Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Caroline Björklund"'
Autor:
Sofia Wallin, Ingrid Øra, Gabriela Prochazka, Johanna Sandgren, Caroline Björklund, Gustaf Ljungman, Hartmut Vogt, Torben Ek, Cornelis M. van Tilburg, Anna Nilsson
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
BackgroundAdvances in treatment of childhood malignancies have improved overall cure rates to 80%. Nevertheless, cancer is still the most common cause of childhood mortality in Sweden. The prognosis is particularly poor for relapse of high-risk malig
Externí odkaz:
https://doaj.org/article/39ec050e766d45bea0317ed219e2a49c
Autor:
Daniel W. Hagey, Egle Kvedaraite, Mira Akber, André Görgens, Joman Javadi, Tatiana von Bahr Greenwood, Caroline Björklund, Selma Olsson Åkefeldt, Tova Hannegård-Hamrin, Henrik Arnell, Katalin Dobra, Nikolas Herold, Mattias Svensson, Samir EL Andaloussi, Jan-Inge Henter, Magda Lourda
Publikováno v:
Haematologica, Vol 108, Iss 9 (2023)
Langerhans cell histiocytosis (LCH) is a potentially life-threatening inflammatory myeloid neoplasia linked to pediatric neurodegeneration, whereby transformed LCH cells form agglomerated lesions in various organs. Although MAP-kinase pathway mutatio
Externí odkaz:
https://doaj.org/article/73b3716c5fc848519e01566ce7fbf090
Autor:
Susanne Fransson, Angela Martinez-Monleon, Mathias Johansson, Rose-Marie Sjöberg, Caroline Björklund, Gustaf Ljungman, Torben Ek, Per Kogner, Tommy Martinsson
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-14 (2020)
Abstract Neuroblastoma is the most common and deadly childhood tumor. Relapsed or refractory neuroblastoma has a very poor prognosis despite recent treatment advances. To investigate genomic alterations associated with relapse and therapy resistance,
Externí odkaz:
https://doaj.org/article/040e279adcf3445389b188aed659660d
Autor:
AnnaCarin Horne, Stefan Hagelberg, Stefan Berg, Tatiana von Bahr Greenwood, Maria Ekelund, Ulf Andersson, Yenan T. Bryceson, Jan-Inge Henter, Peter Erensjö, Samuel C. C. Chiang, Marie Meeths, Caroline Björklund
Publikováno v:
The Journal of Rheumatology. 48:1596-1602
ObjectiveMacrophage activation syndrome (MAS) constitutes 1 subtype of the hyperinflammatory syndrome hemophagocytic lymphohistiocytosis (HLH), and the term MAS-HLH was recently proposed for HLH with underlying autoimmune/autoinflammatory conditions.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2f7586958bb867f2bee54dc7a82f295
https://doi.org/10.3899/jrheum.200941
https://doi.org/10.3899/jrheum.200941
Autor:
Gustaf Ljungman, Per Kogner, Tommy Martinsson, Angela Martinez-Monleon, Caroline Björklund, Torben Ek, Mathias Johansson, Rose-Marie Sjöberg, Susanne Fransson
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-14 (2020)
Scientific Reports
Scientific Reports
Neuroblastoma is the most common and deadly childhood tumor. Relapsed or refractory neuroblastoma has a very poor prognosis despite recent treatment advances. To investigate genomic alterations associated with relapse and therapy resistance, whole-ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c14a0094aa5e197dd67701aeed07c2c
https://doaj.org/article/040e279adcf3445389b188aed659660d
https://doaj.org/article/040e279adcf3445389b188aed659660d
Autor:
Tore Stokland, Magnus Sabel, Benedicte Bang, Henrik Hasle, Steen Rosthøj, Miriam Entesarian, Edvard Nordenskjöld, Samuel C. C. Chiang, Magnus Nordenskjöld, Toivo T. Salmi, Caroline Björklund, Britt-Marie Holmqvist, Ljubica Rajić, Hans-Gustaf Ljunggren, Marie Meeths, Janez Jazbec, Jacek Winiarski, Yenan T. Bryceson, Susan Pfeifer, Bengt Fadeel, Stephanie M. Wood, Heinrich Schlums, Gordana Jakovljević, Jan-Inge Henter
Publikováno v:
Meeths, M, Chiang, S C C, Wood, S M, Entesarian, M, Schlums, H, Bang, B, Nordenskjöld, E, Björklund, C, Jakovljevic, G, Jazbec, J, Hasle, H, Holmqvist, B-M, Rajic, L, Pfeifer, S, Rosthøj, S, Sabel, M, Salmi, T T, Stokland, T, Winiarski, J, Ljunggren, H-G, Fadeel, B, Nordenskjöld, M, Henter, J-I & Bryceson, Y T 2011, ' Familial hemophagocytic lymphohistiocytosis type 3 (FHL3) caused by deep intronic mutation and inversion in UNC13D ', Blood, vol. 118, no. 22, pp. 5783-93 . https://doi.org/10.1182/blood-2011-07-369090
Familial hemophagocytic lymphohistiocytosis (FHL) is an autosomal recessive, often-fatal hyperinflammatory disorder. Mutations in PRF1, UNC13D, STX11, and STXBP2 are causative of FHL2, 3, 4, and 5, respectively. In a majority of suspected FHL patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8deff69498b544057c93df23874e513d
https://doi.org/10.1182/blood-2011-07-369090
https://doi.org/10.1182/blood-2011-07-369090