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	81.	Correction to: Consensus document for the diagnosis of prosthetic joint infections: a joint paper by the EANM, EBJIS, and ESR (with ESCMID endorsement). [electronic resource] by Signore, Alberto Sconfienza, Luca Maria Borens, Olivier Glaudemans, Andor W J M Cassar-Pullicino, Victor N Trampuz, Andrej Winkler, Heinz Gheysens, Olivier Vanhoenacker, Filip M H M Petrosillo, Nicola Jutte, Paul C Publication details: European journal of nuclear medicine and molecular imaging May 2019 In: European journal of nuclear medicine and molecular imaging vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	82.	A new autosomal recessive form of Stickler syndrome is caused by a mutation in the COL9A1 gene. [electronic resource] by Van Camp, Guy Snoeckx, Rikkert L Hilgert, Nele van den Ende, Jenneke Fukuoka, Hisakumi Wagatsuma, Michio Suzuki, Hiroaki Smets, R M Erica Vanhoenacker, Filip Declau, Frank Van de Heyning, Paul Usami, Shin-ichi Producer: 20061019 In: American journal of human genetics vol. 79 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	83.	Indications for a genetic association of a VCP polymorphism with the pathogenesis of sporadic Paget's disease of bone, but not for TNFSF11 (RANKL) and IL-6 polymorphisms. [electronic resource] by Chung, Pui Yan Jenny Beyens, Greet de Freitas, Fenna Boonen, Steven Geusens, Piet Vanhoenacker, Filip Verbruggen, Leon Van Offel, Jan Goemaere, Stefan Zmierczak, Hans-Georg Westhovens, René Devogelaer, Jean-Pierre Van Hul, Wim Producer: 20111013 In: Molecular genetics and metabolism vol. 103 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	84.	The majority of the genetic risk for Paget's disease of bone is explained by genetic variants close to the CSF1, OPTN, TM7SF4, and TNFRSF11A genes. [electronic resource] by Chung, Pui Yan Jenny Beyens, Greet Boonen, Steven Papapoulos, Socrates Geusens, Piet Karperien, Marcel Vanhoenacker, Filip Verbruggen, Leon Fransen, Erik Van Offel, Jan Goemaere, Stefan Zmierczak, Hans-Georg Westhovens, René Devogelaer, Jean-Pierre Van Hul, Wim Producer: 20110121 In: Human genetics vol. 128 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	85.	Diagnosis of peripheral bone and prosthetic joint infections: overview on the consensus documents by the EANM, EBJIS, and ESR (with ESCMID endorsement). [electronic resource] by Sconfienza, Luca Maria Signore, Alberto Cassar-Pullicino, Victor Cataldo, Maria Adriana Gheysens, Olivier Borens, Olivier Trampuz, Andrej Wörtler, Klaus Petrosillo, Nicola Winkler, Heinz Vanhoenacker, Filip M H M Jutte, Paul C Glaudemans, Andor W J M Producer: 20200205 In: European radiology vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	86.	ESSR Consensus Document for Detection, Characterization, and Referral Pathway for Tumors and Tumorlike Lesions of Bone. [electronic resource] by Lalam, Radhesh Bloem, Johan L Noebauer-Huhmann, Iris M Wörtler, Klaus Tagliafico, Alberto Vanhoenacker, Filip Nikodinovska, Violeta Vasilevska Sanal, Hatice Tuba Woude, Henk-Jan van der Papakonstantinou, Olympia Åström, Gunnar Davies, Mark Isaac, Amanda Weber, Marc-André Producer: 20181012 In: Seminars in musculoskeletal radiology vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	87.	