P.C. Remmelzwaal

Arts-onderzoeker

Faculteit Medische Wetenschappen/UMCG

Telefoon:

E-mail:

p.c.remmelzwaal umcg.nl

ORCID Research Portal

Publicaties

First pathogenic deep-intronic SERPINC1 variant causing antithrombin deficiency

Remmelzwaal, P. C., Mulder, R., de Boer-Bergsma, J., Vinke, B., Kooistra, H., Veeger, N., Wierenga, A. T. J., Schuringa, J. J., Lukens, M. & Meijer, K., 12-jul-2026, (Unpublished).

Onderzoeksoutput ›

Novel SERPINC1 variants in hereditary antithrombin deficiency: first pathogenic deep-intronic variant, revealed by multiple genomic and transcriptomic approaches

Remmelzwaal, P. C., Mulder, R., de Boer- Bergsma, J. J., Vinke, A., Kooistra, H. A. M., Veeger, N. J. G. M., Wierenga, A. T. J., Schuringa, J. J., Lukens, M. V. & Meijer, K., aug-2026, In: Journal of Thrombosis and Haemostasis. 24, 8, blz. 2890-2898 9 blz.

Onderzoeksoutput: Article › › peer review

A systematic review on anti-Xa monitoring in the therapeutic use of low-molecular-weight heparins

Jaspers, T. C. C., Remmelzwaal, P. C., Weersink, E. P. S., Meijer, K. & Khorsand, N., okt-2025, In: Journal of Thrombosis and Haemostasis. 23, 10, blz. 3033-3055 23 blz.

Onderzoeksoutput: Article › › peer review

Expanding the phenotype of anauxetic dysplasia caused by biallelic NEPRO mutations: A case report

Remmelzwaal, P. C., Verhagen, M. V., Jongbloed, J. D. H., van den Akker, P. C., Veenstra-Knol, H. E. & Hitzert, M. M., sep-2023, In: American Journal of Medical Genetics. Part A. 191, 9, blz. 2440-2445 6 blz.

Onderzoeksoutput: Article › › peer review