Results 201 to 210 of about 25,453,690 (257)

Pseudopapilledema in neurofibromatosis type 2

American Journal of Ophthalmology, 2000
To report a case of neurofibromatosis type 2 with pseudopapilledema secondary to a prepapillary gliotic membrane.Case report. Results of an ocular examination and fluorescein angiography of a patient are described.Fundus examination of a 14-year-old male with neurofibromatosis type 2 revealed an irregular elevation of the optic nerve and a perifoveal ...
G T, Lueder, J T, Doll
openaire   +2 more sources

Neurofibromatosis 2 in the Pediatric Population

Journal of Child Neurology, 2003
Neurofibromatosis 2 is a severe autosomal dominant disorder characterized by the occurrence of bilateral vestibular schwannomas and other benign tumors of the nervous system. Excellent natural history studies exist for adults with neurofibromatosis 2, but limited outcome data are available for children with neurofibromatosis 2.
Fabio, Nunes, Mia, MacCollin
openaire   +2 more sources

Ocular Abnormalities in Neurofibromatosis 2

Journal of Neuro-Ophthalmology, 1995
To evaluate the ocular abnormalities in patients with clinically diagnosed neurofibromatosis 2 and asymptomatic gene carriers.Probands were ascertained through a surgical otolaryngology practice. In a cross-sectional study, we examined 49 patients with neurofibromatosis 2, 30 offspring of patients, and, as a comparison group, 18 parents and siblings of
N K, Ragge, M E, Baser, J, Klein, A, Nechiporuk, J, Sainz, S M, Pulst, V M, Riccardi   +6 more
openaire   +2 more sources

Neurofibromatosis 2 and malignant mesothelioma

Neurology, 2002
Mutations of the neurofibromatosis 2 (NF2) tumor suppressor gene cause the inherited disorder NF2 and are also common in malignant mesothelioma, which is not a characteristic feature of NF2. The authors report an asbestos-exposed person with NF2 and malignant mesothelioma. Immunohistochemical analysis of the mesothelioma confirmed loss of expression of
M E, Baser, A, De Rienzo, D, Altomare, B R, Balsara, N M, Hedrick, D H, Gutmann, L H, Pitts, R K, Jackler, J R, Testa   +8 more
openaire   +2 more sources

Neurofibromatosis Types 1 and 2

The Neurologist, 2006
Neurofibromatosis types 1 and 2 (NF1 and NF2) are autosomal dominant neurocutaneous disorders with some similarities and many differences. They are frequently discussed together and often confused for one another by clinicians. Both disorders have widely variable presentations and degrees of severity. A thorough understanding of these complex disorders
openaire   +2 more sources

Dorsal root ganglia volume differentiates schwannomatosis and neurofibromatosis 2

Annals of Neurology, 2018
T. Godel, V. Mautner, S. Farschtschi, M. Pham, D. Schwarz, M. Kronlage, Isabel Gugel, S. Heiland, M. Bendszus, P. Bäumer   +9 more
semanticscholar   +1 more source

Neurofibromatosis 2

1995
7th ...
ZOGHBI H. Y., BALLABIO, ANDREA
openaire   +1 more source

Neurofibromatosis 2 (NF2) controls the invasiveness of glioblastoma through YAP-dependent expression of CYR61/CCN1 and miR-296-3p.

Biochimica et Biophysica Acta, 2016
Hong Lee, S. Hwang, Hye Ree Kim, Chang Hoon Shin, K. H. Choi, Je-Gun Joung, Hyeon-ho Kim   +6 more
semanticscholar   +1 more source

Neurofibromatosis type 2

European Journal of Cancer, 1994
G, Thomas, P, Mérel, M, Sanson, K, Hoang-Xuan, J, Zucman, C, Desmaze, T, Melot, A, Aurias, O, Delattre   +8 more
openaire   +2 more sources

The diagnostic evaluation and multidisciplinary management of neurofibromatosis 1 and neurofibromatosis 2.

Journal of the American Medical Association (JAMA), 1997
D. Gutmann, A. Aylsworth, J. Carey, B. Korf, J. Marks, Reed E. Pyeritz, A. Rubenstein, D. Viskochil   +7 more
semanticscholar   +1 more source