His primary areas of study are Immunology, Primary immunodeficiency, Chronic granulomatous disease, Transplantation and Immunodeficiency. His Immunology study combines topics from a wide range of disciplines, such as Signal transduction and RAG2. His biological study spans a wide range of topics, including Immunologic Deficiency Syndromes and Family medicine.
His study looks at the relationship between Chronic granulomatous disease and fields such as NADPH oxidase, as well as how they intersect with chemical problems. His study in Transplantation is interdisciplinary in nature, drawing from both Brain abscess, Abscess, CYBB and Pneumonia. His studies in Immunodeficiency integrate themes in fields like Inflammatory bowel disease and Tyrosine phosphorylation.
His primary scientific interests are in Immunology, Chronic granulomatous disease, Genetic enhancement, Transplantation and Internal medicine. Reinhard Seger frequently studies issues relating to Stem cell and Immunology. His research integrates issues of NADPH oxidase, Busulfan, Inflammation, Disease and Aspergillosis in his study of Chronic granulomatous disease.
His Genetic enhancement study incorporates themes from CD34, Haematopoiesis and Transgene. Reinhard Seger has researched Internal medicine in several fields, including Gastroenterology, Surgery, Histocompatibility and Oncology. In general Primary immunodeficiency, his work in Combined immunodeficiencies is often linked to Expert committee linking many areas of study.
Reinhard Seger mostly deals with Immunology, Chronic granulomatous disease, Primary immunodeficiency, Genetic enhancement and Transplantation. In the field of Immunology, his study on Immunopathology, T cell and Job Syndrome overlaps with subjects such as Primary and Elevated serum IgE. His work deals with themes such as NADPH oxidase, Inflammation, Ulcerative colitis, Therapeutic strategy and Transplantation Conditioning, which intersect with Chronic granulomatous disease.
Primary immunodeficiency and Immunodeficiency are frequently intertwined in his study. His work carried out in the field of Genetic enhancement brings together such families of science as Haematopoiesis, Stem cell, Cell biology, Transgene and Cellular differentiation. His Transplantation study is focused on Surgery and Internal medicine.
His primary areas of investigation include Immunology, Primary immunodeficiency, Chronic granulomatous disease, Expert committee and Combined immunodeficiencies. The study incorporates disciplines such as Caspase 1, P22phox and NADH oxidase in addition to Immunology. The various areas that Reinhard Seger examines in his Primary immunodeficiency study include Immunoglobulin E, Dock8, Immunopathology, Atopy and Genotype.
His research integrates issues of NADPH oxidase, Phagocyte, Genetic enhancement, Transplantation Conditioning and Transplantation in his study of Chronic granulomatous disease. The concepts of his Genetic enhancement study are interwoven with issues in Progenitor cell, Haematopoiesis, Bone marrow and Immune system. He combines subjects such as Autoinflammatory Disorders, Congenital agammaglobulinemia and Immunologic Deficiency Syndromes with his study of Combined immunodeficiencies.
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Chronic Granulomatous Disease: The European Experience
J. Merlijn van den Berg;Elsbeth van Koppen;Anders Åhlin;Bernd H. Belohradsky.
PLOS ONE (2009)
Primary Immunodeficiency Diseases: An Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency
Waleed Al-Herz;Aziz Bousfiha;Jean-Laurent Casanova;Jean-Laurent Casanova;Helen Chapel.
Frontiers in Immunology (2014)
Primary immunodeficiencies: 2009 update
Luigi D. Notarangelo;Alain Fischer;Raif S. Geha;Jean-Laurent Casanova.
The Journal of Allergy and Clinical Immunology (2009)
Restoration of NET formation by gene therapy in CGD controls aspergillosis
Matteo Bianchi;Abdul Hakkim;Volker Brinkmann;Ulrich Siler.
Long-term survival and transplantation of haemopoietic stem cells for immunodeficiencies: report of the European experience 1968–99
Corinne Antoine;Susanna Müller;Andrew Cant;Marina Cavazzana-Calvo.
The Lancet (2003)
Primary immunodeficiency diseases: An update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee
Raif S. Geha;Luigi D. Notarangelo;Jean Laurent Casanova;Helen Chapel.
The Journal of Allergy and Clinical Immunology (2007)
Griscelli Disease Maps to Chromosome 15q21 and Is Associated With Mutations in the myosin-Va Gene
Pastural E;Barrat Fj;Dufourcq-Lagelouse R;Certain S.
Nature Genetics (1997)
Transplantation of hematopoietic stem cells and long-term survival for primary immunodeficiencies in Europe: Entering a new century, do we do better?
Andrew R. Gennery;Andrew R. Gennery;Mary A. Slatter;Mary A. Slatter;Laure Grandin;Pierre Taupin.
The Journal of Allergy and Clinical Immunology (2010)
V(D)J recombination defects in lymphocytes due to RAG mutations: severe immunodeficiency with a spectrum of clinical presentations.
Anna Villa;Cristina Sobacchi;Luigi D. Notarangelo;Fabio Bozzi.
Incidence, severity, and prevention of infections in chronic granulomatous disease
R. Mouy;A. Fischer;E. Vilmer;R. Seger.
The Journal of Pediatrics (1989)
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