Results 51 to 60 of about 8,107 (190)
Epilepsy is a common neurological condition with varied etiological causes, with temporal lobe epilepsy being the most common. Among the varied etiologies of temporal lobe epilepsy, mesial temporal sclerosis is an important one and it presents as ...
Prashanth Raghu +4 more
doaj +1 more source
Radiation induced cavernomas among children with medulloblastoma are common following external beam radiation (XRT) treatment with either photon or proton beams.
S. Joy Trybula +7 more
doaj +1 more source
Peduncular hallucinosis associated with a pontine cavernoma [PDF]
Peduncluar hallucinosis is a rare neurological disorder characterized by visual hallucinations, often described to be vivid and dream-like. While the exact pathophysiology has yet to be elucidated, most cases to date have suggested an etiology stemming ...
Michael Couse +7 more
core +1 more source
ABSTRACT Background Classifying abnormal tongue movements is challenging due to their varied presentations and limited visibility compared to other body parts. Accurate identification of the phenomenology guides physical examination and can point to specific diagnoses.
Nathaniel Bendahan +4 more
wiley +1 more source
Cross-sectional CT image of portal vein thrombosis and cavernoma: A) partial PVT (black arrow) without cavernoma; B) partial PVT (black arrow) with cavernoma (white arrow); C) complete PVT (black arrow) without carvernoma and D) complete PVT (black arrow)
Jianjun Luo (160162) +5 more
core +1 more source
Portal Cavernoma Cholangiopathy [PDF]
Portal cavernoma cholangiopathy is a rare condition, a proper recognition of which is critical. Solid data on this condition are scarce. This review aims at updating current knowledge on its definition, manifestations, diagnosis, and management. A consensus has been reached to prefer the denomination portal cavernoma cholangiopathy for the bile duct ...
openaire +3 more sources
ABSTRACT Neuromyelitis optica spectrum disorder (NMOSD) is a rare autoimmune, demyelinating disorder of the central nervous system. Clinical manifestations include optic neuritis, longitudinally extensive transverse myelitis (LETM) involving three or more vertebral segments, and, in most cases, seropositivity for anti‐aquaporin‐4 antibodies (AQP4‐IgG).
Nikolina Pravdic +7 more
wiley +1 more source
The rare case of optic nerve cavernoma: A case report depicting the diagnostic challenge
The manuscript describes a case of Cavernous Malformation in the optic pathway which is extremely rare, accounting for less than 1% of central nervous system cavernomas.
Rushil Sharma, MD
doaj +1 more source
Surgical Treatment of Cavernous Sinus Cavernomas: Evidence from Vietnam
Cavernous sinus cavernomas, a rare vascular malformation, represents 3% of all benign cavernous sinus tumors. Both clinical and radiological signs are important for differentiating this condition from other cavernous sinus diseases. The best treatment is
Duc-Anh Nguyen +4 more
doaj +1 more source
Rupture of the recurrent thoracic intramedullary spinal cord cavernoma [PDF]
The intramedullary spinal cord cavernoma is a rare vascular disease that occur within spinal cord or intramedullary and account for about 5%-12% of all pathology in the spinal vascular disease. We report a clinical progression of disease and evolution of
Eko Agus Subagio, Eko +3 more
core +1 more source

