Nadine Gretenkort Andersson

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2022
Mark Long-term joint outcomes in adolescents with moderate or severe haemophilia A
Schmidt, David E. ; Michalopoulou, Aikaterini ; Fischer, Kathelijn ; Motwani, Jayashree ; Andersson, Nadine G. ^LU ; Pergantou, Helen and Ranta, Susanna (2022) In Haemophilia 28(6). p.1054-1061
- Contribution to journal › Article
Mark Factor IX antibodies and tolerance in hemophilia B in the Nordic countries - The impact of F9 variants and complications
Kihlberg, Kristina ^LU ; Baghaei, Fariba ; Bruzelius, Maria ; Funding, Eva ^LU ; Holme, Pål Andre ; Lassila, Riitta ; Martin, Myriam ^LU ; Nummi, Vuokko ^LU ; Ranta, Susanna and Strandberg, Karin ^LU , et al. (2022) In Thrombosis Research 217. p.22-32
- Contribution to journal › Article
Mark Silent variant in F8:c.222G>T (p.Thr74Thr) causes a partial exon skipping in a patient with mild hemophilia A
Letelier, Anna ^LU ; Ljung, Rolf ^LU ; Olsson, Anna and Andersson, Nadine G ^LU (2022) In Molecular Genetics & Genomic Medicine 10(1).
- Contribution to journal › Article
2021
Mark Inhibitor incidence in an unselected cohort of previously untreated patients with severe haemophilia B : a PedNet study
Male, Christoph ; Andersson, Nadine G ^LU ; Rafowicz, Anne ; Liesner, Ri ; Kurnik, Karin ; Fischer, Kathelijn ; Platokouki, Helen ; Santagostino, Elena ; Chambost, Hervé and Nolan, Beatrice , et al. (2021) In Haematologica 106(1). p.123-129
- Contribution to journal › Article
2020
Mark Genetic screening of children with suspected inherited bleeding disorders
Andersson, Nadine ^LU ; Rossing, Maria ; Fager Ferrari, Marcus ^LU ; Gabrielaite, Migle ; Leinøe, Eva ; Ljung, Rolf ^LU ; Mårtensson, Annika ^LU ; Norström, Eva ^LU and Zetterberg, Eva ^LU (2020) In Haemophilia 26(2). p.314-324
- Contribution to journal › Article
Mark Novel F8 and F9 gene variants from the PedNet Hemophilia Registry classified according to ACMG/AMP guidelines
Andersson, Nadine G ^LU ; Labarque, Veerle ; Letelier, Anna ^LU ; Mancuso, Maria Elisa ; Bührlen, Martina ; Fischer, Kathelijn ; Kartal-Kaess, Mutlu ; Koskenvuo, Minna ; Mikkelsen, Torben and Ljung, Rolf ^LU (2020) In Human Mutation 41(12). p.2058-2072
- Contribution to journal › Article
Mark Long-term follow-up of neonatal intracranial haemorrhage in children with severe haemophilia
Andersson, Nadine G ^LU ; Wu, Runhui ; Carcao, Manuel ; Claeyssens-Donadel, Ségolène ; Kobelt, Rainer ; Liesner, Ri ; Mäkipernaa, Anne ; Ranta, Susanna and Ljung, Rolf ^LU (2020) In British Journal of Haematology 190(2). p.101-104
- Contribution to journal › Letter
Mark Asymptomatic Right Atrial Thrombosis After Acute Lymphoblastic Leukemia Treatment
Jarvis, Kirsten B ; Andersson, Nadine G ^LU ; Giertz, Mia ; Järvelä, Liisa ; Lindinger, Olle ; Långström, Satu ; Niinimäki, Riitta ; Palmu, Sauli ; Trakymiene, Sonata S and Tuckuviene, Ruta , et al. (2020) In Journal of Pediatric Hematology/Oncology
- Contribution to journal › Article
2019
Mark Mode of delivery in hemophilia : Vaginal delivery and Cesarean section carry similar risks for intracranial hemorrhages and other major bleeds
Andersson, Nadine G ^LU ; Chalmers, Elizabeth A ; Kenet, Gili ; Ljung, Rolf ^LU ; Mäkipernaa, Anne and Chambost, Hervé (2019) In Haematologica 104(10). p.2100-2106
- Contribution to journal › Article
Mark A simplified flow cytometric method for detection of inherited platelet disorders—A comparison to the gold standard light transmission aggregometry
Navred, Kristoffer ; Martin, Myriam ^LU ; Ekdahl, Lina ; Zetterberg, Eva ^LU ; Andersson, Nadine Gretenkort ^LU ; Strandberg, Karin ^LU and Norstrom, Eva ^LU (2019) In PLoS ONE 14(1).
- Contribution to journal › Article