Involvement of PLEKHM1 in osteoclastic vesicular transport and osteopetrosis in incisors absent rats and humans. [electronic resource] by Van Wesenbeeck, Liesbeth Odgren, Paul R Coxon, Fraser P Frattini, Annalisa Moens, Pierre Perdu, Bram MacKay, Carole A Van Hul, Els Timmermans, Jean-Pierre Vanhoenacker, Filip Jacobs, Ruben Peruzzi, Barbara Teti, Anna Helfrich, Miep H Rogers, Michael J Villa, Anna Van Hul, Wim Producer: 20070604 In: The Journal of clinical investigation vol. 117 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	88.	Soft Tissue Tumors in Adults: ESSR-Approved Guidelines for Diagnostic Imaging. [electronic resource] by Noebauer-Huhmann, Iris M Weber, Marc-André Lalam, Radhesh K Trattnig, Siegfried Bohndorf, Klaus Vanhoenacker, Filip Tagliafico, Alberto van Rijswijk, Carla Vilanova, Joan C Afonso, P Diana Breitenseher, Martin Beggs, Ian Robinson, Philip de Jonge, Milko C Krestan, Christian Bloem, Johan L Producer: 20160421 In: Seminars in musculoskeletal radiology vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	89.	Soft Tissue Tumors in Adults: ESSR-Approved Guidelines for Diagnostic Imaging. [electronic resource] by Noebauer-Huhmann, Iris M Weber, Marc-André Lalam, Radhesh K Trattnig, Siegfried Bohndorf, Klaus Vanhoenacker, Filip Tagliafico, Alberto van Rijswijk, Carla Vilanova, Joan C Afonso, P Diana Breitenseher, Martin Beggs, Ian Robinson, Philip de Jonge, Milko C Krestan, Christian Bloem, Johan L Producer: 20161007 In: Seminars in musculoskeletal radiology vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	90.	State-associated changes in longitudinal [ [electronic resource] by De Picker, Livia Ottoy, Julie Verhaeghe, Jeroen Deleye, Steven Wyffels, Leonie Fransen, Erik Kosten, Lauren Sabbe, Bernard Coppens, Violette Timmers, Maarten de Boer, Peter Van Nueten, Luc Op De Beeck, Ken Oberacher, Herbert Vanhoenacker, Filip Ceyssens, Sarah Stroobants, Sigrid Staelens, Steven Morrens, Manuel Producer: 20200225 In: Brain, behavior, and immunity vol. 77 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	91.	Osteopathia striata with cranial sclerosis owing to WTX gene defect. [electronic resource] by Perdu, Bram de Freitas, Fenna Frints, Suzanne G M Schouten, Meyke Schrander-Stumpel, Connie Barbosa, Mafalda Pinto-Basto, Jorge Reis-Lima, Margarida de Vernejoul, Marie-Christine Becker, Kristin Freckmann, Marie-Louise Keymolen, Kathlijn Haan, Eric Savarirayan, Ravi Koenig, Rainer Zabel, Bernhard Vanhoenacker, Filip M Van Hul, Wim Producer: 20100708 In: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	92.	Genetic variation in the TNFRSF11A gene encoding RANK is associated with susceptibility to Paget's disease of bone. [electronic resource] by Chung, Pui Yan Jenny Beyens, Greet Riches, Philip L Van Wesenbeeck, Liesbeth de Freitas, Fenna Jennes, Karen Daroszewska, Anna Fransen, Erik Boonen, Steven Geusens, Piet Vanhoenacker, Filip Verbruggen, Leon Van Offel, Jan Goemaere, Stefan Zmierczak, Hans-Georg Westhovens, René Karperien, Marcel Papapoulos, Socrates Ralston, Stuart H Devogelaer, Jean-Pierre Van Hul, Wim Producer: 20110302 In: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	93.	Loss-of-function mutations in LEMD3 result in osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosis. [electronic resource] by Hellemans, Jan Preobrazhenska, Olena Willaert, Andy Debeer, Philippe Verdonk, Peter C M Costa, Teresa Janssens, Katrien Menten, Bjorn Van Roy, Nadine Vermeulen, Stefan J T Savarirayan, Ravi Van Hul, Wim Vanhoenacker, Filip Huylebroeck, Danny De Paepe, Anne Naeyaert, Jean-Marie Vandesompele, Jo Speleman, Frank Verschueren, Kristin Coucke, Paul J Mortier, Geert R Producer: 20041207 In: Nature genetics vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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