[ 18 F]NaF PET/CT as a Marker for Fibrodysplasia Ossificans Progressiva: From Molecular Mechanisms to Clinical Applications in Bone Disorders by Zwama, Jolien, Rosenberg, Neeltje M, Verheij, Vincent A, Raijmakers, Pieter G H M, Yaqub, Maqsood, Botman, Esmée, de Ruiter, Ruben D, Garrelfs, Mark R, Bökenkamp, Arend, Micha, Dimitra, Schwarte, Lothar A, Teunissen, Bernd P, Lammertsma, Adriaan A, Boellaard, Ronald, Eekhoff, Elisabeth M W

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Identification of a Novel CYP11B2 Variant in a Family with Varying Degrees of Aldosterone Synthase Deficiency by Garrelfs, Mark R., Rinne, Tuula, Hillebrand, Jacquelien J., Lauffer, Peter, Bijlsma, Merijn W., Claahsen-van der Grinten, Hedi L, de Leeuw, Nicole, Finken, Martijn J. J., Rotteveel, Joost, Zwaveling-Soonawala, Nitash, Nieuwdorp, Max, van Trotsenburg, A. S. Paul, Mooij, Christiaan F.

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Transient left bundle branch block and left ventricular dysfunction in a patient with NLRP1-associated autoinflammation with arthritis and dyskeratosis syndrome by Garrelfs, Mark R., Hoppenreijs, Esther, Tanke, Ronald B.

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Eculizumab in Pediatric Dense Deposit Disease by Oosterveld, Michiel J S, Garrelfs, Mark R, Hoppe, Bernd, Florquin, Sandrine, Roelofs, Joris J T H, van den Heuvel, L P, Amann, Kerstin, Davin, Jean-Claude, Bouts, Antonia H M, Schriemer, Pietrik J, Groothoff, Jaap W

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The Phenotypic Spectrum of PNKP-Associated Disease and the Absence of Immunodeficiency and Cancer Predisposition in a Dutch Cohort by Garrelfs, Mark R., Takada, Sanami, Kamsteeg, Erik-Jan, Pegge, Sjoert, Mancini, Grazia, Engelen, Marc, van de Warrenburg, Bart, Rennings, Alexander, van Gaalen, Judith, Peters, Ivo, Weemaes, Corry, van der Burg, Mirjam, Willemsen, Michèl A.

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Neonatal Long-Chain 3-Ketoacyl-CoA Thiolase deficiency: Clinical-biochemical phenotype, sodium-D,L-3-hydroxybutyrate treatment experience and cardiac evaluation using speckle echoc... by Veenvliet, Annemarijne R.J., Garrelfs, Mark R., Udink ten Cate, Floris E.A., Ferdinandusse, Sacha, Denis, Simone, Fuchs, Sabine A., Schwantje, Marit, Geurtzen, Rosa, van Wegberg, Annemiek M.J., Huigen, Marleen C.D.G., Kluijtmans, Leo A.J., Wanders, Ronald J.A., Derks, Terry G.J., de Boer, Lonneke, Houtkooper, Riekelt H., de Vries, Maaike C., van Karnebeek, Clara D.M.

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Adapting to Adulthood: A Review of Transition Strategies for Osteogenesis Imperfecta by Celli, Luca, Garrelfs, Mark R., Sakkers, Ralph J. B., Elting, Mariet W., Celli, Mauro, Bökenkamp, Arend, Smits, Cas, Goderie, Thadé, Smit, Jan Maerten, Schwarte, Lothar A., Schober, Patrick R., Lubbers, Wouter D., Visser, Marieke C., Kievit, Arthur J., van Royen, Barend J., Gilijamse, Marjolijn, Schreuder, Willem H., Rustemeyer, Thomas, Pramana, Angela, Hendrickx, Jan-Jaap, Dahele, Max R., Saeed, Peerooz, Moll, Annette C., Curro–Tafili, Katie R., Ghyczy, Ebba A. E., Dickhoff, Chris, de Leeuw, Robert A., Bonjer, Jaap H., Nieuwenhuijzen, Jakko A., Konings, Thelma C., Engelsman, Anton F., Eeckhout, Augustinus M., van den Aardweg, Joost G., Thoral, Patrick J., Noske, David P., Dubois, Leander, Teunissen, Berend P., Semler, Oliver, Wekre, Lena Lande, Maasalu, Katre, Märtson, Aare, Sangiorgi, Luca, Versacci, Paolo, Riminucci, Mara, Grammatico, Paola, Zambrano, Anna, Martini, Lorena, Castori, Marco, Botman, Esmee, Westerheim, Ingunn, Zhytnik, Lidiia, Micha, Dimitra, Eekhoff, Elisabeth Marelise W.

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18FNaF PET/CT as a Marker for Fibrodysplasia Ossificans Progressiva: From Molecular Mechanisms to Clinical Applications in Bone Disorders by Zwama, Jolien, Rosenberg, Neeltje M, Verheij, Vincent A, Raijmakers, Pieter G H M, Yaqub, Maqsood, Botman, Esmée, de Ruiter, Ruben D, Garrelfs, Mark R, Bökenkamp, Arend, Micha, Dimitra, Schwarte, Lothar A, Teunissen, Bernd P, Lammertsma, Adriaan A, Boellaard, Ronald, Eekhoff, Elisabeth M W

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F]NaF PET/CT as a Marker for Fibrodysplasia Ossificans Progressiva: From Molecular Mechanisms to Clinical Applications in Bone Disorders by Zwama, Jolien, Rosenberg, Neeltje M, Verheij, Vincent A, Raijmakers, Pieter G. H. M, Yaqub, Maqsood, Botman, Esmee, de Ruiter, Ruben D, Garrelfs, Mark R, Bokenkamp, Arend, Micha, Dimitra, Schwarte, Lothar A, Teunissen, Bernd P, Lammertsma, Adriaan A, Boellaard, Ronald, Eekhoff, Elisabeth M. W

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Identification of a Novel CYP11B2 Variant in a Family with Varying Degrees of Aldosterone Synthase Deficiency by Garrelfs, Mark R., Rinne, Tuula, Hillebrand, Jacquelien J., Lauffer, Peter, Bijlsma, Merijn W., Claahsen-van Der Grinten, Hedi L., De Leeuw, Nicole, Finken, Martijn J.J., Rotteveel, Joost, Zwaveling-soonawala, Nitash, Nieuwdorp, Max, Paul vanTrotsenburg, A.S., Mooij, Christiaan F.

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