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Year Number of Results
1988 1
1989 1
1996 1
1997 1
1998 2
2000 2
2001 4
2002 2
2003 1
2004 1
2005 4
2006 1
2007 4
2008 2
2009 3
2010 3
2012 3
2013 4
2014 5
2015 14
2016 3
2017 3
2018 4
2019 2
2020 5
2021 7
2022 5
2023 4
2024 0

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78 results

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Page 1
Feeding problems and gastrointestinal diseases in Down syndrome.
Ravel A, Mircher C, Rebillat AS, Cieuta-Walti C, Megarbane A. Ravel A, et al. Arch Pediatr. 2020 Jan;27(1):53-60. doi: 10.1016/j.arcped.2019.11.008. Epub 2019 Nov 26. Arch Pediatr. 2020. PMID: 31784293 Review.
RESULTS: The anomalies are grouped into three categories: anatomical anomalies: duodenal atresia and stenosis (3.9%), duodenal web and annular pancreas; aberrant right subclavian artery (12% of children with DS with cardiac anomaly); Hirschsprung's disease (2.76%); anorect …
RESULTS: The anomalies are grouped into three categories: anatomical anomalies: duodenal atresia and stenosis (3.9%), duodenal web an …
Cri du chat syndrome: a critical review.
Rodríguez-Caballero A, Torres-Lagares D, Rodríguez-Pérez A, Serrera-Figallo MA, Hernández-Guisado JM, Machuca-Portillo G. Rodríguez-Caballero A, et al. Med Oral Patol Oral Cir Bucal. 2010 May 1;15(3):e473-8. doi: 10.4317/medoral.15.e473. Med Oral Patol Oral Cir Bucal. 2010. PMID: 20038906 Free article. Review.
Our purpose was to review different aspects of this syndrome (concept, epidemiology, aetiology, clinical features, diagnostic methods and prognosis) emphasizing both: the breakthrough in this field introduced by new cytogenetic and molecular techniques, and the orofacial m …
Our purpose was to review different aspects of this syndrome (concept, epidemiology, aetiology, clinical features, diagnostic methods and pr …
Environmental and individual exposure and the risk of congenital anomalies: a review of recent epidemiological evidence.
Baldacci S, Gorini F, Santoro M, Pierini A, Minichilli F, Bianchi F. Baldacci S, et al. Epidemiol Prev. 2018 May-Aug;42(3-4 Suppl 1):1-34. doi: 10.19191/EP18.3-4.S1.P001.057. Epidemiol Prev. 2018. PMID: 30066535 Free article. Review. English.
According to the World Health Organization (WHO), each year approximately 3,2 million of children worldwide are born with a CA and approximately 300,000 newborns with a diagnosis of birth defect die within the first 28 days of life. ...According to the Centre for Disease C …
According to the World Health Organization (WHO), each year approximately 3,2 million of children worldwide are born with a CA and ap …
Evidence-Based Medicine: Cleft Palate.
Woo AS. Woo AS. Plast Reconstr Surg. 2017 Jan;139(1):191e-203e. doi: 10.1097/PRS.0000000000002854. Plast Reconstr Surg. 2017. PMID: 28027255 Review.
LEARNING OBJECTIVES: After studying this article, the participant should be able to: 1. Describe the incidence of cleft palate and risk factors associated with development of an orofacial cleft. 2. ...Establish a treatment plan for individualized care of a …
LEARNING OBJECTIVES: After studying this article, the participant should be able to: 1. Describe the incidence of cleft palate and ri …
Monotherapy treatment of epilepsy in pregnancy: congenital malformation outcomes in the child.
Bromley R, Adab N, Bluett-Duncan M, Clayton-Smith J, Christensen J, Edwards K, Greenhalgh J, Hill RA, Jackson CF, Khanom S, McGinty RN, Tudur Smith C, Pulman J, Marson AG. Bromley R, et al. Cochrane Database Syst Rev. 2023 Aug 29;8(8):CD010224. doi: 10.1002/14651858.CD010224.pub3. Cochrane Database Syst Rev. 2023. PMID: 37647086 Free PMC article. Review.
