Results 101 to 110 of about 2,817,125 (290)

RENAL DEVELOPMENT AND CYSTIC DISEASES [PDF]

open access: yesNephrology Dialysis Transplantation, 2014
C. Cabrera-Lopez   +126 more
openaire   +2 more sources

Senotherapeutics for Knee Osteoarthritis

open access: yesMedicinal Research Reviews, EarlyView.
ABSTRACT Osteoarthritis (OA) is a chronic disease that imposes a significant economic burden and deteriorates quality of life. Nevertheless, current therapeutic options for OA are limited to symptomatic remedies. As such, there is a high interest in novel methods for treating or preventing OA.
Ezgi Duman   +6 more
wiley   +1 more source

Bilateral renal lymphangiectasia: a rare renal cystic disease managed by minimal invasive approach—a case report

open access: yesAfrican Journal of Urology
Background Renal cystic diseases are one of the commonest renal lesions encountered in clinical practice. Although common, most of the cysts are solitary, benign, asymptomatic and seldom clinically significant. But, renal lymphangiectasia is an exception.
Navaneethakrishnan Venkatachalam   +1 more
doaj   +1 more source

Increased prevalence of renal cysts in patients with sickle cell disease

open access: yesBMC Nephrology, 2017
Background Early detection and interventions have enabled patients with sickle cell disease (SCD) to live well into adulthood. Consequently, the chronicity of SCD allows for the insidious manifestation of multisystem complications, including renal damage.
Daveena Meeks   +6 more
doaj   +1 more source

Toxoplasma gondii Infection After Kidney Transplantation: A Case Report and Literature Review

open access: yesOrgan Medicine, EarlyView.
Toxoplasma gondii infection after kidney transplantation is rare and presents with nonspecific clinical manifestations; however, the associated mortality rate is high. We discuss the relevant literature, clinical manifestations, therapeutic regimens, and prognoses of post‐transplantation toxoplasmosis.
Peng Zhang   +8 more
wiley   +1 more source

Maternal Transmission of 17q12 Microdeletion: Intrafamilial Phenotypic Variability and Diagnostic Hurdles—A Case Report

open access: yesDNA
The relatively rare proximal 17q12 microdeletion, including the deletion of the HNF1B gene, is associated with renal cysts and diabetes syndrome (RCAD). This genomic rearrangement results in a wide range of phenotypes, including renal cysts and diabetes,
Susanna Negrisolo   +3 more
doaj   +1 more source

Renal lymphangiectasia

open access: yesAutopsy and Case Reports, 2022
Renal lymphangiectasia (RL), also known as renal lymphangiomatosis, is a rare benign condition characterized by ectasia of peripelvic, perirenal and intrarenal lymphatic vessels.
Sangamitra Rajasekaran   +4 more
doaj  

Integrated Molecular Autopsy in a Highly Consanguineous Perinatal Cohort With Severe Malformations and Strong Genetic Susceptibility

open access: yesPrenatal Diagnosis, EarlyView.
ABSTRACT Objective To evaluate the diagnostic yield of integrated molecular autopsy (IMA) by combining deep post‐mortem phenotyping with exome (ES) and targeted genome sequencing (GS) for prenatally detected anomalies. Method This retrospective study evaluated 28 perinatal cases (22 fetuses, six neonates) with severe anomalies, normal first‐tier ...
Sihem Darouich   +6 more
wiley   +1 more source

Genome-Based Advances in Modeling Renal Ciliopathies and Enhancing Patient Care

open access: yesKidney & Blood Pressure Research
Background: Genetic diseases collectively affect more than 300 million individuals worldwide, posing a significant health burden, as diagnosis is often challenging and therapeutic options are limited.
Floriana Secondulfo   +7 more
doaj   +1 more source

Apigenin Protects Hypertensive Intracerebral Hemorrhage by Regulating Trx1 Through Binding to PRDX2

open access: yesPhytotherapy Research, EarlyView.
ABSTRACT Intracerebral hemorrhage (ICH) remains the most severe stroke subtype with high mortality and disability rates. Although apigenin has shown cerebroprotective potential in preclinical studies, its mechanism of action, particularly in hypertensive ICH, remains poorly understood.
Hao‐chen Xu   +6 more
wiley   +1 more source

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