ILAE classification and definition of epilepsy syndromes with onset in neonates and infants: Position statement by the ILAE Task Force on Nosology and Definitions

SM Zuberi, E Wirrell, E Yozawitz, JM Wilmshurst… - …, 2022 - Wiley Online Library
Abstract The International League Against Epilepsy (ILAE) Task Force on Nosology and
Definitions proposes a classification and definition of epilepsy syndromes in the neonate …

Current concepts in the classification, diagnosis and treatment of hemangiomas and vascular malformations of the head and neck

JA Werner, AA Dünne, BJ Folz, R Rochels… - European archives of …, 2001 - Springer
There are many different classifications of vascular anomalies. As the correct classification of
the vascular lesion has a direct influence on therapy it is difficult to decide which treatment …

Ocular manifestations of Sturge–Weber syndrome

M Silverstein, J Salvin - Current Opinion in Ophthalmology, 2019 - journals.lww.com
Ocular manifestations of Sturge–Weber syndrome : Current Opinion in Ophthalmology Ocular
manifestations of Sturge–Weber syndrome : Current Opinion in Ophthalmology Log in or …

[图书][B] Textbook of clinical neuropsychiatry

D Moore - 2008 - books.google.com
Textbook of Clinical Neuropsychiatry provides a comprehensive, encyclopedic and up to
date coverage of the complete range of neuropsychiatric disorders. The text is clearly written …

[HTML][HTML] Clinical features of Sturge-Weber syndrome

FXP Neto, MAV Junior, LS Ximenes… - Intl Arch …, 2008 - arquivosdeorl.org.br
Introduction: The Syndrome of Sturge-Weber is a rare condition of congenital development,
and is characterized by a neurocutaneous disorder with angiomas wrapping the …

Encephalofacial angiomatosis sparing the occipital lobe and without facial nevus: on the spectrum of Sturge-Weber syndrome variants?

AM Comi, R Fischer, EH Kossoff - Journal of child neurology, 2003 - journals.sagepub.com
We report two cases of leptomeningeal angiomatosis in atypical frontoparietotemporal
locations without an associated facial port-wine stain. Evidence of a leptomeningeal …

Sturge-Weber syndrome: a case report and review of literatures

Z Jing, N Li, X Zhou, J Wang, R Zhang - Chinese Medical …, 2010 - journals.lww.com
Sturge-Weber syndrome (SWS), or encephalo-trigeminal angiomatosis, is a rare, congenital
neurocutaneous syndrome characterized by unilateral facial cutaneous vascular …

Clinical features of Sturge–Weber syndrome without facial nevus: Five novel cases

L Siri, L Giordano, P Accorsi, M Cossu, L Pinelli… - European Journal of …, 2013 - Elsevier
Classic Sturge–Weber syndrome (SWS) is characterized by presence of flammeus nevus
involving the first sensory branch of trigeminal nerve, ipsilateral leptomeningeal …

Sturge-Weber syndrome involved frontoparietal region without facial nevus

C Dilber, HA Tasdemir, A Dagdemir, L Incesu… - Pediatric neurology, 2002 - Elsevier
Classic Sturge-Weber syndrome is characterized by a facial nevus and hamartomatous
lesion in the brain. Hamartomatous lesions are usually located in the ipsilateral occipital …

Migraine-like attacks in child with Sturge-Weber syndrome without facial nevus

G Taddeucci, A Bonuccelli, P Polacco - Pediatric neurology, 2005 - Elsevier
The Sturge-Weber syndrome was recently subdivided into type I (facial and leptomeningeal
angioma, possible glaucoma), type II (facial angioma, without evident endocranial …