Association studies in genetics

Citations 121-130 of 148 total displayed.

Past content (since Jan 2001):

BRIEF COMMUNICATIONS
Possible association of the tau H1/H1 genotype with primary progressive aphasia: M.-J. Sobrido, A. Abu–Khalil, S. Weintraub, N. Johnson, B. Quinn, J. L. Cummings, M.-M. Mesulam, and D. H. Geschwind
Neurology 2003; 60: 862-864. [Abstract] [Full text] [PDF]

ARTICLES
GABA(B) receptor 1 polymorphism (G1465A) is associated with temporal lobe epilepsy: A. Gambardella, I. Manna, A. Labate, R. Chifari, A. La Russa, P. Serra, R. Cittadella, S. Bonavita, V. Andreoli, E. LePiane, F. Sasanelli, A. Di Costanzo, M. Zappia, G. Tedeschi, U. Aguglia, and A. Quattrone
Neurology 2003; 60: 560-563. [Abstract] [Full text] [PDF]

ARTICLES
Infantile ascending hereditary spastic paralysis (IAHSP): Clinical features in 11 families: G. Lesca, E. Eymard–Pierre, F. M. Santorelli, R. Cusmai, M. Di Capua, E. M. Valente, J. Attia–Sobol, H. Plauchu, V. Leuzzi, A. Ponzone, O. Boespflug–Tanguy, and E. Bertini
Neurology 2003; 60: 674-682. [Abstract] [Full text] [PDF]

CLINICAL/SCIENTIFIC NOTES
Pure spastic paraparesis associated with a novel presenilin 1 R278K mutation: A. Assini, L. Terreni, R. Borghi, L. Giliberto, A. Piccini, D. Loqui, S. Fogliarino, G. Forloni, and M. Tabaton
Neurology 2003; 60: 150. [Full text] [PDF]

BRIEF COMMUNICATIONS
The chemokine receptor CCR5 deletion mutation is associated with MS in HLA-DR4–positive Russians: O. O. Favorova, T. V. Andreewski, A. N. Boiko, M. A. Sudomoina, A. D. Alekseenkov, O. G. Kulakova, A. V. Slanova, and E. I. Gusev
Neurology 2002; 59: 1652-1655. [Abstract] [Full text] [PDF]

BRIEF COMMUNICATIONS
Genetic association of ${alpha}$ ₂-macroglobulin polymorphisms with AD in southern Italy: M. Zappia, R. Cittadella, I. Manna, G. Nicoletti, V. Andreoli, S. Bonavita, A. Gambardella, and A. Quattrone
Neurology 2002; 59: 756-758. [Abstract] [Full text] [PDF]

BRIEF COMMUNICATIONS
CSF tau protein phosphorylated at threonine 231 correlates with cognitive decline in MCI subjects: K. Buerger, S. J. Teipel, R. Zinkowski, K. Blennow, H. Arai, R. Engel, K. Hofmann–Kiefer, C. McCulloch, U. Ptok, R. Heun, N. Andreasen, J. DeBernardis, D. Kerkman, H.- J. Moeller, P. Davies, and H. Hampel
Neurology 2002; 59: 627-629. [Abstract] [Full text] [PDF]

BRIEF COMMUNICATIONS
Analysis of tau haplotypes in Pick’s disease: H. R. Morris, M. Baker, K. Yasojima, H. Houlden, M. N. Khan, N. W. Wood, J. Hardy, M. Grossman, J. Trojanowski, T. Revesz, E. H. Bigio, C. Bergeron, J. C. Janssen, P. L. McGeer, M. N. Rossor, A. J. Lees, P. L. Lantos, and M. Hutton
Neurology 2002; 59: 443-445. [Abstract] [Full text] [PDF]

ARTICLES
Evidence for a genetic association between monoamine oxidase A and restless legs syndrome: A. Desautels, G. Turecki, J. Montplaisir, K. Brisebois, A. Sequeira, B. Adam, and G. A. Rouleau
Neurology 2002; 59: 215-219. [Abstract] [Full text] [PDF]

ARTICLES
Contribution of APOE promoter polymorphisms to Alzheimer’s disease risk: J. C. Lambert, L. Araria-Goumidi, L. Myllykangas, C. Ellis, J. C. Wang, M. J. Bullido, J. M. Harris, M. J. Artiga, D. Hernandez, J. M. Kwon, B. Frigard, R. C. Petersen, A. M. Cumming, F. Pasquier, I. Sastre, P. J. Tienari, A. Frank, R. Sulkava, J. C. Morris, D. St. Clair, D. M. Mann, F. Wavrant-DeVrièze, M. Ezquerra-Trabalon, P. Amouyel, J. Hardy, M. Haltia, F. Valdivieso, A. M. Goate, J. Pérez-Tur, C. L. Lendon, and M. C. Chartier-Harlin
Neurology 2002; 59: 59-66. [Abstract] [Full text] [PDF]

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