Results 31 to 40 of about 9,788 (221)
Genetically diagnosed Birt-Hogg-Dubé syndrome and familial cerebral cavernous malformations in the same individual: a case report. [PDF]
, 2016 When faced with an unusual clinical feature in a patient with a Mendelian disorder, the clinician may entertain the possibilities of either the feature representing a novel manifestation of that disorder or the co-existence of a different inherited ...
Skytte, Anne-Bine +2 more
core +2 more sources
Dural Arteriovenous Malformations: A Review of the Literature and a Presentation of the JHN Series [PDF]
, 2010 Dural arteriovenous malformations (DAVMs), also known as dural arteriovenous fistulas, are arteriovenous shunts from a dural arterial supply to a dural venous channel, typically supplied by pachymeningeal arteries and located near a major venous sinus.1 ...
Gonzalez, L. Fernando +5 more
core +2 more sources
Clinical Reasoning: Cerebral cavernous malformations [PDF]
Neurology, 2009 A 40-year-old man presented for management of seizures. His first seizure was 5 years earlier. Evaluation at that time revealed a hemorrhagic lesion near the occipital horn of the left lateral ventricle. Incomplete surgical excision was performed with indeterminate pathology suggestive of an astrocytoma.
Lama M, Chahine, Michel J, Berg
openaire +2 more sources
High-Flow Vascular Malformations in Children. [PDF]
, 2020 Children can have a variety of intracranial vascular anomalies ranging from small and incidental with no clinical consequences to complex lesions that can cause substantial neurologic deficits, heart failure, or profoundly affect development. In contrast
Abla, Adib A +8 more
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Heart of glass anchors Rasip1 at endothelial cell-cell junctions to support vascular integrity. [PDF]
, 2016 Heart of Glass (HEG1), a transmembrane receptor, and Rasip1, an endothelial-specific Rap1-binding protein, are both essential for cardiovascular development.
de Kreuk, Bart-Jan +5 more
core +2 more sources
Indian Journal of Neurosurgery, 2013 Giant cerebral cavernous malformations (GCCMs) are very rare malformations in adults, and they rarely present with raised intracranial pressure due to obstructive hydrocephalus. Around 20 cases of GCCMs have been reported in available literature.
Rajeev Sharma +2 more
doaj +1 more source
Análise da melhor alternativa terapêutica para malformações arteriovenosas durais intracranianas [PDF]
, 2005 The material for this research consisted of 93 patients with dural arteriovenous malformations (DAVMs) who were studied retrospectively with regards to therapeutic success and failure, who had undergone either neurosurgery, or embolization or a ...
Caldas, José Guilherme Mendes Pereira +2 more
core +4 more sources
Cerebral cavernous malformations and epilepsy [PDF]
Neurosurgical Focus, 2006 ✓Seizures and epilepsy are frequent clinical manifestations of cerebral cavernous malformations (CCMs) and represent the most common symptomatic presentation of supratentorial lesions. Clinicians often diagnose CCMs in patients after a first seizure, or in some cases after obtaining neuroimaging studies in patients suffering from chronic epilepsy ...
Issam, Awad, Pascal, Jabbour
openaire +2 more sources
Mosaic RAS/MAPK variants cause sporadic vascular malformations which respond to targeted therapy. [PDF]
, 2018 BACKGROUND: Sporadic vascular malformations (VMs) are complex congenital anomalies of blood vessels that lead to stroke, life-threatening bleeds, disfigurement, overgrowth, and/or pain.
Al-Olabi, L +45 more
core +4 more sources
Multiple cerebral cavernous malformations - a case report [PDF]
Romanian Journal of Neurology, 2013 Cavernomas are frequent low-flow vascular malformations with a characteristic MRI aspect due to their specific morphology. We present the case of a 64-year old male diagnosed in 2008 with multiple cerebral cavernomas and symptomatic epilepsy, who ...
Ana-Maria Vladila +6 more
doaj +1 more source