Research Topics
Species | Karin VargervikSummaryAffiliation: University of California Country: USA Publications
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Detail Information
Publications
Parameters of care for craniosynostosis: dental and orthodontic perspectivesKarin Vargervik
Division of Craniofacial Anomalies, University of California, San Francisco, CA, USA
Am J Orthod Dentofacial Orthop 141:S68-73. 2012..Herein, we present the dental, orthodontic, and surgical care recommendations for those with craniosynostosis, with special emphasis on craniosynostosis syndromes...- Team care for the patient with cleft: UCSF protocols and outcomesKarin Vargervik
Department of Orofacial Sciences, Center for Craniofacial Anomalies, School of Dentistry, University of California at San Francisco, California 94143 044, USA
J Craniofac Surg 20:1668-71. 2009..We present in this article the protocols and treatment outcomes of the University of California at San Francisco... - Volumetric assessment of secondary alveolar bone grafting using cone beam computed tomographySnehlata Oberoi
Center for Craniofacial Anomalies, Department of Orofacial Sciences, University of California at San Francisco, 94143, USA
Cleft Palate Craniofac J 46:503-11. 2009..To assess the radiographic outcome of secondary alveolar bone grafting in individuals with nonsyndromic unilateral or bilateral cleft lip and palate using cone beam computed tomography... - Morphologic and management characteristics of individuals with unilateral cleft lip and palate who required maxillary advancementSnehlata Oberoi
Center for Craniofacial Anomalies, Department of Orofacial Sciences, School of Dentistry, University of California, San Francisco, CA 94143 0442, USA
Cleft Palate Craniofac J 45:42-9. 2008..To delineate factors that may contribute to maxillary hypoplasia requiring maxillary advancement surgery in individuals with nonsyndromic unilateral cleft lip and palate (UCLP)... - Craniofacial team management in Apert syndromeSnehlata Oberoi
Department of Orofacial Sciences, School of Dentistry, University of California at San Francisco, CA, USA
Am J Orthod Dentofacial Orthop 141:S82-7. 2012.... - Hypodontia in Beare-Stevenson syndrome: an example of dental anomalies in FGFR-related craniosynostosis syndromesYou Chen Tao
UCSF School of Dentistry, San Francisco, California, USA
Cleft Palate Craniofac J 47:253-8. 2010..The authors review the current literature to investigate the relationship between dental anomalies and fibroblast growth factor receptor-related mutations in BSS and other craniosynostosis syndromes such as Apert, Crouzon, and Pfeiffer... 
The role of endosseous implants in the management of alveolar cleftsWilliam A Pena
Division of Pediatric Dentistry, University of California, San Francisco, Calif, USA
Pediatr Dent 31:329-33. 2009..Other implant parameters such as surface characteristics and diameter do not seem to influence significantly the long-term longevity of implants placed into grafted alveolar clefts...- Using implants for the growing childArun B Sharma
Department of Preventive and Restorative Dental Sciences, University of California, San Francisco, School of Dentistry, 94143, USA
J Calif Dent Assoc 34:719-24. 2006..In this paper, the authors will discuss the indications for implant placement in the growing child. The decision for implant placement is based not only on growth, but also the number and location of the missing teeth... - Clinical and molecular studies of patients with characteristics of Opitz G/BBB syndrome shows a novel MID1 mutationElena W Y Hsieh
Department of Pediatrics, Division of Genetics, UCSF School of Medicine, San Francisco, California 94143 0748, USA
Am J Med Genet A 146:2337-45. 2008..This mutation affects the PRY domain of the C-terminus of the MID1 protein... - Hemimaxillofacial dysplasia: a variable presentationRagini Porwal
School of Dentistry, University of California at San Francisco, University of California at San Francisco, USA
J Craniofac Surg 19:1554-7. 2008..The reconstruction procedures are detailed, and long-term follow-up findings are described... - Velopharyngeal, speech and dental characteristics as diagnostic aids in 22q11.2 deletion syndromeSnehlata Oberoi
Center for Craniofacial Anomalies, Department of Orofacial Sciences, University of California, San Francisco, School of Dentistry, 94143 044, USA
J Calif Dent Assoc 39:327-32. 2011..There are common findings that can aid the dental practitioner in recognizingthe syndrome and make appropriate referrals... - Velocardiofacial syndrome with single central incisorSnehlata Oberoi
Center for Craniofacial Anomalies, School of Dentistry, University of California, San Francisco, CA 94143, USA
Am J Med Genet A 132:194-7. 2005..A single maxillary central incisor has previously been reported in VCFS, but to our knowledge a single central incisor in the mandible has not been reported previously in this entity... - Acro-dermato-ungual-lacrimal-tooth (ADULT) syndrome: report of a child with phenotypic overlap with ulnar-mammary syndrome and a new mutation in TP63Anne M Slavotinek
Department of Pediatrics, University of California, San Francisco 94143 0748, USA
Am J Med Genet A 138:146-9. 2005..Mutation analysis of TP63 showed a single nucleotide substitution, c.G518A, predicting a novel missense mutation, p.V114M in exon 4. This is the third mutation to be reported in TP63 in ADULT syndrome... - Case reports of oculofaciocardiodental syndrome with unusual dental findingsSnehlata Oberoi
University of California, San Francisco, Center for Craniofacial Anomalies, San Francisco, California 94122, USA
Am J Med Genet A 136:275-7. 2005..4. Mutational analysis in one of our patients showed a deletion of a single nucleotide, c.2613delC, predicting a novel frameshift mutation with a premature stop codon, p.F871Lfs8X... - Frequency of surgical correction for maxillary hypoplasia in cleft lip and palateSnehlata Oberoi
Center for Craniofacial Anomalies, School of Dentistry, University of California at San Francisco, CA 94143 044, USA
J Craniofac Surg 23:1665-7. 2012.... - A novel EFNB1 mutation (c.712delG) in a family with craniofrontonasal syndrome and diaphragmatic herniaJacob Hogue
Department of Pediatrics, University of California, San Francisco, California 94143 0706, USA
Am J Med Genet A 152:2574-7. 2010..The occurrence of congenital diaphragmatic hernia, phenotypic differences between males and females, and utility of molecular testing in craniofrontonasal syndrome are demonstrated... - Hypoplasia and hypodontia in Van der Woude syndromeSnehlata Oberoi
Center for Craniofacial Anomalies, School of Dentistry, University of California, San Francisco, 94143-0640, USA
Cleft Palate Craniofac J 42:459-66. 2005..CONCLUSIONS: Based on these findings, the expectation is that there will be maxillary hypoplasia and hypodontia of greater severity in Van der Woude syndrome than in nonsyndromic clefts... - Phenotypic variation in trismus-pseudocamptodactyly syndrome caused by a recurrent MYH8 mutationKaren Minzer-Conzetti
Department of Pediatrics, Division of Genetics, University of California, San Francisco, California 94143 0748, USA
Clin Dysmorphol 17:1-4. 2008..These findings broaden the phenotype associated with p.R674Q mutations and support the use of MYH8 testing in patients with a clinical diagnosis of TPS syndrome...