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Author/Creator Simons, Annet

1. Complement factor D haplodeficiency is associated with a reduced complement activation speed and diminished bacterial killing. Issue 4 (3rd April 2021)

Authors:
Langereis, Jeroen D; van der Molen, Renate G; de Kat Angelino, Corrie; Henriet, Stefanie S; de Jonge, Marien I; Joosten, Irma; Simons, Annet; Schuurs‐Hoeijmakers, Janneke HM; van Deuren, Marcel; van Aerde, Koen; van der Flier, Michiel
Journal:
Clinical & translational immunology
Issue:
Volume 10:Issue 4(2021)
Page Start:
n/a
Record Type:
Journal Article
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3. Platelet CD34 expression in a patient with a partial deletion of transcription factor subunit CBFB. Issue 6 (8th April 2020)

Authors:
van Bergen, Maaike G.J.M.; Saes, Joline L.; Simons, Annet; Hebeda, Konnie M.; Henskens, Yvonne M.C.; Barteling, Wideke; Huys, Erik; Laros‐van Gorkom, Britta A.P.; Schols, Saskia E.M.; Preijers, Frank W.; Jongmans, Marjolijn C.J.; Jansen, Joop H.; van der Reijden, Bert A.
Journal:
American journal of hematology
Issue:
Volume 95:Issue 6(2020:Jun.)
Page Start:
E136
Record Type:
Journal Article
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4. Primary immunodeficiency associated with chromosomal aberration – an ESID survey. Issue 1 (December 2016)

Authors:
Schatorjé, Ellen; van der Flier, Michiel; Seppänen, Mikko; Browning, Michael; Morsheimer, Megan; Henriet, Stefanie; Neves, João; Vinh, Donald; Alsina, Laia; Grumach, Anete; Soler-Palacin, Pere; Boyce, Thomas; Celmeli, Fatih; Goudouris, Ekaterini; Hayman, Grant; Herriot, Richard; Förster-Waldl, El...
Journal:
Orphanet journal of rare diseases
Issue:
Volume 11:Issue 1(2016)
Page Start:
1
Record Type:
Journal Article
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5. Von Willebrand disease type 2M: Correlation between genotype and phenotype. (21st November 2021)

Authors:
Maas, Dominique P. M. S. M.; Atiq, Ferdows; Blijlevens, Nicole M. A.; Brons, Paul P. T.; Krouwel, Sandy; Laros‐van Gorkom, Britta A. P.; Leebeek, Frank W. G.; Nieuwenhuizen, Laurens; Schoormans, Selene C. M.; Simons, Annet; Meijer, Daniëlle; van Heerde, Waander L.; Schols, Sas...
Journal:
Journal of thrombosis and haemostasis
Issue:
Volume 20:Number 2(2022)
Page Start:
316
Record Type:
Journal Article
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6. Whole exome sequencing in the diagnostic workup of patients with a bleeding diathesis. Issue 1 (15th November 2018)

Authors:
Saes, Joline L.; Simons, Annet; de Munnik, Sonja A.; Nijziel, Marten R.; Blijlevens, Nicole M. A.; Jongmans, Marjolijn C.; van der Reijden, Bert A.; Smit, Yolba; Brons, Paul P.; van Heerde, Waander L.; Schols, Saskia E. M.
Journal:
Haemophilia
Issue:
Volume 25:Issue 1(2019)
Page Start:
127
Record Type:
Journal Article
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