Results 121 to 130 of about 16,202 (282)
BJUI Compass, Volume 7, Issue 3, March 2026.Abstract Objectives This study aims to validate the diagnostic accuracy of a novel urine‐based DNA methylation test in patients with suspected upper tract urothelial carcinoma (UTUC) on CT urography and to assess its potential to eliminate the need for diagnostic ureterorenoscopy (URS) in selected patients, expedite treatment and identify high‐grade ...
Christian Daniel Fankhauser +6 more
wiley +1 more source
Spectrum and outcome of repair of benign biliary strictures
, 2003 Carlos U. Corvera +5 more
openalex +1 more source
Anomalous Origin of the Left Coronary System From the Right Coronary Cusp: A Case Report
Clinical Case Reports, Volume 14, Issue 3, March 2026.ABSTRACT The early recognition of this rare coronary anomaly using multiple imaging modalities such as CCTA provided invaluable information to better stratify the risk, clarify prognosis, and deliver the most appropriate intervention.
Cristian Castillo‐Rodriguez +6 more
wiley +1 more source
Clinical Case Reports, Volume 14, Issue 3, March 2026.ABSTRACT Kartagener's Syndrome (KS), a rare autosomal recessive disorder and a subset of Primary Ciliary Dyskinesia (PCD), is characterized by chronic sinusitis, bronchiectasis, and, in approximately 50% of cases, situs inversus. This condition arises from genetic mutations that impair motile cilia function, leading to defective mucociliary clearance ...
Ibrahim Khalil +3 more
wiley +1 more source
Dilation or biodegradable stent placement for recurrent benign esophageal strictures: a randomized controlled trial [PDF]
, 2018 Daisy Walter +15 more
openalex +1 more source
Clinical Case Reports, Volume 14, Issue 3, March 2026.ABSTRACT We present two patients with > 80 years with type 1 diabetes (T1D), but with minor complications. Their history and risk factors are characterized as are factors conferring resilience against angiopathy. Amazingly, both had clearly detectable C‐peptide.
Åke Sjöholm, Daniel Espes
wiley +1 more source
Treatment of refractory benign gastroenteral strictures with fully covered metal stents [PDF]
, 2021 Amandeep Singh +2 more
openalex +1 more source
Prenatal Diagnosis of Renal Anomalies Associated With a Novel Causative Variant in RAP1B Gene
Clinical Case Reports, Volume 14, Issue 3, March 2026.A case of prenatal renal cystic disease and unilateral renal agenesis is reported. Molecular investigations including TRIO next‐generation sequencing analysis using the Clinical exome sequencing protocol identified the c.179G>T, p.(Gly60Val) “de novo” variant in a heterozygous state in the RAP1B gene.
Adalgisa Cordisco +5 more
wiley +1 more source