Human Fibroblasts as a Model for the Study of Bone Disorders by Lauria Claeys, Nathalie Bravenboer, Elisabeth M. W. Eekhoff, Dimitra Micha

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A Clinical Perspective on Advanced Developments in Bone Biopsy Assessment in Rare Bone Disorders by Sanne Treurniet, Elisabeth M. W. Eekhoff, Felix N. Schmidt, Dimitra Micha, Björn Busse, Nathalie Bravenboer

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Editorial: Innovative Therapies in Bone Biology: What Can Be Learned From Rare Bone Diseases? by Elisabeth M. W. Eekhoff, Teun J. de Vries, Ralph J. B. Sakkers, Wim Van Hul

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Bronchial obstruction in osteogenesis imperfecta can be detected by forced oscillation technique by Silvia Storoni, Silvia Storoni, Sara J. E. Verdonk, Sara J. E. Verdonk, Dimitra Micha, Dimitra Micha, Patrick M. C. Jak, Marianna Bugiani, Elisabeth M. W. Eekhoff, Elisabeth M. W. Eekhoff, Joost G. van den Aardweg

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The intricate mechanism of PLS3 in bone homeostasis and disease by Wenchao Zhong, Wenchao Zhong, Wenchao Zhong, Wenchao Zhong, Janak L. Pathak, Yueting Liang, Yueting Liang, Lidiia Zhytnik, Lidiia Zhytnik, Lidiia Zhytnik, Gerard Pals, Gerard Pals, Elisabeth M. W. Eekhoff, Elisabeth M. W. Eekhoff, Nathalie Bravenboer, Nathalie Bravenboer, Dimitra Micha, Dimitra Micha, Dimitra Micha

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In Vitro Modelling of Osteogenesis Imperfecta with Patient-Derived Induced Mesenchymal Stem Cells by Lauria Claeys, Lidiia Zhytnik, Laura Ventura, Lisanne E. Wisse, Elisabeth M. W. Eekhoff, Gerard Pals, Nathalie Bravenboer, Vivi M. Heine, Dimitra Micha

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Induced Pluripotent Stem Cells to Model Human Fibrodysplasia Ossificans Progressiva by Jie Cai, Valeria V. Orlova, Xiujuan Cai, Elisabeth M.W. Eekhoff, Keqin Zhang, Duanqing Pei, Guangjin Pan, Christine L. Mummery, Peter ten Dijke

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The first family with adult osteogenesis imperfecta caused by a novel homozygous mutation in CREB3L1 by Ferdy K. Cayami, Alessandra Maugeri, Sanne Treurniet, Eva D. Setijowati, Bernd P. Teunissen, Elisabeth M.W. Eekhoff, Gerard Pals, Sultana M. Faradz, Dimitra Micha

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A Systematic Review of the Evidence of Hematopoietic Stem Cell Differentiation to Fibroblasts by Bernard J. Smilde, Esmée Botman, Teun J. de Vries, Ralph de Vries, Dimitra Micha, Ton Schoenmaker, Jeroen J. W. M. Janssen, Elisabeth M. W. Eekhoff

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Relative importance of four functional measures as predictors of 15-year mortality in the older Dutch population by Elisabeth M. W. Eekhoff, Natasja M. van Schoor, Joseph S. Biedermann, Mirjam M. Oosterwerff, Renate de Jongh, Nathalie Bravenboer, Mireille N. M. van Poppel, Dorly J. H. Deeg

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From Genetics to Clinical Implications: A Study of 675 Dutch Osteogenesis Imperfecta Patients by Silvia Storoni, Sara J. E. Verdonk, Lidiia Zhytnik, Gerard Pals, Sanne Treurniet, Mariet W. Elting, Ralph J. B. Sakkers, Joost G. van den Aardweg, Elisabeth M. W. Eekhoff, Dimitra Micha

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International physician survey on management of FOP: a modified Delphi study by Maja Di Rocco, Genevieve Baujat, Marta Bertamino, Matthew Brown, Carmen L. De Cunto, Patricia L. R. Delai, Elisabeth M. W. Eekhoff, Nobuhiko Haga, Edward Hsiao, Richard Keen, Rolf Morhart, Robert J. Pignolo, Frederick S. Kaplan

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Development and Internal Validation of a Multivariable Prediction Model for Adrenocortical-Carcinoma-Specific Mortality by Madeleine H. T. Ettaieb, Sander M. J. van Kuijk, Annelies de Wit-Pastoors, Richard A. Feelders, Eleonora P. M. Corssmit, Elisabeth M. W. Eekhoff, Paul van der Valk, Henri J. L. M. Timmers, Michiel N. Kerstens, Heinz-Josef Klümpen, Rachel S. van Leeuwaarde, Bas Havekes, Harm R. Haak

