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 NCBI Filters

Results by year

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

Year Number of Results
1947 1
1964 1
1968 1
1970 1
1971 3
1972 2
1973 1
1974 6
1975 8
1976 11
1977 4
1978 6
1979 6
1980 10
1981 1
1982 6
1983 5
1984 13
1985 14
1986 13
1987 7
1988 8
1989 15
1990 16
1991 21
1992 16
1993 31
1994 35
1995 28
1996 35
1997 42
1998 25
1999 40
2000 35
2001 42
2002 45
2003 47
2004 38
2005 58
2006 61
2007 36
2008 52
2009 69
2010 71
2011 84
2012 76
2013 83
2014 101
2015 80
2016 53
2017 38
2018 56
2019 40
2020 23
2021 29
2022 29
2023 19
2024 8

Text availability

Article attribute

Article type

Publication date

Search Results

1,529 results

Results by year

Filters applied: . Clear all
Quoted phrase not found in phrase index: "Abnormal palate morphology"
Page 1
The ontogeny of Robin sequence.
Logjes RJH, Breugem CC, Van Haaften G, Paes EC, Sperber GH, van den Boogaard MH, Farlie PG. Logjes RJH, et al. Am J Med Genet A. 2018 Jun;176(6):1349-1368. doi: 10.1002/ajmg.a.38718. Epub 2018 Apr 25. Am J Med Genet A. 2018. PMID: 29696787 Review.
The triad of micrognathia, glossoptosis, and concomitant airway obstruction defined as "Robin sequence" (RS) is caused by oropharyngeal developmental events constrained by a reduced stomadeal space. This sequence of abnormal embryonic development also results in an anatomi …
The triad of micrognathia, glossoptosis, and concomitant airway obstruction defined as "Robin sequence" (RS) is caused by oropharyngeal deve …
Acro-cardio-facial syndrome.
Digilio MC, Dallapiccola B. Digilio MC, et al. Orphanet J Rare Dis. 2010 Sep 29;5:25. doi: 10.1186/1750-1172-5-25. Orphanet J Rare Dis. 2010. PMID: 20920258 Free PMC article. Review.
Acro-cardio-facial syndrome (ACFS) is a rare genetic disorder characterized by split-hand/split-foot malformation (SHFM), facial anomalies, cleft lip/palate, congenital heart defect (CHD), genital anomalies, and mental retardation. ...Management of affected patients …
Acro-cardio-facial syndrome (ACFS) is a rare genetic disorder characterized by split-hand/split-foot malformation (SHFM), facial anomalies, …
Palatal and oral manifestations of Muenke syndrome (FGFR3-related craniosynostosis).
Agochukwu NB, Solomon BD, Doherty ES, Muenke M. Agochukwu NB, et al. J Craniofac Surg. 2012 May;23(3):664-8. doi: 10.1097/SCS.0b013e31824db8bb. J Craniofac Surg. 2012. PMID: 22565872 Free PMC article. Review.
Although Muenke syndrome is the most common syndromic form of craniosynostosis, the frequency of oral and palatal anomalies including high-arched palate, cleft lip with or without cleft palate has not been documented in a patient series of Muenke syndrome to …
Although Muenke syndrome is the most common syndromic form of craniosynostosis, the frequency of oral and palatal anomalies including …
Congenital lesions of epithelial origin.
Hills SE, Maddalozzo J. Hills SE, et al. Otolaryngol Clin North Am. 2015 Feb;48(1):209-23. doi: 10.1016/j.otc.2014.09.014. Otolaryngol Clin North Am. 2015. PMID: 25439555 Review.
Defects of embryologic development give rise to a variety of congenital lesions arising from the epithelium and are among the most common congenital lesions of the head and neck in the pediatric population. This article presents several congenital lesions of …
Defects of embryologic development give rise to a variety of congenital lesions arising from the epithelium and are among the most co …
Palate morphology after unilateral and bilateral cleft lip and palate closure.
Schliephake H, Donnerstag F, Berten JL, Lönquist N. Schliephake H, et al. Int J Oral Maxillofac Surg. 2006 Jan;35(1):25-30. doi: 10.1016/j.ijom.2005.06.007. Epub 2005 Sep 9. Int J Oral Maxillofac Surg. 2006. PMID: 16154317
