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1970 3
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1989 10
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1999 6
2000 13
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2003 11
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2013 13
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401 results

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Page 1
Camurati-Engelmann Disease.
Wallace SE, Wilcox WR. Wallace SE, et al. 2004 Jun 25 [updated 2023 Aug 31]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2004 Jun 25 [updated 2023 Aug 31]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301335 Free Books & Documents. Review.
CLINICAL CHARACTERISTICS: Camurati-Engelmann disease (CED) is characterized by hyperostosis of the long bones and the skull, proximal muscle weakness, limb pain, a wide-based, waddling gait, and joint contractures. ...Surveillance: Assess development of gross …
CLINICAL CHARACTERISTICS: Camurati-Engelmann disease (CED) is characterized by hyperostosis of the long bones and the s …
Camurati-Engelmann Disease.
Van Hul W, Boudin E, Vanhoenacker FM, Mortier G. Van Hul W, et al. Calcif Tissue Int. 2019 May;104(5):554-560. doi: 10.1007/s00223-019-00532-1. Epub 2019 Feb 5. Calcif Tissue Int. 2019. PMID: 30721323 Review.
Camurati-Engelmann disease or progressive diaphyseal dysplasia is a rare autosomal dominant sclerosing bone dysplasia. ...Clinically, the patients suffer from bone pain, easy fatigability, and decreased muscle mass and weakness in the proximal parts of the lo
Camurati-Engelmann disease or progressive diaphyseal dysplasia is a rare autosomal dominant sclerosing bone dysplasia.
Camurati-Engelmann Disease: A Case-Based Review About an Ultrarare Bone Dysplasia.
Klemm P, Aykara I, Lange U. Klemm P, et al. Eur J Rheumatol. 2023 Jan;10(1):34-38. doi: 10.5152/eurjrheum.2023.21115. Eur J Rheumatol. 2023. PMID: 36880809 Free PMC article.
Camurati-Engelmann disease is also associated with myopathy and neurological manifestations. Clinically, Camurati-Engelmann disease typically presents with bone pain in the lower extremities, muscle weakness, and a wobbly, stilted gait. .
Camurati-Engelmann disease is also associated with myopathy and neurological manifestations. Clinically, Camurati
Camurati-Engelmann disease.
de Bonilla Damiá Á, García Gómez FJ. de Bonilla Damiá Á, et al. Reumatol Clin. 2017 Jan-Feb;13(1):48-49. doi: 10.1016/j.reuma.2015.12.004. Epub 2016 Jan 29. Reumatol Clin. 2017. PMID: 26830437 Free article. English, Spanish. No abstract available.
Camurati-Engelmann disease or Ribbing disease.
Dubost JJ, Soubrier M. Dubost JJ, et al. Joint Bone Spine. 2021 May;88(3):105130. doi: 10.1016/j.jbspin.2021.105130. Epub 2021 Jan 20. Joint Bone Spine. 2021. PMID: 33484859 No abstract available.
[Camurati-Engelmann disease].
Kinoshita A. Kinoshita A. Nihon Rinsho. 2015 Dec;73(12):2149-59. Nihon Rinsho. 2015. PMID: 26666167 Review. Japanese.
Camurati-Engelmann disease (CAEND, OMIM 131300) is a rare autosomal dominant, progressive diaphyseal dysplasia, which is characterized by hyperosteosis and sclerosis of the diaphyses of long bones. ...
Camurati-Engelmann disease (CAEND, OMIM 131300) is a rare autosomal dominant, progressive diaphyseal dysplasia, which i
Camurati-Engelmann disease combined with transethmoidal meningoencephalocele: illustrative case.
Yanagihara W, Wada T, Nomura JI, Saura H, Kubo Y, Ogasawara K. Yanagihara W, et al. J Neurosurg Case Lessons. 2022 Feb 28;3(9):CASE21587. doi: 10.3171/CASE21587. Print 2022 Feb 28. J Neurosurg Case Lessons. 2022. PMID: 36130541 Free PMC article.
BACKGROUND: Camurati-Engelmann disease (CED) is a rare disorder characterized by progressive cranial hyperostosis and diaphyseal sclerosis of the long bones. ...
BACKGROUND: Camurati-Engelmann disease (CED) is a rare disorder characterized by progressive cranial hyperostosis and d …
Diagnosing Camurati-Engelmann disease-the age of whole-exome sequencing.
Nagra D, Russell MD, Alveyn E, Birring SS, Elias D, Balachandran S, Galloway JB. Nagra D, et al. Rheumatology (Oxford). 2023 Jul 5;62(7):e221-e222. doi: 10.1093/rheumatology/keac670. Rheumatology (Oxford). 2023. PMID: 36519831 Free PMC article. No abstract available.
Regarding Camurati-Engelmann Disease: To the Editor.
Viana MM, Nunes SV, Fernandes Gomes DCF, de Andrade MAP, de Aguiar MJB. Viana MM, et al. Clin Orthop Surg. 2018 Mar;10(1):116-117. doi: 10.4055/cios.2018.10.1.116. Epub 2018 Feb 27. Clin Orthop Surg. 2018. PMID: 29564056 Free PMC article. No abstract available.
Skull base manifestations of Camurati-Engelmann disease.
Carlson ML, Beatty CW, Neff BA, Link MJ, Driscoll CL. Carlson ML, et al. Arch Otolaryngol Head Neck Surg. 2010 Jun;136(6):566-75. doi: 10.1001/archoto.2010.68. Arch Otolaryngol Head Neck Surg. 2010. PMID: 20566907 Review.
OBJECTIVE: To describe presenting symptoms, evaluation findings, and surgical management of cranial base hyperostosis in patients with Camurati-Engelmann disease (CED). DESIGN: Retrospective study and literature review. ...Although corticosteroids and bisphos …
OBJECTIVE: To describe presenting symptoms, evaluation findings, and surgical management of cranial base hyperostosis in patients with Ca
401 results