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Number of items: 3.

Journal Article

Jonckheere, An I., Huigsloot, Merei, Lammens, Martin ORCID: 0000-0002-3881-6692, Jansen, Jitske, van den Heuvel, Lambert P., Spiekerkoetter, Ute, von Kleist-Retzow, Juergen-Christoph, Forkink, Marleen, Koopman, Werner J. H., Szklarczyk, Radek, Huynen, Martijn A., Fransen, Jack A., Smeitink, Jan A. M. and Rodenburg, Richard J. T. (2011). Restoration of complex V deficiency caused by a novel deletion in the human TMEM70 gene normalizes mitochondrial morphology. Mitochondrion, 11 (6). S. 954 - 964. OXFORD: ELSEVIER SCI LTD. ISSN 1567-7249

Willems, Esther, Lores-Motta, Laura, Zanichelli, Andrea, Suffritti, Chiara, van der Flier, Michiel, van der Molen, Renate G., Langereis, Jeroen D., van Drongelen, Joris, van den Heuvel, Lambert P., Volokhina, Elena, van de Kar, Nicole C. A. J., Keizer-Garritsen, Jenneke, Levin, Michael ORCID: 0000-0003-2767-6919, Herberg, Jethro A., Martinon-Torres, Federico ORCID: 0000-0002-9023-581X, Wessels, Hans J. T. C., de Breuk, Anita, Fauser, Sascha, Hoyng, Carel B., den Hollander, Anneke, I, de Groot, Ronald, van Gool, Alain J., Gloerich, Jolein and de Jonge, Marien, I (2020). Quantitative multiplex profiling of the complement system to diagnose complement-mediated diseases. Clin. Transl. Immunol., 9 (12). HOBOKEN: WILEY. ISSN 2050-0068

de Jong, Sarah ORCID: 0000-0002-3705-3371, de Breuk, Anita, Volokhina, Elena B., Bakker, Bjorn, Garanto, Alejandro ORCID: 0000-0001-5721-1560, Fauser, Sascha, Katti, Suresh, Hoyng, Carel B., Lechanteur, Yara T. E., van den Heuvel, Lambert P. and den Hollander, Anneke, I (2022). Systemic complement levels in patients with age-related macular degeneration carrying rare or low-frequency variants in the CFH gene. Hum. Mol. Genet., 31 (3). S. 455 - 471. OXFORD: OXFORD UNIV PRESS. ISSN 1460-2083

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