Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Julie Damgaard Sandahl"'
Autor:
Julie Damgaard Sandahl, Eva A. Coenen, Erik Forestier, Jochen Harbott, Bertil Johansson, Gitte Kerndrup, Souichi Adachi, Anne Auvrignon, H. Berna Beverloo, Jean-Michel Cayuela, Lucy Chilton, Maarten Fornerod, Valérie de Haas, Christine J. Harrison, Hiroto Inaba, Gertjan J.L. Kaspers, Der-Cherng Liang, Franco Locatelli, Riccardo Masetti, Christine Perot, Susana C. Raimondi, Katarina Reinhardt, Daisuke Tomizawa, Nils von Neuhoff, Marco Zecca, C. Michel Zwaan, Marry M. van den Heuvel-Eibrink, Henrik Hasle
Publikováno v:
Haematologica, Vol 99, Iss 5 (2014)
Acute myeloid leukemia with t(6;9)(p22;q34) is listed as a distinct entity in the 2008 World Health Organization classification, but little is known about the clinical implications of t(6;9)-positive myeloid leukemia in children. This international m
Externí odkaz:
https://doaj.org/article/c2981595332d4bc2ba894d8103bc04b6
Autor:
Barbara De Moerloose, Ninna Bager, Zhanna Kovalova, Berna Beverloo, Bernward Zeller, Eigil Kjeldsen, Julie Damgaard Sandahl, Birgitte Lausen, Olafur G. Jonsson, Eveline S. J. M. de Bont, Kirsi Jahnukainen, Henrik Hasle, Gertjan L. Kaspers, Kadri Saks, Josefine Palle, Ulrika Norén-Nyström, Kristian Løvvik Juul-Dam, Shau-Yin Ha, Jonas Abrahamsson
Publikováno v:
British Journal of Haematology, 183(4), 618-628. Wiley-Blackwell Publishing Ltd
Bager, N, Juul-Dam, K L, Sandahl, J D, Abrahamsson, J, Beverloo, B, de Bont, E S J M, Ha, S-Y, Jahnukainen, K, Jónsson, Ó G, Kaspers, G L, Kovalova, Z, Lausen, B, de Moerloose, B, Noren-Nyström, U, Palle, J, Saks, K, Zeller, B, Kjeldsen, E & Hasle, H 2018, ' Complex and monosomal karyotype are distinct cytogenetic entities with an adverse prognostic impact in paediatric acute myeloid leukaemia. A NOPHO-DBH-AML study ', British Journal of Haematology, vol. 183, no. 4, pp. 618-628 . https://doi.org/10.1111/bjh.15587
Bager, N, Juul-Dam, K L, Sandahl, J D, Abrahamsson, J, Beverloo, B, de Bont, E S J M, Ha, S-Y, Jahnukainen, K, Jónsson, Ó G, Kaspers, G L, Kovalova, Z, Lausen, B, De Moerloose, B, Noren-Nyström, U, Palle, J, Saks, K, Zeller, B, Kjeldsen, E & Hasle, H 2018, ' Complex and monosomal karyotype are distinct cytogenetic entities with an adverse prognostic impact in paediatric acute myeloid leukaemia. A NOPHO-DBH-AML study ', British Journal of Haematology, vol. 183, no. 4, pp. 618-628 . https://doi.org/10.1111/bjh.15587
British Journal of Haematology, 183(4), 618-628. Wiley
British Journal of Haematology, 183(4), 618-628. Wiley-Blackwell
Bager, N, Juul-Dam, K L, Sandahl, J D, Abrahamsson, J, Beverloo, B, de Bont, E S J M, Ha, S-Y, Jahnukainen, K, Jónsson, Ó G, Kaspers, G L, Kovalova, Z, Lausen, B, de Moerloose, B, Noren-Nyström, U, Palle, J, Saks, K, Zeller, B, Kjeldsen, E & Hasle, H 2018, ' Complex and monosomal karyotype are distinct cytogenetic entities with an adverse prognostic impact in paediatric acute myeloid leukaemia. A NOPHO-DBH-AML study ', British Journal of Haematology, vol. 183, no. 4, pp. 618-628 . https://doi.org/10.1111/bjh.15587
Bager, N, Juul-Dam, K L, Sandahl, J D, Abrahamsson, J, Beverloo, B, de Bont, E S J M, Ha, S-Y, Jahnukainen, K, Jónsson, Ó G, Kaspers, G L, Kovalova, Z, Lausen, B, De Moerloose, B, Noren-Nyström, U, Palle, J, Saks, K, Zeller, B, Kjeldsen, E & Hasle, H 2018, ' Complex and monosomal karyotype are distinct cytogenetic entities with an adverse prognostic impact in paediatric acute myeloid leukaemia. A NOPHO-DBH-AML study ', British Journal of Haematology, vol. 183, no. 4, pp. 618-628 . https://doi.org/10.1111/bjh.15587
