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Quoted phrase not found in phrase index: "Abnormality of upper lip vermillion"
Page 1
Precision Dermal Fat Grafting for Vermillion Deficiencies in Patients With Unilateral and Bilateral Cleft Lip.
Cleft Palate Craniofac J. 2020 Jan;57(1):127-131. doi: 10.1177/1055665619864221. Epub 2019 Jul 21.
Cleft Palate Craniofac J. 2020.
PMID: 31327233
OBJECTIVE: Deficiencies of the upper lip vermilion occur with some frequency following repair of unilateral and bilateral clefts of the lip and can compromise the aesthetic outcome. ...This technique combines precise placement of a contoured dermal fat graft …
OBJECTIVE: Deficiencies of the upper lip vermilion occur with some frequency following repair of unilateral and bilateral clef …
The Skoog Lip Repair for Unilateral Cleft Lip Deformity: The Uppsala Experience.
Falk-Delgado A, Lång A, Hakelius M, Skoog V, Nowinski D.
Falk-Delgado A, et al.
Plast Reconstr Surg. 2018 May;141(5):1226-1233. doi: 10.1097/PRS.0000000000004321.
Plast Reconstr Surg. 2018.
PMID: 29697619
The aim of this study was to determine complications after lip surgery and the incidence and indications for lip revisions in all patients born with unilateral cleft lip from 1960 to 2004. METHODS: All patients who were born from 1960 to 2004 with unilateral …
The aim of this study was to determine complications after lip surgery and the incidence and indications for lip revisions in …
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Morphological analysis of the lip and nose following cleft lip repair with simultaneous partial primary rhinoplasty: A prospective study over 4 years.
Kluba S, Bopp C, Bacher M, Reinert S, Krimmel M.
Kluba S, et al.
J Craniomaxillofac Surg. 2015 Jun;43(5):599-605. doi: 10.1016/j.jcms.2015.02.019. Epub 2015 Mar 9.
J Craniomaxillofac Surg. 2015.
PMID: 25843646
Our study analyzed the lip and nose deformities associated with unilateral clefts in a prospective longitudinal study. MATERIAL AND METHODS: A total of 33 patients with a cleft lip or cleft lip and alveolus (UCL) and 46 with a cleft lip and palate (UCL …
Our study analyzed the lip and nose deformities associated with unilateral clefts in a prospective longitudinal study. MATERIAL AND M …
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De novo mutations in beta-catenin (CTNNB1) appear to be a frequent cause of intellectual disability: expanding the mutational and clinical spectrum.
Kuechler A, Willemsen MH, Albrecht B, Bacino CA, Bartholomew DW, van Bokhoven H, van den Boogaard MJ, Bramswig N, Büttner C, Cremer K, Czeschik JC, Engels H, van Gassen K, Graf E, van Haelst M, He W, Hogue JS, Kempers M, Koolen D, Monroe G, de Munnik S, Pastore M, Reis A, Reuter MS, Tegay DH, Veltman J, Visser G, van Hasselt P, Smeets EE, Vissers L, Wieland T, Wissink W, Yntema H, Zink AM, Strom TM, Lüdecke HJ, Kleefstra T, Wieczorek D.
Kuechler A, et al.
Hum Genet. 2015 Jan;134(1):97-109. doi: 10.1007/s00439-014-1498-1. Epub 2014 Oct 19.
Hum Genet. 2015.
PMID: 25326669
All patients have ID, motor delay and speech impairment (both mostly severe) and abnormal muscle tone (truncal hypotonia and distal hypertonia/spasticity). The craniofacial phenotype comprised microcephaly (typically -2 to -4 SD) in 12 of 16 and some overlapping facial fea …
All patients have ID, motor delay and speech impairment (both mostly severe) and abnormal muscle tone (truncal hypotonia and distal h …
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