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Статті в журналах з теми "Craniofacial syndromes"
Schlieder, Daniel, and Michael R. Markiewicz. "Craniofacial Syndromes." Atlas of the Oral and Maxillofacial Surgery Clinics 30, no. 1 (March 2022): 85–99. http://dx.doi.org/10.1016/j.cxom.2021.11.004.
Повний текст джерелаSuri, Mohnish. "Craniofacial syndromes." Seminars in Fetal and Neonatal Medicine 10, no. 3 (June 2005): 243–57. http://dx.doi.org/10.1016/j.siny.2004.12.002.
Повний текст джерелаBuchanan, Edward P., Amy S. Xue, and Larry H. Hollier. "Craniofacial Syndromes." Plastic and Reconstructive Surgery 134, no. 1 (July 2014): 128e—153e. http://dx.doi.org/10.1097/prs.0000000000000308.
Повний текст джерелаKjær, Inger. "Dental Approach to Craniofacial Syndromes: How Can Developmental Fields Show Us a New Way to Understand Pathogenesis?" International Journal of Dentistry 2012 (2012): 1–10. http://dx.doi.org/10.1155/2012/145749.
Повний текст джерелаS, Jeelani. "Craniofacial Abnormalities and Syndromes." Journal of Scientific Dentistry 4, no. 2 (2014): 56–61. http://dx.doi.org/10.5005/jsd-4-2-56.
Повний текст джерелаSchweinler, Bonita. "Orthoptics and Craniofacial Syndromes." American Orthoptic Journal 64, no. 1 (January 2014): 21–23. http://dx.doi.org/10.3368/aoj.64.1.21.
Повний текст джерелаM. Michael Cohen Jr, Sven Kreiborg. "Perspectives on craniofacial syndromes." Acta Odontologica Scandinavica 56, no. 6 (January 1998): 315–20. http://dx.doi.org/10.1080/000163598428239.
Повний текст джерелаForrest, Christopher R., and Richard A. Hopper. "Craniofacial Syndromes and Surgery." Plastic and Reconstructive Surgery 131, no. 1 (January 2013): 86e—109e. http://dx.doi.org/10.1097/prs.0b013e318272c12b.
Повний текст джерелаPosnick, Jeffrey C. "The Craniofacial Dysostosis Syndromes." Clinics in Plastic Surgery 24, no. 3 (July 1997): 429–46. http://dx.doi.org/10.1016/s0094-1298(20)31037-3.
Повний текст джерелаPosnick, Jeffrey C. "The Craniofacial Dysostosis Syndromes." Clinics in Plastic Surgery 21, no. 4 (October 1994): 585–98. http://dx.doi.org/10.1016/s0094-1298(20)30726-4.
Повний текст джерелаДисертації з теми "Craniofacial syndromes"
Cloonan, Yona Keich. "Sleep outcomes in children with craniofacial microsomia /." Thesis, Connect to this title online; UW restricted, 2007. http://hdl.handle.net/1773/10877.
Повний текст джерелаInstrum, Susette M. "Cephalometric comparison of the craniofacial skeletal morphology between Moebius syndrome and non-syndromic controls." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape8/PQDD_0015/MQ46507.pdf.
Повний текст джерелаNguyen, Tung Thanh Wright J. Timothy. "Craniofacial variations in the tricho-dento-osseus syndrome." Chapel Hill, N.C. : University of North Carolina at Chapel Hill, 2008. http://dc.lib.unc.edu/u?/etd,1766.
Повний текст джерелаTitle from electronic title page (viewed Sep. 16, 2008). "... in partial fulfillment of the requirements for the degree of Master of Science in the School of Dentistry Orthodontics." Discipline: Orthodontics; Department/School: Dentistry.
Britto, Jonathan Anthony. "Syndromic craniofacial dysostosis : from genotype to phenotype: studies of FGFR gene expression in human craniofacial development and craniosynostosis." Thesis, University College London (University of London), 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.268446.
Повний текст джерелаGROLLEAU, MERCIER CHRISTINE. "Le syndrome de marden-walker." Lille 2, 1988. http://www.theses.fr/1988LIL2M155.
Повний текст джерелаProudman, Timothy William. "Crouzon syndrome : a clinical and three dimensional radiographic analysis of craniofacial morphology and surgery /." Title page, contents and summary only, 1995. http://web4.library.adelaide.edu.au/theses/09MS/09msp968.pdf.
