Effect of acute hyperglycaemia and/or hyperinsulinaemia on proinflammatory gene expression, cytokine production and neutrophil function in humans von Stegenga, M. E., Crabben, S. N. van der, Dessing, M. C., Pater, J. M., Van Den Pangaart, P. S., De Vos, A. F., Tanck, M. W., Roos, D., Sauerwein, H. P., Van Der Poll, T.

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Mandibuloacral dysplasia type B (MADB): a cohort of eight patients from Suriname with a homozygous founder mutation in ZMPSTE24 (FACE1), clinical diagnostic criteria and management... von Hitzert, M M, van der Crabben, S N, Baldewsingh, G, van Amstel, H K Ploos, van den Wijngaard, A, van Ravenswaaij-Arts, C M A, Zijlmans, C W R

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An update on serine deficiency disorders von van der Crabben, S. N., Verhoeven-Duif, N. M., Brilstra, E. H., Van Maldergem, L., Coskun, T., Rubio-Gozalbo, E., Berger, R., de Koning, T. J.

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BIO FOr CARE: biomarkers of hypertrophic cardiomyopathy development and progression in carriers of Dutch founder truncating MYBPC3 variants—design and status von Jansen, M., Christiaans, I., van der Crabben, S. N., Michels, M., Huurman, R., Hoedemaekers, Y. M., Dooijes, D., Jongbloed, J. D. H., Boven, L. G., Lekanne Deprez, R. H., Wilde, A. A. M., Jans, J. J. M., van der Velden, J., de Boer, R. A., van Tintelen, J. P., Asselbergs, F. W., Baas, A. F.

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Genetic Diagnosis in Sudden Cardiac Death: The Crucial Role of Multidisciplinary Care von van der Crabben, S. N., Komdeur, F. L., Nossent, E. J., Deprez, R. H. Lekanne, Broekhuizen, E. A., van der Werf, C., Vermeer, A. M. C., Niessen, H. W. M., Houweling, A. C.

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Idiopathic ventricular fibrillation: is it a case for genetic testing? von van der Crabben, S. N., Wilde, A. A. M.

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Splice Site Mutations in GH1 Detected in Previously (Genetically) Undiagnosed Families with Congenital Isolated Growth Hormone Deficiency Type II von Kempers, M.J.E., van der Crabben, S.N., de Vroede, M., Alfen-van der Velden, J., Netea-Maier, R.T., Duim, R.A.J., Otten, B.J., Losekoot, M., Wit, J.M.

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Circulating Acylcarnitines Associated with Hypertrophic Cardiomyopathy Severity: an Exploratory Cross-Sectional Study in MYBPC3 Founder Variant Carriers von Jansen, Mark, Schmidt, A. F., Jans, J. J. M., Christiaans, I., van der Crabben, S. N., Hoedemaekers, Y. M., Dooijes, D., Jongbloed, J. D. H., Boven, L. G., Lekanne Deprez, R. H., Wilde, A. A. M., van der Velden, J., de Boer, R. A., van Tintelen, J. P., Asselbergs, F. W., Baas, A. F.

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Mutated PET117 causes complex IV deficiency and is associated with neurodevelopmental regression and medulla oblongata lesions von Renkema, G. H., Visser, G., Baertling, F., Wintjes, L. T., Wolters, V. M., van Montfrans, J., de Kort, G. A. P., Nikkels, P. G. J., van Hasselt, P. M., van der Crabben, S. N., Rodenburg, R. J. T.

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Development of a novel Patient-Reported Outcome Measure (PROM) for adults with an Inherited Cardiac Condition (ICC) von Van Pottelberghe, S, Van Der Crabben, S N, Amin, A S, Wilde, A A, Scheirlynck, E, Nekkebroeck, J, Hes, F, Kupper, N

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Bradycardia in a long QT type 2 family: coinciding KCNH2 and HCN4 variants von Copier, J S, Andrzejczyk, K, Amin, A S, Van Der Crabben, S N, Beekman, L, Bezzina, C R, Verkerk, A O, Lodder, E M

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Effect of cysteine dosage on erythrocyte glutathione synthesis rate in a patient with cystathionine beta synthase deficiency von van der Crabben, S. N., Wijburg, F. A., Ackermans, M. T., Sauerwein, H. P.

