Results 41 to 50 of about 5,302 (181)

The epileptologist's perspective of focal cortical dysplasia type 3: From concept to management

Epilepsia, EarlyView.
Abstract The recent International League Against Epilepsy (ILAE) official and updated classification of focal cortical dysplasia (FCD) includes a third type—FCD type 3—characterized by architectural abnormalities (cortical dyslamination) associated with another “principal” lesion: hippocampal sclerosis (HS), developmental tumors, vascular malformations,
André Palmini, Francine Oliveira, Eliseu Paglioli, Harvey Sarnat, Ricardo Paganin, Ricardo Soder, William Martins, Rafael Paglioli, Thomas Frigeri, Fernanda Schuh, Vicenzo Zarpellon   +10 more
wiley   +1 more source

Case Report of Rasmussen's Encephalitis With a Decade of Refractory Epilepsy and Hemispheric Atrophy

Clinical Case Reports, Volume 14, Issue 2, February 2026.
ABSTRACT Rasmussen's encephalitis (RE) is a rare, chronic inflammatory neurological disorder affecting one cerebral hemisphere and presenting with drug‐resistant epilepsy, progressive hemiparesis, and cognitive decline. This case report describes the clinical course and management of a 21‐year‐old patient with refractory epilepsy and progressive ...
Sajjad Al‐Badri, Aditya Duhan, Rania H. Al‐Taie, Abbas Hamza Abbas, Ayah Abdulgadir, Ibrahim Khalil, Zaryab Bacha, Noran Al‐Gizey   +7 more
wiley   +1 more source

Intelligent Supportive System for People with Profound Intellectual and Multiple Disabilities

Advanced Intelligent Systems, Volume 8, Issue 1, January 2026.
A holistic INSENSION system is developed—a novel intelligent decision support system leveraging state‐of‐the‐art noninvasive audio‐visual sensor technologies together with machine learning algorithms and expert knowledge, to detect and interpret behaviors and communications (nonverbal signals—NVSs) of people with PIMD in challenging real‐world ...
Gašper Slapničar, Michał Kosiedowski, Arkadiusz Radziuk, Erik Dovgan, Torsten Hammann, Meike Engelhardt, Christin Kupitz, Carmen Campomanes‐Alvarez, Dorota Janczewska, Peter Zentel, Mitja Luštrek   +10 more
wiley   +1 more source

Beyond Treatment: The Strategy of Nonintervention in Choroidal Hemangioma

Clinical Case Reports, Volume 14, Issue 1, January 2026.
ABSTRACT The circumscribed choroidal hemangioma (CCH) is a benign congenital eye tumor whose etiology is not clear. A 41‐year‐old female patient came with a 2‐year history of slowly progressive deteriorating vision in her right eye. In the left eye, the best‐corrected visual acuity (BCVA) was 6/6, and counting fingers at 1 m in the right eye.
Humdan Khan, Muhammad Shaheer Bin Faheem, Hurmat Fatima, Asfandyar Asghar, Ahmed Ali Khan, Muhammad Rehan Zahid, Syed Tawassul Hassan, Izzah Shakkel, Muhammad Idrees Khan   +8 more
wiley   +1 more source

Intracerebral hemorrhage in Sturge Weber Syndrome: A case report [PDF]

Romanian Journal of Neurology
Background. Encephalotrigeminal angiomatosis also called Sturge Weber Syndrome (SWS) is neurocutaneous abnormality with angioma affecting the leptomeninges and the face skin, commonly in the eyes and maxillary distribution of trigeminal nerve.
Rizaldy Taslim Pinzon, I Gusti Agung Oka Pratama   +1 more
doaj   +1 more source

Surgical treatment of glaucoma with filtration bleb activation of a patient with Sturge — Weber syndrome: a clinical case

Российский офтальмологический журнал, 2022
Purpose: to describe surgical treatment of glaucoma of a patient with Sturge — Weber — Krabbe syndrome. We present a clinical case of a patient with Sturge — Weber — Krabbe syndrome who sought assistance with us due to secondary stage III glaucoma with ...
T. N. Savranova, V. U. Rozukulov, A. F. Yusupov, D. A. Asadov, S. S. Saidzhonov   +4 more
doaj   +1 more source

Impact of Anesthesia With Propofol on Epileptic Discharges Recorded by Stereo‐Electroencephalography in Pediatric Epilepsy Surgery

CNS Neuroscience &Therapeutics, Volume 32, Issue 1, January 2026.
The number of spikes decreased under anesthesia, particularly within the SOZ, while HFOs increased under anesthesia. However, the extent of the increase did not differ between the SOZ and NSOZ. The number of HFOs appeared to be a more reliable interictal biomarker in ioEEG, particularly in the frontal cortex and cingulate cortex, and was not influenced
Chang Liu, Ping Ding, Tong Zhao, Tinghong Liu, Shijie Wu, Yuxiang Yan, Liu Yuan, Liwei Zhang, Shuli Liang   +8 more
wiley   +1 more source

Secondary Glaucoma in Sturge–Weber Syndrome

Okulistyka
Sturge–Weber syndrome is a congenital neurocutaneous disorder involving abnormalities of blood vessels (hemangiomas) in the brain, face, and eyes. It is not hereditary or genetic, but it is present from birth.
Bożena Romanowska-Dixon, Joanna Kobylarz, Magdalena Dębicka-Kumela, Joanna Kowal, Agnieszka Nowak, Natalia Mackiewicz, Izabella Karska-Basta   +6 more
doaj   +1 more source

Triple pathology in a patient with uncontrolled epilepsy: a case report

Journal of Medical Case Reports
Background Sturge–Weber syndrome is an uncommon neurocutaneous disorder with characteristic vascular lesions, leptomeningeal angiomas, and facial nevi. Seizureis the most prevalent neurological sign of Sturge–Weber syndrome and complications related to ...
Sara Ranji, Behnam Akbari, Melika Javani, Aidin Taghilou, Abbas Tafakhori, Saeideh Salehizadeh, Hoda Naghshineh   +6 more
doaj   +1 more source

Análisis del síndrome de Sturge-Weber: estudio retrospectivo de múltiples variables asociadas

Neurología, 2017
Resumen: Introducción: El síndrome de Sturge-Weber es un trastorno vascular congénito caracterizado por una malformación facial capilar (mancha en vino de Oporto) asociada a malformaciones venosas y capilares en el cerebro y en el ojo.
A.I. Maraña Pérez, M.L. Ruiz-Falcó Rojas, V. Puertas Martín, J. Domínguez Carral, I. Carreras Sáez, A. Duat Rodríguez, V. Sánchez González   +6 more
doaj   +1 more source