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Year Number of Results
1989 1
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1991 1
1994 1
1995 2
1996 1
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1999 2
2000 2
2001 3
2003 4
2005 4
2006 2
2007 2
2008 1
2009 1
2010 3
2011 2
2012 2
2013 2
2014 1
2015 3
2016 3
2017 2
2018 2
2019 3
2020 2
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2023 3
2024 0

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60 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 d …
Femoral stem modularity.
Mertl P, Dehl M. Mertl P, et al. Orthop Traumatol Surg Res. 2020 Feb;106(1S):S35-S42. doi: 10.1016/j.otsr.2019.05.019. Epub 2019 Oct 14. Orthop Traumatol Surg Res. 2020. PMID: 31624033 Free article. Review.
Moreover, it provides no functional advantage, and no longer has a role outside dysplasia and other femoral deformities. Metaphyseal-diaphyseal modularity is not widespread in primary implants, and is it really necessary? ...The connection between a proximal femoral …
Moreover, it provides no functional advantage, and no longer has a role outside dysplasia and other femoral deformities. Metaphyseal- …
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.
In such cases, it can be considered a form of paraneoplastic syndrome. The most prevalent secondary causes of HOA are pulmonary in origin, which is why this condition was formerly referred to as hypertrophic pulmonary osteoarthropathy. ...The authors summarize the pathogen …
In such cases, it can be considered a form of paraneoplastic syndrome. The most prevalent secondary causes of HOA are pulmonary in or …
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 w …
Conditions with abnormal sterol metabolism and different genetic basis have clinical and radiographic features similar to Greenberg dyspl …
Miscellaneous Bone Disorders.
Mughal MZ, Padidela R. Mughal MZ, et al. Endocr Dev. 2015;28:226-246. doi: 10.1159/000381048. Epub 2015 Jun 12. Endocr Dev. 2015. PMID: 26138845 Review.
Imaging features and differential diagnosis of multiple diaphyseal sclerosis: A case report and review of literature.
Cai Y, Lin H, Huang F, Zheng X, Huang Y, Zhang S. Cai Y, et al. Medicine (Baltimore). 2018 Aug;97(33):e11725. doi: 10.1097/MD.0000000000011725. Medicine (Baltimore). 2018. PMID: 30113457 Free PMC article. Review.
RATIONALE: Multiple diaphyseal sclerosis (MDS), known as Ribbing disease, is a rare congenital bone disease resulting from autosomal recessive inheritance. ...LESSONS: MDS is rare and may often be initially misdiagnosed as another type of sclerosing bone dysplasia, …
RATIONALE: Multiple diaphyseal sclerosis (MDS), known as Ribbing disease, is a rare congenital bone disease resulting from autosomal …
Cranio-meta-diaphyseal dysplasia: 25 year follow-up and review of literature.
Dhar SU, Taylor T, Trinh C, Sutton VR. Dhar SU, et al. Am J Med Genet A. 2010 Sep;152A(9):2335-8. doi: 10.1002/ajmg.a.33582. Am J Med Genet A. 2010. PMID: 20684007 Review.
We report here on a 25-year follow-up of cranio-meta-diaphyseal dysplasia in a 31-year-old Caucasian male, who was reported in the literature at the age of 8 years [Langer et al. (1991); Skeletal Radiol 20:37-41]. ...He is the oldest reported patient with this disor …
We report here on a 25-year follow-up of cranio-meta-diaphyseal dysplasia in a 31-year-old Caucasian male, who was reported in …
Sclerosing bone dysplasias--a target-site approach.
Greenspan A. Greenspan A. Skeletal Radiol. 1991;20(8):561-83. doi: 10.1007/BF01106087. Skeletal Radiol. 1991. PMID: 1776023 Review.
The list of conditions constituting this group is relatively short: osteopetrosis (Albers-Schonberg disease), pycnodysostosis (Maroteaux-Lamy disease), enostosis (bone island), osteopoikilosis, osteopathia striata (Voorhoeve disease), progressive diaphyseal dysplasia …
The list of conditions constituting this group is relatively short: osteopetrosis (Albers-Schonberg disease), pycnodysostosis (Maroteaux-Lam …
Sclerosing bone disorders.
de Vernejoul MC. de Vernejoul MC. Best Pract Res Clin Rheumatol. 2008 Mar;22(1):71-83. doi: 10.1016/j.berh.2007.12.011. Best Pract Res Clin Rheumatol. 2008. PMID: 18328982 Review.
Osteocondensation can also be related to increased bone formation. Camurati-Engelman dysplasia is a disabilitating disorder with leg pain and weakness, and thickening of the diaphysis of long bones on x ray. ...Other less common recessive or dominant sclerosing disorders, …
Osteocondensation can also be related to increased bone formation. Camurati-Engelman dysplasia is a disabilitating disorder with leg …
The Erlenmeyer flask bone deformity in the skeletal dysplasias.
Faden MA, Krakow D, Ezgu F, Rimoin DL, Lachman RS. Faden MA, et al. Am J Med Genet A. 2009 Jun;149A(6):1334-45. doi: 10.1002/ajmg.a.32253. Am J Med Genet A. 2009. PMID: 19444897 Free PMC article. Review.
Utilizing a literature review and cohort study of 12 disorders we found 20 distinct disorders were associated with EFD. We interrogated the International Skeletal Dysplasia Registry (ISDR) radiographic database (1988-2007) to determine which skeletal dysplasias or syndrome …
Utilizing a literature review and cohort study of 12 disorders we found 20 distinct disorders were associated with EFD. We interrogated the …
60 results