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Utility of polygenic risk score for prediction of dilated cardiomyopathy and modulation of severity of LV dysfunction among cases von Kramarenko, D R, Jurgens, S J, Ramo, J T, Van Orsouw, C A, Hottenga, J J, Charron, P, Meder, B, Palotie, A, Daly, M, Ellinor, P T, Pinto, Y M, Aragam, K G, Van Der Crabben, S N, Amin, A S, Bezzina, C R

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Hyperglycemia Stimulates Coagulation, Whereas Hyperinsulinemia Impairs Fibrinolysis in Healthy Humans von STEGENGA, Michiel E, VAN DER CRABBEN, Saskia N, LEVI, Marcel, DE VOS, Alex F, TANCK, Michael W, SAUERWEIN, Hans P, VAN DER POLL, Tom

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Circulating Acylcarnitines Associated with Hypertrophic Cardiomyopathy Severity: an Exploratory Cross-Sectional Study in MYBPC3 Founder Variant Carriers von Jansen, Mark, Schmidt, A F, Jans, J J M, Christiaans, I, van der Crabben, S N, Hoedemaekers, Y M, Dooijes, D, Jongbloed, J D H, Boven, L G, Lekanne Deprez, R H, Wilde, A A M, van der Velden, J, de Boer, R A, van Tintelen, J P, Asselbergs, F W, Baas, A F

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Mandibuloacral dysplasia type B , clinical diagnostic criteria and management guidelines von Hitzert, M. M, van der Crabben, S. N, Baldewsingh, G, van Amstel, H. K. Ploos, van den Wijngaard, A, van Ravenswaaij-Arts, C. M. A, Zijlmans, C. W. R

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Mutated PET117 causes complex IV deficiency and is associated with neurodevelopmental regression and medulla oblongata lesions von Renkema, G. Herma, Visser, G, Baertling, F, Wintjes, L. T, Wolters, V. M, van Montfrans, J, de Kort, G. A.P, Nikkels, P. G.J, van Hasselt, P. M, van der Crabben, S. N, Rodenburg, Richard J. T

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The sports cardiology team: personalising athlete care through a comprehensive, multidisciplinary approach von Van Hattum, J, Verwijs, SM, De Vries, ST, Boekholdt, SM, Groenink, M, Van Randen, A, Panhuyzen-Goedkoop, NM, Willems, AR, Knobbe, I, Blom, NA, Van Der Crabben, SN, Bijsterveld, NR, Pinto, YM, Wilde, AAM, Jorstad, HT

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BIO FOr CARE: biomarkers of hypertrophic cardiomyopathy development and progression in carriers of Dutch founder truncating MYBPC3 variants-design and status von Jansen, M, Christiaans, I, van der Crabben, S N, Michels, M, Huurman, R, Hoedemaekers, Y M, Dooijes, D, Jongbloed, J D H, Boven, L G, Lekanne Deprez, R H, Wilde, A A M, Jans, J J M, van der Velden, J, de Boer, R A, van Tintelen, J P, Asselbergs, F W, Baas, A F

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Correction to: De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathy von Klöckner, Chiara, Sticht, Heinrich, Zacher, Pia, Popp, Bernt, Babcock, Holly E., Bakker, Dewi P., Barwick, Katy, Bonfert, Michaela V., Bönnemann, Carsten G., Brilstra, Eva H., Chung, Wendy K., Clarke, Angus J., Devine, Patrick, Donkervoort, Sandra, Fraser, Jamie L., Friedman, Jennifer, Gates, Alyssa, Ghoumid, Jamal, Hobson, Emma, Horvath, Gabriella, Keller-Ramey, Jennifer, Keren, Boris, Kurian, Manju A., Lee, Virgina, Leppig, Kathleen A., Lundgren, Johan, McDonald, Marie T., McLaughlin, Heather M., McTague, Amy, Mefford, Heather C., Mignot, Cyril, Mikati, Mohamad A., Nava, Caroline, Raymond, F. Lucy, Sampson, Julian R., Sanchis-Juan, Alba, Shashi, Vandana, Shieh, Joseph T.C., Shinawi, Marwan, Slavotinek, Anne, Stödberg, Tommy, Stong, Nicholas, Sullivan, Jennifer A., Taylor, Ashley C., Toler, Tomi L., van den Boogaard, Marie-José, van der Crabben, Saskia N., van Gassen, Koen L.I., van Jaarsveld, Richard H., Van Ziffle, Jessica, Wadley, Alexandrea F., Wagner, Matias, Wigby, Kristen, Wortmann, Saskia B., Zarate, Yuri A., Møller, Rikke S., Lemke, Johannes R., Platzer, Konrad

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