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Hemoglobin|April 1, 2010
Forecasting hemoglobinopathy burden through neonatal screening in Omani neonatesSalam Alkindi, Shoaib Al Zadjali, Ali Al Madhani, et al.Immunologic Research|April 9, 2024
Low C4A copy numbers and higher HERV gene insertion contributes to increased risk of SLE, with absence of association with disease phenotype and disease activityChristina Mary Mariaselvam, Gaurav Seth, Chengappa Kavadichanda, et al.Plos One|February 8, 2011
Genetic variation among major human geographic groups supports a peculiar evolutionary trend in PAX9Vanessa R Paixão-Côrtes, Diogo Meyer, Tiago V Pereira, et al.Clinical & Developmental Immunology|June 14, 2013
The association of CD81 polymorphisms with alloimmunization in sickle cell diseaseZohreh Tatari-Calderone, Ryad Tamouza, Gama P Le Bouder, et al.Immunobiology|December 3, 2015
Functional polymorphisms of Monocyte Chemoattractant Protein-1 gene and Pott's disease riskFethi Mecabih, Fatiha Sadouki, Meriem Bennabi, et al.Journal of Infection in Developing Countries|January 14, 2012
The MCP-1 (CCL2) -2518 GG genotype is associated with protection against pulmonary tuberculosis in Moroccan patientsNaima Arji, Marc Busson, Ghali Iraqi, et al.Transplantation|July 9, 2005
Association of HLA-E polymorphism with severe bacterial infection and early transplant-related mortality in matched unrelated bone marrow transplantationRyad Tamouza, Vanderson Rocha, Marc Busson, et al.Immunological Investigations|December 10, 2019
Soluble MICA and anti-MICA Antibodies as Biomarkers of Nasopharyngeal Carcinoma DiseaseArij Ben Chaaben, Nesrine Ouni, Hayet Douik, et al.Movement Disorders : Official Journal of the Movement Disorder Society|July 19, 2012
Association between Parkinson's disease and the HLA-DRB1 locusIsmaïl Ahmed, Ryad Tamouza, Marc Delord, et al.Plos One|March 15, 2019
Correction: Dectin-1 Polymorphism: A Genetic Disease Specifier in Autism Spectrum Disorders?Meriem Bennabi, Richard Delorme, José Oliveira, et al.Pageof 8