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Filip Vanhoenacker

Showing results (81-90 of 96) with videos related to

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European Radiology|August 4, 2004
Accuracy of MRI in characterization of soft tissue tumors and tumor-like lesions. A prospective study in 548 patientsJan L M A Gielen, Arthur M De Schepper, Filip Vanhoenacker, et al.
Insights Into Imaging|February 21, 2012
A comparison between histopathology and findings on magnetic resonance imaging of subcutaneous lipomatous soft-tissue tumorsJohannes Toirkens, Arthur M De Schepper, Filip Vanhoenacker, et al.
Pain Management|March 6, 2026
Beyond the capsule: an integrated perspective on the wide world of frozen shoulder. A collaborative viewpointFabrizio Brindisino, Michel Gcam Mertens, Paul Salamh, et al.
European Radiology|February 9, 2026
ESR Essentials: bone marrow MRI in oncology-practice recommendations by the European Society of Musculoskeletal RadiologyFrédéric E Lecouvet, Lokmane Taihi, Thomas Kirchgesner, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|March 29, 2007
Identification of sex-specific associations between polymorphisms of the osteoprotegerin gene, TNFRSF11B, and Paget's disease of boneGreet Beyens, Anna Daroszewska, Fenna de Freitas, et al.
Molecular Genetics and Metabolism|April 20, 2011
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 polymorphismsPui Yan Jenny Chung, Greet Beyens, Fenna de Freitas, et al.
American Journal of Human Genetics|August 16, 2006
A new autosomal recessive form of Stickler syndrome is caused by a mutation in the COL9A1 geneGuy Van Camp, Rikkert L Snoeckx, Nele Hilgert, et al.
Pathology, Research and Practice|January 25, 2022
Malignant pleural mesothelioma with an EML4-ALK fusion: Expect the unexpected!Fleur Cordier, Joni Van der Meulen, Nadine van Roy, et al.
Human Genetics|September 15, 2010
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 genesPui Yan Jenny Chung, Greet Beyens, Steven Boonen, et al.
Seminars in Musculoskeletal Radiology|October 13, 2017
ESSR Consensus Document for Detection, Characterization, and Referral Pathway for Tumors and Tumorlike Lesions of BoneRadhesh Lalam, Johan L Bloem, Iris M Noebauer-Huhmann, et al.
Pageof 10

Showing results (81-90 of 96) with videos related to

Sort By:
Pageof 10
European Radiology|August 4, 2004
Accuracy of MRI in characterization of soft tissue tumors and tumor-like lesions. A prospective study in 548 patientsJan L M A Gielen, Arthur M De Schepper, Filip Vanhoenacker, et al.
Insights Into Imaging|February 21, 2012
A comparison between histopathology and findings on magnetic resonance imaging of subcutaneous lipomatous soft-tissue tumorsJohannes Toirkens, Arthur M De Schepper, Filip Vanhoenacker, et al.
Pain Management|March 6, 2026
Beyond the capsule: an integrated perspective on the wide world of frozen shoulder. A collaborative viewpointFabrizio Brindisino, Michel Gcam Mertens, Paul Salamh, et al.
European Radiology|February 9, 2026
ESR Essentials: bone marrow MRI in oncology-practice recommendations by the European Society of Musculoskeletal RadiologyFrédéric E Lecouvet, Lokmane Taihi, Thomas Kirchgesner, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|March 29, 2007
Identification of sex-specific associations between polymorphisms of the osteoprotegerin gene, TNFRSF11B, and Paget's disease of boneGreet Beyens, Anna Daroszewska, Fenna de Freitas, et al.
Molecular Genetics and Metabolism|April 20, 2011
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 polymorphismsPui Yan Jenny Chung, Greet Beyens, Fenna de Freitas, et al.
American Journal of Human Genetics|August 16, 2006
A new autosomal recessive form of Stickler syndrome is caused by a mutation in the COL9A1 geneGuy Van Camp, Rikkert L Snoeckx, Nele Hilgert, et al.
Pathology, Research and Practice|January 25, 2022
Malignant pleural mesothelioma with an EML4-ALK fusion: Expect the unexpected!Fleur Cordier, Joni Van der Meulen, Nadine van Roy, et al.
Human Genetics|September 15, 2010
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 genesPui Yan Jenny Chung, Greet Beyens, Steven Boonen, et al.
Seminars in Musculoskeletal Radiology|October 13, 2017
ESSR Consensus Document for Detection, Characterization, and Referral Pathway for Tumors and Tumorlike Lesions of BoneRadhesh Lalam, Johan L Bloem, Iris M Noebauer-Huhmann, et al.
Pageof 10