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

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1987 13
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2007 67
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1,978 results

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Quoted phrase not found in phrase index: "Abnormal long bone morphology"
Page 1
Subchondral bone in osteoarthritis: insight into risk factors and microstructural changes.
Li G, Yin J, Gao J, Cheng TS, Pavlos NJ, Zhang C, Zheng MH. Li G, et al. Arthritis Res Ther. 2013;15(6):223. doi: 10.1186/ar4405. Arthritis Res Ther. 2013. PMID: 24321104 Free PMC article. Review.
Although OA has long been viewed as a primary disorder of articular cartilage, subchondral bone is attracting increasing attention. ...Despite the increase in bone volume fraction, subchondral bone is hypomineralized, due to abnormal bone …
Although OA has long been viewed as a primary disorder of articular cartilage, subchondral bone is attracting increasing atten …
Turner syndrome and osteoporosis.
Augoulea A, Zachou G, Lambrinoudaki I. Augoulea A, et al. Maturitas. 2019 Dec;130:41-49. doi: 10.1016/j.maturitas.2019.09.010. Epub 2019 Sep 25. Maturitas. 2019. PMID: 31706435 Review.
Girls and women with Turner syndrome have lower bone mineral density and a higher fracture rate than healthy individuals. The most important risk factors for osteoporosis are inadequately treated primary ovarian insufficiency, followed by intrinsic bone abnormali …
Girls and women with Turner syndrome have lower bone mineral density and a higher fracture rate than healthy individuals. The most im …
Skeletal Manifestations of Hypoparathyroidism.
Rubin MR. Rubin MR. Bone. 2019 Mar;120:548-555. doi: 10.1016/j.bone.2018.11.012. Epub 2018 Nov 19. Bone. 2019. PMID: 30465918
Chronic PTH deficiency has a marked effect on the skeleton, leading to characteristic decreases in bone remodeling and increases in bone mass. An effect on fracture risk has not been demonstrated, although biochemical, imaging, and histomorphometric data indicate …
Chronic PTH deficiency has a marked effect on the skeleton, leading to characteristic decreases in bone remodeling and increases in …
The suboccipital ligament.
Alabaster K, Fred Bugg M, Splavski B, Boop FA, Arnautovic KI. Alabaster K, et al. J Neurosurg. 2018 Jan;128(1):165-173. doi: 10.3171/2016.10.JNS162161. Epub 2017 Apr 14. J Neurosurg. 2018. PMID: 28409726
OBJECTIVE A fibrous structure located dorsal to the dura at the posterior craniocervical junction stretches horizontally between the bilateral occipital condyles and the upper borders of the C-1 laminae. Partially covered by the occipital bone, this structure is always enc …
OBJECTIVE A fibrous structure located dorsal to the dura at the posterior craniocervical junction stretches horizontally between the bilater …
Monitoring and maintaining bone health in patients with Turner syndrome.
Chiarito M, Brunetti G, D'Amato G, Faienza MF. Chiarito M, et al. Expert Rev Endocrinol Metab. 2020 Nov;15(6):431-438. doi: 10.1080/17446651.2020.1834846. Epub 2020 Oct 19. Expert Rev Endocrinol Metab. 2020. PMID: 33074770 Review.
INTRODUCTION: Subjects affected with Turner Syndrome (TS) suffer low bone mineral density and high risk of fracture from a young age. Estrogen deficiency is considered the main risk factor but other factors, such as intrinsic bone abnormalities, enhanced oste …
INTRODUCTION: Subjects affected with Turner Syndrome (TS) suffer low bone mineral density and high risk of fracture from a young age. …
Miniplate-Augmented Interlaminar Fusion in C1-C2 Screwing.
Huang PJ, Lin JH, Chiang YH. Huang PJ, et al. World Neurosurg. 2020 Jun;138:e634-e641. doi: 10.1016/j.wneu.2020.03.023. Epub 2020 Mar 13. World Neurosurg. 2020. PMID: 32173550
Thus we used the miniplate to stabilize the harvest bone graft on the C1-C2 laminar, which led to a shorter operation time and prevented spinal canal violation. ...Success of fusion was defined as follows: 1) the presence of bone bridging between the bone gra …
Thus we used the miniplate to stabilize the harvest bone graft on the C1-C2 laminar, which led to a shorter operation time and preven …
Management of vaginal agenesis.
Nakhal RS, Creighton SM. Nakhal RS, et al. J Pediatr Adolesc Gynecol. 2012 Dec;25(6):352-7. doi: 10.1016/j.jpag.2011.06.003. Epub 2011 Aug 27. J Pediatr Adolesc Gynecol. 2012. PMID: 21872517 Review.
A variety of surgical options are also available, each with enthusiastic proponents. Long-term outcome studies on most surgical techniques, however, are still lacking and until recently most studies have reported on success rate in terms of anatomical success only, without …
A variety of surgical options are also available, each with enthusiastic proponents. Long-term outcome studies on most surgical techn …
Physical performance of children with longitudinal fibular deficiency (fibular hemimelia).
Morris EJ, Tofts L, Patterson M, Birke O, Adams R, Epps A, Knox K, McKay MJ, Baldwin JN, Burns J, Pacey V. Morris EJ, et al. Disabil Rehabil. 2022 Jun;44(12):2763-2773. doi: 10.1080/09638288.2020.1849420. Epub 2020 Dec 17. Disabil Rehabil. 2022. PMID: 33331793
PURPOSE: Longitudinal fibular deficiency (LFD) is the most common congenital long bone deficiency. This study aimed to objectively assess the physical performance of children and adolescents with LFD compared with unaffected peers, and to examine trends over …
PURPOSE: Longitudinal fibular deficiency (LFD) is the most common congenital long bone deficiency. This study aimed to …
Gracile bone dysplasias.
Kozlowski K, Masel J, Sillence DO, Arbuckle S, Juttnerova V. Kozlowski K, et al. Pediatr Radiol. 2002 Sep;32(9):629-34. doi: 10.1007/s00247-002-0719-2. Epub 2002 Jun 5. Pediatr Radiol. 2002. PMID: 12195301
Gracile bone dysplasias constitute a group of disorders characterised by extremely slender bones with or without fractures. ...Two babies had osteocraniostenosis and one had features of oligohydramnios sequence. The diagnosis in the fourth newborn, which showed thin …
Gracile bone dysplasias constitute a group of disorders characterised by extremely slender bones with or without fractures. .. …
Manifestations of hereditary multiple exostoses.
Stieber JR, Dormans JP. Stieber JR, et al. J Am Acad Orthop Surg. 2005 Mar-Apr;13(2):110-20. doi: 10.5435/00124635-200503000-00004. J Am Acad Orthop Surg. 2005. PMID: 15850368 Review.
The solitary osteochondroma, a common pediatric bone tumor, is a cartilage-capped exostosis. Hereditary multiple exostosis is an autosomal dominant disorder manifested by the presence of multiple osteochondromas. Linkage analysis has implicated mutations in the EXT gene fa …
The solitary osteochondroma, a common pediatric bone tumor, is a cartilage-capped exostosis. Hereditary multiple exostosis is an auto …
1,978 results