Search Results - "Carels, C. E. L."
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Tooth agenesis and orofacial clefting: genetic brothers in arms?
Published in Human genetics (01-12-2016)“…Tooth agenesis and orofacial clefts represent the most common developmental anomalies and their co-occurrence is often reported in patients as well in animal…”
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Dental Development in Hemifacial Microsomia
Published in Journal of dental research (01-12-2010)“…Hemifacial microsomia (HFM) is a congenital disorder marked by facial asymmetry. Whether facial asymmetry accounts for asymmetrical dental development is…”
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Fgf8a mutation affects craniofacial development and skeletal gene expression in zebrafish larvae
Published in Biology open (2019)“…Craniofacial development is tightly regulated and therefore highly vulnerable to disturbance by genetic and environmental factors. Fibroblast growth factors…”
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Prenatal Diagnosis of Craniomaxillofacial Malformations: A Characterization of Phenotypes in Trisomies 13, 18, and 21 by Ultrasound and Pathology
Published in The Cleft palate-craniofacial journal (01-03-2010)“…To determine the relationship between trisomies 13, 18, and 21 and craniofacial malformations detected by prenatal sonography. During a 29-year period (1976…”
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Nasolabial shape and aesthetics in unilateral cleft lip and palate: an analysis of nasolabial shape using a mean 3D facial template
Published in International journal of oral and maxillofacial surgery (01-02-2021)“…The aim of this study was to determine the amount of deviation in nasolabial shape in patients with a cleft compared with an average non-cleft face, and to…”
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Novel IRF6 Mutations Detected in Orofacial Cleft Patients by Targeted Massively Parallel Sequencing
Published in Journal of dental research (01-02-2017)“…Common variants in interferon regulatory factor 6 (IRF6) have been associated with nonsyndromic cleft lip with or without cleft palate (NSCL/P) as well as with…”
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Short Stature in KBG Syndrome: First Responses to Growth Hormone Treatment
Published in Hormone research in paediatrics (01-01-2015)“…KBG syndrome is a rare disorder characterized by intellectual disability and associated with macrodontia of the upper central incisors, specific craniofacial…”
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Novel BCOR mutations in patients with oculofaciocardiodental (OFCD) syndrome
Published in Clinical genetics (01-02-2014)Get full text
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Reduced masticatory function is related to lower satellite cell numbers in masseter muscle
Published in European journal of orthodontics (01-06-2014)“…The physiology of masseter muscles is known to change in response to functional demands, but the effect on the satellite cell (SC) population is not known. In…”
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The anti-epileptic drug valproic acid causes malformations in the developing craniofacial skeleton of zebrafish larvae
Published in Mechanisms of development (01-09-2020)“…Valproic acid (VPA) is an anti-epileptic drug known to cause congenital craniofacial abnormalities, including orofacial clefts (OFC). The exact mechanisms by…”
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Identification of germline mutations in the cancer predisposing gene CDH1 in patients with orofacial clefts
Published in Human molecular genetics (01-03-2013)“…Orofacial clefts (OFC) are among the most common birth defects worldwide. The etiology of non-syndromic OFC is still largely unknown. During embryonic…”
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Prenatal diagnosis of craniomaxillofacial malformations: a characterization of phenotypes in trisomies 13, 18 and 21 by ultrasound and pathology
Published in The Cleft palate-craniofacial journal (01-03-2010)“…OBJECTIVETo determine the relationship between trisomies 13, 18, and 21 and craniofacial malformations detected by prenatal sonography.DESIGNDuring a 29-year…”
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The impact of bisphosphonates on orthodontic treatment
Published in Nederlands tijdschrift voor tandheelkunde (01-04-2012)“…Bisphosphonates are used in the treatment of various diseases which are associated with a disturbance of the balance between bone apposition and degradation…”
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Solitary median maxillary central incisor syndrome
Published in Nederlands tijdschrift voor tandheelkunde (01-09-2014)“…Solitary Median Maxillary Central Incisor syndrome is a rare condition (prevalence 1:50,000), with the characteristic dental feature of a solitary central…”
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Tooth eruption disturbances and syndromes
Published in Nederlands tijdschrift voor tandheelkunde (01-04-2014)“…In the tooth eruption mechanism, various disturbances can appear as a result of gene mutations, a consequence of which can be that tooth eruption does not…”
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Embryonic odontogenesis in vertebrates. A mini-review
Published in Nederlands tijdschrift voor tandheelkunde (01-02-2008)“…Although the molecular cascades that control craniofacial development are still largely unknown, the generation of mutant animal models and the identification…”
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Orthodontics in general dental practice 6. Treatment of Angle Class II/1 malocclusions
Published in Nederlands tijdschrift voor tandheelkunde (01-08-2008)“…Four patients with a Class II/1 malocclusion were treated. Despite their common malocclusion, the 4 patients had a different skeletal and dentofacial…”
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The relationship between malocclusion and masticatory performance
Published in Nederlands tijdschrift voor tandheelkunde (01-07-2008)“…In dentistry 3 aspects may lead to an improvement in the quality of life: pain reduction, aesthetic adjustments, and improvement of masticatory performance…”
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Genetics. Foreword
Published in Nederlands tijdschrift voor tandheelkunde (01-02-2008)Get more information
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Heridity of non-syndromal orofacial clefts
Published in Nederlands tijdschrift voor tandheelkunde (01-02-2008)“…Non-syndromal orofacial clefts are congenital anomalies with a high incidence of heterogeneous origin. The condition is usually multifactorially determined,…”
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