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Journal Abstract Search

175 related items for PubMed ID: 19214502

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  • 29. Camurati-Engelmann disease (progressive diaphyseal dysplasia) in a Moroccan family.
    Simsek S, Janssens K, Kwee ML, Van Hul W, Veenstra J, Netelenbos JC.
    Osteoporos Int; 2005 Sep; 16(9):1167-70. PubMed ID: 15959620
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  • 31. Progressive diaphyseal dysplasia (Engelmann disease(: scintigraphic-radiographic-clinical correlations.
    Kumar B, Murphy WA, Whyte MP.
    Radiology; 1981 Jul; 140(1):87-92. PubMed ID: 6454165
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  • 32. Clinical characteristics and identification of a novel TGFB1 variant in three unrelated Chinese families with Camurati-Engelmann disease.
    Tao XH, Yang XG, Wang ZY, Xu Y, Lin XY, Xu T, Zhang ZL, Yue H.
    Mol Genet Genomic Med; 2022 May; 10(5):e1922. PubMed ID: 35315241
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  • 33. A new LRP6 variant and Camurati-Engelmann-like disease.
    Pickering ME, Ltaief-Boudrigua A, Feurer E, Collet C, Chapurlat R.
    Bone; 2021 Feb; 143():115706. PubMed ID: 33164853
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  • 34. [Value of various radiological study results in the follow-up of Camurati-Engelmann disease].
    Wilhelm KR, Lenarz T, Weise D, Baldauf G, Fritz P, Bihl H.
    Rofo; 1987 Sep; 147(3):278-82. PubMed ID: 2823332
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  • 35. Bone scintigraphy demonstrating Engelmann's disease.
    Sty JR, Babbitt DP, Starshak RJ.
    Clin Nucl Med; 1978 Feb; 3(2):69-70. PubMed ID: 657659
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  • 36. Camurati-Engelmann disease (progressive diaphyseal dysplasia): reports of an Indian kindred.
    Bhadada SK, Sridhar S, Steenackers E, Dhiman V, Mortier G, Bhansali A, Van Hul W.
    Calcif Tissue Int; 2014 Feb; 94(2):240-7. PubMed ID: 24154985
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  • 40. Camurati-Engelmann disease: unique variant featuring a novel mutation in TGFβ1 encoding transforming growth factor beta 1 and a missense change in TNFSF11 encoding RANK ligand.
    Whyte MP, Totty WG, Novack DV, Zhang X, Wenkert D, Mumm S.
    J Bone Miner Res; 2011 May; 26(5):920-33. PubMed ID: 21541994
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