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Gene expression studies
Citations 1-10 of 33 total displayed.
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Most recent content
(10 Nov 2009):
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- EDITORIALS
Pathologic intracellular signaling in childhood pilocytic astrocytomas
- Scott L. Pomeroy
Neurology 2009; 73: 1522-1523.
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- ARTICLES
Alterations of BRAF and HIPK2 loci predominate in sporadic pilocytic astrocytoma
- J. Yu, H. Deshmukh, R. J. Gutmann, R. J. Emnett, F. J. Rodriguez, M. A. Watson, R. Nagarajan, and D. H. Gutmann
Neurology 2009; 73: 1526-1531.
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Past content
(since Oct 2002):
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- EDITORIALS
Pathologic intracellular signaling in childhood pilocytic astrocytomas
- Scott L. Pomeroy
Neurology first published on October 7, 2009 as doi: WNL.0b013e3181c1850e.
Rapid PDF
- ARTICLES
Alterations of BRAF and HIPK2 loci predominate in sporadic pilocytic astrocytoma
- J. Yu, H. Deshmukh, R. J. Gutmann, R. J. Emnett, F. J. Rodriguez, M. A. Watson, R. Nagarajan, and D. H. Gutmann
Neurology first published on September 30, 2009 as doi: WNL.0b013e3181c0664a.
[Abstract]
Rapid PDF
- ARTICLES
Bevacizumab and chemotherapy for recurrent glioblastoma: A single-institution experience
- P. L. Nghiemphu, W. Liu, Y. Lee, T. Than, C. Graham, A. Lai, R. M. Green, W. B. Pope, L. M. Liau, P. S. Mischel, S. F. Nelson, R. Elashoff, and T. F. Cloughesy
Neurology 2009; 72: 1217-1222.
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- ARTICLES
A mechanism for low penetrance in an ALS family with a novel SOD1 deletion
- L. Zinman, H. N. Liu, C. Sato, Y. Wakutani, A. F. Marvelle, D. Moreno, K. E. Morrison, K. L. Mohlke, J. Bilbao, J. Robertson, and E. Rogaeva
Neurology 2009; 72: 1153-1159.
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A novel Frabin (FGD4) nonsense mutation p.R275X associated with phenotypic variability in CMT4H
- Henry Houlden, Simon Hammans, Haider Katifi, and Mary M. Reilly
Neurology 2009; 72: 617-620.
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 -Internexin expression identifies 1p19q codeleted gliomas
- F. Ducray, E. Crinière, A. Idbaih, K. Mokhtari, Y. Marie, S. Paris, S. Navarro, F. Laigle-Donadey, C. Dehais, J. Thillet, K. Hoang-Xuan, J. -Y. Delattre, and M. Sanson
Neurology 2009; 72: 156-161.
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- EDITORIALS
Hereditary motor neuropathy and heat shock proteins: A shocking transformation
- Clifton Gooch and Michael Shy
Neurology 2008; 71: 1656-1657.
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- ARTICLES
Autosomal recessive myosclerosis myopathy is a collagen VI disorder
- L. Merlini, E. Martoni, P. Grumati, P. Sabatelli, S. Squarzoni, A. Urciuolo, A. Ferlini, F. Gualandi, and P. Bonaldo
Neurology 2008; 71: 1245-1253.
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