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Year Number of Results
2008 1
2009 2
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2011 1
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Page 1
[The high phenotypic variability of RYR1 gene mutations].
Islam Kediha M, Nouioua S, Tazir M, Sternberg D, Lunardi J, Ali Pacha L. Islam Kediha M, et al. Among authors: ali pacha l. Med Sci (Paris). 2022 Dec;38 Hors série n° 1:46-48. doi: 10.1051/medsci/2022178. Epub 2023 Jan 16. Med Sci (Paris). 2022. PMID: 36649637 Free article. French.
Clinical management and disease-modifying treatment for amyotrophic lateral sclerosis in African hospital centers: the TROPALS study.
Luna J, Jost J, Diagana M, Ait Aissa L, Tazir M, Ali Pacha L, Kacem I, Gouider R, Henning F, Basse A, Cisse O, Balogou AK, Kombate D, Agbetou M, Houinato D, Gnonlonfoun DD, Millogo A, Agba T, Belo M, Sengxeu N, Hamidou B, Preux PM, Benoit M, Couratier P; Tropals Collaboration. Luna J, et al. Among authors: ali pacha l. Amyotroph Lateral Scler Frontotemporal Degener. 2022 May;23(3-4):279-283. doi: 10.1080/21678421.2021.1961806. Epub 2021 Aug 28. Amyotroph Lateral Scler Frontotemporal Degener. 2022. PMID: 34459327
Clinical features and prognosis of amyotrophic lateral sclerosis in Africa: the TROPALS study.
Luna J, Diagana M, Ait Aissa L, Tazir M, Ali Pacha L, Kacem I, Gouider R, Henning F, Basse A, Cisse O, Balogou AAK, Kombate D, Agbetou M, Houinato D, Millogo A, Agba T, Belo M, Penoty M, Raymondeau-Moustafa M, Hamidou B, Couratier P, Preux PM, Marin B; TROPALS Collaboration. Luna J, et al. Among authors: ali pacha l. J Neurol Neurosurg Psychiatry. 2019 Jan;90(1):20-29. doi: 10.1136/jnnp-2018-318469. Epub 2018 Sep 21. J Neurol Neurosurg Psychiatry. 2019. PMID: 30242088
In-vitro immunomodulatory effects of nicotine on Nitric Oxide, interleukin 1β and interleukin 37 production in human peripheral blood mononuclear cells (PBMC) from patients with Behçet disease.
Ghozali N, Belguendouz H, Messaoudene D, Hadjimi Z, Ihammichene S, Chekaoui A, Benchabane S, Terahi M, Kediha I, Ali Pacha L, Touil-Boukoffa C. Ghozali N, et al. Among authors: ali pacha l. Int Immunopharmacol. 2021 Dec;101(Pt A):108189. doi: 10.1016/j.intimp.2021.108189. Epub 2021 Oct 1. Int Immunopharmacol. 2021. PMID: 34601327
Molecular diagnosis of known recessive ataxias by homozygosity mapping with SNP arrays.
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 FM, Tazir M, Koenig M. H'mida-Ben Brahim D, et al. Among authors: ali pacha l. J Neurol. 2011 Jan;258(1):56-67. doi: 10.1007/s00415-010-5682-5. Epub 2010 Aug 27. J Neurol. 2011. PMID: 20798953
Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients.
Anheim M, Monga B, Fleury M, Charles P, Barbot C, Salih M, Delaunoy JP, 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. Anheim M, et al. Among authors: ali pacha l. Brain. 2009 Oct;132(Pt 10):2688-98. doi: 10.1093/brain/awp211. Epub 2009 Aug 20. Brain. 2009. PMID: 19696032
Ataxia with oculomotor apraxia type 2: a clinical and genetic study of 19 patients.
Tazir M, Ali-Pacha L, M'Zahem A, Delaunoy JP, Fritsch M, Nouioua S, Benhassine T, Assami S, Grid D, Vallat JM, Hamri A, Koenig M. Tazir M, et al. Among authors: ali pacha l. J Neurol Sci. 2009 Mar 15;278(1-2):77-81. doi: 10.1016/j.jns.2008.12.004. Epub 2009 Jan 11. J Neurol Sci. 2009. PMID: 19141356
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