Year |
Citation |
Score |
2020 |
Van de Voorde N, Mortier GR, Vanhoenacker FM. Fibrous Dysplasia, Paget's Disease of Bone, and Other Uncommon Sclerotic Bone Lesions of the Craniofacial Bones. Seminars in Musculoskeletal Radiology. 24: 570-578. PMID 33036044 DOI: 10.1055/s-0039-3400292 |
0.351 |
|
2019 |
Van Hul W, Boudin E, Vanhoenacker FM, Mortier G. Camurati-Engelmann Disease. Calcified Tissue International. PMID 30721323 DOI: 10.1007/s00223-019-00532-1 |
0.378 |
|
2013 |
Vancauwenberghe T, Vanhoenacker F, Doninck JV, Declercq H. Periosteal chondroma of the proximal tibia mimicking Osgood-schlatter’s disease Journal of the Belgian Society of Radiology. 96: 30. DOI: 10.5334/JBR-BTR.178 |
0.365 |
|
2010 |
Perdu B, de Freitas F, Frints SG, Schouten M, Schrander-Stumpel C, Barbosa M, Pinto-Basto J, Reis-Lima M, de Vernejoul MC, Becker K, Freckmann ML, Keymolen K, Haan E, Savarirayan R, Koenig R, ... ... Vanhoenacker FM, et al. Osteopathia striata with cranial sclerosis owing to WTX gene defect. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 25: 82-90. PMID 20209645 DOI: 10.1359/jbmr.090707 |
0.318 |
|
2009 |
Chung⁎ P, Beyens G, Riches P, Van Wesenbeeck L, Jennes K, Daroszewska A, Boonen S, Geusens P, Vanhoenacker F, Verbruggen L, Van Offel J, Goemaere S, Zmierczak H, Westhovens R, Karperien M, et al. Genetic variation in the TNFRSF11A (RANK) gene contributes to the risk to develop sporadic Paget's disease of bone Bone. 44: S347-S348. DOI: 10.1016/J.BONE.2009.03.161 |
0.329 |
|
2005 |
Janssens K, Vanhoenacker F, Bonduelle M, Verbruggen L, Van Maldergem L, Ralston S, Guañabens N, Migone N, Wientroub S, Divizia MT, Bergmann C, Bennett C, Simsek S, Melançon S, Cundy T, et al. Camurati-Engelmann disease: review of the clinical, radiological, and molecular data of 24 families and implications for diagnosis and treatment. Journal of Medical Genetics. 43: 1-11. PMID 15894597 DOI: 10.1136/jmg.2005.033522 |
0.345 |
|
2005 |
Janssens K, de Vernejoul MC, de Freitas F, Vanhoenacker F, Van Hul W. An intermediate form of juvenile Paget's disease caused by a truncating TNFRSF11B mutation. Bone. 36: 542-8. PMID 15777670 DOI: 10.1016/J.BONE.2004.12.004 |
0.321 |
|
2004 |
Janssens K, Thompson E, Vanhoenacker F, Savarirayan R, Morris L, Dobbie A, Van Hul W. Macrocephaly and sclerosis of the tubular bones in an isolated patient: a mild case of craniodiaphyseal dysplasia? Clinical Dysmorphology. 12: 245-50. PMID 14564212 DOI: 10.1097/00019605-200310000-00007 |
0.402 |
|
2003 |
Wergedal JE, Veskovic K, Hellan M, Nyght C, Balemans W, Libanati C, Vanhoenacker FM, Tan J, Baylink DJ, Van Hul W. Patients with Van Buchem disease, an osteosclerotic genetic disease, have elevated bone formation markers, higher bone density, and greater derived polar moment of inertia than normal. The Journal of Clinical Endocrinology and Metabolism. 88: 5778-83. PMID 14671168 DOI: 10.1210/jc.2003-030201 |
0.692 |
|
2003 |
Vanhoenacker FM, Balemans W, Tan GJ, Dikkers FG, De Schepper AM, Mathysen DG, Bernaerts A, Hul WV. Van Buchem disease: lifetime evolution of radioclinical features. Skeletal Radiology. 32: 708-18. PMID 14520501 DOI: 10.1007/s00256-003-0675-4 |
0.462 |
|
2003 |
Vanhoenacker FM, Janssens K, Van Hul W, Gershoni-Baruch R, Brik R, De Schepper AM. Camurati-Engelmann disease. Review of radioclinical features. Acta Radiologica (Stockholm, Sweden : 1987). 44: 430-4. PMID 12846694 DOI: 10.1034/J.1600-0455.2003.00088.X |
0.429 |
|
2003 |