Повний текст джерелаPerkiömäki, M. R. (Marja Riitta). "Craniofacial shape and dimensions as indicators of orofacial clefting and palatal form:a study on cleft lip and palate and Turner syndrome families." Doctoral thesis, University of Oulu, 2008. http://urn.fi/urn:isbn:9789514288708.
Повний текст джерелаGould, Rebekah. "Dose and time dependence of alcohol exposure in relation to craniofacial dysmorphisms in fetal alcohol syndrome." Thesis, Boston University, 2013. https://hdl.handle.net/2144/21158.
Повний текст джерелаThe National Institutes of Health defines Fetal Alcohol Syndrome (FAS) as a debilitating collection of birth defects that include craniofacial dysmorphisms, neurological and motor insufficiencies, growth retardation, and behavioral and social discrepancies. Characteristic craniofacial abnormalities, which include smooth philtrum, thin vermillion border, short palpebral fissures, and microcephaly, are used as a diagnostic tool for FAS. There is agreement across the literature that the characteristic craniofacial dysmorphisms are induced as a result of prenatal alcohol exposure in very specific doses, and during very particular time periods during embryonic development. However, ambiguity still exists about the critical time and dose relationship of prenatal alcohol exposure in the production of FAS. In regards to the critical timing, researchers have concluded that prenatal alcohol exposure during the second half of the first trimester, defined as days 43-94 postconception, was found to cause an increased incidence of smooth philtrum, thin vermillion border, microcephaly and reduced birth weight. Conversely, other studies found that prenatal alcohol exposure on day 7 of gestation in mice, which corresponds to week 3 of human gestation, induced craniofacial abnormalities comparable to those seen in humans with FAS. In regards to the critical dose, there is a linear relationship between the dose of prenatal alcohol exposure and the incidence of FAS-related craniofacial abnormalities, with no safe threshold. It was also found that a binge pattern of drinking was more significantly associated with the craniofacial abnormalities seen in FAS than a continuous or less condensed pattern of drinking, even if the binge pattern involved a smaller absolute dose of alcohol. These results regarding both dose and pattern on prenatal alcohol exposure, suggest that binge-drinking patterns are most significantly associated with craniofacial abnormalities if consumed before pregnancy or during late pregnancy, whereas absolute high doses of alcohol in a non-binge pattern were most significantly associated with craniofacial abnormalities in the first trimester. Further research is required for clarification of the critical time and dose relationships involved in the production of the characteristic craniofacial dysmorphisms seen in FAS. A definite conclusion will aid in the public education and prevention programs for FAS if solid information can be provided about the harms of alcohol consumption during pregnancy in regards to timing and dose.
2031-01-01
Naidoo, Sudeshi. "Fetal alcohol syndrome in the Western Cape : craniofacial and oral manifestations : a case control study." Thesis, Stellenbosch : Stellenbosch University, 2003. http://hdl.handle.net/10019.1/53425.
Повний текст джерелаENGLISH ABSTRACT: Introduction: Fetal alcohol syndrome (FAS) consists of multi-system abnormalities and is caused by the excessive intake of alcohol during pregnancy. The teratogenic effect of alcohol on the human fetus has now been established beyond reasonable doubt and FAS is the most important human teratogenic condition known today. The syndrome, first described by Lemoine in1968 in the French literature and in the English literature by Jones and Smith in 1973, has since been corroborated by numerous animal and human studies. This study has grown out of several epidemiological, prenatal and infant studies in areas of the Western Cape that are currently being undertaken by the Foundation for Alcohol Related Research (FARR). Preliminary data from studies in Wellington have confirmed that a significant proportion of school-entry children have FAS. The prevalence ofF AS in this community exceeds that for Down syndrome by a factor of30 times. The frequency ofFAS in high-risk populations of the Western Cape is the highest reported anywhere in the world. With this background, and the paucity of FAS literature related to dentistry, the aim of this study was to determine the craniofacial and oral manifestations ofF AS in a sample of school-going children in the Western Cape. Methodology: This study is a descriptive, case-control, cross-sectional study using a random cluster sampling method. On the day of examination, children were weighed, and their height and head circumference were measured. They then had photographs and radiographs taken, followed by an oral examination. For each child, the following information was recorded on the data capture sheet: date of birth, gender, head circumference, weight and height, enamel opacities, dental fluorosis, plaque index, gingival bleeding index, dentition status, oral mucosal lesions and dentofacial anomalies. Results: The total sample of90 children with diagnosed FAS and 90 controls, were matched for age, gender and social class. There were no significant age differences between the two groups (p=0.3363) and the mean ages were 8.9 and 9.1 for the FAS and control groups respectively. Head circumference (HC) differed significantly between the two groups (p
Opper, Björn. "Compromised affect and learning associated with Crouzon syndrome a clinical case study /." Pretoria : [s.n.], 2006. http://upetd.up.ac.za/thesis/available/etd-10022007-132545/.
