Results 201 to 210 of about 72,082 (267)

Traumatic Transverse Aortic Arch Pseudoaneurysm in a Pediatric Patient. [PDF]

JACC Case Rep
Maza Portuondo L, Li B, Chakiath M, Halickman R, Pedroso F, Infante J, Forbess J.   +6 more
europepmc   +1 more source

Identification of the Genomic Etiology of Unexplained Congenital Problems in Pediatric Patients: First Reported Case With Coffin–Siris Syndrome and Sialuria From India

Clinical Case Reports, Volume 14, Issue 9, September 2026.
ABSTRACT Coffin–Siris syndrome (CSS) (OMIM:614608) is a rare genetic disorder characterized by global developmental delay (GDD), speech impediment, coarse facial features, and hypoplastic or absent fifth fingernails/toenails. Genetic variants in the SMARCB1 gene are associated with CSS, benign tumors (schwannomas), and rhabdoid tumor predisposition ...
Aparna Bhanushali, Archana Kawalakatt, Smita Kulkarni, Preethi Nair, Ankita Mali, Ashlesha Pradhan, Anirvan Chatterjee   +6 more
wiley   +1 more source

Escalating Diameter Buddy Balloon in Transcatheter Aortic Valve Implantation With Complex Aortic Arch. [PDF]

Catheter Cardiovasc Interv
Paolucci L, Scarpelli M, Maselli D, Briguori C.   +3 more
europepmc   +1 more source

Rapid Diagnosis and Surgical Management of Catastrophic Stanford Type A Acute Aortic Dissection Resulting in Successful Lung Donation: A Case Report

Clinical Case Reports, Volume 14, Issue 9, September 2026.
ABSTRACT This case highlights that rapid diagnosis and emergency surgical repair for catastrophic Stanford Type A acute aortic dissection may preserve the opportunity for successful lung donation even when neurological recovery is impossible. Transthoracic echocardiography played a critical role in establishing the diagnosis when computed tomography ...
Koki Yokawa, Ryota Abe, Tomonori Higuma, Kazunori Yoshida, Hidefumi Obo, Makoto Kadotani, Hidetaka Wakiyama   +6 more
wiley   +1 more source

Safety and Feasibility of In Situ Fenestration in the Aortic Arch: A Prospective Single-Center Observational Cohort Study. [PDF]

J Clin Med
Kolvenbach R, Shu C, Lica ER.
europepmc   +1 more source

Congenital Absence of the Left Pulmonary Artery Associated With Right‐Sided Aortic Arch Presenting as Hemoptysis in an Adult: A Case Report

Clinical Case Reports, Volume 14, Issue 9, September 2026.
ABSTRACT Congenital unilateral absence of the pulmonary artery is a rare vascular anomaly that may remain undiagnosed until adulthood. Patients can present with unexplained hemoptysis, recurrent respiratory infections, or pulmonary hypertension. Contrast‐enhanced CT plays a crucial role in diagnosis, evaluation of collateral circulation, and guiding ...
Tayyaba Kauser, Asma Khan, Asma Sattar, Syed Muhammed Salman Hassan, Masroor Raza, Sarim Hassan Shahab, Fazal Habib   +6 more
wiley   +1 more source

Impact of Antegrade Selective Cerebral Perfusion Flow Ranges on Clinical and Neurological Outcomes in Aortic Arch Surgery. [PDF]

Interdiscip Cardiovasc Thorac Surg
Piperata A, Van den Eynde J, Castagnini S, Carotenuto F, Garofalo R, Snaidero S, Leone A, Di Marco L, Pacini D.   +8 more
europepmc   +1 more source

Premature Ductus Arteriosus Constriction and Pulmonary Trunk Dilation in a Case of Non‐Immune Hydrops Fetalis With Trisomy 21

Clinical Case Reports, Volume 14, Issue 9, September 2026.
ABSTRACT Premature constriction of the ductus arteriosus accompanied by the dilation of the pulmonary trunk constitutes a rare congenital heart anomaly that may be underestimated and can result in fetal hydrops and ultimately death if not treated; therefore, it necessitates fetal post‐mortem evaluation in all cases of legal abortion or fetal death.
Nazari Mohadeseh, Hejrati Zinatosadat, Pajokh Mojde   +2 more
wiley   +1 more source

Single-Stage Repair of Complex Congenital Aortic Arch Pathology With Dissection and Aneurysm in an Adult. [PDF]

JACC Case Rep
Ahmad N, Chen X, Huang Y, Li J, Wang Y, Zhang Q, Huang L.   +6 more
europepmc   +1 more source

Plasma exosomal miR‐339‐3p promotes myocardial remodeling in chronic heart failure by regulating USP25‐mediated DDX58 deubiquitination

Journal of Cell Communication and Signaling, Volume 20, Issue 3, September 2026.
In the patients of chronic heart failure (HF), miR‐339‐3p derived from plasma exosomes can target ubiquitin‐specific protease 25, inhibiting its K48‐linked deubiquitination modification of DDX58, leading to increased ubiquitination and degradation of DDX58.
Guoqiang Jing, Ting Xu, Yuhong Ma
wiley   +1 more source