Hans Christian Erichsen

Førsteamanuensis - Pediatri
Bilde av Hans Christian Erichsen
English version of this page
Brukernavn
Besøksadresse Kirkeveien 166 Bygg 9 None 0450 OSLO
Postadresse Postboks 4956 Nydalen 0424 OSLO

Publikasjoner

  • Kellner, Erinn S; Krupski, Christa; Kuehn, Hye Sun; Rosenzweig, Sergio D.; Yoshida, Nao; Kojima, Seiji; Boutboul, David; Latour, Sylvain; Barlogis, Vincent; Galambrun, Claire; Stray-Pedersen, Asbjørg; Erichsen, Hans Christian & Marsh, Rebecca A (2019). Allogeneic hematopoietic stem cell transplant outcomes for patients with dominant negative IKZF1/IKAROS mutations. Journal of Allergy and Clinical Immunology.  ISSN 0091-6749.  144(1), s 339- 342 . doi: 10.1016/j.jaci.2019.03.025
  • Lam, Michael T.; Coppola, Simona; Krumbach, Oliver H.F.; Prencipe, Giuseppe; Insalaco, Antonella; Cifaldi, Cristina; Brigida, Immacolata; Zara, Erika; Scala, Serena; Di Cesare, Silvia; Martinelli, Simone; Di Rocco, Martina; Pascarella, Antonia; Niceta, Marcello; Pantaleoni, Francesca; Ciolfi, Andrea; Netter, Petra; Carisey, Alexandre; Diehl, Michael; Akbarzadeh, Mohammad; Conti, Francesca; Merli, Pietro; Pastore, Anna; Mortera, Stefano Levi; Camerini, Serena; Farina, Luciapia; Buchholzer, Marcel; Pannone, Luca; Cao, Tram N.; Coban-Akdemir, Zeynep H.; Jhangiani, Shalini N.; Muzny, Donna M.; Gibbs, Richard A.; Basso-Ricci, Luca; Chiriaco, Maria; Dvorsky, Radovan; Putignani, Lorenza; Carsetti, Rita; Janning, Petra; Stray-Pedersen, Asbjørg; Erichsen, Hans Christian; Horne, AnnaCarin; Bryceson, Yenan; Torralba-Raga, Lamberto; Ramme, Kim; Rosti, Vittorio; Bracaglia, Claudia; Messia, Virginia; Palma, Paolo; Finocchi, Andrea; Locatelli, Franco; Chinn, Ivan K.; Lupski, James R.; Mace, Emily M.; Cancrini, Caterina; Aiuti, Alessandro; Ahmadian, Mohammad R.; Orange, Jordan S.; De Benedetti, Fabrizio & Tartaglia, Marco (2019). A novel disorder involving dyshematopoiesis, inflammation, and HLH due to aberrant CDC42 function. Journal of Experimental Medicine.  ISSN 0022-1007.  216(12), s 2778- 2799 . doi: 10.1084/jem.20190147
  • Volpi, Stefano; Cicalese, Maria Pia; Tuijnenburg, Paul; Tool, Anton TJ; Cuadrado, Eloy; Abu-Halaweh, Marwan; Ahanchian, Hamid; Alzyoud, Raed; Akdemir, Zeynep Coban; Barzaghi, Federica; Blank, Alexander; Boisson, Bertrand; Bottino, Cristina; Brigida, Immacolata; Caorsi, Roberta; Casanova, Jean-Laurent; Chiesa, Sabrina; Chinn, Ivan Kingyue; Duckers, Gregor; Enders, Anselm; Erichsen, Hans Christian; Forbes, Lisa R.; Gambin, Tomasz; Gattorno, Marco; Karimiani, Ehsan Ghayoor; Giliani, Silvia; Gold, Michael; Jacobsen, Eva Marie; Jansen, Machiel H; King, Jovanka R; Laxer, Ronald M; Lupski, James R.; Mace, Emily M.; Marcenaro, Stefania; Maroofian, Reza; Meijer, Alexander B.; Niehues, Tim; Notarangelo, Luigi D.; Orange, Jordan S.; Pannicke, Ulrich; Pearson, Chris; Picco, Paolo; Quinn, Patrick J; Schulz, Ansgar; Seeborg, Filiz; Stray-Pedersen, Asbjørg; Tawamie, Hasan; Van Leeuwen, Esther; Aiuti, Alessandro; Yeung, Rae S.M.; Schwarz, Klaus & Kuijpers, Taco W. (2019). A combined immunodeficiency with severe infections, inflammation, and allergy caused by ARPC1B deficiency. Journal of Allergy and Clinical Immunology.  ISSN 0091-6749.  143(6), s 2296- 2299 . doi: 10.1016/j.jaci.2019.02.003
  • Davies, E. Graham; Cheung, Melissa; Gilmour, Kimberly; Maimaris, Jesmeen; Curry, Joe; Furmanski, Anna; Sebire, Neil; Halliday, Neil; Mengrelis, Konstantinos; Adams, Stuart; Bernatoniene, Jolanta; Bremner, Ronald; Browning, Michael; Devlin, Blythe; Erichsen, Hans Christian; Gaspar, H Bobby; Hutchison, Lizzie; Ip, Winnie; Ifversen, Marianne; Leahy, T Ronan; McCarthy, Elizabeth; Moshous, Despina; Neuling, Kim; Pac, Malgorzata; Papadopol, Alina; Parsley, Kathryn L; Poliani, Luigi; Ricciardelli, Ida; Sansom, David M; Voor, Tiia; Worth, Austen; Crompton, Tessa; Markert, M Louise & Thrasher, Adrian J (2017). Thymus transplantation for complete DiGeorge syndrome: European experience. Journal of Allergy and Clinical Immunology.  ISSN 0091-6749.  140(6), s 1660- 1670.e16 . doi: 10.1016/j.jaci.2017.03.020
