|
All Genetics
Citations 1-10 of 676 total displayed.
|
Most recent content
(3 Nov 2009):
|
- ARTICLES
The heritability and genetics of frontotemporal lobar degeneration
- J. D. Rohrer, R. Guerreiro, J. Vandrovcova, J. Uphill, D. Reiman, J. Beck, A. M. Isaacs, A. Authier, R. Ferrari, N. C. Fox, I.R.A. Mackenzie, J. D. Warren, R. de Silva, J. Holton, T. Revesz, J. Hardy, S. Mead, and M. N. Rossor
Neurology 2009; 73: 1451-1456.
[Abstract]
[Full text]
[PDF]
- CLINICAL/SCIENTIFIC NOTES
MGMT METHYLATION IS A PROGNOSTIC BIOMARKER IN ELDERLY PATIENTS WITH NEWLY DIAGNOSED GLIOBLASTOMA
- E. R. Gerstner, S. Yip, D. L. Wang, D. N. Louis, A. J. Iafrate, and T. T. Batchelor
Neurology 2009; 73: 1509-1510.
[Full text]
[PDF]
|
Past content
(since Jan 2001):
|
- ARTICLES
"Frontotemporoparietal" dementia: Clinical phenotype associated with the c.709-1G>A PGRN mutation
- F. Moreno, B. Indakoetxea, M. Barandiaran, A. Alzualde, A. Gabilondo, A. Estanga, J. Ruiz, M. Ruibal, A. Bergareche, J. F. Martí-Massó, and A. López de Munain
Neurology 2009; 73: 1367-1374.
[Abstract]
[Full text]
[PDF]
- CLINICAL/SCIENTIFIC NOTES
DEVELOPMENT OF MESIAL TEMPORAL LOBE EPILEPSY IN CHOREA-ACANTHOCYTOSIS
- R. Scheid, B. Bader, D. V. Ott, A. Merkenschlager, and A. Danek
Neurology 2009; 73: 1419-1422.
[Full text]
[PDF]
- HISTORICAL NEUROLOGY
Abraham Lincoln did not have type 5 spinocerebellar ataxia
- John G. Sotos
Neurology 2009; 73: 1328-1332.
[Full text]
[PDF]
- EDITORIALS
Another gene for ALS: Mutations in sporadic cases and the rare variant hypothesis
- Kevin Talbot
Neurology 2009; 73: 1172-1173.
[Full text]
[PDF]
- ARTICLES
Mutations in FUS cause FALS and SALS in French and French Canadian populations
- V. V. Belzil, P. N. Valdmanis, P. A. Dion, H. Daoud, E. Kabashi, A. Noreau, J. Gauthier, for the S2D team, P. Hince, A. Desjarlais, J. -P. Bouchard, L. Lacomblez, F. Salachas, P. -F. Pradat, W. Camu, V. Meininger, N. Dupré, and G. A. Rouleau
Neurology 2009; 73: 1176-1179.
[Abstract]
[Full text]
[PDF]
- ARTICLES
Analysis of FUS gene mutation in familial amyotrophic lateral sclerosis within an Italian cohort
- N. Ticozzi, V. Silani, A. L. LeClerc, P. Keagle, C. Gellera, A. Ratti, F. Taroni, T. J. Kwiatkowski, Jr, D. M. McKenna-Yasek, P. C. Sapp, R. H. Brown, Jr, and J. E. Landers
Neurology 2009; 73: 1180-1185.
[Abstract]
[Full text]
[PDF]
- ARTICLES
SPG15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosum
- C. Goizet, A. Boukhris, D. Maltete, L. Guyant-Maréchal, J. Truchetto, E. Mundwiller, S. Hanein, P. Jonveaux, F. Roelens, J. Loureiro, E. Godet, S. Forlani, J. Melki, M. Auer-Grumbach, J. C. Fernandez, P. Martin-Hardy, I. Sibon, G. Sole, I. Orignac, C. Mhiri, P. Coutinho, A. Durr, A. Brice, and G. Stevanin
Neurology 2009; 73: 1111-1119.
[Abstract]
[Full text]
[PDF]
- ARTICLES
Apolipoprotein genotype does not influence MS severity, cognition, or brain atrophy
- A. van der Walt, J. Stankovich, M. Bahlo, B. V. Taylor, I.A.F. van der Mei, S. J. Foote, T. J. Kilpatrick, J. P. Rubio, and H. Butzkueven
Neurology 2009; 73: 1018-1025.
[Abstract]
[Full text]
[PDF]
|
|
