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Quoted phrase not found in phrase index: "Thickened cortex of long bones"
Page 1
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.
DIAGNOSES: MDS is characterized radiographically by a fusiform widening of the diaphyseal portion of the long bones, which is caused by a thickening of the cortex with obstruction of the medullary cavity. The pathologies are observed utilizing d …
DIAGNOSES: MDS is characterized radiographically by a fusiform widening of the diaphyseal portion of the long bones, which is …
The ulnar interosseous tuberosity exists: a radiological and descriptive cadaveric study.
Rougereau G, Langlais T, Valteau B, Creze M, Soubeyrand M. Rougereau G, et al. Surg Radiol Anat. 2021 Oct;43(10):1609-1617. doi: 10.1007/s00276-021-02792-9. Epub 2021 Jul 6. Surg Radiol Anat. 2021. PMID: 34228179

The mean tuberosity length was 107.5 mm ( 18.2), without any significant gender influence. It corresponded to a thickening (6.9 mm then 4.6 mm above and 3.9 mm below; p < 0.0001) of the ulnar interosseous cortex. ...CONCLUSION: Tuberositas interossea ulnarii exis

…
The mean tuberosity length was 107.5 mm ( 18.2), without any significant gender influence. It corresponded to a thickening (6.9 mm th …
Treatment of fibrous dysplasia of bone with intravenous pamidronate: long-term effectiveness and evaluation of predictors of response to treatment.
Chapurlat RD, Hugueny P, Delmas PD, Meunier PJ. Chapurlat RD, et al. Bone. 2004 Jul;35(1):235-42. doi: 10.1016/j.bone.2004.03.004. Bone. 2004. PMID: 15207763
Fibrous dysplasia (FD) of bone is a rare but potentially severe bone disease that often entails fractures, deformities, and bone pain. ...We found that pain intensity significantly decreased with treatment in the 44 patients who had bone pain at baseli …
Fibrous dysplasia (FD) of bone is a rare but potentially severe bone disease that often entails fractures, deformities, and …
Novel mutation in LRP5 gene cause rare osteosclerosis: cases studies and literature review.
Zhao D, Sun L, Zheng W, Hu J, Zhou B, Wang O, Jiang Y, Xia W, Xing X, Li M. Zhao D, et al. Mol Genet Genomics. 2023 May;298(3):683-692. doi: 10.1007/s00438-023-02008-2. Epub 2023 Mar 27. Mol Genet Genomics. 2023. PMID: 36971833 Free PMC article. Review.
Three patients with increased bone mineral density or thickened bone cortex were included, who were 30-year-old, 22-year-old and 50-year-old men, respectively. ...The latter two patients showed enlargement of the mandible and enlarged osseous prominenc …
Three patients with increased bone mineral density or thickened bone cortex were included, who were 30-year-old, …
Structural analysis of the Kresna 11 Homo erectus femoral shaft (Sangiran, Java).
Puymerail L, Ruff CB, Bondioli L, Widianto H, Trinkaus E, Macchiarelli R. Puymerail L, et al. J Hum Evol. 2012 Nov;63(5):741-9. doi: 10.1016/j.jhevol.2012.08.003. Epub 2012 Oct 1. J Hum Evol. 2012. PMID: 23036460
The biomechanical characterization of lower limb long bones in the chrono-ecogeographically diverse species Homo erectus is a fundamental step for assessing evolutionary changes in locomotor mode and body shape that occurred within the genus Homo. ...Synthetic funct …
The biomechanical characterization of lower limb long bones in the chrono-ecogeographically diverse species Homo erectus is a …
Clinical characteristics and treatment outcomes in Camurati-Engelmann disease: A case series.
Kim YM, Kang E, Choi JH, Kim GH, Yoo HW, Lee BH. Kim YM, et al. Medicine (Baltimore). 2018 Apr;97(14):e0309. doi: 10.1097/MD.0000000000010309. Medicine (Baltimore). 2018. PMID: 29620655 Free PMC article.
