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

Year Number of Results
1968 1
1971 2
1972 2
1974 3
1975 3
1976 5
1977 2
1978 5
1979 2
1980 7
1981 1
1982 3
1983 3
1984 2
1985 9
1986 11
1987 4
1988 10
1989 5
1990 8
1991 10
1992 5
1993 10
1994 14
1995 16
1996 15
1997 23
1998 18
1999 19
2000 21
2001 25
2002 28
2003 21
2004 21
2005 27
2006 30
2007 16
2008 26
2009 39
2010 34
2011 27
2012 33
2013 36
2014 33
2015 38
2016 37
2017 29
2018 33
2019 27
2020 28
2021 20
2022 8
2023 10
2024 3

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785 results

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Quoted phrase not found in phrase index: "Abnormal long bone morphology"
Page 1
Complete Androgen Insensitivity Syndrome: From Bench to Bed.
Tyutyusheva N, Mancini I, Baroncelli GI, D'Elios S, Peroni D, Meriggiola MC, Bertelloni S. Tyutyusheva N, et al. Int J Mol Sci. 2021 Jan 27;22(3):1264. doi: 10.3390/ijms22031264. Int J Mol Sci. 2021. PMID: 33514065 Free PMC article. Review.
Basic research will lead to the consideration of new issues to improve long-term well-being (such as bone health, immune and metabolic aspects and cardiovascular risk). An expert multidisciplinary approach is mandatory to increase the long-term quality of lif …
Basic research will lead to the consideration of new issues to improve long-term well-being (such as bone health, immune and m …
Effects of continuing or stopping alendronate after 5 years of treatment: the Fracture Intervention Trial Long-term Extension (FLEX): a randomized trial.
Black DM, Schwartz AV, Ensrud KE, Cauley JA, Levis S, Quandt SA, Satterfield S, Wallace RB, Bauer DC, Palermo L, Wehren LE, Lombardi A, Santora AC, Cummings SR; FLEX Research Group. Black DM, et al. JAMA. 2006 Dec 27;296(24):2927-38. doi: 10.1001/jama.296.24.2927. JAMA. 2006. PMID: 17190893 Clinical Trial.
OBJECTIVE: To compare the effects of discontinuing alendronate treatment after 5 years vs continuing for 10 years. DESIGN AND SETTING: Randomized, double-blind trial conducted at 10 US clinical centers that participated in the Fracture Intervention Trial
OBJECTIVE: To compare the effects of discontinuing alendronate treatment after 5 years vs continuing for 10 years. DESIGN AND SETTING: Ra
Swyer syndrome.
King TF, Conway GS. King TF, et al. Curr Opin Endocrinol Diabetes Obes. 2014 Dec;21(6):504-10. doi: 10.1097/MED.0000000000000113. Curr Opin Endocrinol Diabetes Obes. 2014. PMID: 25314337 Review.
PURPOSE OF REVIEW: This review focuses on the pathogenesis, diagnosis, management and long-term outcomes of disorders of sex development, specifically women with Swyer syndrome (46,XY complete gonadal dysgenesis). ...SUMMARY: Further pathogenic gene mutations are likely to …
PURPOSE OF REVIEW: This review focuses on the pathogenesis, diagnosis, management and long-term outcomes of disorders of sex developm …
Thalidomide and neurotrophism.
Soper JR, Bonar SF, O'Sullivan DJ, McCredie J, Willert HG. Soper JR, et al. Skeletal Radiol. 2019 Apr;48(4):517-525. doi: 10.1007/s00256-018-3086-2. Epub 2018 Oct 19. Skeletal Radiol. 2019. PMID: 30341712 Free PMC article. Review.
BACKGROUND: Following the thalidomide disaster (1958-62), Henkel and Willert analysed the pattern of dysmelia in the long bones (J Bone Joint Surg Br. 51:399-414, 1969) and the extremities, Willert and Henkel (Z Orthop Ihre Grenzgeb. 107:663-75, 1970). ...In …
BACKGROUND: Following the thalidomide disaster (1958-62), Henkel and Willert analysed the pattern of dysmelia in the long bones
Mineralized tissues in hypophosphatemic rickets.
