The scientist’s investigation covers issues in Immunology, Immunodeficiency, Internal medicine, Gene and Missense mutation. His Immunology research is multidisciplinary, incorporating elements of Heterozygote advantage and Genotype. In his study, Ectodermal dysplasia, Frameshift mutation, Nonsense mutation and Acute leukemia is strongly linked to Severe combined immunodeficiency, which falls under the umbrella field of Immunodeficiency.
His work deals with themes such as Gastroenterology and Surgery, which intersect with Internal medicine. His Missense mutation research is multidisciplinary, incorporating perspectives in Cancer research, X chromosome and Gene mutation. He interconnects Busulfan, Transplantation and Pneumonia in the investigation of issues within Chronic granulomatous disease.
His main research concerns Immunology, Internal medicine, Pediatrics, Surgery and Immunodeficiency. His Immunology study often links to related topics such as Transplantation. His studies deal with areas such as Gastroenterology, Endocrinology, Viral load and Oncology as well as Internal medicine.
His biological study spans a wide range of topics, including Incidence and Diphtheria, Vaccination. Particularly relevant to Complication is his body of work in Surgery. His work investigates the relationship between Immunopathology and topics such as Acquired immunodeficiency syndrome that intersect with problems in Virology.
His primary scientific interests are in Immunology, Hematopoietic stem cell transplantation, Primary immunodeficiency, Internal medicine and Pediatrics. His studies link Inflammatory bowel disease with Immunology. His Hematopoietic stem cell transplantation study combines topics from a wide range of disciplines, such as Regimen, Age of onset, Retrospective cohort study and Immunodeficiency.
His Primary immunodeficiency research includes themes of Hypogammaglobulinemia, Adverse effect, Bronchiectasis and Virology. His Internal medicine research is multidisciplinary, relying on both Gastroenterology, Surgery and Oncology. The concepts of his Pediatrics study are interwoven with issues in Tolerability, Quality of life and Common variable immunodeficiency.
Bernd H. Belohradsky spends much of his time researching Immunology, Hematopoietic stem cell transplantation, Primary immunodeficiency, Internal medicine and Mutation. His studies in Immunology integrate themes in fields like Germline mutation and Pediatrics. His Hematopoietic stem cell transplantation research includes elements of Malignancy, Cohort study, Enteritis, Inflammatory bowel disease and Immunodeficiency.
The various areas that Bernd H. Belohradsky examines in his Primary immunodeficiency study include Cancer research, Virology, CD28, Hypogammaglobulinemia and Signal transduction. His research investigates the link between Internal medicine and topics such as Surgery that cross with problems in Cumulative incidence. The Mutation study combines topics in areas such as Cell culture, Therapeutic approach, Interleukin 10 and Age of onset.
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Insertional oncogenesis in 4 patients after retrovirus-mediated gene therapy of SCID-X1
Salima Hacein-Bey-Abina;Alexandrine Garrigue;Gary P. Wang;Jean Soulier.
Journal of Clinical Investigation (2008)
Gain-of-function human STAT1 mutations impair IL-17 immunity and underlie chronic mucocutaneous candidiasis
Luyan Liu;Satoshi Okada;Xiao Fei Kong;Alexandra Y. Kreins.
Journal of Experimental Medicine (2011)
Efficacy of Gene Therapy for X-Linked Severe Combined Immunodeficiency
Salima Hacein-Bey-Abina;Julia Hauer;Annick Lim;Capucine Picard.
The New England Journal of Medicine (2010)
Chronic Granulomatous Disease: The European Experience
J. Merlijn van den Berg;Elsbeth van Koppen;Anders Åhlin;Bernd H. Belohradsky.
PLOS ONE (2009)
Human Tyrosine Kinase 2 Deficiency Reveals Its Requisite Roles in Multiple Cytokine Signals Involved in Innate and Acquired Immunity
Yoshiyuki Minegishi;Masako Saito;Tomohiro Morio;Ken Watanabe.
Positional cloning of the gene for Nijmegen breakage syndrome
Shinya Matsuura;Hiroshi Tauchi;Asako Nakamura;Noriko Kondo.
Nature Genetics (1998)
Clinical picture and treatment of 2212 patients with common variable immunodeficiency
Benjamin Gathmann;Nizar Mahlaoui;Laurence Gérard;Eric Oksenhendler.
The Journal of Allergy and Clinical Immunology (2014)
Genetic Linkage of Hyper-IgE Syndrome to Chromosome 4
Bodo Grimbacher;Alejandro A. Schäffer;Steven M. Holland;Joie Davis.
American Journal of Human Genetics (1999)
Autosomal recessive hyperimmunoglobulin E syndrome: a distinct disease entity
Eleonore D. Renner;Jennifer M. Puck;Steven M. Holland;Markus Schmitt.
The Journal of Pediatrics (2004)
Treatment of chronic granulomatous disease with myeloablative conditioning and an unmodified hemopoietic allograft: a survey of the European experience, 1985-2000.
Reinhard A. Seger;Tayfun Gungor;Bernd H. Belohradsky;Stephane Blanche.
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