Results 91 to 100 of about 6,027 (196)

The Epidemiology and Clinical Presentation of the Acute Imbalance Syndrome (AIS)—A Systematic Review and Meta‐Analysis

European Journal of Neurology, Volume 33, Issue 6, June 2026.
ABSTRACT Objectives The acute imbalance syndrome (AIS) refers to acute‐onset and persistent vertigo, dizziness and/or imbalance without nystagmus, reflecting a subset of the acute vestibular syndrome (AVS) with or without nystagmus. While AVS with nystagmus is well characterized and the approach to these patients is validated, much less is known about ...
Konstantin Schmidt, Andreas Zwergal, Diego Kaski, Alexander Andrea Tarnutzer   +3 more
wiley   +1 more source

Risk of Clinical Events in Presymptomatic Familial Cerebral Cavernous Malformations

European Journal of Neurology, Volume 33, Issue 6, June 2026.
ABSTRACT Background and Purpose Familial cerebral cavernous malformations (fCCM) may cause focal neurological deficits (FND) due to hemorrhagic or non‐hemorrhagic events and epileptic seizures (ES). With the widespread use of magnetic resonance imaging (MRI) and genetic testing, diagnosis is now frequently established at a presymptomatic stage, before ...
Constantina Rodica Popa, Dominique Hervé, Nassira Alili, Estelle Dubus, Abbas Taleb, Fanny Fernandes, Florence Riant, Elisabeth Tournier Lasserve, Louis Lambert, Hugues Chabriat, Stéphanie Guey   +10 more
wiley   +1 more source

Familial cerebral cavernous malformation syndrome in Serbian family

, 2018
Cavernomas are benign vascular malformations, and about 50% of all cases are multiple. The hereditary form of brain cavernomas is uncommon, and it is certainly under diagnosed. Another entity is familial cerebral cavernous malformation syndrome.
Vuk, Aleksić, Miroljub, Jovančević, Vladimir, Miladinović, Marko, Samardžić, Marko, Rapaić, Igor, Popović, Aleksandar, Mandarić, Milenko, Stanić, Miljan, Mihajlović, Milan, Spaić, Nemanja, Aleksić   +10 more
core   +1 more source

Krit1 Missense Mutations Lead to Splicing Errors in Cerebral Cavernous Malformation

, 2002
At least 40% of families affected with cerebral cavernous malformation have a mutation in Krit1. We previously identified two point mutations in Krit1 leading to changes in amino acids (D137G and Q210E) in two different families.
Siegel, Adrian M., Verlaan, Dominique J., Rouleau, Guy A.   +2 more
core   +1 more source

Predicting Epileptogenic Tubers in Patients With Tuberous Sclerosis Complex Using a Fusion Model Integrating Lesion Network Mapping and Machine Learning

Annals of Clinical and Translational Neurology, Volume 13, Issue 5, Page 972-983, May 2026.
ABSTRACT Objective Accurate localization of epileptogenic tubers (ETs) in patients with tuberous sclerosis complex (TSC) is essential but challenging, as these tubers lack distinct pathological or genetic markers to differentiate them from other cortical tubers.
Tinghong Liu, Qi Wang, Suhui Kuang, Dezhi Cao, Ping Ding, Shaohui Zhang, Haihua Wei, Zhirong Wei, Jinshan Xu, Xinyu Huang, Bing Liu, Shuli Liang   +11 more
wiley   +1 more source

Nature, frequency and natural history of intracranial cavernous malformations in adults [PDF]

, 2014
Scottish Intracranial Vascular Malformation Study was the first prospective, population-based study of the major types of intracranial vascular malformations; arteriovenous, cavernous and venous malformations including dural fistulae and carotid ...
Hall, Julie Maria
core  

Cerebral cavernous malformation: new molecular and clinical insights.

, 2006
Cerebral cavernous malformation (CCM) is a vascular malformation causing neurological problems, such as headaches, seizures, focal neurological deficits, and cerebral haemorrhages.
Revencu, Nicole, Vikkula, Miikka
core   +1 more source

Structural Basis for the Unique Heterodimeric Assembly between Cerebral Cavernous Malformation 3 and Germinal Center Kinase III

, 2013
SummaryDefects in cerebral cavernous malformation protein CCM3 result in cerebral cavernous malformation (CCM), a common vascular lesion of the human CNS. CCM3 functions as an adaptor protein that interacts with various signal proteins.
Wang, Da-Cheng, Ding, Jingjin, Zhang, Ying, Xu, Xueyong, Wang, Xiaoyan   +4 more
core   +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