Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Michaël V. Lukens"'
Autor:
Anouk M. La Rose, Venetia Bazioti, Joanne A. Hoogerland, Arthur F. Svendsen, Anouk G. Groenen, Martijn van Faassen, Martijn G.S. Rutten, Niels J. Kloosterhuis, Bertien Dethmers-Ausema, J. Hendrik Nijland, Gilles Mithieux, Fabienne Rajas, Folkert Kuipers, Michaël V. Lukens, Oliver Soehnlein, Maaike H. Oosterveer, Marit Westerterp
Publikováno v:
Molecular Metabolism, Vol 53, Iss , Pp 101265- (2021)
Objective: Glycogen storage disease type 1a (GSD Ia) is a rare inherited metabolic disorder caused by mutations in the glucose-6-phosphatase (G6PC1) gene. When untreated, GSD Ia leads to severe fasting-induced hypoglycemia. Although current intensive
Externí odkaz:
https://doaj.org/article/96f72353a8d648dbb58c1f3c0cd8e578
Autor:
Louise H Hooimeijer MD, Marjet A Stein-Wit MD, Marja AJ Voskuilen RN, Michaël V Lukens PhD, Karina Meijer MD, PhD, Anja BU Mäkelburg MD, PhD, Rienk YJ Tamminga MD, PhD
Publikováno v:
Clinical and Applied Thrombosis/Hemostasis, Vol 29 (2023)
In 2018, Refacto AF R , a B-domain-deleted third-generation FVIII concentrate, became our preferential product. After the introduction, the development of inhibitors was prospectively monitored; retrospectively, we sought for risk factors in the pati
Externí odkaz:
https://doaj.org/article/940ec3bfb93740f6aef3d62772b9fb28
Autor:
Isidor Minović, Martin R. Schipperus, Anja B. U. Mäkelburg, Kornelis Meijer, Michaël V. Lukens, Jenny E. Kootstra‐Ros, Frans van der Heide, Ilhama Abbasova, Ruben H. J. de Kleine, Johan H. Meekers, André B. Mulder
Publikováno v:
British Journal of Haematology, 200(1), 109-112. Wiley
Autor:
Mirthe H. Links, Joop D. Lefrandt, Ton Lisman, Trynke van der Boom, Michaël V. Lukens, Karina Meijer, Thera P. Links, Wouter T. Zandee
Publikováno v:
Thyroid, 33(2), 203-213. MARY ANN LIEBERT, INC
BACKGROUND: During treatment for differentiated thyroid carcinoma (DTC) patients go from euthyroidism to severe hypothyroidism to subclinical hyperthyroidism induced by thyroid hormone suppression therapy (THST). Severe hypothyroidism may induce a te
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8cbcc78ce867640e64d20472ecfd749
https://research.rug.nl/en/publications/dbfa9959-9eaa-42f5-b2c8-29d8699517dc
https://research.rug.nl/en/publications/dbfa9959-9eaa-42f5-b2c8-29d8699517dc
Autor:
Michaël V. Lukens, Martine J. Hollestelle, Piet Meijer, Sjef J van de Leur, Nathalie C. V. Péquériaux, Moniek P.M. de Maat, Ryanne A Arisz
Publikováno v:
International Journal of Laboratory Hematology, 44(2), 407-413. Wiley-Blackwell Publishing Ltd
International journal of laboratory hematology, 44(2), 407-413. Wiley
International journal of laboratory hematology, 44(2), 407-413. Wiley
Introduction: The high incidence of thrombotic events in patients with COVID-19 affects health care worldwide and results in an increased workload in haemostasis laboratories due to more frequent testing of D-dimer, haemostatic parameters and anti-Xa
Autor:
Sophie Wiewel-Verschueren, Janny H. Dekker, Karina Meijer, Joep W van Borselen, Marlies Y. Bongers, Michaël V. Lukens, Pleun Beelen, Marian J van den Brink
Publikováno v:
Haemophilia, 27(6):14392, E756-E759. Wiley
Haemophilia, 27(6):14392, e756-e759. Wiley
Haemophilia, 27(6):14392, e756-e759. Wiley
Autor:
Bertien Dethmers-Ausema, Niels J. Kloosterhuis, Folkert Kuipers, Gilles Mithieux, Anouk M. La Rose, Martijn G S Rutten, Oliver Soehnlein, Joanne A Hoogerland, J Hendrik Nijland, Marit Westerterp, Fabienne Rajas, Maaike H. Oosterveer, Arthur Flohr Svendsen, Venetia Bazioti, Michaël V. Lukens, Martijn van Faassen, Anouk G. Groenen
Publikováno v:
Molecular metabolism
Molecular metabolism, Elsevier, 2021, pp.101265. ⟨10.1016/j.molmet.2021.101265⟩
Molecular metabolism, 53:101265, 1-14. ELSEVIER SCIENCE BV
Molecular Metabolism, Vol 53, Iss, Pp 101265-(2021)
Molecular Metabolism
Molecular metabolism, Elsevier, 2021, pp.101265. ⟨10.1016/j.molmet.2021.101265⟩
Molecular metabolism, 53:101265, 1-14. ELSEVIER SCIENCE BV
Molecular Metabolism, Vol 53, Iss, Pp 101265-(2021)
Molecular Metabolism
Objective Glycogen storage disease type 1a (GSD Ia) is a rare inherited metabolic disorder caused by mutations in the glucose-6-phosphatase (G6PC1) gene. When untreated, GSD Ia leads to severe fasting-induced hypoglycemia. Although current intensive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0fee94b82da6e1129feb4ffc5aac411
https://www.hal.inserm.fr/inserm-03257584/document
https://www.hal.inserm.fr/inserm-03257584/document
Autor:
Jessie S Luken, Jaap Jan Zwaginga, Johanna G. van der Bom, Mart P. Janssen, Peter C. Ligthart, Henk Schonewille, Claudia C. Folman, Masja de Haas, C. Ellen van der Schoot, Johan H Meekers, Michaël V. Lukens
Publikováno v:
Transfusion, 1-9. Wiley
STARTPAGE=1;ENDPAGE=9;ISSN=0041-1132;TITLE=Transfusion
Transfusion, 61(3), 713-721. WILEY
Transfusion
Transfusion, 61(3), 713-721. Wiley-Blackwell
STARTPAGE=1;ENDPAGE=9;ISSN=0041-1132;TITLE=Transfusion
Transfusion, 61(3), 713-721. WILEY
Transfusion
Transfusion, 61(3), 713-721. Wiley-Blackwell
Background: During pregnancy, maternal red blood cell (RBC) antibodies can lead to life-threatening fetal hemolysis and anemia. Women can become immunized by a pregnancy or an unmatched transfusion. Our aim was to quantify the effect of a nationwide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d01c5459194d31f0f7afd204c705d79
https://research.rug.nl/en/publications/ea473598-2bd4-44e1-b059-9c54526ac76a
https://research.rug.nl/en/publications/ea473598-2bd4-44e1-b059-9c54526ac76a
Publikováno v:
Thrombosis and Haemostasis, 121(2), 242-245. GEORG THIEME VERLAG KG
Autor:
Martijn V Verhagen, Helene L. Hooimeijer, Michaël V. Lukens, Marjet A Stein-Wit, Rienk Y. J. Tamminga, Karina Meijer
Publikováno v:
Haemophilia, 26(3), e138-e140. Wiley