Повний текст джерелаКниги з теми "Craniofacial syndromes"
B, Cassidy Suzanne, and Allanson Judith E, eds. Management of genetic syndromes. 2nd ed. Hoboken, N.J: Wiley-Liss, 2005.
Знайти повний текст джерелаYates, David M., and Michael R. Markiewicz, eds. Craniofacial Microsomia and Treacher Collins Syndrome. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-84733-3.
Повний текст джерелаInstrum, Susette M. Cephalometric comparison of the craniofacial skeletal morphology between mobius syndrome and non-syndromic controls. [Toronto: University of Toronto, Faculty of Dentistry], 1999.
Знайти повний текст джерелаInstrum, Susette M. Craniofacial morphology and malocclusion in individuals with Mobius syndrome. [Toronto: University of Toronto, Faculty of Dentistry], 1998.
Знайти повний текст джерелаSelnes, J. Eric. Cephalometric comparison of craniofacial morphology between velocardiofacial syndrome with confirmed 22q 11.2 microdeletions : isolated cleft palate and non-syndromic children. [Toronto: University of Toronto, Faculty of Dentistry], 1997.
Знайти повний текст джерелаParker, James N., and Philip M. Parker. Treacher Collins syndrome: A bibliography and dictionary for physicians, patients, and genome researchers [to Internet references]. San Diego, CA: ICON Health Publications, 2007.
Знайти повний текст джерелаManagement of Genetic Syndromes. 2nd ed. Wiley-Liss, 2004.
Знайти повний текст джерелаCassidy, Suzanne B., and Judith E. Allanson. Management of Genetic Syndromes. Wiley & Sons, Incorporated, John, 2010.
Знайти повний текст джерелаCassidy, Suzanne B., and Judith E. Allanson. Management of Genetic Syndromes. Wiley & Sons, Incorporated, John, 2005.
Знайти повний текст джерелаHopkins, Paul, and Laura Ryan. Difficult Airway. Edited by Erin S. Williams, Olutoyin A. Olutoye, Catherine P. Seipel, and Titilopemi A. O. Aina. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190678333.003.0015.
Повний текст джерелаЧастини книг з теми "Craniofacial syndromes"
Gruber, Elizabeth Anne, and Michael Stephen Dover. "Craniofacial Syndromes." In Clinical Embryology, 133–42. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-319-26158-4_16.
Повний текст джерелаMavridis, Ι. Ν., W. S. B. Wimalachandra, and D. Rodrigues. "Craniofacial Syndromes." In Pediatric Neurosurgery for Clinicians, 147–61. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-80522-7_10.
Повний текст джерелаYang, Robin, Jordan W. Swanson, and Christopher M. Cielo. "Craniofacial Syndromes." In Pediatric Sleep Medicine, 655–65. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-65574-7_54.
Повний текст джерелаLangevin, Claude-Jean, Earl Gage, and Frank Papay. "Craniofacial Clefts and Craniofacial Syndromes." In Plastic and Reconstructive Surgery, 253–64. London: Springer London, 2010. http://dx.doi.org/10.1007/978-1-84882-513-0_19.
Повний текст джерелаFrancis-West, P. H., L. Robson, and Darell J. R. Evans. "Human Craniofacial Syndromes." In Craniofacial Development The Tissue and Molecular Interactions That Control Development of the Head, 87–98. Berlin, Heidelberg: Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-642-55570-1_8.
Повний текст джерелаTaub, Peter J., and Paymon Sanati-Mehrizy. "Craniofacial Surgery: Craniosynostosis and Craniofacial Syndromes." In Tips and Tricks in Plastic Surgery, 477–86. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-78028-9_28.
