Advertisement
Neurology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH SEARCH RESULT
 QUICK SEARCH:   [advanced]


     


Chromosomes

Citations 1-10 of 10 total displayed.

Most recent content (13 Jan 2009):

ARTICLES
{alpha}-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. [Abstract] [Full text] [PDF]  

Past content (since Jun 2003):

ARTICLES
Sensorimotor integration is abnormal in asymptomatic Parkin mutation carriers: A TMS study
T. Bäumer, P. P. Pramstaller, H. R. Siebner, S. Schippling, J. Hagenah, M. Peller, C. Gerloff, C. Klein, and A. Münchau
Neurology 2007; 69: 1976-1981. [Abstract] [Full text] [PDF]  

ARTICLES
Temozolomide for low-grade gliomas: Predictive impact of 1p/19q loss on response and outcome
G. Kaloshi, A. Benouaich-Amiel, F. Diakite, S. Taillibert, J. Lejeune, F. Laigle-Donadey, M.-A Renard, W. Iraqi, A. Idbaih, S. Paris, L. Capelle, H. Duffau, P. Cornu, J.-M Simon, K. Mokhtari, M. Polivka, A. Omuro, A. Carpentier, M. Sanson, J.-Y Delattre, and K. Hoang-Xuan
Neurology 2007; 68: 1831-1836. [Abstract] [Full text] [PDF]  

ARTICLES
Pathologic pain distorts visuospatial perception
M. Sumitani, M. Shibata, T. Iwakura, Y. Matsuda, G. Sakaue, T. Inoue, T. Mashimo, and S. Miyauchi
Neurology 2007; 68: 152-154. [Abstract] [Full text] [PDF]  

EDITORIALS
Migraine and cognitive function: Some reassuring news
Mitchell S.V. Elkind and Ann I. Scher
Neurology 2005; 64: 590-591. [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
SCN4A-associated hypokalemic periodic paralysis merits a trial of acetazolamide
S. L. Venance, K. Jurkat-Rott, F. Lehmann-Horn, and R. Tawil
Neurology 2004; 63: 1977. [Full text] [PDF]  

ARTICLES
PET evidence for a role of the basal ganglia in patients with ring chromosome 20 epilepsy
A. Biraben, F. Semah, M. -J. Ribeiro, G. Douaud, P. Remy, and A. Depaulis
Neurology 2004; 63: 73-77. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
Severe epilepsy, retardation, and dysmorphic features with a 2q deletion including SCN1A and SCN2A
S. Pereira, J. P. Vieira, F. Barroca, P. Roll, R. Carvalhas, P. Cau, S. Sequeira, P. Genton, and P. Szepetowski
Neurology 2004; 63: 191-192. [Full text] [PDF]  

ARTICLES
Temporal cortex hypermetabolism in Down syndrome prior to the onset of dementia
R. J. Haier, M. T. Alkire, N. S. White, M. R. Uncapher, E. Head, I. T. Lott, and C. W. Cotman
Neurology 2003; 61: 1673-1679. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Telomerase reactivation in malignant gliomas and loss of heterozygosity on 10p15.1
P. Leuraud, L. Aguirre-Cruz, K. Hoang-Xuan, E. Crinière, M-L. Tanguy, J-L. Golmard, M. Kujas, J-Y. Delattre, and M. Sanson
Neurology 2003; 60: 1820-1822. [Abstract] [Full text] [PDF]  

* Collected Resources Home

* 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


HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH SEARCH RESULT
Copyright © 2009 by AAN Enterprises, Inc.
Advertisement