Results 61 to 70 of about 21,956 (166)
Pituitary Adenoma Presenting as Cranial Nerve III Palsy and Hemifacial Pain [PDF]
Pituitary adenomas are common neoplasms arising from the pituitary adenohypophyseal cell. They can be classified by cell type, size and as nonfunctioning or functioning based on the secretion of pituitary hormones.
Maduka, Peter +3 more
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Ocular manifestations in Gorlin-Goltz syndrome
Background Gorlin-Goltz syndrome, also known as nevoid basal cell carcinoma syndrome, is a rare genetic disorder that is transmitted in an autosomal dominant manner with complete penetrance and variable expressivity. It is caused in 85% of the cases with
Antonietta Moramarco +8 more
doaj +1 more source
Evaluating optic system compression in sellar tumors: A novel application of quantitative pupillometry [PDF]
<jats:title>Abstract</jats:title> <jats:sec> <jats:title>Introduction</jats:title> <jats:p>Tumorous growths in the sellar region pose significant clinical challenges due to their ...
Walter, Johannes +5 more
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Neurofibromatosis type 1 (NF1) is a complex neurocutaneous disorder with an increased susceptibility to develop both benign and malignant tumors but with a wide spectrum of inter and intrafamilial clinical variability.
Alkindy Adila +4 more
doaj +1 more source
We hereby report the case of a patient with optic nerve sheath meningioma (ONSM), whose diagnosis and multidisciplinary management was guided by the use of Gallium-68 (68Ga)-labeled dodecanetetraacetic acid-tyrosine-3-octreotate (DOTATATE) positron ...
Karine A. Al Feghali +5 more
doaj +1 more source
Advances in the Management of Skull Base Meningioma [PDF]
Meningioma is among the most common intracranial neoplasms of adulthood and may be the most common primary intracranial tumor. While many tumors are asymptomatic and remain so throughout life, meningiomas of the skull base will frequently cause visual or
Prem S. Subramanian
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Neurosurgical implications of neurofibromatosis Type I in children [PDF]
Neurofibromatosis Type 1 (NF1) is one of the most common inherited diseases in humans. It is caused by a mutation in the NF1 gene on chromosome 17, and is associated with numerous central and peripheral nervous system manifestations.
Komotar, Ricardo +2 more
core +1 more source
Pediatric extranasal, EBV-negative, extranodal natural killer/T-cell lymphoma; case report
Extranodal natural killer/T-cell lymphomas (ENKTCL) are rare, aggressive neoplasms primarily occurring in adults of Asian or Native American descent. Most are associated with Epstein-Barr virus (EBV) and originate in the nasopharyngeal region. We present
Rachel Gallant, Osman Khan
doaj +1 more source
Treatment of refractory pituitary neoplasms with temozolomide in three patients [PDF]
BACKGROUND: There is relatively little information regarding the efficacy of temozolomide (TMZ) for pituitary adenomas; less than 100 cases treated with TMZ are reported, with a variable response rate of 50-75%, depending on response criteria.
Rogers, Lisa +2 more
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A screen for genes regulating neuroblast activity in Drosophila. [PDF]
Following embryogenesis, the morphology of the CNS becomes dramatically remodelled to reflect the different locomotive and sensory requirements of the adult relative to the larva. This is largely achieved through the varying spatio-temporal proliferation
Pendred, J.
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