Results 31 to 40 of about 276,553 (236)

Editorial [PDF]

open access: yesJournal of Neurosurgery: Pediatrics, 2010
Ding and colleagues at the University of Virginia provide an analysis of 444 patients who had stereotactic radiosurgery for an arteriovenous malformation (AVM) without evidence of prior symptomatic hemorrhage.1 The series included patients with a mean AVM volume of 4.2 cm3 (about 2 cm in diameter), but only 14% of the AVMs were in deep brain locations.
openaire   +3 more sources

Uterine arteriovenous malformation [PDF]

open access: yesBMJ Case Reports, 2013
Uterine arteriovenous malformation (AVM) is a little known condition of which, to date, very few cases have been described. It has a very diverse symptomatology, even though in most cases, it is diagnosed during a severe and acute haemorrhagic event. Its treatment can vary from expectant management to hysterectomy; however, current evidence suggests ...
Francisco Sellers   +3 more
openaire   +3 more sources

Novel planning pipeline utilizing the Surgical Theater system for pediatric epilepsy surgery

open access: yesEpilepsia Open, EarlyView.
Abstract Objective Advances in the analysis and collation of radiographic datasets have enhanced presurgical planning for various neurosurgical procedures, including clipping of cerebral aneurysms, surgical resection of tumors, and arteriovenous malformation management.
Lisa B. E. Shields   +4 more
wiley   +1 more source

A unique case of prenatal diagnosis of vascular Ehlers‐Danlos syndrome

open access: yesInternational Journal of Gynecology &Obstetrics, EarlyView.
Abstract We present a rare instance of prenatal diagnosis of vEDS without a family history. The suspicion of a genetic syndrome arose from an incidental ultrasound finding of a facial anomaly—previously associated with vEDS in adulthood but never described prenatally.
Emma Bertucci   +5 more
wiley   +1 more source

Use of endovascular embolization to treat a ruptured arteriovenous malformation in a pregnant woman: a case report

open access: yesJournal of Medical Case Reports, 2012
IntroductionPregnancy has been linked to increased rates of arteriovenous malformation rupture. This link remains a matter of debate and very few studies have addressed the management of arteriovenous malformation in pregnancy.
W. Jermakowicz   +3 more
semanticscholar   +1 more source

From multi‐omics to precision medicine in intracranial aneurysm: Biomarker discovery and multimodal integration

open access: yesInterdisciplinary Medicine, EarlyView.
This review explores intracranial aneurysm biomarker discovery through multi‐omics. It reveals key genes, proteins, and metabolites, and shows how machine‐learning‐based multi‐modal integration may aid diagnosis and treatment. Abstract Despite extensive research, currently, no biomarkers are available for clinical use in intracranial aneurysm (IA ...
Jiaxin Zhang   +4 more
wiley   +1 more source

Klippel‐Trénaunay‐Weber Syndrome: Prenatal Diagnosis and Review of the Literature

open access: yesJournal of Clinical Ultrasound, Volume 53, Issue 3, Page 535-546, March/April 2025.
This meta‐analysis demonstrates the high diagnostic accuracy of SZ‐CEUS for differentiating between malignant and benign focal liver lesions, as well as for HCC from non‐HCC lesions. The study shows better performance for smaller lesions and those with a higher proportion of malignancy.
Giuliana Orlandi   +13 more
wiley   +1 more source

PELVIC ARTERIOVENOUS MALFORMATIONS [PDF]

open access: yesAmerican Journal of Roentgenology, 1968
Two young men with congenital pelvic arteriovenous malformations are reported. Both had local Symptoms related to the presence of a mass. Angiographic studies were diagnostic and essential in guiding treatment.
Harold A. Mitty   +2 more
openaire   +3 more sources

An incidental finding of mesenteric hematoma in a patient with a new diagnosis of inflammatory bowel disease

open access: yesJPGN Reports, EarlyView.
Abstract Mesenteric hematomas (MHs) are relatively rare and are characterized by localized bleeding in the mesenteric vascular tree presenting with abdominal pain, vomiting, abdominal distension, masses, and hypotension. We report a case of a MH which was incidentally found in a 10‐year‐old patient with a new diagnosis of ulcerative colitis (UC).
Breanna Brown   +2 more
wiley   +1 more source

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