Hendrickx, Rik

De Novo Loss-of-Function Mutations in CHD2 Cause a Fever-Sensitive Myoclonic Epileptic Encephalopathy Sharing Features with Dravet Syndrome

Suls, A., Jaehn, J. A., Kecskés, A., Weber, Y., Weckhuysen, S., Craiu, D. C., Siekierska, A., Djémié, T., Afrikanova, T., Gormley, P., et al. (2013) · The American Journal of Human Genetics

Epilepsy research and treatmentIon channel regulation and function

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Allosteric inhibition of trypanosomatid pyruvate kinases by a camelid single-domain antibody

Pinto Torres, J. E., Claes, M., Hendrickx, R., Yuan, M., Smiejkowska, N., Van Wielendaele, P., Hacisuleyman, A., De Winter, H., Muyldermans, S., Michels, P. A., et al. (2024) · eLife

Trypanosoma species research and implicationsMonoclonal and Polyclonal Antibodies Research

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Allosteric inhibition of trypanosomatid pyruvate kinases by a camelid single-domain antibody

Pinto Torres, J. E., Claes, M., Hendrickx, R., Yuan, M., Smiejkowska, N., Van Wielendaele, P., Hacisuleyman, A., De Winter, H., Muyldermans, S., Michels, P. A., et al. (2025) · eLife

Trypanosoma species research and implicationsMonoclonal and Polyclonal Antibodies Research

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