T
Tore G. Abrahamsen
Researcher at Oslo University Hospital
Publications - 91
Citations - 4571
Tore G. Abrahamsen is an academic researcher from Oslo University Hospital. The author has contributed to research in topics: Immunodeficiency & Aspergillus fumigatus. The author has an hindex of 34, co-authored 91 publications receiving 4217 citations. Previous affiliations of Tore G. Abrahamsen include Rikshospitalet–Radiumhospitalet & University of Oslo.
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Journal ArticleDOI
Clinical spectrum of X-linked hyper-IgM syndrome
Jacov Levy,Teresa Espanol-Boren,Carolin Thomas,Alain Fischer,Pier-Angelo Tovo,Pierre Bordigoni,Igor B. Resnick,Anders Fasth,Maija Baer,Lina Gomez,E.A.M. Sanders,Marie-Dominique Tabone,Dominique Plantaz,Amos Etzioni,V. Monafo,Mario Abinun,Lennart Hammarström,Tore G. Abrahamsen,Allison Jones,Adam Finn,Timo Klemola,Esther DeVries,Ozden Sanal,Manuel C. Peitsch,Luigi D. Notarangelo +24 more
TL;DR: Although lymphocyte counts and in vitro proliferation to mitogens were normal, a defective in vitro proliferative response to antigens was observed in some patients, and additional defects of cell-mediated immunity may be presumed on the basis of current knowledge of CD40-ligand function.
Journal ArticleDOI
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,Mario Abinun,Tore G. Abrahamsen,Peter D. Arkwright,Michal Baniyash,Edward G. Brooks,Mary Ellen Conley,Patricia Cortes,Marzia Duse,Anders Fasth,Alexandra M. Filipovich,Anthony J. Infante,Alison L Jones,Evelina Mazzolari,Susanna M. Müller,Srdjan Pasic,Gideon Rechavi,Maria Grazia Sacco,Sandro Santagata,Marlis L. Schroeder,Reinhard Seger,Dario Strina,Alberto G. Ugazio,Jouni Väliaho,Mauno Vihinen,Larry B. Vogler,Hans D. Ochs,Paolo Vezzoni,Wilhelm Friedrich,Klaus Schwarz +32 more
TL;DR: The clinical and immunologic phenotypes of patients bearing mutations in RAGs are more diverse than previously thought and that this variability is related, in part, to the specific type of RAG mutation.
Journal ArticleDOI
Late-Onset Septicemia in a Norwegian National Cohort of Extremely Premature Infants Receiving Very Early Full Human Milk Feeding
Arild Rønnestad,Tore G. Abrahamsen,Sverre Medbø,Hallvard Reigstad,Kristin Lossius,Per Ivar Kaaresen,Thore Egeland,Inger Elise Engelund,Lorentz M. Irgens,Trond Markestad +9 more
TL;DR: The main difference, compared with other studies, was the feeding practice, and the data suggest that very early FEF with human milk significantly reduces the risk of LOS among extremely premature infants.
Journal ArticleDOI
Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders.
Asbjørg Stray-Pedersen,Hanne Sørmo Sorte,Pubudu S. Samarakoon,Tomasz Gambin,Tomasz Gambin,Ivan K. Chinn,Zeynep Coban Akdemir,Hans Christian Erichsen,Lisa R. Forbes,Shen Gu,Bo Yuan,Shalini N. Jhangiani,Donna M. Muzny,Olaug K. Rødningen,Ying Sheng,Sarah K. Nicholas,Lenora M. Noroski,Filiz O. Seeborg,Carla M. Davis,Debra Canter,Emily M. Mace,Timothy J. Vece,Carl E. Allen,Harshal Abhyankar,Philip M. Boone,Christine R. Beck,Wojciech Wiszniewski,Børre Fevang,Pål Aukrust,Geir E. Tjønnfjord,Tobias Gedde-Dahl,Henrik Hjorth-Hansen,Ingunn Dybedal,Ingvild Nordøy,Silje F. Jørgensen,Tore G. Abrahamsen,Torstein Øverland,Anne Grete Bechensteen,Vegard Skogen,Liv T. N. Osnes,Mari Ann Kulseth,Trine Prescott,Cecilie F. Rustad,Ketil Heimdal,John W. Belmont,Nicholas L. Rider,Javier Chinen,Tram N. Cao,Eric A. Smith,María Soledad Caldirola,Liliana Bezrodnik,Saul Oswaldo Lugo Reyes,Francisco Javier Espinosa Rosales,Nina Denisse Guerrero-Cursaru,Luis A. Pedroza,Cecilia Poli,Cecilia Poli,José Luis Franco,Claudia Milena Trujillo Vargas,Juan Carlos Aldave Becerra,Nicola A.M. Wright,Thomas B. Issekutz,Andrew C. Issekutz,Jordan K. Abbott,Jason W. Caldwell,Diana K. Bayer,Alice Y. Chan,Alessandro Aiuti,Caterina Cancrini,Eva Holmberg,Christina E. West,Magnus K. O. Burstedt,Ender Karaca,Gozde Yesil,Gozde Yesil,Hasibe Artac,Yavuz Bayram,Mehmed M. Atik,Mohammad K. Eldomery,Mohammad S. Ehlayel,Stephen Jolles,Berit Flatø,Alison A. Bertuch,I. Celine Hanson,Victor Wei Zhang,Lee-Jun C. Wong,Jianhong Hu,Magdalena Walkiewicz,Yaping Yang,Christine M. Eng,Eric Boerwinkle,Eric Boerwinkle,Richard A. Gibbs,William T. Shearer,Robert Lyle,Jordan S. Orange,James R. Lupski +96 more
TL;DR: This high‐throughput genomic approach enabled detection of disease‐related variants in unexpected genes; permitted detection of low‐grade constitutional, somatic, and revertant mosaicism; and provided evidence of a mutational burden in mixed PIDD immunophenotypes.
Journal ArticleDOI
Primary immunodeficiency diseases in Norway.
TL;DR: Compared to previous reports from other European countries, there is a smaller proportion of antibody deficiencies due to few IgA deficiencies registered and a large proportion of complement deficienciesdue to many patients with hereditary angioedema.