Повний текст джерелаEstrellado-Cruz, Wendy, and Robert C. Beckerman. "Children with Craniofacial Syndromes." In Sleep Disordered Breathing in Children, 337–48. Totowa, NJ: Humana Press, 2012. http://dx.doi.org/10.1007/978-1-60761-725-9_25.
Повний текст джерелаMiller, Marilyn T., and Anna Newlin. "Craniofacial Syndromes and Malformations." In Pediatric Ophthalmology and Strabismus, 705–39. New York, NY: Springer New York, 2003. http://dx.doi.org/10.1007/978-0-387-21753-6_41.
Повний текст джерелаKreiborg, Sven, Howard Aduss, and M. Michael Cohen. "Apert’s and Crouzon’s Syndromes Contrasted: Qualitative Craniofacial X-Ray Findings." In Craniofacial Surgery, 91–95. Berlin, Heidelberg: Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-82875-1_20.
Повний текст джерелаPassos-Bueno, Maria Rita, Andréa L. Sertié, Fernanda S. Jehee, Roberto Fanganiello, and Erika Yeh. "Genetics of Craniosynostosis: Genes, Syndromes, Mutations and Genotype-Phenotype Correlations." In Craniofacial Sutures, 107–43. Basel: S. KARGER AG, 2008. http://dx.doi.org/10.1159/000115035.
Повний текст джерелаТези доповідей конференцій з теми "Craniofacial syndromes"
PUCCIARELLI, Valentina, Marina CODARI, Chiara INVERNIZZI, Simona BERTOLI, Alberto BATTEZZATI, Ramona DE AMICIS, Valentina DE GIORGIS, Pierangelo VEGGIOTTI, and Chiarella SFORZA. "Three-Dimensional Craniofacial Features of Glut1 Deficiency Syndrome Patients." In 6th International Conference on 3D Body Scanning Technologies, Lugano, Switzerland, 27-28 October 2015. Ascona, Switzerland: Hometrica Consulting - Dr. Nicola D'Apuzzo, 2015. http://dx.doi.org/10.15221/15.061.
Повний текст джерелаDOLCI, Claudia, Valentina PUCCIARELLI, Marina CODARI, Susan MARELLI, Giuliana TRIFIRO, Alessandro PINI, and Chiarella SFORZA. "3D Morphometric Evaluation of Craniofacial Features in Adult Subjects with Marfan Syndrome." In 7th International Conference on 3D Body Scanning Technologies, Lugano, Switzerland, 30 Nov.-1 Dec. 2016. Ascona, Switzerland: Hometrica Consulting - Dr. Nicola D'Apuzzo, 2016. http://dx.doi.org/10.15221/16.098.
Повний текст джерелаLoo, Lucas, Luke Smith, and Juling Ong. "1124 Assessing changes in the upper airway using 3-dimensional segmentation after craniofacial distraction surgery in children with syndromic craniofacial anomalies." In Royal College of Paediatrics and Child Health, Abstracts of the RCPCH Conference, Liverpool, 28–30 June 2022. BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health, 2022. http://dx.doi.org/10.1136/archdischild-2022-rcpch.399.
Повний текст джерелаDOLCI, Claudia, Valentina PUCCIARELLI, Marina CODARI, Daniele M. GIBELLI, Susan MARELLI, Giuliana TRIFIRO, Alessandro PINI, and Chiarellag SFORZA. "3D Craniofacial Morphometric Analysis of Young Subjects with Marfan Syndrome: A Preliminary Report." In 6th International Conference on 3D Body Scanning Technologies, Lugano, Switzerland, 27-28 October 2015. Ascona, Switzerland: Hometrica Consulting - Dr. Nicola D'Apuzzo, 2015. http://dx.doi.org/10.15221/15.054.
Повний текст джерелаSilva, Bruno Custódio, Gisele Delazeri, Ana Luíza Kolling Konopka, Giulia Righetti Tuppini Vargas, Paulo Ricardo Gazzola Zen, and Rafael Fabiano Machado Rosa. "Report of a family affected by fragile X syndrome and type 1 diabetes mellitus." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.076.
Повний текст джерелаWarrick, Amanda E., J. Douglas Swarts, and Samir N. Ghadiali. "Fluid Structure Interactions in the Eustachain Tube Under Normal and Pathological Conditions." In ASME 2007 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2007. http://dx.doi.org/10.1115/sbc2007-175328.
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