Results 81 to 90 of about 116,920 (234)

Vascular Disc Anomalies - Retinal Arteriovenous Malformations

, 1973
Retinal arteriovenous malformations. Anatomy: Optic disc. Pathology: Retinal arteriovenous malformation. Disease/Diagnosis: Retinal arteriovenous malformation.
William F. Hoyt, MD
core  

Stereotactic radiosurgery for arteriovenous malformations, Part 4:management of basal ganglia and thalamus arteriovenous malformations

, 2012
The authors conducted a study to define the long-term outcomes and risks of stereotactic radiosurgery (SRS) for arteriovenous malformations (AVMs) of the basal ganglia and ...
Flickinger, John C, Kondziolka, Douglas, Lunsford, L Dade, Huai-che Yang, Douglas Kondziolka, Yang, Huai-che, Niranjan, Ajay, John C. Flickinger, Hideyuki Kano, Thomas J. Flannery, Ajay Niranjan, Flannery, Thomas J, Novotny, Josef, L. Dade Lunsford, Kano, Hideyuki, Josef Novotny   +15 more
core   +1 more source

Arteriovenous malformations embolization in the modern era: case series report [PDF]

, 2021
Background: Cerebral arteriovenous malformations are complex high-flow lesions that can result in devastating neurological injury when they hemorrhage.
Parpaut, Vladimir, Davidov, Ghenadie, Zapuhlih, Grigore, Preguza, Ion, Galearschi, Vasile   +4 more
core   +1 more source

Assessment of Growth in Cardio‐Facio‐Cutaneous Syndrome

American Journal of Medical Genetics Part A, Volume 200, Issue 11, Page 2443-2453, November 2026.
ABSTRACT Cardio‐facio‐cutaneous (CFC) syndrome is a rare, multiple congenital anomaly disorder in which individuals commonly experience faltering growth; however, systematic analysis of growth parameters in this disorder has not been performed. We recruited 69 participants with CFC through CFC International and collected data on assessing height ...
Kari Johnston, Sandesh C. S. Nagamani, Bradley S. Miller, Katherine A. Rauen, Richard D. Boyce, Salma Musaad, Pilar L. Magoulas   +6 more
wiley   +1 more source

Arteriovenous malformation in mice and men

, 2008
Arteriovenous malformations are the most dangerous vascular malformations and extremely difficult to treat. While most of them are sporadic, some are associated with autosomal dominant disorders, such as hereditary hemorrhagic telangiectasia, PTEN ...
Boon, Laurence M., Revencu, Nicole, Vikkula, Miikka   +2 more
core  

Risk factors associated with cerebral complications in patients with pulmonary arteriovenous malformations (n = 55).

, 2022
Risk factors associated with cerebral complications in patients with pulmonary arteriovenous malformations (n = 55).
Young-Ok Na (14204628), Jae-Kyeong Lee (10099045), Yong-Soo Kwon (754013), In-Jae Oh (2967396), Hyung-Joo Oh (4264765), Bo-Gun Kho (14204634), Hong-Joon Shin (2967390), Hwa Kyung Park (14204631), Yu-Il Kim (798679), Tae-Ok Kim (3183162), Sung-Chul Lim (226845), Cheol-Kyu Park (2967393), Young-Chul Kim (2967387), Ha-Young Park (556116)   +13 more
core   +1 more source

Sleeve lobectomy for an arteriovenous malformation in the bronchus intermedius in a child

Journal of Pediatric Surgery Case Reports, 2019
Arteriovenous malformations within the tracheobronchial tree in pediatric patients uncommonly present as hemoptysis, and can usually be treated with percutaneous transcatheter embolization.
Aditya Sengupta, Othman Aljohani, Howaida El-Said, Aparna Rao, Matthew Brigger, Raghav Murthy   +5 more
doaj   +1 more source

A Comprehensive In Vitro Approach for Assessing the Physiological Degradation of Medical Implants: The Silkothane Arteriovenous Graft Case Study

Advanced NanoBiomed Research, Volume 6, Issue 11, November 2026.
Evaluating the degradation of absorbable medical devices in vitro demands physiologically relevant conditions. This study presents a comprehensive framework applied to a three‐layered silk fibroin/polyurethane arteriovenous graft, employing human enzymes at physiological concentrations over 6 months. Multiparametric analyses of both graft structure and
Cristina Oldani, Alice Caldiroli, Federica Barzaghi, Nina Bono, Gabriele Candiani, Stefania Adele Riboldi   +5 more
wiley   +1 more source

Prenatal Diagnosis of Recurrent Fetal Intracranial Hemorrhage and a Maternally Inherited COL4A1 Variant of Uncertain Significance: A Case Report With Maternal Reverse Phenotyping

Clinical Case Reports, Volume 14, Issue 11, November 2026.
ABSTRACT A 33‐year‐old woman with two consecutive pregnancies affected by fetal left periventricular germinal matrix hemorrhage (Grade IV) and progressive ventriculomegaly underwent trio whole‐exome sequencing. A heterozygous COL4A1 c.4249G>C (p.Gly1417Arg) variant, classified as a variant of uncertain significance, was identified in the fetus of the ...
Wei Shi, Hongjing Xu, Caihong Pu, Yuanzhong Liang, Ting Zhao, Xueli Wang, Zhenxing Liu, Chunhua Zhang, Ting Li, Fengquan He   +9 more
wiley   +1 more source

Deep Intramuscular Vascular Malformations in Pediatric Klippel–Trenaunay Syndrome Mimicking Maffucci Syndrome: A Case Report

Clinical Case Reports, Volume 14, Issue 11, November 2026.
ABSTRACT Klippel‐Trenaunay syndrome (KTS) is a rare congenital vascular overgrowth disorder characterized by capillary and venous or lymphatic malformations with limb hypertrophy. Deep intramuscular involvement in children is uncommon and may resemble other vascular‐overgrowth syndromes.
Syeda Simrah Shah, Barka Sajid, Muzainah Tabassum, Mirha Ali, Taher Janoowala, Tehreem Farooq, Muhammad Ahsan, Mirza Mohammad Ali Baig, Mirza Daniyal Baig, Mohammed Hammad Jaber Amin   +9 more
wiley   +1 more source