C. Boulet, H. Madani, L. Lenchik, F. Vanhoenacker, D. S. Amalnath, J. de Mey, M. De Maeseneer: Sclerosing bone dysplasias: genetic, clinical and radiology update of hereditary and non-hereditary disorders. In: The British journal of radiology. Band 89, Nummer 1062, Juni 2016, S. 20150349, doi:10.1259/bjr.20150349, PMID 26898950, PMC 5258139 (freier Volltext) (Review).
A. Greenspan: Sclerosing bone dysplasias–a target-site approach. In: Skeletal radiology. Band 20, Nummer 8, 1991, S. 561–583, doi:10.1007/BF01106087, PMID 1776023 (Review).
A. M. Zicari, L. Tarani, D. Perotti, L. Papetti, F. Nicita, N. Liberati, A. Spalice, G. Salvatori, F. Guaraldi, M. Duse: WTX R353X mutation in a family with osteopathia striata and cranial sclerosis (OS-CS): case report and literature review of the disease clinical, genetic and radiological features. In: Italian journal of pediatrics. Band 38, Juni 2012, S. 27, doi:10.1186/1824-7288-38-27, PMID 22716240, PMC 3416731 (freier Volltext) (Review).
J. A. Gehweiler, W. R. Bland, T. S. Carden, R. H. Daffner: Osteopathia striata–Voorhoeve's disease. Review of the roentgen manifestations. In: The American journal of roentgenology, radium therapy, and nuclear medicine. Band 118, Nummer 2, Juni 1973, S. 450–455, doi:10.2214/ajr.118.2.450, PMID 4541298.
F. M. Vanhoenacker, L. H. De Beuckeleer, W. Van Hul, W. Balemans, G. J. Tan, S. C. Hill, A. M. De Schepper: Sclerosing bone dysplasias: genetic and radioclinical features. In: European radiology. Band 10, Nummer 9, 2000, S. 1423–1433, doi:10.1007/s003300000495, PMID 10997431 (Review).
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C. Boulet, H. Madani, L. Lenchik, F. Vanhoenacker, D. S. Amalnath, J. de Mey, M. De Maeseneer: Sclerosing bone dysplasias: genetic, clinical and radiology update of hereditary and non-hereditary disorders. In: The British journal of radiology. Band 89, Nummer 1062, Juni 2016, S. 20150349, doi:10.1259/bjr.20150349, PMID 26898950, PMC 5258139 (freier Volltext) (Review).
A. Greenspan: Sclerosing bone dysplasias–a target-site approach. In: Skeletal radiology. Band 20, Nummer 8, 1991, S. 561–583, doi:10.1007/BF01106087, PMID 1776023 (Review).
A. M. Zicari, L. Tarani, D. Perotti, L. Papetti, F. Nicita, N. Liberati, A. Spalice, G. Salvatori, F. Guaraldi, M. Duse: WTX R353X mutation in a family with osteopathia striata and cranial sclerosis (OS-CS): case report and literature review of the disease clinical, genetic and radiological features. In: Italian journal of pediatrics. Band 38, Juni 2012, S. 27, doi:10.1186/1824-7288-38-27, PMID 22716240, PMC 3416731 (freier Volltext) (Review).
J. A. Gehweiler, W. R. Bland, T. S. Carden, R. H. Daffner: Osteopathia striata–Voorhoeve's disease. Review of the roentgen manifestations. In: The American journal of roentgenology, radium therapy, and nuclear medicine. Band 118, Nummer 2, Juni 1973, S. 450–455, doi:10.2214/ajr.118.2.450, PMID 4541298.
F. M. Vanhoenacker, L. H. De Beuckeleer, W. Van Hul, W. Balemans, G. J. Tan, S. C. Hill, A. M. De Schepper: Sclerosing bone dysplasias: genetic and radioclinical features. In: European radiology. Band 10, Nummer 9, 2000, S. 1423–1433, doi:10.1007/s003300000495, PMID 10997431 (Review).
