Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

100 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Identification of a novel locus on chromosome 2q13, which predisposes to clinical vertebral fractures independently of bone density.
Alonso N, Estrada K, Albagha OME, Herrera L, Reppe S, Olstad OK, Gautvik KM, Ryan NM, Evans KL, Nielson CM, Hsu YH, Kiel DP, Markozannes G, Ntzani EE, Evangelou E, Feenstra B, Liu X, Melbye M, Masi L, Brandi ML, Riches P, Daroszewska A, Olmos JM, Valero C, Castillo J, Riancho JA, Husted LB, Langdahl BL, Brown MA, Duncan EL, Kaptoge S, Khaw KT, Usategui-Martín R, Del Pino-Montes J, González-Sarmiento R, Lewis JR, Prince RL, D'Amelio P, García-Giralt N, Nogués X, Mencej-Bedrac S, Marc J, Wolstein O, Eisman JA, Oei L, Medina-Gómez C, Schraut KE, Navarro P, Wilson JF, Davies G, Starr J, Deary I, Tanaka T, Ferrucci L, Gianfrancesco F, Gennari L, Lucas G, Elosua R, Uitterlinden AG, Rivadeneira F, Ralston SH. Alonso N, et al. Ann Rheum Dis. 2018 Mar;77(3):378-385. doi: 10.1136/annrheumdis-2017-212469. Epub 2017 Nov 23. Ann Rheum Dis. 2018. PMID: 29170203 Free PMC article.
Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.
Albagha OM, Visconti MR, Alonso N, Langston AL, Cundy T, Dargie R, Dunlop MG, Fraser WD, Hooper MJ, Isaia G, Nicholson GC, del Pino Montes J, Gonzalez-Sarmiento R, di Stefano M, Tenesa A, Walsh JP, Ralston SH. Albagha OM, et al. Nat Genet. 2010 Jun;42(6):520-4. doi: 10.1038/ng.562. Epub 2010 May 2. Nat Genet. 2010. PMID: 20436471 Free PMC article.
Clinical and Genetic Advances in Paget's Disease of Bone: a Review.
Alonso N, Calero-Paniagua I, Del Pino-Montes J. Alonso N, et al. Clin Rev Bone Miner Metab. 2017;15(1):37-48. doi: 10.1007/s12018-016-9226-0. Epub 2016 Dec 19. Clin Rev Bone Miner Metab. 2017. PMID: 28255281 Free PMC article. Review.
Common susceptibility alleles and SQSTM1 mutations predict disease extent and severity in a multinational study of patients with Paget's disease.
Albagha OM, Visconti MR, Alonso N, Wani S, Goodman K, Fraser WD, Gennari L, Merlotti D, Gianfrancesco F, Esposito T, Rendina D, di Stefano M, Isaia G, Brandi ML, Giusti F, Del Pino-Montes J, Corral-Gudino L, Gonzalez-Sarmiento R, Ward L, Rea SL, Ratajczak T, Walsh JP, Ralston SH. Albagha OM, et al. J Bone Miner Res. 2013 Nov;28(11):2338-46. doi: 10.1002/jbmr.1975. J Bone Miner Res. 2013. PMID: 23658060 Free article.
VAV3 Gene Polymorphism Is Associated with Paget's Disease of Bone.
Usategui-Martín R, Calero-Paniagua I, García-Aparicio J, Corral-Gudino L, Del Pino Montes J, González Sarmiento R. Usategui-Martín R, et al. Genet Test Mol Biomarkers. 2016 Jun;20(6):335-7. doi: 10.1089/gtmb.2015.0292. Epub 2016 May 12. Genet Test Mol Biomarkers. 2016. PMID: 27172236 Free PMC article.
Polymorphisms in autophagy genes are associated with paget disease of bone.
Usategui-Martín R, García-Aparicio J, Corral-Gudino L, Calero-Paniagua I, Del Pino-Montes J, González Sarmiento R. Usategui-Martín R, et al. PLoS One. 2015 Jun 1;10(6):e0128984. doi: 10.1371/journal.pone.0128984. eCollection 2015. PLoS One. 2015. PMID: 26030385 Free PMC article.
Bisphosphonates for Paget's disease of bone in adults.
Corral-Gudino L, Tan AJ, Del Pino-Montes J, Ralston SH. Corral-Gudino L, et al. Cochrane Database Syst Rev. 2017 Dec 1;12(12):CD004956. doi: 10.1002/14651858.CD004956.pub3. Cochrane Database Syst Rev. 2017. PMID: 29192423 Free PMC article. Review.
100 results