Results 71 to 80 of about 8,539 (170)

Intramedullary cavernoma: a surgical resection technique

, 2017
Intramedullary spinal cavernoma is a rare vascular disease constituting 5-12% of all spinal vascular tumors. The clinical course is usually characterized either by an acute neurological deterioration, recurrent episodes of neurological deficits or by a ...
Giammattei, L, Di Meco, F, Messerer, M, Prada, F   +3 more
core   +1 more source

Microsurgical removal of a cavernous malformation on the midbrain dorsal surface using the supracerebellar infratentorial approach: a clinical case

Сеченовский вестник
Common surgical approaches to the dorsal midbrain include: the occipital transtentorial, supracerebellar infratentorial, posterior subtemporal, and the tonsilloveal transaqueductal approaches.Case report. A 38-year-old man presented with mild right-sided
N. O. Rahimov, K. J. Rakhmonov, D. R. Sanginov, M. A. Khasanov   +3 more
doaj   +1 more source

Cavernoma de la órbita

, 2009
Cuatro imágenes de un cavernoma de la órbita.Four pictures of a cavernoma in the ...
Iglesias Rozas, José Rafael, 1942-
core  

Intraventricular Cavernoma

, 2018
Intraventricular cavernomas (IVC) are rare entities. We report a case of incidentally detected intraventricular cavernoma (IVC) in frontal horn of the lateral ventricle in which the diagnosis was established by typical magnetic resonance imaging (MRI ...
Kumar Savith, Savith Kumar
core   +1 more source

High Levels of Receptor Tyrosine Kinases in CCM3-Deficient Cells Increase Their Susceptibility to Tyrosine Kinase Inhibition

Biomedicines, 2020
Cerebral cavernous malformations (CCMs) are vascular malformations that can be the result of the deficiency of one of the CCM genes. Their only present treatment is surgical removal, which is not always possible, and an alternative pharmacological ...
Miriam Sartages, Ebel Floridia, Mar García-Colomer, Cristina Iglesias, Manuel Macía, Patricia Peñas, Pierre-Olivier Couraud, Ignacio A. Romero, Babette Weksler, Celia M. Pombo, Juan Zalvide   +10 more
doaj   +1 more source

Spinal cord cavernoma — operative strategy and results in 30 patients

, 2012
Background Many case reports and small series addressing the surgical management of spinal cord cavernoma have been published. However, only few larger series that would allow identifying operative strategies exist.
Gilsbach, Joachim, Gilsbach, Joachim Michael, Rohde, Veit, Psychogios, Marios, Wachter, Dorothee   +4 more
core   +1 more source

KRIT1 heterozygous mutations are sufficient to induce a pathological phenotype in patient-derived iPSC models of cerebral cavernous malformation

Cell Reports
Summary: Cerebral cavernous malformation (CCM) is a neurovascular disease distinguished by clusters of leaky, mulberry-like blood vessels. KRIT1 bi-allelic loss-of-function mutations in endothelial cells are known to trigger brain cavernomas; however ...
Maximiliano Arce, Iza Erzar, Fan Yang, Neeharika Senthilkumar, Favour C. Onyeogaziri, Dario Ronchi, Frida C. Ahlstrand, Nora Noll, Roberta Lugano, Mark Richards, Elisa Scola, Monica Corada, Francesca Lazzaroni, Linda Meggiolaro, Jens Schuster, Niklas Dahl, Mika Niemelä, Behnam Rezai Jahromi, Anna Dimberg, Silvia Lanfraconi, Roberto Latini, Peetra U. Magnusson   +21 more
doaj   +1 more source

Routinely Performed Serial Follow-Up Imaging in Asymptomatic Patients With Multiple Cerebral Cavernous Malformations Has No Influence on Surgical Decision Making

Frontiers in Neurology, 2018
Background: The best strategy to perform follow-up of patients with multiple cerebral cavernous malformations (mCCM) is unclear due to the unpredictable clinical course. Still, serial radiological follow-up is often performed.
Julia Velz, Julia Velz, Martin Nikolaus Stienen, Martin Nikolaus Stienen, Marian Christoph Neidert, Marian Christoph Neidert, Yang Yang, Yang Yang, Luca Regli, Luca Regli, Oliver Bozinov, Oliver Bozinov   +11 more
doaj   +1 more source

Cavernoma en paciente con epilepsia

, 2009
Imagen de un cavernoma en un paciente con epilepsia.Picture of a cavernoma in a patient with ...
Iglesias Rozas, José Rafael, 1942-
core  

Cavernoma in a young adult: a case report

Egyptian Journal of Neurosurgery
Cavernomas or cavernous malformations of the central nervous system are acquired or hereditary vascular anomalies. Although they are present in 0.1–0.5% in the general population, they are usually asymptomatic and undetected until symptoms occur.
Hina Ali, Samar Zaki, Ehsan Bari, Sara Khowaja   +3 more
doaj   +1 more source