ANNEE 2011
Alouache S, Kada M, Messai Y, Estepa V, Torres C, Bakour R.
Antibiotic Resistance and Extended-Spectrum β-Lactamases in Isolated Bacteria from Seawater of Algiers Beaches (Algeria).
Microbes Environ. 2011 Nov 16. [Epub ahead of print]
ABDELHAKIM AOUF, YAMINA MESSAI, MOHAMMED S. SALAMA, HALA M. ABOUSHADY, MERVAT G. EL-ANANY, SOUHILA ALOUACHE, RABAH BAKOUR
Resistance to β-lactams of human and veterinary Salmonella isolates in Egypt and Algeria. Soumis et accepté à African Journal of Microbiology Research (2011).
– BABA AHMED Z. , AYAD A. , MESLI E. , MESSAI Y. , BAKOUR R. , DRISSI M. Dissemination of CTX-M-15 extented-spectrum β-lactamases in Enterobacteriaceae in the ICU of Tlemcen hospital (Algeria). Soumis et accepté à Eastern Mediterranean Health Journal (2011).
– M. DRISSI, Z. BABA AHMED et BAKOUR R.
Sensibilité de Pseudomonas aeruginosa aux antibiotiques au niveau du service de neurochirurgie du CHU de Tlemcen. Phénotype de résistance aux béta-lactamines. Médecine Maghreb, 2011 ; 184 : 23-27
ANNEE 2010
F. CHERBAL, R. BAKOUR, S. ADANE, K. BOUALGA, G. BENAIS-PONT, AND P. MAILLET. BRCA1 and BRCA2 germline mutations screening in Algerian breast/ovarian cancer families. Dis. Markers, 2010 ; 28(6) : 377-84.
Lesage, S., Patin, E., Condroyer, C., Leutenegger, A.L., Lohmann, E., Giladi, N., Bar-Shira, A., Belarbi, S., Hecham, N., Pollak, P., Ouvrard-Hernandez, A.M., Bardien, S., Carr, J., Benhassine, T., Tomiyama, H., Pirkevi, C., Hamadouche, T., Cazeneuve, C., Basak, A.N., Hattori, N., Dürr, A., Tazir, M., Orr-Urtreger, A., Quintana-Murci, L., Brice, A. and the French Parkinson’s Disease Genetics Study Group (2010) Parkinson’s disease-related LRRK2 G2019S mutation results from independent mutational events in humans. Hum. Mol. Genet. 19:1998-2004.
H’mida-Ben Brahim, D., M’zahem, A., Assoum, M., Bouhlal, Y., Fattori, F., Anheim, M., Ali-Pacha, L., Ferrat, F., Chaouch, M., Lagier-Tourenne, C., Drouot, N., Thibaut, C., Benhassine, T., Sifi, Y., Stoppa-Lyonnet, D., N’guyen, K., Poujet, J., Hamri, A., Hentati, F., Amouri, R., Santorelli, F.M., Tazir, M., and Koenig, M. (2010) Molecular diagnosis of known recessive ataxias by homozygosity mapping with SNP arrays. J. Neurol. 258 : 56-67.
Belarbi, S., Hecham, N., Lesage, S., Kediha, M.I., Smail, N., Benhassine, T., Ysmail-Dahlouk, F., Lohman, E., Benhabyles, B., Hamadouche, T., Assami, S., Brice, A., et Tazir, M. (2010) LRRK2 G2019S mutation in Parkinson’s disease : A neuropsychological and neuropsychiatric study in a large Algerian cohort. Parkinsonism Relat. Disord. 16 : 676-679.
ANNEE 2009
Iabadene H., Messai, Y., Ammari, H., Alouache, S., Verdet, C., Bakour, R., Arlet, G. Prevalence of plasmid-mediated AmpC !-lactamases among Enterobacteriaceae in Algiers hospitals. Int J Antimicrob Agents, 2009 ; 34(4) : 340-2.
Iabadene H., Messai, Y., Ammari, H., Alouache, S., Verdet, C., Bakour, R., Arlet, G. Prevalence of plasmid-mediated AmpC !-lactamases among Enterobacteriaceae in Algiers hospitals. Int J Antimicrob Agents, 2009 ; 34(4) : 340-2.
Iabadene, H., Bakour, R., Messai, Y., Da Costa, Arlet, G. Détection des gènes blaCTX-M-14 et aac (3)-II chez Salmonella enterica sérotype Kedougou en Algérie. Médecine et maladies infectieuses. 39 (2009) 806–807
Ammar-Khodja F, Faugère V, Baux D, Giannesini C, Léonard S, Makrelouf M, Malek R, Djennaoui D, Zenati A, Claustres M, Roux AF. Molecular screening of deafness in Algeria : high genetic heterogeneity involving DFNB1 and the Usher loci, DFNB2/USH1B, DFNB12/USH1D and DFNB23/USH1F. Eur J Med Genet. 2009 52(4):174-9.
