Retention of herpes simplex virus type II sequences in bglII n-transformed cells after co-transfection with a selectable marker.

Por Saavedra, C, Kessous-Elbaz, A
Publicado em 1985

Neuronal expression of human immunodeficiency virus type 1 env proteins in transgenic mice: distribution in the central nervous system and pathological alterations.

Por Berrada, F, Ma, D, Michaud, J, Doucet, G, Giroux, L, Kessous-Elbaz, A
Publicado em 1995

Detection of polymerase chain reaction-amplified human immunodeficiency virus type 1 proviral DNA with a digoxigenin-labeled RNA probe and an enzyme-linked immunoassay.

Por He, Y, Coutlée, F, Saint-Antoine, P, Olivier, C, Voyer, H, Kessous-Elbaz, A
Publicado em 1993

Association of polymorphisms in the Tau and Saitohin genes with Parkinson's disease

Por Levecque, C, Elbaz, A, Clavel, J, Vidal, J, Amouyel, P, Alperovitch, A, Tzourio, C, Chartier-Harlin, M
Publicado em 2004

Evaluation of infection with human immunodeficiency virus type 1 by using nonisotopic solution hybridization for detection of polymerase chain reaction-amplified proviral DNA.

Por Coutlée, F, Saint-Antoine, P, Olivier, C, Voyer, H, Kessous-Elbaz, A, Berrada, F, Bégin, P, Giroux, L, Viscidi, R
Publicado em 1991

Excess non-psychiatric hospitalizations among employees with mental disorders: a 10-year prospective study of the GAZEL cohort

Por Azevedo Da Silva, M, Lemogne, C, Melchior, M, Zins, M, Van Der Waerden, J, Consoli, S M, Goldberg, M, Elbaz, A, Singh-Manoux, A, Nabi, H
Publicado no Acta Psychiatr Scand (2015)

Mutation in DHP receptor alpha 1 subunit (CACLN1A3) gene in a Dutch family with hypokalaemic periodic paralysis.

Por Boerman, R H, Ophoff, R A, Links, T P, van Eijk, R, Sandkuijl, L A, Elbaz, A, Vale-Santos, J E, Wintzen, A R, van Deutekom, J C, Isles, D E
Publicado em 1995

Hypokalemic Periodic Paralysis and the Dihydropyridine Receptor (CACNLIA3): Genotype/Phenotype Correlations for two Predominant Mutations and Evidence for the Absence of a Founder...

Por Elbaz, A., Vale-Santos, J., Jurkat-Rott, K., Lapie, P., Ophoff, R. A., Bady, B., Links, T. P., Piussan, C., Vila, A., Monnier, N., Padberg, G. W., Abe, K., Feingold, N., Guimaraes, J., Wintzen, A. R., van der Hoeven, J. H., Saudubray, J. M., Grunfeld, J. P., Lenoir, G., Nivet, H., Echenne, B., Frants, R. R., Fardeau, M., Lehmann-Horn, F., Fontaine, B.
Publicado em 1995

Specifically neuropathic Gaucher's mutations accelerate cognitive decline in Parkinson's

Por Liu, Ganqiang, Boot, Brendon, Locascio, Joseph J., Jansen, Iris E., Winder‐Rhodes, Sophie, Eberly, Shirley, Elbaz, Alexis, Brice, Alexis, Ravina, Bernard, van Hilten, Jacobus J., Cormier‐Dequaire, Florence, Corvol, Jean‐Christophe, Barker, Roger A., Heutink, Peter, Marinus, Johan, Williams‐Gray, Caroline H., Scherzer, Clemens R., Scherzer, C., Hyman, B.T., Ivinson, A.J., Trisini‐Lipsanopoulos, A., Franco, D., Burke, K., Sudarsky, L.R., Hayes, M.T., Umeh, C.C., Growdon, J.H., Schwarzschild, M.A., Hung, A.Y., Flaherty, A.W., Wills, A.‐M., Mejia, N.I., Gomperts, S.N., Khurana, V., Selkoe, D.J., Yi, T., Page, K., Liao, Z., Barker, R., Foltynie, T., Williams‐Gray, C.H., Mason, S., Winder‐Rhodes, S., Barker, R., Williams‐Gray, C.H., Breen, D., Cummins, G., Evans, J., Winder‐Rhodes, S., Corvol, J.‐C., Brice, A., Elbaz, A., Mallet, A., Vidailhet, M., Bonnet, A.‐M., Bonnet, C., Grabli, D., Hartmann, A., Klebe, S., Lacomblez, L., Mangone, G., Bourdain, F., Brandel, J.‐P., Derkinderen, P., Durif, F., Mesnage, V., Pico, F., Rascol, O., Forlani, S., Lesage, S., Tahiri, K., van Hilten, J.J., Marinus, J., Liao, Z., Page, K., Franco, D., Duong, K., Yi, T., Trisini‐Lipsanopoulos, A., Dong, X., Sudarsky, L.R., Hutten, S.J., Amr, S.S., Shoulson, I., Tanner, C.M., Lang, A.E., Nalls, M.A.
Publicado no Ann Neurol (2016)