British Journal of Haematology, 183(4), 618-628. Wiley
British Journal of Haematology, 183(4), 618-628. Wiley-Blackwell
Data on occurrence, genetic characteristics and prognostic impact of complex and monosomal karyotype (CK/MK) in children with acute myeloid leukaemia (AML) are scarce. We studied CK and MK in a large unselected cohort of childhood AML patients diagno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a9e5916363a37e49a2149640bc18903
https://doi.org/10.1111/bjh.15587
https://doi.org/10.1111/bjh.15587
Autor:
Julie Damgaard Sandahl, Eigil Kjeldsen, Jonas Abrahamsson, Henrik Hasle, Peter H. Asdahl, Kirsi Jahnukainen, Bernward Zeller, Olafur G. Jonsson, Erik Forestier, Josefine Palle, Jesper Heldrup, Birgitte Lausen, Anne Cathrine Lund Laursen, Shau Yin Ha
Publikováno v:
Genes, Chromosomes and Cancer. 55:719-726
Trisomy 8 (+8) is a common cytogenetic aberration in acute myeloid leukemia (AML); however, the impact of +8 in pediatric AML is largely unknown. We retrospectively investigated 609 patients from t ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::05af52d4c2c3fcb2e11847e951bebe45
https://doi.org/10.1002/gcc.22373
https://doi.org/10.1002/gcc.22373
Autor:
Julie Damgaard Sandahl, Riccardo Masetti, Mareike Rasche, Dirk Reinhardt, Gabor G. Kovacs, Susana C. Raimondi, Franco Locatelli, Henrik Hasle, Kristian Løvvik Juul-Dam, Jonas Abrahamsson, Guy Leverger, Ulrika Norén-Nyström, E. Anders Kolb, Bernward Zeller, Eigil Kjeldsen, Kirsi Jahnukainen, Daisuke Tomizawa, Anne Hammer, Walentyna Balwierz, Irén Haltrich, Tomohiko Taki, Audrey Guilmatre
Publikováno v:
Hammer, A S B, Juul-Dam, K L, Sandahl, J D, Hasle, H & Kjeldsen, E 2018, ' Hypodiploidy in Childhood Acute Myeloid Leukemia: A Retrospective Cohort Study within the International Berlin-Frankfurt-Münster Study Group ' . https://doi.org/10.1182/blood-2018-99-109988
Background: Despite major improvements in survival, relapse is still a frequent and severe event in pediatric acute myeloid leukemia (AML). Cytogenetic abnormalities represent important predictors of outcome. Improved risk stratification encompassing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8df69d747083e9c9e4df8529f42ebc3
https://pure.au.dk/portal/da/publications/hypodiploidy-in-childhood-acute-myeloid-leukemia-a-retrospective-cohort-study-within-the-international-berlinfrankfurtmunster-study-group(1271c67a-d38f-4b7a-883e-39075507b166).html
https://pure.au.dk/portal/da/publications/hypodiploidy-in-childhood-acute-myeloid-leukemia-a-retrospective-cohort-study-within-the-international-berlinfrankfurtmunster-study-group(1271c67a-d38f-4b7a-883e-39075507b166).html
Autor:
Julie Damgaard Sandahl, Hélène Bruyère
Publikováno v:
Atlas of Genetics and Cytogenetics in Oncology and Haematology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d5784deab5846a381ac59f438336f4c
https://doi.org/10.4267/2042/68740
https://doi.org/10.4267/2042/68740
Autor:
Julie Damgaard Sandahl, Henrik Hasle
Publikováno v:
Atlas of Genetics and Cytogenetics in Oncology and Haematology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::50e82c4c90af0a6a61a2c0bd77a963c9
https://doi.org/10.4267/2042/68533
https://doi.org/10.4267/2042/68533
Autor:
Kirsi Jahnukainen, Shau-Yin Ha, Josefine Palle, Eigil Kjeldsen, Olafur G. Jonsson, Erik Forestier, Bernward Zeller, Jesper Heldrup, Jonas Abrahamsson, Birgitte Lausen, Julie Damgaard Sandahl, Henrik Hasle
