Results 71 to 80 of about 3,472 (237)

Anomalias congénitas com interesse médico-legal [PDF]

, 2017
Cada vez mais se recorre à Medicina Dentária Forense para identificação de cadáveres, isto porque esta área se tem mostrado prática e eficaz na determinação da sua identidade, principalmente em casos em que o corpo esteja em avançado estágio de ...
Trabúlo, Ana Carolina Ramos Tomé Almeida
core  

Periodontal and orthodontic management of impacted canines

Periodontology 2000, EarlyView.
Abstract The maxillary and mandibular canines are described by many clinicians as the “cornerstone” of the arch. When in their optimal position, they play a critical role in providing a well‐balanced occlusal scheme that contributes toward functional as well as neuromuscular stability, harmony, esthetics, and dentofacial balance.
Mohammad Qali, Chenshuang Li, Chun‐Hsi Chung, Nipul Tanna   +3 more
wiley   +1 more source

Fixture-abutment connection surface and micro-gap measurements by 3D micro-tomographic technique analysis [PDF]

, 2012
X-ray micro-tomography (micro-CT) is a miniaturized form of conventional computed axial tomography (CAT) able to investigate small radio-opaque objects at a-few-microns high resolution, in a non-destructive, non-invasive, and tri-dimensional way ...
Baggi, L, Bedini, R, Di Carlo, F, Di Girolamo, M, Meleo, D, Pecci, R   +5 more
core   +2 more sources

Genotypes and Phenotypes of Patients With TSPEAR‐Related Disorder: Evidence of a Predominant Dental Phenotype

American Journal of Medical Genetics Part A, Volume 200, Issue 4, Page 790-799, April 2026.
ABSTRACT TSPEAR (chr. 21q22.3) encodes a protein involved in tooth development and is predominantly expressed in the enamel knot. Biallelic loss of function variants in TSPEAR cause ectodermal dysplasia, tooth agenesis and sensorineural hearing loss. However, the role of TSPEAR in auditory processes is unclear.
Debora Vergani, Lucia Tiberi, Annarita Giliberti, Elia Dirupo, Laila Zaroili, Francesco Brancati, Michela Brena, Stefano Caraffi, Chiara De Luca, Livia Garavelli, Anna Virginia Gulino, Milena Mariani, Marzia Pollazzon, Angelo Selicorni, Samuela Landini, Ilaria Sani, Rosangela Artuso, Angela Peron   +17 more
wiley   +1 more source

Agenesias dentarias: en busca de las alteraciones genéticas responsables de la falta de desarrollo [PDF]

, 2004
En conjunto, las agenesias dentarias son la malformación cráneofacial más frecuente. Su prevalencia alcanza el 20% en la dentición permanente, y su expresión puede variar desde la ausencia de una sola pieza, generalmente un tercer molar, hasta la de toda
Kolenc Fusé, Francisco Javier
core  

The Homeobox Genes: Classification, Regulation, Biological Functions, and Diseases

MedComm, Volume 7, Issue 4, April 2026.
Overview of the homeobox gene superfamily and its pathophysiological roles. The homeobox superfamily comprises several major classes, including ANTP, PRD, TALE, LIM, POU, and others. Among these, the HOX clusters (A–D) play critical roles in embryonic development specifically in conferring cellular identity, regulating morphogenesis, and guiding axial ...
Maedeh Dadzadi, Shahin Ramazi, Mona Darvazi, Sepideh Yoosefi, Melika Abbasi, Shirin Farsad   +5 more
wiley   +1 more source

Analysis of width/height ratio and gingival zenith in patients with bilateral agenesis of maxillary lateral incisor

Dental Press Journal of Orthodontics, 2012
OBJECTIVE: The purpose of this study was to evaluate the width/length ratio and the gingival zenith (GZ), by means of dental casts and digital caliper, in patients with missing maxillary lateral incisors after treatment.
Núbia Inocencya Pavesi Pini, Luciana Manzotti De-Marchi, Bruno Frazão Gribel, Adilson Luiz Ramos, Laurindo Zanco Furquim, Renata Corrêa Pascotto   +5 more
doaj   +1 more source

Presencia de osteopatologías en el yacimiento de Venta Micena (Orce, Granada, España) [PDF]

, 2014
En el yacimiento del Pleistoceno inferior de Venta Micena (Orce, prov. Granada), datado en 1,5-1,6 millones de años, se han identificado abundantes elementos fósiles de grandes mamíferos que presentan patologíasóseas, las cuales corresponden en su mayor ...
Espigares, María Patrocinio, Martínez-Navarro, Bienvenido, Marín Garrido, Antonio, Palmqvist, Paul, Ros-Montoya, Sergio   +4 more
core  

Detection of the Heterozygous Recurrent MAX p.(Arg60Gln) Variant in Two Females Confirms and Expands the Phenotypic Spectrum of Polydactyly–Macrocephaly Syndrome

Clinical Genetics, Volume 109, Issue 4, Page 788-795, April 2026.
We identified a recurrent heterozygous MAX c.179G>A:p.Arg60Gln variant in two unrelated females affected with the emerging phenotypes of MAX‐associated polydactyly‐macrocephaly syndrome. We propose that genitourinary abnormalities, including Mayer–Rokitanski–Kuster–Hauser syndrome in one individual, are an expansion of the known phenotypes associated ...
Iftekhar A. Showpnil, Neta Feinstein‐Goren, Lior Greenbaum, Ortal Barel, Daniel C. Koboldt, Samantha A. Brugmann, Kathryn Nicole Weaver, Anne Slavotinek, Ben Pode‐Shakked, Rolf W. Stottmann   +9 more
wiley   +1 more source

Dental agenesis: review of the literature and report of two cases

Revista Facultad de Odontología Universidad de Antioquia, 2006
Tooth agenesis is the most common anomaly of craniofacial development. The purpose of this report is to present a brief review of literature about tooth agenesis, which includes: terminology, etiology, prevalence, associated syndromes and dental ...
Luz Ángela Arboleda-A. , Jacqueline Echeverri-E. , Luz Ángela Restrepo-P. , Martha Lucía Marín-B. , Gonzalo Vásquez-P. , July Catalina Gómez-M., Hugo Alexánder Manco-G. , Clara María Pérez-S. , Elizabeth Taborda-F.   +8 more
doaj