Vanhoenacker FM, Janssens K, Van Hul W, Gershoni-Baruch R, Brik R, De Schepper AM. Camurati-engelmann disease: Review of radioclinical features Acta Radiologica. 44: 430-434. DOI: 10.1080/j.1600-0455.2003.00088.x |
0.352 |
|
2002 |
Hul EV, Gram J, Bollerslev J, Wesenbeeck LV, Mathysen D, Andersen PE, Vanhoenacker F, Hul WV. Localization of the Gene Causing Autosomal Dominant Osteopetrosis Type I to Chromosome 11q12‐13 Journal of Bone and Mineral Research. 17: 1111-1117. PMID 12054167 DOI: 10.1359/Jbmr.2002.17.6.1111 |
0.581 |
|
2002 |
Van Hul W, Vanhoenacker F, Balemans W, Janssens K, De Schepper AM. Molecular and radiological diagnosis of sclerosing bone dysplasias. European Journal of Radiology. 40: 198-207. PMID 11731208 DOI: 10.1016/S0720-048X(01)00400-4 |
0.325 |
|
2002 |
Ozsarlak O, Schepens E, Parizel PM, Van Goethem JW, Vanhoenacker F, De Schepper AM, Martin JJ. Hereditary neuromuscular diseases. European Journal of Radiology. 40: 184-97. PMID 11731207 DOI: 10.1016/S0720-048X(01)00399-0 |
0.33 |
|
2001 |
Wuyts W, Van Wesenbeeck L, Morales-Piga A, Ralston S, Hocking L, Vanhoenacker F, Westhovens R, Verbruggen L, Anderson D, Hughes A, Van Hul W. Evaluation of the role of RANK and OPG genes in Paget's disease of bone. Bone. 28: 104-7. PMID 11165949 DOI: 10.1016/S8756-3282(00)00411-7 |
0.356 |
|
2000 |
Janssens K, Gershoni-Baruch R, Guañabens N, Migone N, Ralston S, Bonduelle M, Lissens W, Van Maldergem L, Vanhoenacker F, Verbruggen L, Van Hul W. Mutations in the gene encoding the latency-associated peptide of TGF-beta 1 cause Camurati-Engelmann disease. Nature Genetics. 26: 273-5. PMID 11062463 DOI: 10.1038/81563 |
0.358 |
|
2000 |
Vanhoenacker FM, De Beuckeleer LH, Van Hul W, Balemans W, Tan GJ, Hill SC, De Schepper AM. Sclerosing bone dysplasias: Genetic arid radioclinical features European Radiology. 10: 1423-1433. PMID 10997431 DOI: 10.1007/s003300000495 |
0.429 |
|
2000 |
Janssens K, Gershoni-Baruch R, Van Hul E, Brik R, Guañabens N, Migone N, Verbruggen LA, Ralston SH, Bonduelle M, Van Maldergem L, Vanhoenacker F, Van Hul W. Localisation of the gene causing diaphyseal dysplasia Camurati-Engelmann to chromosome 19q13. Journal of Medical Genetics. 37: 245-9. PMID 10745041 DOI: 10.1136/jmg.37.4.245 |
0.406 |
|
2000 |
Vanhoenacker F, Vandevenne J, De Schepper A, De Leersnijder J. Regarding “Adventitial cystic disease: a unifying hypothesis” Journal of Vascular Surgery. 31: 621-622. DOI: 10.1067/MVA.2000.104415 |
0.33 |
|
1999 |
Balemans W, Van Den Ende J, Paes-Alves AF, Dikkers FG, Willems PJ, Vanhoenacker F, De Almeida-Melo N, Alves CF, Stratakis CA, Hill SC, Van Hul W. Localization of the gene for sclerosteosis to the van Buchem disease- gene region on chromosome 17q12-q21 American Journal of Human Genetics. 64: 1661-1669. PMID 10330353 DOI: 10.1086/302416 |
0.401 |
|
1998 |
Van Hul W, Balemans W, Van Hul E, Dikkers FG, Obee H, Stokroos RJ, Hildering P, Vanhoenacker F, Van Camp G, Willems PJ. Van Buchem disease (hyperostosis corticalis generalisata) maps to chromosome 17q12-q21. American Journal of Human Genetics. 62: 391-9. PMID 9463328 DOI: 10.1086/301721 |
0.439 |
|
1997 |
Van Hul W, Bollerslev J, Gram J, Van Hul E, Wuyts W, Benichou O, Vanhoenacker F, Willems PJ. Localization of a gene for autosomal dominant osteopetrosis (Albers-Schönberg disease) to chromosome 1p21. American Journal of Human Genetics. 61: 363-9. PMID 9311741 DOI: 10.1086/514844 |
0.41 |
|
Show low-probability matches. |