Results 101 to 110 of about 8,444 (208)

Late‐onset epilepsy of unknown etiology is more treatment‐responsive than acquired lesional late‐onset epilepsy

Epilepsia Open, Volume 10, Issue 6, Page 1847-1859, December 2025.
Abstract Objective Late‐onset epilepsy of unknown etiology (LOEU) carries an elevated risk of dementia, suggesting that it may represent an early manifestation of neurodegenerative or cerebrovascular disease. Direct comparisons between LOEU and acquired lesional late‐onset epilepsy (LOE) may elucidate clinical features specific to LOEU.
L. Brian Hickman, Bhavya Pandey, Alexander Fish, Mohit Bandla, Adnan Husein, Corinne Allas, Harika Kottakota, Lauren Herzog, Keith Vossel, John M. Stern   +9 more
wiley   +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

Cerebral Cavernous Malformations [PDF]

Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques, 2000
I, Fleetwood, W, Hu, M, Hudon
openaire   +2 more sources

Upregulation of transmembrane endothelial junction proteins in human cerebral cavernous malformations [PDF]

, 2010
OBJECT: Cerebral cavernous malformations (CCMs) are among the most prevalent cerebrovascular malformations, and endothelial cells seem to play a major role in the disease.
Chappell PM, Felbor U, Hilder TL, Revencu N, Robinson JR, Stahl S, Tsukita S, Vestweber D, Zhu Y   +8 more
core   +1 more source

Pediatric intracranial dural arteriovenous fistulas: age-related differences in clinical features, angioarchitecture, and treatment outcomes. [PDF]

, 2016
OBJECTIVE Intracranial dural arteriovenous fistulas (DAVFs) are rare in children. This study sought to better characterize DAVF presentation, angioarchitecture, and treatment outcomes.
Amans, Matthew R, Cooke, Daniel L, Dowd, Christopher F, Fullerton, Heather J, Halbach, Van V, Hetts, Steven W, Higashida, Randall T, Maluste, Neil, Moftakhar, Parham   +8 more
core   +1 more source

Intraoperative Neurophysiological Monitoring for Endoscopic Endonasal Approaches to the Skull Base: A Technical Guide. [PDF]

, 2016
Intraoperative neurophysiological monitoring during endoscopic, endonasal approaches to the skull base is both feasible and safe. Numerous reports have recently emerged from the literature evaluating the efficacy of different neuromonitoring tests during
Doan, Adam T., Evans, James J., Kenning, Tyler J., Lober, Robert M., Matsumoto, Craig I., Singh, Harminder, Vogel, Richard W.   +6 more
core   +3 more sources

Cerebral cavernous malformations associated to meningioma: High penetrance in a novel family mutated in the PDCD10 gene [PDF]

, 2015
Multiple familial meningiomas occur in rare genetic syndromes, particularly neurofibromatosis type 2. The association of meningiomas and cerebral cavernous malformations (CCMs) has been reported in few patients in the medical literature.
Al-Shahi Salman R, Batra S, de Champfleur NM, DeAngelis LM, Haasdijk RA, Labauge P, Lehnhardt FG, Marosi C, Riant F, Riemenschneider MJ, Schröder W, Shen Y, Spiegler S, Whittle IR, Zabramski JM   +14 more
core   +1 more source

Familial Cerebral Cavernous Malformations [PDF]

Stroke, 2019
Atif, Zafar, Syed A, Quadri, Mudassir, Farooqui, Asad, Ikram, Myranda, Robinson, Blaine L, Hart, Marc C, Mabray, Catherine, Vigil, Alan T, Tang, Mark L, Kahn, Howard, Yonas, Michael T, Lawton, Helen, Kim, Leslie, Morrison   +13 more
openaire   +2 more sources

Complications of Decompressive Craniectomy [PDF]

, 2012
Introduction: Persistent elevation of intracranial pressure (ICP), if untreated, may lead to brain ischemia or lack of brain oxygen and even brain death.1-6,10 When standard treatments for elevated ICP are exhausted without any signs of improvement ...
Ho, BS, Sandra, Jallo, MD, PhD, Jack, Maltenfort, PhD, Mitchell, Ooi, MD, Yinn C., Sheikh, MBBS, Muhamad A.   +4 more
core   +2 more sources

Natural history of familial cerebral cavernous malformations: the CCM_Italia cohort study

Frontiers in Neurology
BackgroundFamilial cerebral cavernous malformations (fCCMs) are a rare genetic autosomal dominant cerebrovascular disease characterized by multiple cerebral and spinal angiomas. The condition is caused by mutations in KRIT1 (CCM1), CCM2 (malcavernin), or
Silvia Lanfranconi, Elisa Scola, Deborah Novelli, Anna Poggesi, Anna Poggesi, Francesca Pescini, Marco Pavanello, Ferruccio Romano, Quintino Giorgio D’Alessandris, Walter Marani, Francesco Signorelli, Giorgio Iaconetta, Giovanni Torelli, Enrico Fainardi, Mariasavina Severino, Luigi Gianmaria Remore, Luigi Gianmaria Remore, Giulio Andrea Bertani, Giorgio Conte, Valeria Capra, Antonella Vasamì, Enrico Nicolis, Giorgia Contino, Dario Ronchi, Dario Ronchi, Maria Chiara Palmieri, Alessandra Previtali, Pier Paolo Mattogno, Carmelo Lucio Sturiale, Maria Elena Solarino, Rita Caliulo, Maria Teresa Bozzi, Filippo Fratini, Filippo Fratini, Elisa R. Zanier, Roberto Latini, Jennifer Marie Theresia Anna Meessen, Marco Locatelli, Marco Locatelli, and the CCM_Italia investigators   +39 more
doaj   +1 more source