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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1954 1
1977 2
1979 1
1980 1
1981 1
1982 2
1983 1
1985 2
1986 1
1987 3
1989 1
1993 2
1994 1
1995 1
1998 1
1999 2
2000 2
2001 1
2002 1
2003 2
2004 1
2005 1
2007 2
2009 2
2011 1
2012 1
2013 1
2014 1
2016 3
2017 3
2019 1
2020 1
2021 1
2022 1
2023 1
2024 0

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48 results

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Page 1
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. ...
Camurati-Engelmann disease or progressive diaphyseal dysplasia is a rare autosomal dominant sclerosing bone dysplasia. ...
Proband and the Brother.
B S, Kotha JP. B S, et al. J Assoc Physicians India. 2023 Jan;71(1):1. J Assoc Physicians India. 2023. PMID: 37116016
As patient brother had limp since childhood genetic disorders were and a provisional diagnosis of sclerotic bone disease probable Progressive diaphyseal dysplasia was considered. PET-CT was done which revealed abnormal osteoblastic activity in both femurs, focal hyp …
As patient brother had limp since childhood genetic disorders were and a provisional diagnosis of sclerotic bone disease probable Progressiv …
Hypertrophic Osteoarthropathy: Clinical and Imaging Features.
Yap FY, Skalski MR, Patel DB, Schein AJ, White EA, Tomasian A, Masih S, Matcuk GR Jr. Yap FY, et al. Radiographics. 2017 Jan-Feb;37(1):157-195. doi: 10.1148/rg.2017160052. Epub 2016 Dec 9. Radiographics. 2017. PMID: 27935768 Review.
The authors summarize the pathogenesis, classification, causes, and symptoms and signs of HOA, including the genetics underlying the primary form (pachydermoperiostosis); describe key findings of HOA found at various imaging modalities, with examples of underlying causative condi …
The authors summarize the pathogenesis, classification, causes, and symptoms and signs of HOA, including the genetics underlying the primary …
Engelmann's disease.
Krohel GB, Wirth CR. Krohel GB, et al. Am J Ophthalmol. 1977 Oct;84(4):520-5. doi: 10.1016/0002-9394(77)90445-7. Am J Ophthalmol. 1977. PMID: 910856
A 5-year-old boy with diaphyseal dysplasia who exhibited marked involvement of the cranial bones developed marked disk edema in a one-year period. ...
A 5-year-old boy with diaphyseal dysplasia who exhibited marked involvement of the cranial bones developed marked disk edema i …
Sclerosing bone dysplasias: genetic, clinical and radiology update of hereditary and non-hereditary disorders.
Boulet C, Madani H, Lenchik L, Vanhoenacker F, Amalnath DS, de Mey J, De Maeseneer M. Boulet C, et al. Br J Radiol. 2016 Jun;89(1062):20150349. doi: 10.1259/bjr.20150349. Epub 2016 Feb 22. Br J Radiol. 2016. PMID: 26898950 Free PMC article. Review.
Hereditary bony dysplasias include osteopoikilosis, osteopathia striata, osteopetrosis, progressive diaphyseal dysplasia, hereditary multiple diaphyseal sclerosis and pyknodysostosis. ...
Hereditary bony dysplasias include osteopoikilosis, osteopathia striata, osteopetrosis, progressive diaphyseal dysplasia, here …
Sclerosing bone dysplasias: review and differentiation from other causes of osteosclerosis.
Ihde LL, Forrester DM, Gottsegen CJ, Masih S, Patel DB, Vachon LA, White EA, Matcuk GR Jr. Ihde LL, et al. Radiographics. 2011 Nov-Dec;31(7):1865-82. doi: 10.1148/rg.317115093. Radiographics. 2011. PMID: 22084176 Review.
Several genes have been discovered that, when disrupted, result in specific types of hereditary sclerosing bone dysplasia (osteopetrosis, pyknodysostosis, osteopoikilosis, osteopathia striata, progressive diaphyseal dysplasia, hereditary multiple diaphyseal sclerosi …
Several genes have been discovered that, when disrupted, result in specific types of hereditary sclerosing bone dysplasia (osteopetrosis, py …
Cortical lesions of the tibia: characteristic appearances at conventional radiography.
Levine SM, Lambiase RE, Petchprapa CN. Levine SM, et al. Radiographics. 2003 Jan-Feb;23(1):157-77. doi: 10.1148/rg.231015088. Radiographics. 2003. PMID: 12533651 Review.
Lesions that cause cortical proliferation include osteochondroma, stress fracture, osteoid osteoma, periosteal osteogenic sarcoma, diaphyseal dysplasia, venous stasis, cellulitis, chronic osteomyelitis, osteopathia striatum, and melorheostosis. ...
Lesions that cause cortical proliferation include osteochondroma, stress fracture, osteoid osteoma, periosteal osteogenic sarcoma, diaphy …
Sclerosing bone dysplasias: genetic and radioclinical features.
Vanhoenacker FM, De Beuckeleer LH, Van Hul W, Balemans W, Tan GJ, Hill SC, De Schepper AM. Vanhoenacker FM, et al. Eur Radiol. 2000;10(9):1423-33. doi: 10.1007/s003300000495. Eur Radiol. 2000. PMID: 10997431 Review.
Within each group, further differentiation can be made by distinctive clinical findings and by mode of inheritance: (a) dysplasias of endochondral bone formation: osteopetrosis (Albers-Schonberg disease), pycnodysostosis, enostosis, osteopoikilosis, osteopathia striata (Voorhoeve …
Within each group, further differentiation can be made by distinctive clinical findings and by mode of inheritance: (a) dysplasias of endoch …
A new case of Greenberg dysplasia and literature review suggest that Greenberg dysplasia, dappled diaphyseal dysplasia, and Astley-Kendall dysplasia are allelic disorders.
Gregersen PA, McKay V, Walsh M, Brown E, McGillivray G, Savarirayan R. Gregersen PA, et al. Mol Genet Genomic Med. 2020 Jun;8(6):e1173. doi: 10.1002/mgg3.1173. Epub 2020 Apr 18. Mol Genet Genomic Med. 2020. PMID: 32304187 Free PMC article. Review.
Conditions with abnormal sterol metabolism and different genetic basis have clinical and radiographic features similar to Greenberg dysplasia, for example X-linked dominant chondrodysplasia punctata, Conradi-Hunermann type, and CHILD syndrome, and other conditions with unknown ge …
Conditions with abnormal sterol metabolism and different genetic basis have clinical and radiographic features similar to Greenberg dysplasi …
Progressive diaphyseal dysplasia (Camurati-Engelmann): radiographic follow-up and CT findings.
Kaftori JK, Kleinhaus U, Naveh Y. Kaftori JK, et al. Radiology. 1987 Sep;164(3):777-82. doi: 10.1148/radiology.164.3.3615880. Radiology. 1987. PMID: 3615880
Sixteen patients with progressive diaphyseal dysplasia (PDD) and aged six months to 76 years were examined. ...
Sixteen patients with progressive diaphyseal dysplasia (PDD) and aged six months to 76 years were examined. ...
48 results