Zobrazeno 1 - 10
of 304
pro vyhledávání: '"G Kerndrup"'
Autor:
Carina A. Rosenberg, Mathias Hauerslev, Matthew A. Rodrigues, Marie Bill, G. Kerndrup, Maja Ludvigsen, Peter Hokland
Publikováno v:
Rosenberg, C A, Bill, M, Rodrigues, M A, Hauerslev, M, Kerndrup, G B, Hokland, P & Ludvigsen, M 2021, ' Exploring dyserythropoiesis in patients with myelodysplastic syndrome by imaging flow cytometry and machine-learning assisted morphometrics ', Cytometry. Part B: Clinical Cytometry, vol. 100, no. 5, pp. 554-567 . https://doi.org/10.1002/cyto.b.21975
BACKGROUND: The hallmark of myelodysplastic syndrome (MDS) remains dysplasia in the bone marrow (BM). However, diagnosing MDS may be challenging and subject to inter-observer variability. Thus, there is an unmet need for novel objective, standardized
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e8d2fa38a1f574f15b9e40d1ef7331a
https://pure.au.dk/portal/da/publications/exploring-dyserythropoiesis-in-patients-with-myelodysplastic-syndrome-by-imaging-flow-cytometry-and-machinelearning-assisted-morphometrics(0adc6867-29ac-4629-99dd-6cec2508e532).html
https://pure.au.dk/portal/da/publications/exploring-dyserythropoiesis-in-patients-with-myelodysplastic-syndrome-by-imaging-flow-cytometry-and-machinelearning-assisted-morphometrics(0adc6867-29ac-4629-99dd-6cec2508e532).html
Autor:
Marcus Celik Hansen, Maja Ludvigsen, Ina Kathrine Lykke Ewald, G. Kerndrup, Johannes Frasez Soerensen, Marie Bill, Peter Hokland, Lene Hyldahl Ebbesen, Anne Stidsholt Roug, Carina A. Rosenberg, Anni Aggerholm
Publikováno v:
Soerensen, J F, Aggerholm, A, Kerndrup, G B, Hansen, M C, Ewald, I K L, Bill, M, Ebbesen, L H, Rosenberg, C A, Hokland, P, Ludvigsen, M & Stidsholt Roug, A 2020, ' Clonal hematopoiesis predicts development of therapy-related myeloid neoplasms post-autologous stem cell transplantation ', Blood advances, vol. 4, no. 5, pp. 885-892 . https://doi.org/10.1182/bloodadvances.2019001157
Soerensen, J F, Aggerholm, A, Kerndrup, G B, Hansen, M C, Ewald, I K L, Bill, M, Ebbesen, L H, Rosenberg, C A, Hokland, P, Ludvigsen, M & Stidsholt Roug, A 2020, ' Clonal hematopoiesis predicts development of therapy-related myeloid neoplasms post-autologous stem cell transplantation ', Blood Advances, vol. 4, no. 5, pp. 885-892 . https://doi.org/10.1182/bloodadvances.2019001157
Soerensen, J F, Aggerholm, A, Kerndrup, G B, Hansen, M C, Ewald, I K L, Bill, M, Ebbesen, L H, Rosenberg, C A, Hokland, P, Ludvigsen, M & Stidsholt Roug, A 2020, ' Clonal hematopoiesis predicts development of therapy-related myeloid neoplasms post-autologous stem cell transplantation ', Blood Advances, vol. 4, no. 5, pp. 885-892 . https://doi.org/10.1182/bloodadvances.2019001157
Therapy-related myeloid neoplasms (tMN) develop after exposure to cytotoxic and radiation therapy, and due to their adverse prognosis, it is of paramount interest to identify patients at high risk. The presence of clonal hematopoiesis has been shown
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3dfa61d6b3a49c67ea473f48530d20e
https://vbn.aau.dk/ws/files/336993392/advancesadv2019001157.pdf
https://vbn.aau.dk/ws/files/336993392/advancesadv2019001157.pdf
Autor:
Johannes Frasez Sørensen, Maja Ludvigsen, Peter Hokland, Anne Stidsholt Roug, G. Kerndrup, Marcus Høy Hansen, Lene Hyldahl Ebbesen, Anni Aggerholm
Publikováno v:
Blood. 136:15-16
Introduction: Clonal hematopoiesis (CH) denotes somatic mutations in genes related to myeloid neoplasms present at any variant allele frequency (VAF). Clonal hematopoiesis increases the risk of cardiovascular disease, de novo myeloid neoplasms and th