Robinson ME, AlQuorain H, Murshed M, Rauch F. Robinson ME, et al. Pediatr Nephrol. 2020 Oct;35(10):1843-1854. doi: 10.1007/s00467-019-04290-y. Epub 2019 Aug 8. Pediatr Nephrol. 2020. PMID: 31392510 Review.
The bone tissue immediately adjacent to osteocytes often remains unmineralized ("periosteocytic lesions"), highlighting the osteocyte defect in this disorder. Common clinical features of XLH include deformities of the lower extremities, short stature, enthesopathies …
The bone tissue immediately adjacent to osteocytes often remains unmineralized ("periosteocytic lesions"), highlighting the osteocyte …
Dental impact of anti-fibroblast growth factor 23 therapy in X-linked hypophosphatemia.
Lira Dos Santos EJ, Nakajima K, Po J, Hanai A, Zhukouskaya V, Biosse Duplan M, Linglart A, Shimada T, Chaussain C, Bardet C. Lira Dos Santos EJ, et al. Int J Oral Sci. 2023 Dec 6;15(1):53. doi: 10.1038/s41368-023-00259-8. Int J Oral Sci. 2023. PMID: 38052774 Free PMC article.
Elevated fibroblast growth factor 23 (FGF23) in X-linked hypophosphatemia (XLH) results in rickets and phosphate wasting, manifesting by severe bone and dental abnormalities. Burosumab, a FGF23-neutralizing antibody, an alternative to conventional treatment (phospho …
Elevated fibroblast growth factor 23 (FGF23) in X-linked hypophosphatemia (XLH) results in rickets and phosphate wasting, manifesting by sev …
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 …
Dental materials for cleft palate repair.
Sharif F, Ur Rehman I, Muhammad N, MacNeil S. Sharif F, et al. Mater Sci Eng C Mater Biol Appl. 2016 Apr 1;61:1018-28. doi: 10.1016/j.msec.2015.12.019. Epub 2015 Dec 11. Mater Sci Eng C Mater Biol Appl. 2016. PMID: 26838929 Review.
Numerous bone and soft tissue grafting techniques are followed to repair cleft of lip and palate (CLP) defects. ...Any data available on the surgical interventions to repair alveolar or palatal cleft, with natural or synthetic graft materials was included in this review. T …
Numerous bone and soft tissue grafting techniques are followed to repair cleft of lip and palate (CLP) defects. ...Any data available …
Cellular and Molecular Alterations Underlying Abnormal Bone Growth in X-Linked Hypophosphatemia.
Fuente R, García-Bengoa M, Fernández-Iglesias Á, Gil-Peña H, Santos F, López JM. Fuente R, et al. Int J Mol Sci. 2022 Jan 15;23(2):934. doi: 10.3390/ijms23020934. Int J Mol Sci. 2022. PMID: 35055123 Free PMC article. Review.
X-linked hypophosphatemia (XLH), the most common form of hereditary hypophosphatemic rickets, is caused by inactivating mutations of the phosphate-regulating endopeptidase gene (PHEX). XLH is mainly characterized by short stature, bone deformities and rickets, while in hyp …
X-linked hypophosphatemia (XLH), the most common form of hereditary hypophosphatemic rickets, is caused by inactivating mutations of the pho …
Short- and Long-Term Outcomes by Procedure Type for Nonsagittal Single-Suture Craniosynostosis.
Bennett KG, Hespe GE, Vercler CJ, Buchman SR. Bennett KG, et al. J Craniofac Surg. 2019 Mar/Apr;30(2):458-464. doi: 10.1097/SCS.0000000000005129. J Craniofac Surg. 2019. PMID: 30640851 Free PMC article. Review.
CONCLUSION: Studies comparing long-term outcomes between different surgical techniques for single-suture craniosynostosis remain deficient. The development of standardized outcome measures is essential, and prospective, multicenter studies are necessary to assess the lo
CONCLUSION: Studies comparing long-term outcomes between different surgical techniques for single-suture craniosynostosis remain defi …
785 results