Search Results - "Salah, Sofiane"

HLA-E circulating and genetic determinants in schizophrenia and bipolar disorder by Boukouaci, Wahid, Lajnef, Mohamed, Richard, Jean-Romain, Wu, Ching-Lien, Bouassida, Jihène, Rafik, Ismail, Foiselle, Marianne, Straczek, Céline, Mezouad, Esma, Naamoune, Soumia, Salah, Sofiane, Bencharif, Mohamed Amin, Ben Chaaben, Arij, Barau, Caroline, Le Corvoisier, Philippe, Leboyer, Marion, Tamouza, Ryad

“…Schizophrenia (SZ) and bipolar disorders (BD) are severe mental illnesses that lack reliable biomarkers to guide diagnosis and management. As immune…”
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Low peripheral mitochondrial DNA copy number during manic episodes of bipolar disorders is associated with disease severity and inflammation by Angrand, Loïc, Boukouaci, Wahid, Lajnef, Mohamed, Richard, Jean-Romain, Andreazza, Ana, Wu, Chieng-Lien, Bouassida, Jihène, Rafik, Ismail, Foiselle, Marianne, Mezouad, Esma, Naamoune, Soumia, Chami, Leila, Mihoub, Ons, Salah, Sofiane, Benchaaben, Arij, Le Corvoisier, Philippe, Barau, Caroline, Costes, Bruno, Yolken, Robert, Crepeaux, Guillemette, Leboyer, Marion, Tamouza, Ryad

“…•BD are underpinned by dysimmunity and oxidative stress/ cellular senescence.•Mitchondria are at the cross road between stress, senescence and…”
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Universalis Calcinosis in Adult Dermatomyositis: An "Anti-NXP2 Syndrome" by Fodil, Dalila, Meyer, Alain, Salah, Sofiane Samir, Sibilia, Jean, Attal, Nabila, Tafiani-Lefkir, Salima

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Universalis Calcinosis in Adult Dermatomyositis by Fodil, Dalila, Meyer, Alain, Salah, Sofiane Samir, Sibilia, Jean, Attal, Nabila, Tafiani-Lefkir, Salima

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Functional polymorphisms of Monocyte Chemoattractant Protein-1 gene and Pott’s disease risk by Mecabih, Fethi, Sadouki, Fatiha, Bennabi, Meriem, Salah, Sofiane, Boukouaci, Wahid, Amroun, Habiba, Fortier, Catherine, Marzais, François, Charron, Dominique, Djoudi, Hachemi, Abbadi, Mohamed Cherif, Krishnamoorthy, Rajagopal, Tamouza, Ryad

“…Abstract Objective Monocyte Chemoattractant Protein-1 (MCP-1/CCL2), a key player in immune-mediated responses against Mycobacterium tuberculosis , is encoded…”
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Cytokine expression and cytokine-based T cell profiling in South Indian rheumatoid arthritis by Mariaselvam, Christina Mary, Aoki, Masayuki, Salah, Sofiane, Boukouaci, Wahid, Moins-Teisserenc, Hélène, Charron, Dominique, Krishnamoorthy, Rajagopal, Tamouza, Ryad, Negi, Vir Singh

“…Abstract Rheumatoid arthritis (RA), a chronic inflammatory disease affects up to 1% of the general population. Early diagnosis and treatment are limited by the…”
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Genetic diversity of TLR2, TLR4, and VDR loci and pulmonary tuberculosis in Moroccan patients by Arji, Naima, Busson, Marc, Iraqi, Ghali, Bourkadi, Jamal Eddine, Benjouad, Abdelaziz, Bouayad, Abdellatif, Mariaselvam, Christina, Salah, Sofiane, Fortier, Catherine, Amokrane, Kahina, Marzais, François, Boukouaci, Wahid, Krishnamoorthy, Rajagopal, Charron, Dominique, El Aouad, Rajae, Tamouza, Ryad

“…Toll-like receptors (TLRs) 2, 4, and the vitamin D receptor (VDR) are central components of the innate and adaptive immunity against Mycobacterium tuberculosis…”
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Polymorphisms in oxidative stress-related genes are associated with nasopharyngeal carcinoma susceptibility by Ben Chaaben, Arij, Mariaselvam, Christina, Salah, Sofiane, Busson, Marc, Dulphy, Nicolas, Douik, Hayet, Ghanem, Abderraouf, Boukaouci, Wahid, Al Daccak, Reem, Mamoghli, Tesnim, Harzallah, Latifa, Bouassida, Jihene, Fortier, Catherine, Gritli, Said, Hamida, Jeannette Ben, Charron, Dominique, Krishnamoorthy, Rajagopal, Guemira, Fethi, Tamouza, Ryad

“…Abstract Nasopharyngeal carcinoma (NPC) is a complex multifactorial disorder involving both genetic and environmental factors. Polymorphisms of genes encoding…”
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Association of HLA-E01:01/01:03 polymorphism with methotrexate-based treatment response in South Indian rheumatoid arthritis patients by Mariaselvam, Christina Mary, Sundaresh, Aparna, Ben Chaaben, Arij, Salah, Sofiane, Fortier, Catherine, Charron, Dominique, Krishnamoorthy, Rajagopal, Tamouza, Ryad, Negi, Vir Singh

“…Abstract Objectives Non-classical HLA-E molecules may influence the disease susceptibility and phenotype including treatment response in chronic inflammatory…”
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Le syndrome de Sneddon et péripartum : binôme non fortuit by Mati, Mounia, Hakem, Djanette, Lassouaoui, Sonia, Chouikrat, Nadia, Berrah, Abdelkrim, Salah, Sofiane-Samir, Attal, Nadia, Slimani, Nabila, Slimani, Nabila

“…Le syndrome de Sneddon est une entité rare qui associe un livédo pathologique et des manifestations neurologiques ischémiques récidivantes, exposant au risque…”
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Algerian Registry for Inborn Errors of Immunity in Children: Report of 887 Children (1985–2021) by Yagoubi, Abdelghani, Tahiat, Azzeddine, Touri, Nabila Souad, Ladj, Mohamed Samir, Drali, Ouardia, Belaid, Brahim, Mohand-Oussaid, Ayda, Dehimi, Abdelhak, Belbouab, Reda, Ferhani, Yacine, Melzi, Souhila, Guedouar, Assia, Hakem, Saliha, Khemici, Ouardia, Inouri, Yacine, Meddour, Yanis, Dib, Saadeddine, Mansouri, Zohra, Iddir, Samir, Boufersaoui, Abderrahmane, Boudiaf, Houda, Bouhdjila, Abderrachid, Ibsaine, Ouardia, Maouche, Hachemi, Dahlouk, Djazia, Mekki, Azzedine, Bioud, Belkacem, Bouzerar, Zair, Zeroual, Zoulikha, Benhassine, Fadila, Bekkat-Berkani, Dahila, Naamoune, Soumeya, Salah, Samir Sofiane, Chaib, Samia, Attal, Nabila, Bensaadi, Nadia, Bouchair, Nadira, Cherif, Nacira, Kedji, Leila, Bendeddouche, Salih, Atif, Mohamed Lamine, Djenouhat, Kamel, Kechout, Nadia, Djidjik, Reda, Benhalla, Keltoum Nafissa, Smati, Leila, Boukari, Rachida

“…Introduction Inborn errors of immunity (IEI) represent a heterogeneous large group of genetic disorders characterized by susceptibility of affected individuals…”
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