Autor:
Signe Spetalen, Bernward Zeller, Ludmila Gorunova, Lil Sofie Ording Müller, Marit Hellebostad, G. Kerndrup, Anne Tierens, Sverre Heim, Ioannis Panagopoulos, Liv T. N. Osnes, Kristin Andersen
Publikováno v:
Experimental Hematology & Oncology
Background The chromosomal translocation t(11;19)(q23;p13) with a breakpoint within subband 19p13.1 is found mainly in acute myeloid leukemia (AML) and results in the MLL-ELL fusion gene. Variations in the structure of MLL-ELL seem to influence the l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3919ec18afd901039ee27ad310a15c73
http://hdl.handle.net/10852/49666
http://hdl.handle.net/10852/49666
Autor:
Mathias Hauerslev, Marie Bill, Carina A. Rosenberg, Peter Hokland, G. Kerndrup, Maja Ludvigsen
Publikováno v:
Blood. 132:5508-5508
Introduction In myelodysplastic syndrome (MDS), multicolor flow cytometry (FC) offers a supplement to the morphological, cytogenetic and molecular evaluation of the hematopoietic lineages in the bone marrow (BM). In addition to providing a robust enu
Autor:
G. Pallesen, G. Kerndrup
Publikováno v:
Scandinavian Journal of Haematology. 27:99-107
During a 4-year period 24 cases of malignant non-Hodgkin's lymphomas were proposed to be of the Burkitt-type (BL) by at least 1 of 5 pathologists of the lymphoma Registry in Jutland, Denmark. When the histological material was critically reviewed the
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 9, Iss Suppl 1, p P300 (2011)
Pediatric Rheumatology Online Journal
Pediatric Rheumatology Online Journal
Background Majeed syndrome is a rare, syndromic form of chronic recurrent multifocal osteomyelitis (CRMO) first described in 1989. The syndrome starts during infancy with recurrent relapses of osteomyelitis typically associated with fever, congenital
Autor:
Victor Pastor Loyola, Markus Schmugge, Miguel Hernandez-Marti, Albert Català, Barbara De Moerloose, Bartlomiej P Przychodzen, Jan Starý, Roos J. Leguit, Shinsuke Hirabayashi, Riccardo Masetti, G. Kerndrup, Michael Dworzak, Vit Campr, Franco Locatelli, Marek Ussowicz, Pascale Paepe, Ingrid Simonitsch-Klupp, Maureen OxSullivan, Rita Devito, Marcin W. Wlodarski, Owen P. Smith, Marry M. van den Heuvel-Eibrink, Axel Karow, Jadwiga Maldyk, Jaroslaw P. Maciejewski, Brigitte Strahm, Irith Baumann, Emilia J Kozyra, Henrik Hasle, Charlotte M. Niemeyer
Publikováno v:
Blood. 126:1662-1662
Childhood myelodysplastic syndromes (MDS) belong to a rare group of disorders of aberrant clonal hematopoiesis manifesting throughout entire childhood and adolescence. We had previously established that GATA2 germline mutations can be considered the
Autor:
G. Kerndrup, Roos J Leguit, I Baumann, V de Haas, Vit Campr, S. Behrendt, Ingrid Furlan, C.M. Niemeyer, M. Ftihrer, P. De Paepe, Judit Csomor, Stephan Schwarz, Peter Noellke
Publikováno v:
Leukemia Research. 35:S1
5q syndrome was first described in 1974 by Van den Berghe who reported the consistent association of the deletion of the long arm of chromosome 5 [del(5q)] with haematological abnormalities: macrocytosis, anaemia, normal or high platelet count and hy
Publikováno v:
British Journal of Surgery. 79:1327-1329
The ability of splenic tissue to regenerate when implanted in an isolated segment of small intestine with intact circulation was studied in six pigs. After total splenectomy, 10 per cent of the weight of the spleen was implanted in a 10–15-cm long