Works by Henter, Jan-Inge

Results: 108
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    Patients with both Langerhans cell histiocytosis and Crohn's disease highlight a common role of interleukin‐23.

    Published in:
    Acta Paediatrica, 2021, v. 110, n. 4, p. 1315, doi. 10.1111/apa.15590
    By:
    • Kvedaraite, Egle;
    • Lourda, Magda;
    • Han, HongYa;
    • Tesi, Bianca;
    • Mitchell, Jenée;
    • Ideström, Maja;
    • Mouratidou, Natalia;
    • Rassidakis, George;
    • Bahr Greenwood, Tatiana;
    • Cohen‐Aubart, Fleur;
    • Jädersten, Martin;
    • Åkefeldt, Selma Olsson;
    • Svensson, Mattias;
    • Kannourakis, George;
    • Bryceson, Yenan T.;
    • Haroche, Julien;
    • Henter, Jan‐Inge
    Publication type:
    Article
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    The need for worldwide policy and action plans for rare diseases.

    Published in:
    Acta Paediatrica, 2012, v. 101, n. 8, p. 805, doi. 10.1111/j.1651-2227.2012.02705.x
    By:
    • Forman, John;
    • Taruscio, Domenica;
    • Llera, Virginia A.;
    • Barrera, Luis A.;
    • Coté, Timothy R.;
    • Edfjäll, Catarina;
    • Gavhed, Désirée;
    • Haffner, Marlene E.;
    • Nishimura, Yukiko;
    • Posada, Manuel;
    • Tambuyzer, Erik;
    • Groft, Stephen C.;
    • Henter, Jan-Inge
    Publication type:
    Article
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    HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease).

    Published in:
    Nature Genetics, 2007, v. 39, n. 1, p. 86, doi. 10.1038/ng1940
    By:
    • Klein, Christoph;
    • Grudzien, Magda;
    • Appaswamy, Giridharan;
    • Germeshausen, Manuela;
    • Sandrock, Inga;
    • Schäffer, Alejandro A.;
    • Rathinam, Chozhavendan;
    • Boztug, Kaan;
    • Schwinzer, Beate;
    • Rezaei, Nima;
    • Bohn, Georg;
    • Melin, Malin;
    • Carlsson, Göran;
    • Fadeel, Bengt;
    • Dahl, Niklas;
    • Palmblad, Jan;
    • Henter, Jan-Inge;
    • Zeidler, Cornelia;
    • Grimbacher, Bodo;
    • Welte, Karl
    Publication type:
    Article
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    2016 Classification Criteria for Macrophage Activation Syndrome Complicating Systemic Juvenile Idiopathic Arthritis: A European League Against Rheumatism/American College of Rheumatology/Paediatric Rheumatology International Trials Organisation Collaborative Initiative

    Published in:
    Arthritis & Rheumatology, 2016, v. 68, n. 3, p. 566, doi. 10.1002/art.39332
    By:
    • Ravelli, Angelo;
    • Minoia, Francesca;
    • Davì, Sergio;
    • Horne, AnnaCarin;
    • Bovis, Francesca;
    • Pistorio, Angela;
    • Aricò, Maurizio;
    • Avcin, Tadej;
    • Behrens, Edward M.;
    • De Benedetti, Fabrizio;
    • Filipovic, Lisa;
    • Grom, Alexei A.;
    • Henter, Jan‐Inge;
    • Ilowite, Norman T.;
    • Jordan, Michael B.;
    • Khubchandani, Raju;
    • Kitoh, Toshiyuki;
    • Lehmberg, Kai;
    • Lovell, Daniel J.;
    • Miettunen, Paivi
    Publication type:
    Article
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    Response to mitogen‐activated protein kinase inhibition of neurodegeneration in Langerhans cell histiocytosis monitored by cerebrospinal fluid neurofilament light as a biomarker: a pilot study.

    Published in:
    British Journal of Haematology, 2022, v. 196, n. 1, p. 248, doi. 10.1111/bjh.17781
    By:
    • Henter, Jan‐Inge;
    • Kvedaraite, Egle;
    • Martín Muñoz, Daniel;
    • Cheng Munthe‐Kaas, Monica;
    • Zeller, Bernward;
    • Nystad, Tove A.;
    • Björklund, Caroline;
    • Donnér, Isabella;
    • Lourda, Magda;
    • Zetterberg, Henrik;
    • Blennow, Kaj;
    • Herold, Nikolas;
    • Gavhed, Désirée;
    • von Bahr Greenwood, Tatiana
    Publication type:
    Article
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    Clinical presentation of Griscelli syndrome type 2 and spectrum of RAB27A mutations.

    Published in:
    Pediatric Blood & Cancer, 2010, v. 54, n. 4, p. 563, doi. 10.1002/pbc.22357
    By:
    • Meeths, Marie;
    • Bryceson, Yenan T.;
    • Rudd, Eva;
    • Zheng, Chengyun;
    • Wood, Stephanie M.;
    • Ramme, Kim;
    • Beutel, Karin;
    • Hasle, Henrik;
    • Heilmann, Carsten;
    • Hultenby, Kjell;
    • Ljunggren, Hans-Gustaf;
    • Fadeel, Bengt;
    • Nordenskjöld, Magnus;
    • Henter, Jan-Inge
    Publication type:
    Article
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    Chondrodysplasia and growth failure in children after early hematopoietic stem cell transplantation for non‐oncologic disorders.

    Published in:
    American Journal of Medical Genetics. Part A, 2021, v. 185, n. 2, p. 517, doi. 10.1002/ajmg.a.62021
    By:
    • Botto, Lorenzo D.;
    • Meeths, Marie;
    • Campos‐Xavier, Belinda;
    • Bergamaschi, Rosalba;
    • Mazzanti, Laura;
    • Scarano, Emanuela;
    • Finocchi, Andrea;
    • Cancrini, Caterina;
    • Zirn, Birgit;
    • Kühnle, Ingrid;
    • Kramm, Christof Maria;
    • Alanay, Yasemin;
    • Jones, Wendy D.;
    • Irving, Melita;
    • Sabir, Ataf;
    • Henter, Jan‐Inge;
    • Borgström, Birgit;
    • Nordgren, Ann;
    • Hammarsjö, Anna;
    • Putti, Caterina
    Publication type:
    Article
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