Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Evelina, Kratunova"'
Publikováno v:
Ophthalmic Genet
PURPOSE: To evaluate retinal function in a family presenting with Jalili syndrome due to a previously unreported variant in CNNM4. METHODS: A family of three sisters with a novel CNNM4 variant, c.482T>C p.(Leu161Pro), and ten visually normal, age-sim
Publikováno v:
Ophthalmic Genetics. 43:268-276
Publikováno v:
Journal of Clinical Pediatric Dentistry. 45:193-198
Loeys-Dietz Syndrome (LDS) is a rare connective tissue disorder with an autosomal dominant pattern of inheritance, linked to heterozygous mutations in six genes from the transforming growth factor beta receptor complex. The classical syndrome charact
Publikováno v:
The Cleft Palate Craniofacial Journal. :105566562311701
Objective The objectives of this study were to assess the oral health status and parental perception of oral health needs of pediatric patients in an urban Craniofacial Center. Design This research utilized a prospective cross-sectional matched study
Autor:
Rachel, Vorwaller, Evelina, Kratunova, Marcio A, da Fonseca, Satish B, Alapati, Brittaney, Hill, Clark, Stanford
Publikováno v:
Pediatric dentistry. 43(6)
Autor:
Evelina, Kratunova
Publikováno v:
Pediatric dentistry. 43(6)
Publikováno v:
Journal of dentistry for children (Chicago, Ill.). 88(3)
Publikováno v:
Pediatric dentistry. 43(5)
Publikováno v:
Journal of dentistry for children (Chicago, Ill.). 88(2)
Publikováno v:
Journal of dental educationREFERENCES.
PURPOSE/OBJECTIVES To evaluate patient attendance for moderate sedation (MS) at a university-based pediatric dental clinic; to identify factors with negative impact on MS being completed and to assess for associations between no-show appointments and