Haematology patient care

M Bartels
Person: Associate Professor - medical, Assistant Professor - medical
20032026

103 Article
10 Review article
9 Meeting Abstract
8 Comment/Letter to the editor
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Germline LCP1 mutations cause immunodeficiency with neutropenia, monocytopenia, lymphopenia and defective cytokinesis
van Bergen, T., Bosch, D., Bellanné-Chantelot, C., Mulet-Lazaro, R., Bledsoe, J. R., Chen, L., de Looper, H. W. J., van Dijk, C., Ter Borg, M., Bindels, E., Hoogenboezem, R., Roovers, O., Olofsen, P. A., Bartels, M., van Montfrans, J. M., Breed, P., Salzer, E., Holierhoek, M. G., Nelken, B. & Beaupain, B. & 7 others, Fleming, M. D., Shimamura, A., Raaijmakers, M. H. G. P., Donadieu, J., Newburger, P. E., Touw, I. P. & Aalbers, A. M., 10 Feb 2026, In: Blood Advances. 10, 3, p. 627-641 15 p.
Research output: Contribution to journal › Article › Academic › peer-review

Open Access
File
2 Downloads (Pure)
In-depth analysis of osmotic gradient ektacytometry parameters across different genotypes in hereditary spherocytosis
de Wilde, J. R. A., Kuppens, G. Z. L., Boesveld, M. E., van Vuren, A. J., van Solinge, W. W., Waanders, E., van Beers, E. J., Rab, M. A. E., Bartels, M. & van Wijk, R., May 2026, In: British Journal of Haematology. 208, 5, p. 1785-1796 12 p.
Research output: Contribution to journal › Article › Academic › peer-review

Open Access
File
Mechanistic Consequences of Piezo1 Gain-of-Function Variants for Decreased Red Cell Survival in Hereditary Xerocytosis
Makhro, A., Huisjes, R., Seiler, E., Qiao, M., Bartels, M., Hegemann, I., Eppenberger, P., Bender, N., Dorn, I., Bogdanova, A., van Wijk, R. & Kaestner, L., Mar 2026, In: American journal of hematology. 101, 3, p. 619-622 4 p.
Research output: Contribution to journal › Letter › Academic › peer-review

Open Access
File

1 Downloads (Pure)

3 Participation in conference
3 Participation in workshop, seminar, course
2 Invited talk
1 Publication peer-review

Gata1 defects: a DBA subgroup or a distinct disease?
Bartels, M. (Speaker)
7 Oct 2017
Activity: Talk or presentation › Invited talk › Academic
Severe Congenital Neutropenia International Registry (SCNIR)
Bartels, M. (Organiser)
22 Sept 2017 → 23 Sept 2017
Activity: Participating in or organising an event › Participation in workshop, seminar, course › Academic
22nd Congress of European Hematology Association
Versluijs, A. (Participant)
22 May 2017 → 25 May 2017
Activity: Participating in or organising an event › Participation in conference › Academic

De rol van ijzer in de functie van het jonge immuunsysteem: wel of niet suppleren?
Boes, M. (Recipient) & Bartels, M. (Recipient), 18 May 2018
Prize: Fellowship awarded competitively

Haematology patient care

Collaborations and top research areas from the last five years

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M Bartels

Germline LCP1 mutations cause immunodeficiency with neutropenia, monocytopenia, lymphopenia and defective cytokinesis

In-depth analysis of osmotic gradient ektacytometry parameters across different genotypes in hereditary spherocytosis

Mechanistic Consequences of Piezo1 Gain-of-Function Variants for Decreased Red Cell Survival in Hereditary Xerocytosis

Gata1 defects: a DBA subgroup or a distinct disease?

Severe Congenital Neutropenia International Registry (SCNIR)

22nd Congress of European Hematology Association

De rol van ijzer in de functie van het jonge immuunsysteem: wel of niet suppleren?

Haematology patient care

Collaborations and top research areas from the last five years

Profiles

Research output

Activities

Prizes