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Journal Abstract Search

155 related items for PubMed ID: 20566907

  • 1. Skull base manifestations of Camurati-Engelmann disease.
    Carlson ML, Beatty CW, Neff BA, Link MJ, Driscoll CL.
    Arch Otolaryngol Head Neck Surg; 2010 Jun; 136(6):566-75. PubMed ID: 20566907
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  • 2. Repeat Intracranial Expansion After Skull Regrowth in Hyperostotic Disease: Technical Note.
    Wong T, Herschman Y, Patel NV, Patel T, Hanft S.
    World Neurosurg; 2017 Jun; 102():555-560. PubMed ID: 28137547
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  • 4. Decompression of the internal auditory canal via the retrosigmoid approach in a patient with Camurati-Engelmann disease: illustrative case.
    Achahbar SE, Somers T, Van Havenbergh T.
    J Neurosurg Case Lessons; 2021 Jan 25; 1(4):. PubMed ID: 36131584
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  • 6. Aggressive cranial vault decompression for cranial hyperostosis: technical case report of two cases.
    Mocco J, Komotar RJ, Zacharia BE, Feldstein NA, Bruce JN.
    Neurosurgery; 2005 Jul 25; 57(1 Suppl):E212; discussion E212. PubMed ID: 15987595
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  • 11. Mild Camurati‑Engelamann disease presenting with exophthalmos as the first and only manifestation: A case report.
    Jiajue R, Wu B, Jiang Y, Wang O, Li M, Xing X, Xia W.
    Mol Med Rep; 2016 Sep 25; 14(3):2710-6. PubMed ID: 27484238
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  • 12. Phenotypic manifestations and management of hyperostosis cranialis interna, a hereditary bone dysplasia affecting the calvaria and the skull base.
    Waterval JJ, Stokroos RJ, Bauer NJ, De Bondt RB, Manni JJ.
    Am J Med Genet A; 2010 Mar 25; 152A(3):547-55. PubMed ID: 20140965
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  • 13. Bilateral visual loss in craniodiaphysial dysplasia.
    Kim CH, Oh DE, Kim YD.
    Am J Ophthalmol; 2006 Feb 25; 141(2):398-9. PubMed ID: 16458710
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  • 14. [Observations on the Camurati-Engelmann syndrome. Demonstration of changes of the petrous bone using high-resolution computed tomography].
    Dannenmaier B, Weber B.
    Rofo; 1989 Aug 25; 151(2):175-8. PubMed ID: 2548243
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  • 16. Significant Improvement After Surgery for a Symptomatic Osteoblastoma in a Patient with Camurati-Engelmann Disease: Case Report and Literature Review.
    Yonezawa H, Hayashi K, Yamamoto N, Takeuchi A, Tada K, Miwa S, Igarashi K, Kimura H, Aoki Y, Morinaga S, Araki Y, Asano Y, Sakurakichi K, Ikeda H, Nojima T, Tsuchiya H.
    Calcif Tissue Int; 2021 Jun 25; 108(6):819-824. PubMed ID: 33555353
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  • 19. Camurati-Engelmann disease (progressive hereditary craniodiaphyseal dysplasia). Case report.
    Yen JK, Bourke RS, Popp AJ, Wirth CR.
    J Neurosurg; 1978 Jan 25; 48(1):138-42. PubMed ID: 619016
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  • 20. [Otolaryngological aspects of Camurati-Engelmann disease (progressive diaphyseal dysplasia): review of literature and report of one case].
    Paludetti G, Galli A, Lombardi R, Almadori G, Pujolas FX, Maurizi M.
    Acta Otorrinolaringol Esp; 1994 Jan 25; 45(3):207-13. PubMed ID: 8068367
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