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1963
2025

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

Year Number of Results
1963 2
1964 2
1965 1
1967 1
1968 3
1969 2
1971 2
1972 5
1973 3
1974 6
1975 6
1976 3
1977 3
1978 3
1979 3
1980 3
1981 5
1982 3
1983 1
1984 1
1985 7
1986 3
1987 3
1988 8
1989 9
1990 11
1991 14
1992 12
1993 14
1994 11
1995 18
1996 18
1997 22
1998 13
1999 5
2000 14
2001 18
2002 9
2003 9
2004 11
2005 11
2006 15
2007 12
2008 11
2009 5
2010 10
2011 14
2012 14
2013 14
2014 25
2015 21
2016 15
2017 13
2018 14
2019 22
2020 17
2021 18
2022 17
2023 18
2024 13
2025 0

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549 results

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Page 1
Treacher Collins Syndrome.
Aljerian A, Gilardino MS. Aljerian A, et al. Clin Plast Surg. 2019 Apr;46(2):197-205. doi: 10.1016/j.cps.2018.11.005. Epub 2019 Jan 30. Clin Plast Surg. 2019. PMID: 30851751 Review.
Treacher Collins syndrome is a rare genetic disorder of craniofacial development with a highly variable phenotype. The disorder displays an intricate underlying dysmorphology. ...Standard craniofacial procedures for bony and soft tissue reconstruction are used. This …
Treacher Collins syndrome is a rare genetic disorder of craniofacial development with a highly variable phenotype. The disorder displ …
The etiology, clinical features, and treatment options of hemifacial microsomia.
Luo S, Sun H, Bian Q, Liu Z, Wang X. Luo S, et al. Oral Dis. 2023 Sep;29(6):2449-2462. doi: 10.1111/odi.14508. Epub 2023 Mar 13. Oral Dis. 2023. PMID: 36648381 Review.
To organize the possible up-to-date information on the etiology, craniofacial phenotypes, and therapeutic alternatives in order to fully comprehend the HFM. ...The commonly used clinical classification for HFM is OMENS, OMENS-plus, and SAT. Other craniofacial anomal …
To organize the possible up-to-date information on the etiology, craniofacial phenotypes, and therapeutic alternatives in order to fu …
Goldenhar syndrome: current perspectives.
Bogusiak K, Puch A, Arkuszewski P. Bogusiak K, et al. World J Pediatr. 2017 Oct;13(5):405-415. doi: 10.1007/s12519-017-0048-z. Epub 2017 Jun 15. World J Pediatr. 2017. PMID: 28623555 Review.
Craniofacial Microsomia.
Birgfeld C, Heike C. Birgfeld C, et al. Clin Plast Surg. 2019 Apr;46(2):207-221. doi: 10.1016/j.cps.2018.12.001. Clin Plast Surg. 2019. PMID: 30851752 Review.
Clinicians use different diagnostic terms for patients with underdevelopment of facial features arising from the embryonic first and second pharyngeal arches, including first and second branchial arch syndrome, otomandibular dysostosis, oculoauriculovertebral syndrome, and …
Clinicians use different diagnostic terms for patients with underdevelopment of facial features arising from the embryonic first and second …
Craniosynostosis syndromes.
Dicus Brookes C, Golden BA, Turvey TA. Dicus Brookes C, et al. Atlas Oral Maxillofac Surg Clin North Am. 2014 Sep;22(2):103-10. doi: 10.1016/j.cxom.2014.04.001. Atlas Oral Maxillofac Surg Clin North Am. 2014. PMID: 25171992 Review. No abstract available.
Freeman-Burian syndrome.
Poling MI, Dufresne CR, Chamberlain RL. Poling MI, et al. Orphanet J Rare Dis. 2019 Jan 10;14(1):14. doi: 10.1186/s13023-018-0984-2. Orphanet J Rare Dis. 2019. PMID: 30630514 Free PMC article. Review.
CLINICAL DESCRIPTION: Freeman-Burian syndrome (FBS) is a rare congenital myopathic craniofacial syndrome. Considerable variability in severity is seen, but diagnosis requires the following: microstomia, whistling-face appearance (pursed lips), H or V-shaped chin defect, an …
CLINICAL DESCRIPTION: Freeman-Burian syndrome (FBS) is a rare congenital myopathic craniofacial syndrome. Considerable variability in …
Syndromic Craniosynostosis.
Wang JC, Nagy L, Demke JC. Wang JC, et al. Facial Plast Surg Clin North Am. 2016 Nov;24(4):531-543. doi: 10.1016/j.fsc.2016.06.008. Facial Plast Surg Clin North Am. 2016. PMID: 27712819 Review.
Syndromic craniosynostosis affects up to 1:30,000 live births with characteristic craniofacial growth restrictions, deformities, and other associated abnormalities, such as carpal-pedal anomalies and cognitive function impairment. ...
Syndromic craniosynostosis affects up to 1:30,000 live births with characteristic craniofacial growth restrictions, deformities, and …
State-of-the-Art Hypertelorism Management.
Shakir S, Hoppe IC, Taylor JA. Shakir S, et al. Clin Plast Surg. 2019 Apr;46(2):185-195. doi: 10.1016/j.cps.2018.11.004. Epub 2019 Jan 9. Clin Plast Surg. 2019. PMID: 30851750 Review.
549 results