Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Karin P. M. van Galen"'
Autor:
Ferdows Atiq, Johan Boender, Waander L. van Heerde, Juan M. Tellez Garcia, Selene C. Schoormans, Sandy Krouwel, Marjon H. Cnossen, Britta A. P. Laros-van Gorkom, Joke de Meris, Karin Fijnvandraat, Johanna G. van der Bom, Karina Meijer, Karin P. M. van Galen, Jeroen Eikenboom, Frank W. G. Leebeek, for the WiN Study Group
Publikováno v:
HemaSphere, Vol 6, Iss 6, p e718 (2022)
Genotyping is not routinely performed at diagnosis of von Willebrand disease (VWD). Therefore, the association between genetic variants and pathogenic mechanism or the clinical and laboratory phenotype is unknown in most patients, especially in type
Externí odkaz:
https://doaj.org/article/b94cb49d3709414589c99a1f377839d1
Autor:
Wobke E. M. van Dijk, Robert J. J. van Es, Maria E. P. Correa, Roger E. G. Schutgens, Karin P. M. van Galen
Publikováno v:
TH Open, Vol 05, Iss 04, Pp e489-e502 (2021)
Background Dentoalveolar procedures in immune thrombocytopenia (ITP) pose a risk of bleeding due to thrombocytopenia and infection due to immunosuppressive treatments. We aimed to systematically review the safety and management of dentoalveolar proce
Externí odkaz:
https://doaj.org/article/1975cd99e95b4cb3988950abdc64553e
Autor:
Johan Boender, Ferdows Atiq, Marjon H. Cnossen, Johanna G. van der Bom, Karin Fijnvandraat, Joke de Meris, Moniek P. M. de Maat, Karin P. M. van Galen, Britta A. P. Laros-van Gorkom, Karina Meijer, Jeroen Eikenboom, Frank W. G. Leebeek, for the WiN study group
Publikováno v:
HemaSphere, Vol 5, Iss 3, p e542 (2021)
Von Willebrand factor (VWF) multimer analysis is important in the classification of von Willebrand disease (VWD). Current visual VWF multimer analysis is time consuming and inaccurate in detecting subtle changes in multimer patterns. Although VWF mul
Externí odkaz:
https://doaj.org/article/9417f6e0e8384b96a65c589f3b60f36d
Autor:
Olav Versloot, Ellen Kemler, Johan Blokzijl, Merel Timmer, Marleen Schuuring, Karin P. M. van Galen, Idske Cornelia L. Kremer Hovinga, Paul R. van der Valk, Lize F. D. van Vulpen, Roger E. G. Schutgens, Casper F. van Koppenhagen, Janjaap van der Net, Kathelijn Fischer
Publikováno v:
Haemophilia.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::535aecae77710b8bfecba82dd41ff22f
https://doi.org/10.1111/hae.14800
https://doi.org/10.1111/hae.14800
Autor:
Maria Elvira Pizzigatti Correa, Wobke E. M. van Dijk, Roger E. G. Schutgens, Karin P M van Galen, Robert J.J. van Es
Publikováno v:
TH Open, Vol 05, Iss 04, Pp e489-e502 (2021)
TH Open: Companion Journal to Thrombosis and Haemostasis
TH Open: Companion Journal to Thrombosis and Haemostasis
Background Dentoalveolar procedures in immune thrombocytopenia (ITP) pose a risk of bleeding due to thrombocytopenia and infection due to immunosuppressive treatments. We aimed to systematically review the safety and management of dentoalveolar proce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5392855f01f12a6beac4a2cf46f7b1ec
https://doi.org/10.1055/a-1641-7770
https://doi.org/10.1055/a-1641-7770
Autor:
Catherine Bagot, Allied Disorders, Michelle Lavin, Ellen van Loon, Debra Pollard, Roseline d'Oiron, Rezan Abdul-Kadir, Petra Elfvinge, Declan Noone, Eveline P. Mauser-Bunschoten, Krista Fischer, Naja Skouw-Rasmussen, Keith Gomez, Karin P M van Galen, Kate Khair
Publikováno v:
Haemophilia. 27:837-847
Introduction Despite increasing awareness of issues faced by women and girls with inherited BDs (WGBD), standards of care are lacking, with disparities in diagnosis and treatment for WGBD across Europe. We aimed to develop practical principles of car
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48e3c3dd7a32b299299ee5cc4a1af272
https://doi.org/10.1111/hae.14379
https://doi.org/10.1111/hae.14379
Autor:
Roshni Kulkarni, Karin P M van Galen, Maha Othman, Robert F. Sidonio, Paula D. James, Dawn Rotellini, Rezan Abdul-Kadir, Roseline d'Oiron, Peter A. Kouides, Flora Peyvandi, Johnny Mahlangu, Rochelle Winikoff
Publikováno v:
Journal of Thrombosis and Haemostasis
Hemophilia A and B predominantly attracts clinical attention in males due to X‐linked inheritance, introducing a bias toward female carriers to be asymptomatic. This common misconception is contradicted by an increasing body of evidence with consis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d425820a7cf4bc0e8ab6475292631f11
http://europepmc.org/articles/PMC8361713
http://europepmc.org/articles/PMC8361713
Autor:
Wobke E. M. van Dijk, Marieke C. Punt, Karin P. M. van Galen, Jeanette van Leeuwen, A. Titia Lely, Roger E. G. Schutgens
Publikováno v:
British journal of haematology. 198(4)
Immune thrombocytopenia (ITP) may cause menstrual problems. This cross-sectional study assessed menstrual problems in premenopausal chronic ITP women by several questionnaires, including the pictorial bleeding assessment calendar (PBAC; score ≥100
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe984b9f38a108de1f117097af61f799
https://pubmed.ncbi.nlm.nih.gov/35662003
https://pubmed.ncbi.nlm.nih.gov/35662003
Autor:
Roseline d'Oiron, Ellen Laan, Karin P M van Galen, Eveline P. Mauser-Bunschoten, Lotte Haverman, Manon E L Degenaar, Dietje E. Fransen van de Putte, Rezan A. Kadir, Petra Elfvinge, Lorynn Teela
Publikováno v:
Haemophilia, 27(3), 463-469. Wiley-Blackwell
Haemophilia
Haemophilia
Introduction Multidisciplinary management of women‐specific bleeding is important to preserve quality of life, healthy reproduction and social participation of women and girls with bleeding disorders (WBD). Aim To support appropriate multidisciplin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8d7f88b0d9cd7e44efe09849b356c75
https://doi.org/10.1111/hae.14221
https://doi.org/10.1111/hae.14221
Autor:
Krista Fischer, Karin P M van Galen, Marieke C Punt, Mariette H E Driessens, Tanja H Aalders, Kitty W. M. Bloemenkamp, Marlies H Schrijvers
Publikováno v:
Journal of Thrombosis and Haemostasis
Background Hemophilia carriers (HCs) face specific psychosocial challenges related to pregnancy, caused by their inherited bleeding disorder. Optimal support from healthcare providers can only be realized by exploring medical and psychological health
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2821316f26c7bead00439f57eb3fb4df
https://doi.org/10.1111/jth.14825
https://doi.org/10.1111/jth.14825