Zobrazeno 1 - 10
of 296
pro vyhledávání: '"Gerald A, Campbell"'
Autor:
Samantha Stubbs, BS, Haris Vakil, BS, Gary D. Lewis, MD, Sarah A. Westergaard, MD, Gerald A. Campbell, MD, PhD, Todd A. Swanson, MD, PhD
Publikováno v:
Interdisciplinary Neurosurgery, Vol 14, Iss , Pp 139-141 (2018)
Only 1% of melanomas present with isolated involvement of the central nervous system. Primary melanoma of the spinal cord is especially rare. There are only a handful of cases reported and only one reported during pregnancy. The patient was a 27-year
Externí odkaz:
https://doaj.org/article/873b0c9422e24d36b4837f559172b192
Publikováno v:
Case Reports in Pathology, Vol 2018 (2018)
Introduction. Plexiform schwannoma is a rare variant of schwannoma that accounts for only 5% of all schwannomas. Herein, we present a rare case of plexiform schwannoma of the tongue in a pediatric patient with neurofibromatosis type 2 (NF2). Case Pre
Externí odkaz:
https://doaj.org/article/9215f8e8ccc140c4904ec74cde0a88ee
Autor:
Gregg N Milligan, Vanessa V Sarathy, Ernesto Infante, Li Li, Gerald A Campbell, P Robert Beatty, Eva Harris, Alan D T Barrett, Nigel Bourne
Publikováno v:
PLoS ONE, Vol 10, Iss 5, p e0125476 (2015)
Dengue is a mosquito-borne disease of global public health significance that is caused by four serologically and genetically related viruses (DENV-1 to DENV-4). Most human DENV infections are asymptomatic, but clinical cases can range in severity fro
Externí odkaz:
https://doaj.org/article/ecbc5b4f2c6b4fecbcf52264b3055192
Publikováno v:
Neurobiology of Disease, Vol 18, Iss 2, Pp 385-389 (2005)
Canavan disease (CD) is a neurodegenerative disorder characterized by the spongy degeneration of the white matter of the brain. Aspartoacylase (ASPA) gene mutation resulting enzyme deficiency is the basic cause of CD. Whether the ASPA defect in CD af
Externí odkaz:
https://doaj.org/article/f66377650f354bff9fa79f4478ffced7
Publikováno v:
Acad Forensic Pathol
Sarcoidosis is a noncaseating granulomatous disease of unknown etiology. The incidence is 11 per 100 000 white individuals and 34 per 100 000 black individuals. Cardiac involvement is seen in 2% to 5% of patients with systemic sarcoidosis and is ofte
Autor:
Diep Tran, Suzanne Zein-Eldin Powell, Rajyalakshmi Luthra, Adriana Olar, Maria N. Garnovskaya, Gregory N. Fuller, Adekunle M. Adesina, Jawad Manekia, Vidya Mehta, Kenneth D. Aldape, Benjamin Ellezam, Erik P. Sulman, Carrie A. Mohila, Annekathrin Reinhardt, Gerald A. Campbell
Publikováno v:
Clinical Neuropathology. 38:59-73
Introduction Pilocytic astrocytoma (PA) with anaplastic features (PAAF) is a rare entity associated with decreased survival. It is characterized by hypercellularity, atypia, brisk mitotic activity, variable necrosis, and association with a classic PA
Publikováno v:
Cureus
Metastatic lesions to the choroid plexus, although far less common than colloid cysts, can present very similarly both symptomatically and radiographically. Choroid plexus metastases are most common in the lateral ventricles, however, when they occur
Publikováno v:
Cureus
We report a rare case of ecchordosis physaliphora presenting with headache, nausea, and diplopia. On neurological examination, the patient was found to have left abducens nerve palsy. CT of the head without contrast was unremarkable. Brain MRI demons
Publikováno v:
Cureus
Infections of the lumbar spine can have serious sequelae, including neurological deficits, paralysis, and death. Prolonged infection can result in fracture of the vertebrae, local abscesses, and infiltration and compression of local vascular structur