Results 31 to 40 of about 97,266 (336)

Neurofibromatosis 2

open access: yesMedical Journal of Dr. D.Y. Patil University, 2015
Neurofibromatosis 2 is a rare autosomal dominant neurocutaneous disorder classically characterized by bilateral acoustic schwannomas. Multiple other central, as well as peripheral central nervous system neoplasms as meningiomas and ependymomas, are also ...
Abhijit M Patil   +3 more
doaj   +1 more source

Tumors in von Hippel–Lindau Syndrome: From Head to Toe—Comprehensive State-of-the-Art Review [PDF]

open access: yes, 2018
Von Hippel–Lindau syndrome (VHL) is an autosomal-dominant hereditary tumor disease that arises owing to germline mutations in the VHL gene, located on the short arm of chromosome 3.
Bhalla, Sanjeev   +6 more
core   +1 more source

Surgical treatment of lumbar extradural chondroma in a dog - case report
Tratamento cirúrgico de condroma extradural lombar em cão - relato de caso

open access: yesSemina: Ciências Agrárias, 2013
Neoplasms originating in the spinal canal are uncommon in small animal veterinary clinic, but when present can cause significant neurological signs. Anatomically, these neoplasms can be classified as extradural, intradural-extramedullary and medullary ...
Paulo Vinícius Tertuliano Marinho   +5 more
doaj   +1 more source

Effect of screening abdominal ultrasound examination on the decision to pursue advanced diagnostic tests and treatment in dogs with neurologic disease. [PDF]

open access: yes, 2015
BackgroundAbdominal ultrasound examinations (AUS) are commonly performed before advanced neurodiagnostics to screen for diseases that might affect diagnostic plans and prognosis.ObjectivesDescribe the type and frequency of abnormalities found by AUS in ...
Blair, WH   +5 more
core   +1 more source

Management of primary spinal chondrosarcoma: report of two cases causing cord compression Manejo dos condrosarcomas espinhais primários: relato de dois casos causando compressão medular

open access: yesArquivos de Neuro-Psiquiatria, 2004
Chondrosarcomas are malignant tumors that rarely grow inside the spinal canal. Prognosis depends on histological features, patient's age and surgical margins free from tumor. Response to radio and chemotherapy is poor. Ideal treatment consists of total "
Daniel Monte-Serrat Prevedello   +4 more
doaj   +1 more source

Near-miss Thoracic Spine Solitary Plasmacytoma with Neurological Deficit during Pregnancy: A Case Report [PDF]

open access: yesMalaysian Orthopaedic Journal, 2022
Solitary plasmacytoma (SPC) account for only 5% of plasma cell neoplasms, and the literature hardly reports spinal SPC with a neurological deficit.
Teh KH   +4 more
doaj   +1 more source

Primary cerebellopontine angle melanocytoma: review. [PDF]

open access: yes, 2012
Introduction Primary cerebellopontine angle melanocytomas (PCPAMs) are very rare. Their natural history and prognosis are not fully understood. We reviewed the literature and add a new case to analyze PCPAM's presentation, radiological features, and ...
Elashaal, R   +3 more
core   +1 more source

Spinal Cord Ependymomas [PDF]

open access: yes, 2009
Intradural or primary spinal cord tumors (SCT) are rare. However, when these lesions grow, compression of the spinal cord can lead to limb dysfunction, motor or sensory loss, and possibly death.
Blyzniuk, Carol, BSN, RN   +1 more
core   +2 more sources

Comparison of Single or Double Titanium Mesh Cage for Anterior Reconstruction After Total En Bloc Spondylectomy for Thoracic and Lumbar Spinal Tumors [PDF]

open access: yesNeurospine
Objective To compare the clinical efficacy of anterior column reconstruction using single or double titanium mesh cage (TMC) after total en bloc spondylectomy (TES) of thoracic and lumbar spinal tumors.
Ao Leng   +8 more
doaj   +1 more source

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