Elie Haddad focuses on Internal medicine, Immunology, Gastroenterology, Bone marrow and Transplantation. In general Internal medicine, his work in Immunosuppression is often linked to TRPM linking many areas of study. His Immunology research is multidisciplinary, relying on both Hemophagocytic lymphohistiocytosis, Cyclophosphamide and Cell biology.
His Gastroenterology research includes themes of Autoimmune hemolytic anemia, Macrophage activation syndrome, Lupus erythematosus, Complication and Lupus anticoagulant. His biological study deals with issues like Immunodeficiency, which deal with fields such as Immune dysregulation. His Transplantation study combines topics in areas such as Severe combined immunodeficiency, Transplantation Conditioning and Retrospective cohort study.
Elie Haddad mainly investigates Immunology, Internal medicine, Immune system, Transplantation and Pediatrics. His Immunology research integrates issues from Hematopoietic stem cell transplantation and Pathology. His research integrates issues of Survival rate and Severe combined immunodeficiency in his study of Hematopoietic stem cell transplantation.
As a part of the same scientific family, Elie Haddad mostly works in the field of Internal medicine, focusing on Surgery and, on occasion, Disease. His Transplantation study incorporates themes from Transplantation Conditioning and Survival analysis. His work investigates the relationship between Pediatrics and topics such as Cohort that intersect with problems in Arthritis.
His primary areas of study are Immune system, Cancer research, Internal medicine, Haematopoiesis and Stem cell. His Immune system study is concerned with Immunology in general. His Immunology research incorporates themes from Viral replication, Stimulation and Heterogeneous group.
His Internal medicine study combines topics from a wide range of disciplines, such as Gastroenterology, Oncology and Familial Hemophagocytic Lymphohistiocytosis. He usually deals with Survival rate and limits it to topics linked to Wiskott–Aldrich syndrome and Hematopoietic stem cell transplantation. His studies deal with areas such as Transplantation Conditioning and Severe combined immunodeficiency as well as Hematopoietic stem cell transplantation.
Elie Haddad mainly focuses on Immunology, Hematopoietic stem cell transplantation, Internal medicine, Severe combined immunodeficiency and Extramural. His work carried out in the field of Immunology brings together such families of science as Stimulation and Ligand. The various areas that Elie Haddad examines in his Hematopoietic stem cell transplantation study include Transplantation Conditioning, Wiskott–Aldrich syndrome and Inflammatory bowel disease.
The concepts of his Internal medicine study are interwoven with issues in Gastroenterology and UNC13D. His research in Severe combined immunodeficiency tackles topics such as Cohort which are related to areas like Pediatrics. Elie Haddad works mostly in the field of Phenotype, limiting it down to topics relating to Immune system and, in certain cases, Hematopoietic cell.
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Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family.
Karl P Schlingmann;Stefanie Weber;Melanie Peters;Lene Niemann Nejsum.
Nature Genetics (2002)
Transplantation Outcomes for Severe Combined Immunodeficiency, 2000–2009
Sung Yun Pai;Brent R. Logan;Linda M. Griffith;Rebecca H. Buckley.
The New England Journal of Medicine (2014)
Early and prolonged intravenous immunoglobulin replacement therapy in childhood agammaglobulinemia: a retrospective survey of 31 patients.
Pierre Quartier;Marianne Debré;Jacques De Blic;Rodolphe de Sauverzac.
The Journal of Pediatrics (1999)
Long-Term Immune Reconstitution and Outcome After HLA-Nonidentical T-Cell–Depleted Bone Marrow Transplantation for Severe Combined Immunodeficiency: A European Retrospective Study of 116 Patients
Elie Haddad;Paul Landais;Wilhelm Friedrich;Bert Gerritsen.
Blood (1998)
Autoimmunity in Wiskott-Aldrich syndrome: risk factors, clinical features, and outcome in a single-center cohort of 55 patients.
Sophie Dupuis-Girod;Jacques Medioni;Elie Haddad;Pierre Quartier.
Pediatrics (2003)
Long-term outcome and lineage-specific chimerism in 194 patients with Wiskott-Aldrich syndrome treated by hematopoietic cell transplantation in the period 1980-2009: an international collaborative study
Daniele Moratto;Silvia Giliani;Carmem Bonfim;Evelina Mazzolari.
Blood (2011)
Efficacy of cyclosporine A in the treatment of macrophage activation syndrome in juvenile arthritis: Report of five cases
Richard Mouy;Jean-Louis Stephan;Pascal Pillet;Elie Haddad.
The Journal of Pediatrics (1996)
Frequency and Severity of Central Nervous System Lesions in Hemophagocytic Lymphohistiocytosis
Elie Haddad;Maria-Luisa Sulis;Nada Jabado;Stephane Blanche.
Blood (1997)
X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management, and outcome of the disease
Claire Booth;Kimberly C. Gilmour;Paul Veys;Andrew R. Gennery.
Blood (2011)
Reduced-intensity conditioning and HLA-matched haemopoietic stem-cell transplantation in patients with chronic granulomatous disease: a prospective multicentre study
Tayfun Güngör;Pierre Teira;Mary Slatter;Georg Stussi.
The Lancet (2014)
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