Publikováno v:
Sandahl, J D, Kjeldsen, E, Abrahamsson, J, Ha, S-Y, Heldrup, J, Jahnukainen, K, Jónsson, Ó G, Lausen, B, Palle, J, Zeller, B, Forestier, E & Hasle, H 2015, ' The applicability of the WHO classification in paediatric AML. A NOPHO-AML study ', British Journal of Haematology, vol. 169, no. 6, pp. 859-67 . https://doi.org/10.1111/bjh.13366
The World Health Organization (WHO) classification of myeloid leukaemia was revised in 2008. It incorporates newly recognized entities and emphasizes the pivotal role of cytogenetic abnormalities. The aim of this study was to evaluate the usability o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a92a83cea3d78527af67facab8c6b1da
https://doi.org/10.1111/bjh.13366
https://doi.org/10.1111/bjh.13366
Autor:
Julie Damgaard Sandahl, Henrik Hasle, Erik Forestier, Bernward Zeller, Jesper Heldrup, Shau-Yin Ha, Kirsi Jahnukainen, Jonas Abrahamsson, Eigil Kjeldsen, Birgitte Lausen, Olafur G. Jonsson, Josefine Palle
Publikováno v:
Genes, Chromosomes and Cancer. 53:667-675
We report the first large series (n=596) of pediatric acute myeloid leukemia (AML) focusing on modal numbers (MN) from the population-based NOPHO-AML trials. Abnormal karyotypes were present in 452 ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::411a800a48afa9b94bea3e2ad620b69d
https://doi.org/10.1002/gcc.22177
https://doi.org/10.1002/gcc.22177
Autor:
Erik Forestier, Kirsi Jahnukainen, Heidi Kristine Støve, Josefine Palle, Julie Damgaard Sandahl, Henrik Hasle, Bernward Zeller, Shau-Yin Ha, Jonas Abrahamsson, Peter H. Asdahl, Olafur G. Jonsson, Birgitte Lausen
Publikováno v:
Støve, H K, Sandahl, J D, Abrahamsson, J, Asdahl, P H, Forestier, E, Ha, S-Y, Jahnukainen, K, Jonsson, O G, Lausen, B, Palle, J, Zeller, B & Hasle, H 2017, ' Extramedullary leukemia in children with acute myeloid leukemia : A population-based cohort study from the Nordic Society of Pediatric Hematology and Oncology (NOPHO) ', Pediatric Blood & Cancer, vol. 64, no. 12 . https://doi.org/10.1002/pbc.26520
BACKGROUND: The prognostic significance of extramedullary leukemia (EML) in childhood acute myeloid leukemia is not clarified.PROCEDURE: This population-based study included 315 children from the NOPHO-AML 2004 trial.RESULTS: At diagnosis, 73 (23%) p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7960ad936981649bf09885f7ad3068d5
https://pure.au.dk/portal/da/publications/extramedullary-leukemia-in-children-with-acute-myeloid-leukemia(e9084606-353c-4794-bbab-a728ac43d0db).html
https://pure.au.dk/portal/da/publications/extramedullary-leukemia-in-children-with-acute-myeloid-leukemia(e9084606-353c-4794-bbab-a728ac43d0db).html
Autor:
Anne Cathrine Lund, Laursen, Julie Damgaard, Sandahl, Eigil, Kjeldsen, Jonas, Abrahamsson, Peter, Asdahl, Shau-Yin, Ha, Jesper, Heldrup, Kirsi, Jahnukainen, Ólafur G, Jónsson, Birgitte, Lausen, Josefine, Palle, Bernward, Zeller, Erik, Forestier, Henrik, Hasle
Publikováno v:
Genes, chromosomescancer. 55(9)
Trisomy 8 (+8) is a common cytogenetic aberration in acute myeloid leukemia (AML); however, the impact of +8 in pediatric AML is largely unknown. We retrospectively investigated 609 patients from the NOPHO-AML database to determine the clinical and c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::96da51e5203aeed6a68b32c12ac30646
https://pubmed.ncbi.nlm.nih.gov/27153159
https://pubmed.ncbi.nlm.nih.gov/27153159