-ADPKD patients with acute pneumonia. Design.
Carlos Franco Palacios   +8 more
doaj   +2 more sources

Exome sequencing of Saudi Arabian patients with ADPKD

open access: yesRenal Failure, 2019
Purpose: Autosomal dominant polycystic kidney disease (ADPKD) is characterized by progressive development of kidney cysts and enlargement and dysfunction of the kidneys. The Consortium of Radiologic Imaging Studies of the Polycystic Kidney Disease (CRISP)
Fahad A. Al-Muhanna   +19 more
doaj   +2 more sources

MR Brain Screening in ADPKD Patients [PDF]

open access: yes, 2021
Background Adult polycystic kidney disease (ADPKD) still represents a major cause of renal failure and intracranial aneurisms (IA) have a higher prevalence in ADPKD than in the general population.
M. Seri   +16 more
core   +1 more source

Patient perspectives on ADPKD [PDF]

open access: yes, 2023
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.
Ong, A.C.M., Harris, T., Gittus, M.
core   +1 more source

aksg87/adpkd-segmentation-pytorch: ADPKD Segmentation models v1.0

open access: yes, 2021
ADPKD Segmentation models v1.0 Training pipeline implementation. Inference script with best model and checkpoint. Extensive experiment documentation via Tensorboard runs and YAML config files. Total kidney volume metric calculation.
Akshay Goel
core   +1 more source

Urinary proteomic biomarkers for diagnosis and risk stratification of autosomal dominant polycystic kidney disease: a multicentric study [PDF]

open access: yes, 2013
Treatment options for autosomal dominant polycystic kidney disease (ADPKD) will likely become available in the near future, hence reliable diagnostic and prognostic biomarkers for the disease are strongly needed.
Torres, Vicente E.   +101 more
core   +2 more sources

Giant Bilateral Adrenal Myelolipoma: Case Report

open access: yesIndian Journal of Endocrinology and Metabolism, 2020
Adrenal myelolipomas are nonfunctional tumors that are usually asymptomatic; however, they have been known to coexist with other endocrine disorders, such as Cushing's syndrome, congenital adrenal hyperplasia (CAH), Conn's syndrome, and pheochromocytoma.
B Rathna Roger   +3 more
doaj   +1 more source

The BC ADPKD Network: A Comprehensive Provincial Approach to Support Specialized and Locally Delivered Multidisciplinary ADPKD Care

open access: yesCanadian Journal of Kidney Health and Disease, 2021
Purpose: With evolving evidence around the progression, assessment, and management of autosomal dominant polycystic kidney disease (ADPKD), care of the disease has become increasingly complex.
M. Bevilacqua   +6 more
doaj   +1 more source

RECURRENT HAPLOTYPE IN ADPKD PATIENTS WITH THE SAME GERMLINE NONSENSE MUTATION IN THE PKD2 GENE [PDF]

open access: yes, 2022
openLa malattia autosomica dominante del Rene Policistico (Autosomal Dominant Polycystic Kidney Disease, ADPKD) è la più comune malattia genetica renale nella popolazione mondiale e in Europa è la quarta causa di CKD (Chronic Kidney Disease) che ...
RADONIC, SARA
core  

Cardiac structural and functional findings in Persian cats with autosomal dominant polycystic kidney disease [PDF]

open access: yesCiência Rural, 2020
: Autosomal dominant polycystic kidney disease (ADPKD) has been related to left ventricular structural and functional abnormalities in human patients. The present study aimed to evaluate the cardiac structural and functional findings in Persian cats with
Juliana Mariotti Guerra   +10 more
doaj   +1 more source

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