Results 171 to 180 of about 7,157 (217)
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Familial cerebral cavernous angiomas

Neurological Research, 1990
Three families with two or more members affected by cavernous angiomas of the brain are described and the other 17 reported in the literature are reviewed. The familial occurrence of cerebral cavernous angiomas has been considered a rare event; nevertheless, the experience of the authors (positive familiarity in three patients where two or more ...
GANGEMI, MICHELANGELO   +5 more
openaire   +3 more sources

Genetics of cavernous angiomas

The Lancet Neurology, 2007
Cerebral cavernous malformations (CCM) are vascular malformations that can occur as a sporadic or a familial autosomal dominant disorder. Clinical and cerebral MRI data on large series of patients with a genetic form of the disease are now available. In addition, three CCM genes have been identified: CCM1/KRIT1, CCM2/MGC4607, and CCM3/PDCD10.
Pierre, Labauge   +3 more
openaire   +2 more sources

Cavernous Angioma of the Cavernous Sinus: Case Report

Neurosurgery, 1990
Abstract An unusual case of cavernous angioma in the cavernous sinus (“cavernous cavernoma”) is presented. The acute onset of symptoms simulated Tolosa-Hunt syndrome, and after neuroradiological investigations, the suspected diagnosis was an intracavernous meningioma.
A, Sepehrnia   +4 more
openaire   +2 more sources

Multiple Intracranial Cavernous Angiomas With a Trigonal Cavernous Angioma Mimicking Glioma

Journal of Craniofacial Surgery, 2018
Abstract Intracranial cavernous angiomas (CAs) are hamartomatous vascular malformations consisting of thin-walled vascular channels located within the brain, but typically lacking intervening neural parenchyma, large feeding arteries, or draining veins.
Jie, Wu   +3 more
openaire   +2 more sources

Cavernous Angiomas, Cavernous Malformations

2017
Cavernous angiomas, cavernous malformations, were allocated into the group of true malformations in the international histological classification of tumors of the central nervous system only in 1979. Before this, cavernous angiomas (CAs) were regarded as tumors. CAs represent the system of communicating vascular cavities with various sizes and sinusoid
Mikhail Dolgushin   +2 more
openaire   +1 more source

Intradural extramedullary cavernous angioma

Neurosurgery, 1991
Abstract Cavernous angiomas represent 5 to 12% of spinal vascular malformations and usually are located at the vertebral body level with possible extension into the extradural space. The intradural intramedullary cavernoma occurs in about 3% of cases, whereas extramedullary localization is extremely rare.
L, Mastronardi   +5 more
openaire   +2 more sources

CAVERNOUS ANGIOMAS

Neurosurgery, 1987
J, Vaquero, J, Salazar, R, Martínez
  +5 more sources

INCIDENTAL CAVERNOUS ANGİOMA

2020
Introduction: Besides developmental venous anomaly (DVA), arteriovenous malformation (AVM) and capillary telangiectasia, cavernomas are one of the vascular malformations of the central nervous system. In this case report, we present a case diagnosed with cavernous angioma in the left posterior frontal region, who presented to our emergency department ...
EKMEKYAPAR, Tuba   +3 more
openaire   +1 more source

Brainstem Cavernous Angioma

Otology & Neurotology, 2003
Elizabeth H, Toh   +2 more
openaire   +2 more sources

Giant Cavernous Angioma

Pediatric Neurosurgery, 2001
H G, Brumblay   +3 more
openaire   +2 more sources

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