Tazir M., Ali-Pacha L., M’zahem A., Delaunoy J.P., Fritsch M., Nouioua S., Benhassine T., Assami S., Grid D., Vallat J.M., Hamri A., Koenig M. Ataxia with oculomotor apraxia type 2 : A clinical and genetic study of 19 patients. J. Neurol. Sci. 2009 ; 278 : 77-81.
Anheim M., Monga B., Fleury M., Charles P., Barbot C., Salih M., Delaunoy J.P., Fritsch M., Arning L., Synofzik M., Schöls L., Sequeiros J., Goizet C., Marelli C., Le Ber I., Koht J., Gazulla J., De Bleecker J., Mukhtar M., Drouot N., Ali-Pacha L., Benhassine T., Chbicheb M., M’Zahem A., Hamri A., Chabrol B., Pouget J., Murphy R., Watanabe M., Coutinho P., Tazir M., Durr A., Brice A., Tranchant C., Koenig M. Ataxia with oculomotor apraxia type 2 : clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients. Brain. 2009 ; 132 : 2688-2698.
Population structure and geographical subdivision of the Leishmania major vector Phlebotomus papatasi as revealed by microsatellite variation.
O Hamarsheh, W Presber, MR Yaghoobi-Ershadi, A Amro, A Al-Jawabreh, S Sawalha, A Al-Lahem, ML Das, S Guernaoui, N Seridi, RC Dhiman, Y Hashiguchi, J Ghrab, M Hassan, and G Schonian
Med Vet Entomol, 2009 ; 23(1) : 69-77.
ANNEE 2008
Iabadene H., Messai Y., Ammari H., Ramdani-Bouguessa N., Lounes S., Bakour R., Arlet G. Dissemination of ESBL and Qnr determinants in Enterobacter cloacae in Algeria. Journal of Antimicrobial Chemotherapy. 2008 ; 62 : 133 – 136.
Messai Y., Iabadene H., Benhassine T., Alouache S., Tazir M., Gautier V., Arlet G., Bakour R. Prevalence and characterization of extended-spectrum ß-lactamases in Klebsiella pneumoniae in Algiers hospitals (Algeria). Pathologie Biologie. 2008 ; 56 : 319–325
Drissi M., Baba Ahmed Z., Dehecq B., Bakour R., Plésiat P., Hocquet D. Antibiotic susceptibility and mechanisms of β-lactam resistance among clinical strains of Pseudomonas aeruginosa : First report in Algeria. Médecine et Maladies Infectieuses.2008 ; 38 :187–191
Hamadouche T., Poitelon Y., Genin E., Chaouch M., Tazir M., Kassouri N., Nouioua S., Chaouch A., Boccaccio I., Benhassine T., De Sandre-Giovannoli A., Grid D., Lévy N., Delague V. Founder effect and estimation of the age of the c.892C>T (p.Arg298Cys) mutation in LMNA associated to Charcot-Marie-Tooth subtype CMT2B1 in families from North Western Africa. Ann. Hum. Genet. 2008 ; 72 : 590-597.
Lagier-Tourenne C., Tazir M., Lopez L.C., Quinzii C.M., Assoum M., Drouot N., Busso C., Makri S., Ali-Pacha L., Benhassine T., Anheim M., Lynch D.R., Thibault C., Plewniak F., Bianchetti L., Tranchant C., Poch O., DiMauro S., Mandel J.L., Barros M.H., Hirano M., Koenig M. ADCK3, an ancestral kinase, is mutated in a form of recessive ataxia associated with coenzyme Q10 deficiency. Am. J. Hum. Genet. 2008 ; 82 : 661-672.
Lesage S., Belarbi S., Troiano A., Condroyer C., Hecham N., Pollak P., Lohman E., Benhassine T., Ysmail-Dahlouk F., Dürr A., Tazir M., Brice A., the French Parkinson’s Disease Genetics Study Group. Is the common LRRK2 G2019S mutation related to dyskinesias in North African Parkinson disease ? Neurology 2008 ; 71 : 1550-1552.
Genetic polymorphism of Algerian Leishmania infantum strains revealed by multilocus microsatellite analysis. N Seridi, A Amro, K Kuhls, M Belkaid, C Zidane, A Al-Jawabreh, and G Schonian Microbes Infect, 2008 ; 10 : 1309-15.
Application of PCR-RFLP for the exploration of the molecular diversity of Leishmania infantum in Algeria. N Seridi, M Belkaid, W Quispe-Tintaya, C Zidane, and JC Dujardin Trans R Soc Trop Med Hyg, 2008 ; 102(6) : 556-63.