Ptychographic transmission microscopy in three dimensions using a multi-slice approach von MAIDEN, A. M, HUMPHRY, M. J, RODENBURG, J. M

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Iron deficiency impairs contractility of human cardiomyocytes through decreased mitochondrial function von Hoes, Martijn F., Grote Beverborg, Niels, Kijlstra, J. David, Kuipers, Jeroen, Swinkels, Dorine W., Giepmans, Ben N.G., Rodenburg, Richard J., van Veldhuisen, Dirk J., de Boer, Rudolf A., van der Meer, Peter

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Biochemical diagnosis of mitochondrial disorders von Rodenburg, Richard J. T.

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Ptychographic electron microscopy using high-angle dark-field scattering for sub-nanometre resolution imaging von Humphry, M.J., Kraus, B., Hurst, A.C., Maiden, A.M., Rodenburg, J.M.

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Mitochondrial complex I-linked disease von Rodenburg, Richard J.

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Soft X-ray spectromicroscopy using ptychography with randomly phased illumination von Maiden, A.M., Morrison, G.R., Kaulich, B., Gianoncelli, A., Rodenburg, J.M.

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Ptychographic microscope for three-dimensional imaging von Godden, T M, Suman, R, Humphry, M J, Rodenburg, J M, Maiden, A M

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Cancer survivors' needs during various treatment phases after multimodal treatment for colon cancer - is there a role for eHealth? von den Bakker, C M, Schaafsma, F G, Huirne, J A F, Consten, E C J, Stockmann, H B A C, Rodenburg, C J, de Klerk, G J, Bonjer, H J, Anema, J R

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An annealing algorithm to correct positioning errors in ptychography von Maiden, A.M., Humphry, M.J., Sarahan, M.C., Kraus, B., Rodenburg, J.M.

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Spectrophotometric Assay for Complex I of the Respiratory Chain in Tissue Samples and Cultured Fibroblasts von Janssen, Antoon J.M, Trijbels, Frans J.M, Sengers, Rob C.A, Smeitink, Jan A.M, van den Heuvel, Lambert P, Wintjes, Liesbeth T.M, Stoltenborg-Hogenkamp, Berendien J.M, Rodenburg, Richard J.T

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Statin-Induced Myopathy Is Associated with Mitochondrial Complex III Inhibition von Schirris, Tom J.J., Renkema, G. Herma, Ritschel, Tina, Voermans, Nicol C., Bilos, Albert, van Engelen, Baziel G.M., Brandt, Ulrich, Koopman, Werner J.H., Beyrath, Julien D., Rodenburg, Richard J., Willems, Peter H.G.M., Smeitink, Jan A.M., Russel, Frans G.M.

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A core outcome set for hyperemesis gravidarum research: an international consensus study von Jansen, LAW, Koot, MH, van‘t Hooft, J, Dean, CR, Duffy, JMN, Ganzevoort, W, Gauw, N, Goes, BY, Rodenburg, J, Roseboom, TJ, Painter, RC, Grooten, IJ

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Gene identification in the congenital disorders of glycosylation type I by whole-exome sequencing von TIMAL, Sharita, HOISCHEN, Alexander, GILISSEN, Christian, RODENBURG, Richard J, EIDHOF, Ilse, VAN DEN HEUVEL, Lambert, THIEL, Christian, WEVERS, Ron A, MORAVA, Eva, VELTMAN, Joris, LEFEBER, Dirk J, LEHLE, Ludwig, ADAMOWICZ, Maciej, HUIJBEN, Karin, SYKUT-CEGIELSKA, Jolanta, PAPROCKA, Justyna, JAMROZ, Ewa, VAN SPRONSEN, Francjan J, KÖRNER, Christian

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Statins Affect Skeletal Muscle Performance: Evidence for Disturbances in Energy Metabolism von Allard, Neeltje A E, Schirris, Tom J J, Verheggen, Rebecca J, Russel, Frans G M, Rodenburg, Richard J, Smeitink, Jan A M, Thompson, Paul D, Hopman, Maria T E, Timmers, Silvie

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Characterisation of an Adult Zebrafish Model for SDHB -Associated Phaeochromocytomas and Paragangliomas von Miltenburg, Jasmijn B, Gorissen, Marnix, van Outersterp, Inge, Versteeg, Iris, Nowak, Alex, Rodenburg, Richard J, van Herwaarden, Antonius E, Olthaar, Andre J, Kusters, Benno, Conrad, Catleen, Timmers, Henri J L M, Dona, Margo

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The functional genomics laboratory: functional validation of genetic variants von Rodenburg, Richard J.

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Mutations in RARS cause hypomyelination von Wolf, Nicole I., Salomons, Gajja S., Rodenburg, Richard J., Pouwels, Petra J. W., Schieving, Jolanda H., Derks, Terry G. J., Fock, Johanna M., Rump, Patrick, van Beek, Daphne M., van der Knaap, Marjo S., Waisfisz, Quinten

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Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number von Thompson, Kyle, Majd, Homa, Dallabona, Cristina, Reinson, Karit, King, Martin S., Alston, Charlotte L., He, Langping, Lodi, Tiziana, Jones, Simon A., Fattal-Valevski, Aviva, Fraenkel, Nitay D., Saada, Ann, Haham, Alon, Isohanni, Pirjo, Vara, Roshni, Barbosa, Inês A., Simpson, Michael A., Deshpande, Charu, Puusepp, Sanna, Bonnen, Penelope E., Rodenburg, Richard J., Suomalainen, Anu, Õunap, Katrin, Elpeleg, Orly, Ferrero, Ileana, McFarland, Robert, Kunji, Edmund R.S., Taylor, Robert W.

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Mutations in APOPT1, Encoding a Mitochondrial Protein, Cause Cavitating Leukoencephalopathy with Cytochrome c Oxidase Deficiency von Melchionda, Laura, Haack, Tobias B., Hardy, Steven, Abbink, Truus E.M., Fernandez-Vizarra, Erika, Lamantea, Eleonora, Marchet, Silvia, Morandi, Lucia, Moggio, Maurizio, Carrozzo, Rosalba, Torraco, Alessandra, Diodato, Daria, Strom, Tim M., Meitinger, Thomas, Tekturk, Pinar, Yapici, Zuhal, Al-Murshedi, Fathiya, Stevens, René, Rodenburg, Richard J., Lamperti, Costanza, Ardissone, Anna, Moroni, Isabella, Uziel, Graziella, Prokisch, Holger, Taylor, Robert W., Bertini, Enrico, van der Knaap, Marjo S., Ghezzi, Daniele, Zeviani, Massimo

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TMEM199 Deficiency Is a Disorder of Golgi Homeostasis Characterized by Elevated Aminotransferases, Alkaline Phosphatase, and Cholesterol and Abnormal Glycosylation von Jansen, Jos C., Timal, Sharita, van Scherpenzeel, Monique, Michelakakis, Helen, Vicogne, Dorothée, Ashikov, Angel, Moraitou, Marina, Hoischen, Alexander, Huijben, Karin, Steenbergen, Gerry, van den Boogert, Marjolein A.W., Porta, Francesco, Calvo, Pier Luigi, Mavrikou, Mersyni, Cenacchi, Giovanna, van den Bogaart, Geert, Salomon, Jody, Holleboom, Adriaan G., Rodenburg, Richard J., Drenth, Joost P.H., Huynen, Martijn A., Wevers, Ron A., Morava, Eva, Foulquier, François, Veltman, Joris A., Lefeber, Dirk J.

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