  • Sorte, Hanne Sørmo; Osnes, Liv T. N.; Fevang, Børre; Aukrust, Pål; Erichsen, Hans Christian; Backe, Paul Hoff; Abrahamsen, Tore G; Kittang, Ole Bjørn; Øverland, Torstein; Jhangiani, Shalini N.; Muzny, Donna M.; Vigeland, Magnus Dehli; Samarakoon, Pubudu Saneth; Gambin, Tomasz; Akdemir, Zeynep H.C.; Gibbs, Richard A.; Rødningen, Olaug Kristin; Lyle, Robert; Lupski, James R. & Stray-Pedersen, Asbjørg (2016). A potential founder variant in CARMIL2/RLTPR in three Norwegian families with warts, molluscum contagiosum, and T-cell dysfunction. Molecular Genetics & Genomic Medicine.  ISSN 2324-9269.  4(6), s 604- 616 . doi: 10.1002/mgg3.237
  • Stray-Pedersen, Asbjørg; Sorte, Hanne Sørmo; Samarakoon, Pubudu Saneth; Gambin, Tomasz; Chinn, Ivan K.; Akdemir, Zeynep H.C.; Erichsen, Hans Christian; Forbes, Lisa R.; Gu, Shen; Yuan, Bo; Jhangiani, Shalini N.; Muzny, Donna M.; Rødningen, Olaug Kristin; Sheng, Ying; Nicholas, S.; Noroski, Lenora M.; Seeborg, FO; Davis, Carla M.; Canter, Debra L.; Mace, Emily M.; Vece, Timothy J.; Allen, Carl E.; Abhyankar, Harshal A.; Boone, Philip M.; Beck, Christine R.; Wiszniewski, Wojciech; Fevang, Børre; Aukrust, Pål; Tjønnfjord, Geir Erland; Gedde-Dahl, Tobias Jr.; Hjorth-Hansen, Henrik; Dybedal, Ingunn; Nordøy, Ingvild; Jørgensen, Silje Fjellgård; Abrahamsen, Tore G; Øverland, Torstein; Bechensteen, Anne Grete; Skogen, Vegard; Osnes, Liv T. N.; Kulseth, Mari Ann; Prescott, Trine; Rustad, Cecilie; Heimdal, Ketil Riddervold; Belmont, John W.; Rider, Nicholas L.; Chinen, Javier; Cao, Tram N.; Smith, Eric A.; Caldirola, Maria Soledad; Bezrodnik, Liliana & Flatø, Berit (2016). Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders. Journal of Allergy and Clinical Immunology.  ISSN 0091-6749.  139(1), s 232- 245 . doi: 10.1016/j.jaci.2016.05.042
  • Tesi, Bianca; Lagerstedt-Robinson, Kristina; Chiang, Samuel C.C.; Bdira, Eya Ben; Abboud, Miguel; Belen, Burcu; Devecioglu, Omer; Fadoo, Zehra; Yeoh, Allen E.J.; Erichsen, Hans Christian; Möttönen, Merja; Akar, Himmet Haluk; Hästbacka, Johanna; Kaya, Zuhre; Nunes, Susana; Patiroglu, Turkan; Sabel, Magnus; Saribeyoglu, Ebru Tugrul; Tvedt, Tor Henrik Anderson; Unal, Ekrem; Unal, Sule; Unuvar, Aysegul; Meeths, Marie; Henter, Jan-Inge; Nordenskjöld, Magnus & Bryceson, Yenan (2015). Targeted high-throughput sequencing for genetic diagnostics of hemophagocytic lymphohistiocytosis. Genome Medicine.  ISSN 1756-994X.  7:130 . doi: 10.1186/s13073-015-0244-1
  • Stray-Pedersen, Asbjørg; Backe, Paul Hoff; Sorte, Hanne Sørmo; Mørkrid, Lars; Chokshi, N.Y.; Erichsen, Hans Christian; Gambin, Tomasz; Elgstøen, Katja B. Prestø; Bjørås, Magnar; Wlodarski, Marcin W.; Krüger, Marcus; Jhangiani, Shalini N.; Muzny, Donna M.; Patel, Ankita; Raymond, Kimiyo M.; Sasa, Ghadir S.; Krance, Robert A.; Martinez, Caridad A.; Abraham, Shirley M.; Speckmann, Carsten; Ehl, Stephan; Hall, Patricia; Forbes, Lisa R.; Merckoll, Else; Westvik, Jostein; Nishimura, Gen; Rustad, Cecilie; Abrahamsen, Tore G; Rønnestad, Arild Erlend; Osnes, Liv T. N.; Egeland, Torstein; Rødningen, Olaug Kristin; Beck, Christine R.; Boerwinkle, Eric A.; Gibbs, Richard A.; Lupski, James R.; Orange, Jordan S.; Lausch, Ekkehart & Hanson, I. Celine (2014). PGM3 mutations cause a congenital disorder of glycosylation with severe immunodeficiency and skeletal dysplasia. American Journal of Human Genetics.  ISSN 0002-9297.  95(1), s 96- 107 . doi: 10.1016/j.ajhg.2014.05.007