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Influence of Receptor Polymorphisms on the Response to α-Adrenergic Receptor Blockers in Pheochromocytoma Patients by Annika M. A. Berends, Mathieu S. Bolhuis, Ilja M. Nolte, Edward Buitenwerf, Thera P. Links, Henri J. L. M. Timmers, Richard A. Feelders, Elisabeth M. W. Eekhoff, Eleonora P. M. Corssmit, Peter H. Bisschop, Harm R. Haak, Ron H. N. van Schaik, Samira el Bouazzaoui, Bob Wilffert, Michiel N. Kerstens

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Health-Related Quality of Life in Adrenocortical Carcinoma: Development of the Disease-Specific Questionnaire ACC-QOL and Results from the PROFILES Registry by Rebecca V. Steenaard, Thomas M. A. Kerkhofs, Myrte Zijlstra, Floortje Mols, Michiel N. Kerstens, Henry J. L. M. Timmers, Rachel S. van Leeuwaarde, Koen M. A. Dreijerink, Elisabeth M. W. Eekhoff, Els J. M. Nieveen van Dijkum, Eleonora P. M. Corssmit, Ellen Kapiteijn, Marjolein N. T. Kremers, Richard A. Feelders, Harm R. Haak

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Microarchitecture of Heterotopic Ossification in Fibrodysplasia Ossificans Progressiva: An HR-pQCT Case Series by Esmée Botman, Melissa S. A. M. Bevers, Melissa S. A. M. Bevers, Melissa S. A. M. Bevers, Caroline E. Wyers, Caroline E. Wyers, Caroline E. Wyers, Bert van Rietbergen, Bert van Rietbergen, Bernd P. Teunissen, Pieter G. Raijmakers, Jan Coen Netelenbos, Joop P. van den Bergh, Joop P. van den Bergh, Joop P. van den Bergh, Joop P. van den Bergh, Elisabeth M. W. Eekhoff

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Fibrodysplasia Ossificans Progressiva: What Have We Achieved and Where Are We Now? Follow-up to the 2015 Lorentz Workshop by Ruben D. de Ruiter, Bernard J. Smilde, Gerard Pals, Nathalie Bravenboer, Petra Knaus, Ton Schoenmaker, Esmée Botman, Gonzalo Sánchez-Duffhues, Maurizio Pacifici, Robert J. Pignolo, Eileen M. Shore, Marjolein van Egmond, Hans Van Oosterwyck, Hans Van Oosterwyck, Frederick S. Kaplan, Edward C. Hsiao, Paul B. Yu, Renata Bocciardi, Carmen Laura De Cunto, Patricia Longo Ribeiro Delai, Teun J. de Vries, Susanne Hilderbrandt, Susanne Hilderbrandt, Richard T. Jaspers, Richard Keen, Peter Koolwijk, Rolf Morhart, Jan C. Netelenbos, Thomas Rustemeyer, Christiaan Scott, Clemens Stockklausner, Peter ten Dijke, James Triffit, Francesc Ventura, Roberto Ravazzolo, Dimitra Micha, Elisabeth M. W. Eekhoff

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Correction: Common Variants in the Type 2 Diabetes Gene Are Associated with Impairments in Insulin Secretion During Hyperglycaemic Glucose Clamp. by Jana V. van Vliet-Ostaptchouk, Timon W. van Haeften, Gijs W. D. Landman, Erwin Reiling, Nanne Kleefstra, Henk J. G. Bilo, Olaf H. Klungel, Anthonius de Boer, Cleo C. van Diemen, Cisca Wijmenga, H. Marike Boezen, Jacqueline M. Dekker, Esther van 't Riet, Giel Nijpels, Laura M. C. Welschen, Hata Zavrelova, Elinda J. Bruin, Clara C. Elbers, Florianne Bauer, N. Charlotte Onland-Moret, Yvonne T. van der Schouw, Diederick E. Grobbee, Annemieke M. W. Spijkerman, Daphne L. van der A, Annemarie M. Simonis-Bik, Elisabeth M. W. Eekhoff, Michaela Diamant, Mark H. H. Kramer, Dorret I. Boomsma, Eco J. de Geus, Gonneke Willemsen, P. Eline Slagboom, Marten H. Hofker, Leen M. 't Hart

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Common variants in the type 2 diabetes KCNQ1 gene are associated with impairments in insulin secretion during hyperglycaemic glucose clamp. by Jana V van Vliet-Ostaptchouk, Timon W van Haeften, Gijs W D Landman, Erwin Reiling, Nanne Kleefstra, Henk J G Bilo, Olaf H Klungel, Anthonius de Boer, Cleo C van Diemen, Cisca Wijmenga, H Marike Boezen, Jacqueline M Dekker, Esther van 't Riet, Giel Nijpels, Laura M C Welschen, Hata Zavrelova, Elinda J Bruin, Clara C Elbers, Florianne Bauer, N Charlotte Onland-Moret, Yvonne T van der Schouw, Diederick E Grobbee, Annemieke M W Spijkerman, Daphne L van der A, Annemarie M Simonis-Bik, Elisabeth M W Eekhoff, Michaela Diamant, Mark H H Kramer, Dorret I Boomsma, Eco J de Geus, Gonneke Willemsen, P Eline Slagboom, Marten H Hofker, Leen M 't Hart

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