The aim of the present study was to compare the morphology of the hard palate of patients with uni- and bilateral cleft lip and palate after palatoplasty using vomer and palatal pedicled flaps with the palatal morphology of non-cleft indi …
The aim of the present study was to compare the morphology of the hard palate of patients with uni- and bilateral cleft lip an …
Gingivoperiosteoplasty and midfacial growth.
Wood RJ, Grayson BH, Cutting CB. Wood RJ, et al. Cleft Palate Craniofac J. 1997 Jan;34(1):17-20. doi: 10.1597/1545-1569_1997_034_0017_gamg_2.3.co_2. Cleft Palate Craniofac J. 1997. PMID: 9003907
Twenty-five consecutively treated patients who presented with complete unilateral clefts of the primary and secondary palate were included in the study. Of these, 20 patients were available for 6-year follow-up cephalometric documentation and review. ...We were unable to o …
Twenty-five consecutively treated patients who presented with complete unilateral clefts of the primary and secondary palate were inc …
Management of knee deformities in children with arthrogryposis.
Lampasi M, Antonioli D, Donzelli O. Lampasi M, et al. Musculoskelet Surg. 2012 Dec;96(3):161-9. doi: 10.1007/s12306-012-0218-z. Epub 2012 Aug 9. Musculoskelet Surg. 2012. PMID: 22875688 Review.
Arthrogryposis includes heterogeneous disorders, characterized by congenital contractures of multiple joints. Knee involvement is very common (38-90 % of patients with amyoplasia) ranging from soft-tissue contractures (in flexion or hyperextension) to subluxation and dislo …
Arthrogryposis includes heterogeneous disorders, characterized by congenital contractures of multiple joints. Knee involvement is ver …
The spectrum of orofacial clefting.
Eppley BL, van Aalst JA, Robey A, Havlik RJ, Sadove AM. Eppley BL, et al. Plast Reconstr Surg. 2005 Jun;115(7):101e-114e. doi: 10.1097/01.prs.0000164494.45986.91. Plast Reconstr Surg. 2005. PMID: 15923821 Review.
BACKGROUND: Clefts of the orofacial region are among the most common congenital facial defects. The clinical presentation is usually that of a lateral cleft of the lip through the philtrum with or without extension through the palatal shelves. However, atypical form …
BACKGROUND: Clefts of the orofacial region are among the most common congenital facial defects. The clinical presentation is usually …
Holoprosencephaly in neonates.
Ram SP, Noor AR, Mahbar Z, Krishna TN. Ram SP, et al. Int J Pediatr Otorhinolaryngol. 1994 Mar;29(1):65-71. doi: 10.1016/0165-5876(94)90110-4. Int J Pediatr Otorhinolaryngol. 1994. PMID: 8169049
A single nostril associated with alobar holoprosencephaly is a rare congenital lesion. This paper reports two female term neonates with holoprosencephaly. ...The other neonate had cleft lip and palate and recurrent convulsions. Both neonates had gross motor and deve …
A single nostril associated with alobar holoprosencephaly is a rare congenital lesion. This paper reports two female term neonates wi …
A systematic review comparing Furlow double-opposing Z-plasty and straight-line intravelar veloplasty methods of cleft palate repair.
Timbang MR, Gharb BB, Rampazzo A, Papay F, Zins J, Doumit G. Timbang MR, et al. Plast Reconstr Surg. 2014 Nov;134(5):1014-1022. doi: 10.1097/PRS.0000000000000637. Plast Reconstr Surg. 2014. PMID: 25347635 Review.
The exclusion criteria were as follows: syndromic patients, no description or poor description of the technique used, data not stratified by cleft palate type, two-stage cleft palate repair, average age at repair younger than 9 months or older than 18 months, and ag …
The exclusion criteria were as follows: syndromic patients, no description or poor description of the technique used, data not stratified by …
1,529 results