The MCM risk for children of women without epilepsy was 2.1% (95% CI 1.5 to 3.0) in cohort studies and 3.3% (95% CI 1.5 to 7.1) in health record studies. ...For phenobarbital exposure, the prevalence was 6.3% (95% CI 4.8 to 8.3) and 8.8% (95% CI …
The MCM risk for children of women without epilepsy was 2.1% (95% CI 1.5 to 3.0) in cohort studies and 3.3% (95% CI 1.5 …
Caries in children with and without orofacial clefting: A systematic review and meta-analysis.
Grewcock RE, Innes NPT, Mossey PA, Robertson MD. Grewcock RE, et al. Oral Dis. 2022 Jul;28(5):1400-1411. doi: 10.1111/odi.14183. Epub 2022 Mar 22. Oral Dis. 2022. PMID: 35263806 Free PMC article. Review.
For dmfs (n = 1095 children; 6 groups), CL/P mean = 4; sd = 3.5 and no CL/P mean = 3; sd = 2.8. For % caries experience (n = 1094 children; 7 groups), CL/P mean = 65%; sd = 20.8 and no CL/P mean = 52%; sd = 28.1. ...Studies' risk of bias was high (n = 7), medium (n- …
For dmfs (n = 1095 children; 6 groups), CL/P mean = 4; sd = 3.5 and no CL/P mean = 3; sd = 2.8. For % caries experience (n = 1 …
p63-associated disorders.
Rinne T, Brunner HG, van Bokhoven H. Rinne T, et al. Cell Cycle. 2007 Feb 1;6(3):262-8. doi: 10.4161/cc.6.3.3796. Epub 2007 Feb 3. Cell Cycle. 2007. PMID: 17224651 Free article. Review.
Heterozygous mutations in the transcription factor gene p63 are causative for several syndromes, with ectodermal dysplasia, orofacial clefting and limb malformations as the key characteristics. Different combinations of these features are seen in five different synd …
Heterozygous mutations in the transcription factor gene p63 are causative for several syndromes, with ectodermal dysplasia, orofacial
Orofacial cleft management by short-term surgical missions in South America: literature review.
Best DL, Gauger TL, Dolan JM, Donnelly LA, Ranganathan K, Ulloa-Marin C, Sung-Hsieh HH. Best DL, et al. Int J Oral Maxillofac Surg. 2018 Nov;47(11):1373-1380. doi: 10.1016/j.ijom.2018.05.025. Epub 2018 Jun 23. Int J Oral Maxillofac Surg. 2018. PMID: 29945819 Review.
There is a growing demand for surgical care in South America, particularly for patients with congenital orofacial clefts (OFCs). Short-term surgical missions (STSMs) have emerged as a means to deliver surgical expertise and alleviate this demand. ...Descriptive stat …
There is a growing demand for surgical care in South America, particularly for patients with congenital orofacial clefts (OFCs …
Toward an orofacial gene regulatory network.
Kousa YA, Schutte BC. Kousa YA, et al. Dev Dyn. 2016 Mar;245(3):220-32. doi: 10.1002/dvdy.24341. Epub 2015 Sep 17. Dev Dyn. 2016. PMID: 26332872 Free PMC article. Review.
Orofacial clefting is a common birth defect with significant morbidity. ...Among these, variants in interferon regulatory factor 6 (IRF6) cause syndromic orofacial clefting and contribute risk toward isolated cleft lip and palate (1/700 live bir
Orofacial clefting is a common birth defect with significant morbidity. ...Among these, variants in interferon regulatory fact
Tooth abnormalities associated with non-syndromic cleft lip and palate: systematic review and meta-analysis.
Fonseca-Souza G, de Oliveira LB, Wambier LM, Scariot R, Feltrin-Souza J. Fonseca-Souza G, et al. Clin Oral Investig. 2022 Aug;26(8):5089-5103. doi: 10.1007/s00784-022-04540-8. Epub 2022 Jun 21. Clin Oral Investig. 2022. PMID: 35729285 Review.
OBJECTIVE: To evaluate the association between orofacial clefts (OFC) and tooth abnormalities (TA). METHODS: We searched PubMed, Scopus, Web of Science, Cochrane Library, LILACS, and BBO, and in the gray literature and selected observational studies that evaluated t …
OBJECTIVE: To evaluate the association between orofacial clefts (OFC) and tooth abnormalities (TA). METHODS: We searched PubMe …
78 results