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

Year Number of Results
1989 2
1993 1
2000 1
2002 1
2003 1
2005 1
2006 1
2007 1
2008 2
2009 2
2010 2
2011 2
2012 3
2013 3
2015 1
2016 3
2017 1
2021 1
2024 0

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26 results

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Page 1
Brain infections.
Sarrazin JL, Bonneville F, Martin-Blondel G. Sarrazin JL, et al. Diagn Interv Imaging. 2012 Jun;93(6):473-90. doi: 10.1016/j.diii.2012.04.020. Epub 2012 Jun 5. Diagn Interv Imaging. 2012. PMID: 22677301 Free article. Review.
In addition, in a certain number of cases, the type of infection is not known and it is up to the MRI via use of an exhaustive technique to diagnose an infectious origin when faced with a mass syndrome. This technical mastery, associated with knowledge of major brai …
In addition, in a certain number of cases, the type of infection is not known and it is up to the MRI via use of an exhaustive technique to …
Surgical treatment of adrenal carcinoma.
Gaujoux S, Weinandt M, Bonnet S, Reslinger V, Bertherat J, Dousset B. Gaujoux S, et al. J Visc Surg. 2017 Oct;154(5):335-343. doi: 10.1016/j.jviscsurg.2017.06.010. Epub 2017 Jul 25. J Visc Surg. 2017. PMID: 28754418 Free article. Review.
Adrenocortical carcinoma (ACC) is a rare disease with a poor prognosis. The presence of a mass syndrome or signs of hormonal hypersecretion often lead to its discovery, but more and more frequently, adrenocortical malignancy is fortuitously discovered as an incident …
Adrenocortical carcinoma (ACC) is a rare disease with a poor prognosis. The presence of a mass syndrome or signs of hormonal h …
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.
Other less common recessive or dominant sclerosing disorders, such as endosteal hyperostosis, sclerostosis, van Buchen disease and high bone mass syndrome, are due to mutations in two genes (LRP5 and SOST) of the Wnt pathway that induce increased osteoblast activity …
Other less common recessive or dominant sclerosing disorders, such as endosteal hyperostosis, sclerostosis, van Buchen disease and high bone …
Perioperative anaesthetic management of mediastinal mass in adults.
Erdös G, Tzanova I. Erdös G, et al. Eur J Anaesthesiol. 2009 Aug;26(8):627-32. doi: 10.1097/EJA.0b013e328324b7f8. Eur J Anaesthesiol. 2009. PMID: 19384235 Review.
Mediastinal mass syndrome remains an anaesthetic challenge that cannot be underestimated. ...The aim of this article is to summarize the genesis of and the diagnostic options for mediastinal mass syndrome and to provide a solid detailed methodology for …
Mediastinal mass syndrome remains an anaesthetic challenge that cannot be underestimated. ...The aim of this article is to sum …
Heritable sclerosing bone disorders: presentation and new molecular mechanisms.
de Vernejoul MC, Kornak U. de Vernejoul MC, et al. Ann N Y Acad Sci. 2010 Mar;1192:269-77. doi: 10.1111/j.1749-6632.2009.05244.x. Ann N Y Acad Sci. 2010. PMID: 20392246 Review.
Rare recessive or dominant sclerosing disorders, such as endosteal hyperostosis, sclerosteosis, van Buchem disease, high bone-mass syndrome, and osteopathia striata, are caused by mutations in genes involved in the Wnt pathway, which regulates osteoblast differentia …
Rare recessive or dominant sclerosing disorders, such as endosteal hyperostosis, sclerosteosis, van Buchem disease, high bone-mass
Genetic disorders of the elastic fiber system.
Milewicz DM, Urbán Z, Boyd C. Milewicz DM, et al. Matrix Biol. 2000 Nov;19(6):471-80. doi: 10.1016/s0945-053x(00)00099-8. Matrix Biol. 2000. PMID: 11068201 Review.
The following disorders will be discussed in this review: supravalvular aortic stenosis; Williams-Beuren syndrome; cutis laxa; Marfan syndrome; ectopia lentis; familial thoracic aortic aneurysms and dissections; MASS syndrome; isolated skeletal features of Marfan sy …
The following disorders will be discussed in this review: supravalvular aortic stenosis; Williams-Beuren syndrome; cutis laxa; Marfan syndro …
Lrp5 and bone formation : A serotonin-dependent pathway.
Yadav VK, Ducy P. Yadav VK, et al. Ann N Y Acad Sci. 2010 Mar;1192:103-9. doi: 10.1111/j.1749-6632.2009.05312.x. Ann N Y Acad Sci. 2010. PMID: 20392224 Review.
Lrp5, the mutated gene in osteoporosis pseudoglioma (OPPG) and the high bone-mass syndrome (HBM), regulates bone formation, while beta-catenin, the molecular node of Wnt signaling, regulates bone resorption, suggesting that Lrp5 could act in a Wnt-independent manner …
Lrp5, the mutated gene in osteoporosis pseudoglioma (OPPG) and the high bone-mass syndrome (HBM), regulates bone formation, wh …
Genetic control of susceptibility to osteoporosis.
Ralston SH. Ralston SH. J Clin Endocrinol Metab. 2002 Jun;87(6):2460-6. doi: 10.1210/jcem.87.6.8621. J Clin Endocrinol Metab. 2002. PMID: 12050200 Review.
Examples are the osteoporosis-pseudoglioma syndrome, caused by inactivating mutations in the lipoprotein receptor-related protein 5 gene and the high bone mass syndrome, caused by activating mutations of the same gene. Genome-wide linkage studies in man have identif …
Examples are the osteoporosis-pseudoglioma syndrome, caused by inactivating mutations in the lipoprotein receptor-related protein 5 gene and …
The masticator space: from anatomy to pathology.
Faye N, Lafitte F, Williams M, Guermazi A, Sahli-Amor M, Chiras J, Dion E. Faye N, et al. J Neuroradiol. 2009 Jun;36(3):121-30. doi: 10.1016/j.neurad.2008.08.005. Epub 2008 Oct 5. J Neuroradiol. 2009. PMID: 18835644 Review.
Multidetector CT and MRI enable precise study of the space, its communications with other deep spaces and the etiology of any mass syndrome. Understanding the anatomy of the masticator space and how it links up with the other deep facial spaces helps the radiologist …
Multidetector CT and MRI enable precise study of the space, its communications with other deep spaces and the etiology of any mass
26 results