Results 91 to 100 of about 10,298 (208)

Imaging Diagnosis of Neonatal Umbilical Arteriovenous Malformation Complicated with Portosystemic Shunt [PDF]

open access: yesAdvanced Ultrasound in Diagnosis and Therapy
In the last twenty years, there were less than 10 cases of umbilical arteriovenous malformations have been reported, which usually had single complication, included mild cardiac dilatation, pulmonary hypertension, hemorrhagic shock, and hepatic damage ...
Zhang Minyu, Jia Baocheng, Huang Liuming
doaj   +1 more source

Somatic activating mutations in Pik3ca cause sporadic venous malformations in mice and humans. [PDF]

open access: yes, 2016
Venous malformations (VMs) are painful and deforming vascular lesions composed of dilated vascular channels, which are present from birth. Mutations in the TEK gene, encoding the tyrosine kinase receptor TIE2, are found in about half of sporadic ...
Angulo-Urarte, Ana   +27 more
core   +2 more sources

New Right‐To‐Left Shunt Through a Patent Foramen Ovale Following Abdominal Surgery

open access: yesClinical Case Reports, Volume 14, Issue 3, March 2026.
ABSTRACT In the setting of new platypnea‐orthodeoxia syndrome, early consideration of right‐to‐left shunting via a patent foramen ovale is critical for effective management.
Jack Franke   +5 more
wiley   +1 more source

Endovascular treatment of pulmonary arteriovenous malformations in hereditary haemorrhagic telangiectasia. [PDF]

open access: yes, 2015
PRINCIPLES: To assess the efficiency and complication rates of vaso-occlusion of pulmonary arteriovenous malformations (PAVMs) in Rendu-Osler-Weber disease (hereditary haemorrhagic telangectasia; HHT).
Aebischer, N.   +5 more
core   +1 more source

LKB1–AMPK Signaling Pathway in Cardiovascular and Other Diseases

open access: yesMedComm, Volume 7, Issue 3, March 2026.
The LKB1–AMPK pathway has a central regulatory role in various diseases. Dysfunction of this pathway can lead to pathological processes in cardiovascular diseases (atrial fibrillation, myocardial infarction, myocardial hypertrophy, atherosclerosis), metabolic diseases (diabetes and kidney disease), neurodegenerative diseases (Alzheimer's disease ...
Zhuo Chen, Qin Yang, Guo‐Wei He
wiley   +1 more source

Complications After Treatment of Head and Neck Venous Malformations With Sodium Tetradecyl Sulfate Foam [PDF]

open access: yes, 2017
The aim of this study was to evaluate complications in patients with head and neck venous malformations (VMs) treated with foam sclerotherapy using sodium tetradecyl sulfate (STS)
Bardazzi Alessandro   +6 more
core   +1 more source

Advances and Prospects of Stereotactic Radiosurgery and Stereotactic Ablative Body Radiotherapy: Evolving Paradigms in Precision Oncology

open access: yesMed Research, Volume 2, Issue 1, Page 157-180, March 2026.
The graphical abstract outlines the progressive development and impact of stereotactic radiosurgery (SRS) and stereotactic body radiotherapy (SBRT). Technological Evolution illustrates the transition from brachytherapy with single‐dose, LDR/HDR schedules to fractionated radiotherapy, three‐dimensional conformal radiotherapy (3DCRT) and Gamma Knife ...
Jing Zhang   +10 more
wiley   +1 more source

Four‐Dimensional Computed Tomography Differentiates Congenital Right Pulmonary Vein Atresia From Suspected Arteriovenous Malformation: A Case Report

open access: yesRespirology Case Reports, Volume 14, Issue 3, March 2026.
Congenital pulmonary vein atresia (PVA) is a rare condition often associated with vascular anomalies and complex pulmonary hemodynamics. We present a case in which 4D‐CT effectively differentiated congenital right PVA, presenting with a varix and abnormal vein, from a suspected pulmonary arteriovenous malformation.
Takahiro Arano   +9 more
wiley   +1 more source

PULMONARY ARTERIOVENOUS MALFORMATION: STILL A SURGICAL CONSIDERATION [PDF]

open access: yesActa Medica Iranica, 1998
Pulmonary arteriovenous malformations are rare clinical entities thai are associated with right to left shunts, and are often clinically presented by the triad of dyspnea, cyanosis, and digital clubbing.
S. Shahidnoorai M.Rahbar
doaj   +1 more source

Genetically diagnosed Birt-Hogg-Dubé syndrome and familial cerebral cavernous malformations in the same individual: a case report. [PDF]

open access: yes, 2016
When faced with an unusual clinical feature in a patient with a Mendelian disorder, the clinician may entertain the possibilities of either the feature representing a novel manifestation of that disorder or the co-existence of a different inherited ...
Skytte, Anne-Bine   +2 more
core   +2 more sources

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