Results 111 to 120 of about 867,107 (207)

Malignant Transformation in Oral Potentially Malignant Disorders

Oral Diseases, EarlyView.
ABSTRACT Background In 2020, the World Health Organization (WHO) Collaborating Centre for Oral Cancer convened an international expert workshop to establish an updated consensus on the nomenclature and classification of oral potentially malignant disorders (OPMDs).
Miguel Ángel González‐Moles, Pablo Ramos‐García, Saman Warnakulasuriya   +2 more
wiley   +1 more source

Clinical characteristics of the proband with non-syndromic oligodontia.

, 2015
(A) Clinical phenotype of the proband. (B) Panoramic radiograph of the participant. (C) Schematic presentation of congenitally missing teeth of the proband. * Position of a missing tooth;? Undetermined position of a missing tooth.
Hailan Feng (487918), Tingting Ding (800448), Haochen Liu (487914), Yuan Zhan (800449)   +3 more
core   +1 more source

Prevalence and clinical characteristics of missing teeth among dental students at Albanian University: a cross-sectional study

Annali di Stomatologia
Missing teeth are one of the most common clinical and public health concerns. They can affect quality of life by compromising esthetics and function. Therefore, early diagnosis may reduce their consequences.
Valbona Disha, Eni Disha, Esmeralda Murtini, Blerina Zeza, Bora Zaimi, Elizana Petrela   +5 more
doaj   +1 more source

Genetic risk variants implicate impaired maintenance and repair of periodontal tissues as causal for periodontitis—A synthesis of recent findings

Periodontology 2000, EarlyView.
AbstractPeriodontitis is a complex inflammatory disease in which the host genome, in conjunction with extrinsic factors, determines susceptibility and progression. Genetic predisposition is the strongest risk factor in the first decades of life. As people age, chronic exposure to the periodontal microbiome puts a strain on the proper maintenance of ...
Arne S. Schaefer, Luigi Nibali, Noha Zoheir, Niki M. Moutsopoulos, Bruno G. Loos   +4 more
wiley   +1 more source

Association of MSX1 gene polymorphisms and maxillary lateral incisor agenesis in Non-syndromic cleft lip and/or palate individuals

Journal of Oral Biology and Craniofacial Research
Background: To investigate the association between MSX1 gene polymorphisms and maxillary lateral incisor agenesis with and without Non Syndromic Cleft lip and palate (NSCL/P) in a South Indian population.
Dhanyashri Kamalakannan, Vignesh Kailasam, Sridevi Padmanaban, Solomon F.D. Paul, Gnanasambandan Ramanathan   +4 more
doaj   +1 more source

Long‐term stability of horizontal bone augmentation at implant sites

Periodontology 2000, EarlyView.
Abstract Horizontal bone augmentation is a fundamental surgical procedure in regenerative implant dentistry. In recent decades, this procedure has evolved, enabling clinicians to achieve predictable and stable horizontal bone augmentation that supports dental implant restorations.
Jia‐Hui Fu, Hui Jia Sophia Choo, Ding‐Sen Ong, Henry Kwek   +3 more
wiley   +1 more source

Congenitally missing teeth

Tässä kirjallisuuskatsauksessa on käsitelty synnynnäisten hammaspuutosten esiintyvyyttä, etiologiaa ja liitännäisongelmia maito- ja pysyvässä hampaistossa. Lisäksi on esitelty hampaan normaali kehittyminen.
Leinonen, Sara
core  

Definition and recommendations for trial methods for evaluating dentin hypersensitivity: A hybrid AI‐assisted scoping review and Delphi consensus process

Periodontology 2000, EarlyView.
Abstract Background Dentin hypersensitivity (DH) is a common yet inconsistently defined condition impacting oral health and quality of life. Variability in diagnostic criteria and trial methodologies has limited comparability of previous research. Objectives To map current definitions, diagnostic frameworks, and clinical trial methodologies in DH ...
Alexander J. Pollard, Tom J. Pollard, Anne‐Marie Glenny, Jan Clarkson, Tanya Walsh, Maria Davies, Thomas Sounack, Matthew Wright, Joon Seong, Joshua Twigg, Rupert Austin, Rossana Izzetti, Crystal Marruganti, Robert Newcombe, Rebecca Bullock, Nicola X. West   +15 more
wiley   +1 more source

Oral abnormalities in the Ellis-van Creveld syndrome

Indian Journal of Dental Research, 2010
Ellis-van Creveld (EvC) syndrome is an autosomal recessive disorder, mainly affecting the ectodermal components such as, enamel, nail, and hair. The gene for EvC syndrome is located on chromosome 4p16.
Babaji Prashant
doaj  

Oral health and systemic health outcomes: A call for interdisciplinary action

Periodontology 2000, EarlyView.
Abstract Objectives To make the case, from periodontology and dental public health, for interdisciplinary action on oral and systemic health, and to set out recommendations for practice, policy, education, and research. Materials and Methods A joint working group of the European Federation of Periodontology (EFP) and the European Association of Dental ...
Moritz Kebschull, Ryan T. Demmer, Nigel Pitts, Huda Yusuf, Gitana Rederiene, Nikolaos Donos, Wim Teughels, Raman Bedi, Orsolya Nemeth, Mia Rakic, Stéphanie Tubert‐Jeannin, Raimondo Ascione, Francesco D'Aiuto, James Deschner, Thomas Dietrich, Mili Doshi, Julian Fisher, Ramón Juanatey, Phoebus Madianos, Katalin Nagy, Barry Quinn, Saulė Skinkytė, Lina Stangvaltaite‐Mouhat, Maria van den Muijsenbergh, Josep Vilaseca, Nicola West, Anton Sculean, Andreas Stavropoulos, Kenneth Eaton, Joint EFP/EADPH Working Group   +29 more
wiley   +1 more source