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Neurology
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Neurofibromatosis

Citations 11-20 of 32 total displayed.

Past content (since May 2001):

BRIEF COMMUNICATIONS
Matrilin-2 expression distinguishes clinically relevant subsets of pilocytic astrocytoma
M. K. Sharma, M. A. Watson, M. Lyman, A. Perry, K. D. Aldape, F. Deák, and D. H. Gutmann
Neurology 2006; 66: 127-130. [Abstract] [Full text] [PDF]  

ARTICLES
The nature and frequency of cognitive deficits in children with neurofibromatosis type 1
Shelley L. Hyman, Arthur Shores, and Kathryn N. North
Neurology 2005; 65: 1037-1044. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
Vascular dysplasia in neurofibromatosis type 2
Aisling M. Ryan, Michael Hurley, Paul Brennan, and Joan T. Moroney
Neurology 2005; 65: 163-a-164-a. [Full text] [PDF]  

VIEWS & REVIEWS
Diagnostic criteria for schwannomatosis
M. MacCollin, E. A. Chiocca, D. G. Evans, J. M. Friedman, R. Horvitz, D. Jaramillo, M. Lev, V. F. Mautner, M. Niimura, S. R. Plotkin, C. N. Sang, A. Stemmer-Rachamimov, and E. S. Roach
Neurology 2005; 64: 1838-1845. [Abstract] [Full text] [PDF]  

NEUROIMAGES
Plexiform neurofibromas of the brachial plexuses
Boguslaw Paradowski, Malgorzata Bilinska, Marek Sasiadek, and Michal Jelen
Neurology 2005; 64: 1943. [Full text] [PDF]  

BRIEF COMMUNICATIONS
Cerebrovascular abnormalities in a population of children with neurofibromatosis type 1
Tena L. Rosser, Gilbert Vezina, and Roger J. Packer
Neurology 2005; 64: 553-555. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Late-onset optic pathway tumors in children with neurofibromatosis 1
R. Listernick, R. E. Ferner, L. Piersall, S. Sharif, D. H. Gutmann, and J. Charrow
Neurology 2004; 63: 1944-1946. [Abstract] [Full text] [PDF]  

NEUROIMAGES
Clinical picture of bilateral vestibular schwannomas, sudden bilateral hearing loss, and aviation
Daniel G. Healy and Nicholas W. Wood
Neurology 2004; 63: 933. [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
Multiple meningiomas in brain and lung due to acquired mutation of the NF2 gene
O. Eckstein, A. Stemmer-Rachamimov, F. Nunes, D. Hoch, R. Ojemann, and M. MacCollin
Neurology 2004; 62: 1904-1905. [Full text] [PDF]  

ARTICLES
Neurofibromatosis type 1: Motor and cognitive function and T2-weighted MRI hyperintensities
R. Feldmann, J. Denecke, M. Grenzebach, G. Schuierer, and J. Weglage
Neurology 2003; 61: 1725-1728. [Abstract] [Full text] [PDF]  

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* Related collections:
 Genetics
 All Genetics
 Neurofibromatosis
 Other neurocutaneous disorders
 Genetic linkage
 Association studies in genetics
 Gene expression studies
 Gene therapy
 Mitochondrial disorders
 Ion channel gene defects
 Spinocerebellar ataxia
 Trinucleotide repeat diseases
 Chromosomes


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