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  • Stray-Pedersen, Asbjørg; Backe, Paul Hoff; Sorte, Hanne Sørmo; Mørkrid, Lars; Chokshi, N.Y.; Erichsen, Hans Christian; Gambin, Tomasz; Elgstøen, Katja B. Prestø; Bjørås, Magnar; Wlodarski, M.W.; Krüger, M.; Jhangiani, Shalini N.; Muzny, DM; Patel, A.; Raymond, K.M.; Sasa, G. S.; Krance, R.A.; Martinez, C. A.; Abraham, S. M.; Speckmann, C.; Ehl, S.; Hall, P; Forbes, L.R.; Merckoll, Else; Westvik, Jostein; Nishimura, Gen; Rustad, C. F.; Abrahamsen, TG; Rønnestad, Arild; Osnes, LT; Egeland, T; Rødningen, OK; Beck, C.R.; Boerwinkle, E; Gibbs, R.A.; Lupski, J.R; Orange, JS; Lausch, E. & Hanson, IC (2014). A congenital disorder of glycosylation, with lymphopenia, neutropenia, and skeletal dysplasia, caused by mutations in the gene encoding phosphoglucomutase 3 (PGM3)..
  • Stray-Pedersen, Asbjørg; Sorte, Hanne Sørmo; Rødningen, Olaug Kristin; Lyle, Robert; Gonzaga-Jauregui, C G; Hanson, C I; Noroski, L M; Nicholas, S.; Erichsen, Hans Christian; Abrahamsen, Tore G; Flatø, Berit; Osnes, Liv T. N.; Heimdal, Ketil Riddervold; Undlien, Dag Erik; Lupski, J.R & Shearer, W T (2012). THE UTILITY OF EXOME SEQUENCING IN PRIMARY IMMUNODEFICIENCY DISEASES AND IMMUNODYSREGULATIVE DISORDERS. Journal of Clinical Immunology.  ISSN 0271-9142.  32(Supp. 1), s 184- 185
  • Abrahamsen, Tore G & Erichsen, Hans Christian (2007). Single Nucleotide Polymorphisms in Genes Encoding Vitamin C Transport Proteins and Inflammatory Cytokines: Risk of Colon Adenoma and Preterm Birth. Dissertation for the degree of Dr.Med.. 477. Vis sammendrag

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Publisert 12. feb. 2019 10:35 - Sist endret 12. feb. 2019 10:35

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