Results 161 to 170 of about 59,833 (291)

Pelvi‐Ureteric Junction Obstruction in a Solitary Functioning Kidney in Children: An Unfavourable Combination

open access: yesActa Paediatrica, Volume 115, Issue 1, Page 196-201, January 2026.
ABSTRACT Aim Solitary functioning kidney (SFK) is linked to chronic kidney disease (CKD) in children, particularly when associated with congenital anomalies of the kidney and urinary tract (CAKUT). Pelvi‐ureteric junction obstruction (PUJO) is the most frequent obstructive uropathy in SFK.
Mathilde Grapin   +9 more
wiley   +1 more source

Percutaneous nephrostomy, ureteral stent or primary ureteroscopy with stone removal for the treatment of hydronephrosis secondary to ureteric calculi: A prospective evaluation of the impact on complications, stone management and health-related QoL

open access: gold, 2020
Ricardo Rodrigues   +9 more
openalex   +1 more source

Autosplenectomy in a Patient With Autoimmune Polyglandular Syndrome Type 2 (APS‐2)

open access: yesCase Reports in Endocrinology, Volume 2026, Issue 1, 2026.
Autoimmune glandular syndrome type 2 is a complex genetic condition where a triad of endocrinopathies is involved, namely, Addison’s disease, type 1 diabetes, and/or autoimmune thyroid disorder. The disease predisposes one to a variety of other autoimmune associations.
Luqman S. Fauzi   +4 more
wiley   +1 more source

Causes and outcome of prenatally diagnosed hydronephrosis

open access: yesSaudi Journal of Kidney Diseases and Transplantation, 2009
Hydronephrosis is the most common abnormal finding in the urinary tract on prenatal screening with ultrasonography (U/S). Hydronephrosis may be obstructive or non-obstructive; obstructive lesions are more harmful to the developing kidneys. The aim of the
Ahmadzadeh Ali   +2 more
doaj  

Hypokalemic Periodic Paralysis Associated With a Rare CACNA1S Variant (p.Leu1243Val): Expanding the Mutational Spectrum

open access: yesCase Reports in Genetics, Volume 2026, Issue 1, 2026.
Background Hypokalemic periodic paralysis (HypoPP) is a rare skeletal muscle channelopathy, most often caused by mutations in CACNA1S or SCN4A. Most pathogenic CACNA1S mutations affect arginine residues in S4 voltage‐sensor domains, but other variants remain poorly understood.
Mark Abi Nader, Balraj Mittal
wiley   +1 more source

Unmasking the Culprit of Profound Hyponatremia in an Infant

open access: yesCase Reports in Pediatrics, Volume 2026, Issue 1, 2026.
Infants with severe hyponatremia (Na < 120) and an abdominal mass require an astute clinical evaluation and often represent a medical emergency. We report a case of a 2‐month‐old White female, born full term, presenting with a two‐day history of decreased oral intake and urinary output, who was found to have severe hyponatremia with notable abdominal ...
Bayan Matarneh   +3 more
wiley   +1 more source

Advanced Urologic Cancer Consensus Conference (AUC3) 2025: Expert consensus on the management of renal cell and urinary tract cancers

open access: yesCA: A Cancer Journal for Clinicians, Volume 76, Issue 1, January/February 2026.
Abstract The therapeutic landscape for renal cell carcinoma (RCC) and urinary tract cancer (UTC) has transformed dramatically, creating complexity in treatment selection and sequencing. The 2025 Advanced Urologic Cancer Consensus Conference was convened to establish evidence‐based expert consensus recommendations for optimal management.
Rana R. McKay   +53 more
wiley   +1 more source

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