BACKGROUND: Camurati-Engelmann disease is an extremely rare disease characterized by hyperostosis of multiple long bones. This condition is caused by heterozygous mutations in the TGFB1 gene. ...Skeletal survey showed diaphyseal expansion with diffuse cortical th …
BACKGROUND: Camurati-Engelmann disease is an extremely rare disease characterized by hyperostosis of multiple long bones. This …
Atypical subtrochanteric and diaphyseal femoral fractures: report of a task force of the American Society for Bone and Mineral Research.
Shane E, Burr D, Ebeling PR, Abrahamsen B, Adler RA, Brown TD, Cheung AM, Cosman F, Curtis JR, Dell R, Dempster D, Einhorn TA, Genant HK, Geusens P, Klaushofer K, Koval K, Lane JM, McKiernan F, McKinney R, Ng A, Nieves J, O'Keefe R, Papapoulos S, Sen HT, van der Meulen MC, Weinstein RS, Whyte M; American Society for Bone and Mineral Research. Shane E, et al. J Bone Miner Res. 2010 Nov;25(11):2267-94. doi: 10.1002/jbmr.253. J Bone Miner Res. 2010. PMID: 20842676 Free article.
Reports linking long-term use of bisphosphonates (BPs) with atypical fractures of the femur led the leadership of the American Society for Bone and Mineral Research (ASBMR) to appoint a task force to address key questions related to this problem. ...The task force d …
Reports linking long-term use of bisphosphonates (BPs) with atypical fractures of the femur led the leadership of the American Societ …
Valgus deformity after fibular resection in children.
González-Herranz P, del Río A, Burgos J, López-Mondejar JA, Rapariz JM. González-Herranz P, et al. J Pediatr Orthop. 2003 Jan-Feb;23(1):55-9. J Pediatr Orthop. 2003. PMID: 12499944
Representative radiologic findings were distal migration of the fibula head in 75% (but without clinical relevance), thickening of the external tibial cortex in 20%, talar tilt in 45%, proximal migration of the lateral malleolus in 55%, and diaphyseal valgus of the …
Representative radiologic findings were distal migration of the fibula head in 75% (but without clinical relevance), thickening of th …
Brain malformation with loss of normal FGFR3 expression in thanatophoric dysplasia type I.
Itoh K, Pooh R, Kanemura Y, Yamasaki M, Fushiki S. Itoh K, et al. Neuropathology. 2013 Dec;33(6):663-6. doi: 10.1111/neup.12036. Epub 2013 Apr 1. Neuropathology. 2013. PMID: 23551494
In this case, fetal ultrasonography at the 18th week of gestation led to a prenatal diagnosis of TD1 with characteristic bone features. The subject was stillborn at the 21st week of gestation, showing marked shortening of the long bones, small thorax and curv …
In this case, fetal ultrasonography at the 18th week of gestation led to a prenatal diagnosis of TD1 with characteristic bone feature …
Aneurysmal bone cysts: treatment with direct percutaneous Ethibloc injection: long-term results.
Falappa P, Fassari FM, Fanelli A, Genovese E, Ascani E, Crostelli M, Salsano V, Montanaro A, Di Lazzaro A, Serra F. Falappa P, et al. Cardiovasc Intervent Radiol. 2002 Jul-Aug;25(4):282-90. doi: 10.1007/s00270-001-0062-2. Epub 2002 May 20. Cardiovasc Intervent Radiol. 2002. PMID: 12016517
PURPOSE: To assess the efficacy and long-term results of Ethibloc treatment in aneurysmal bone cysts (ABC). ...RESULTS AND CONCLUSIONS: All images demonstrated a remarkable shrinkage of the cystic lesion and bone cortex thickening. In all patien …
PURPOSE: To assess the efficacy and long-term results of Ethibloc treatment in aneurysmal bone cysts (ABC). ...RESULTS AND CON …
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