Results 71 to 80 of about 3,300 (225)

Parameter Populasi Kerang Lumpur Tropis Anodontia Edentula Di Ekosistem Mangrove [PDF]

open access: yes, 2009
Population Parameters of Tropical Mudflat Clam, (Anodontia edentula) in MangroveEcosystem. Over a 12 months period (Januari 2005 – Desember 2005), population parameters oftropical mudflat clam, (Anodonta edentula) in mangrove ecosystem were determined ...
Natan, Y. (Yuliana)
core  

The Incidence of the Tooth Agenesis in Students of Dentistry at Palacký University in Olomouc

open access: yesČeská Stomatologie a Praktické Zubní Lékařství, 2015
Aim of the study: Tooth agenesis is very often developmental anomaly. The prevalence of this disorder differs depending on several factors. Different results can be observed in populations on different continents, in different races and genders, and in ...
L. Kramerová   +3 more
doaj   +1 more source

Auto-percepção dos portadores de Amelogênese Imperfeita e Displasia [PDF]

open access: yes, 2012
TCC (graduação) - Universidade Federal de Santa Catarina. Centro de Ciências da Saúde. Odontologia.A Amelogênese Imperfeita é um distúrbio hereditário caracterizado pela formação anormal de esmalte, o que gera dentes com alteração de cor, sensibilidade e
Klita, Ana Paula Haisi
core  

Conservative interdisciplinary management for a congenitally missing maxillary lateral incisor in an adolescent patient

open access: yesAustralian Dental Journal, Volume 69, Issue 4, Page 267-277, December 2024.
Abstract A congenitally missing lateral incisor tooth is commonly associated with both short and long‐term clinical dilemmas, particularly for a growing patient. A unilaterally missing maxillary lateral incisor tooth creates a significant dental asymmetry in the critical aesthetic zone of the smile and potentially increases the difficulty of any ...
R Hmud, DC‐V Ong
wiley   +1 more source

Ectodermal Dysplasia - Connections and Implantation

open access: yesČeská Stomatologie a Praktické Zubní Lékařství, 2009
Ectodermal dysplasia is a disease of strong familial disposition. There is a broad scale of subtypes with more or less expressed signs. The diagnostics is of high significance as well as the associated missing teeth.
P. Prachár   +4 more
doaj  

Hypodontia in the permanent dentition: a study of its prevalence in Malaysian children

open access: yesAustralasian Orthodontic Journal, 1989
An investigation of the prevalence and distribution of hypodontia was carried out in Malaysian children between the ages of five to fifteen years. Hypodontia occurred in 2.8 per cent of these children.
Nik-Hussein Nik Moriah
doaj   +1 more source

Displasia Ektodermal Hipohidrotik

open access: yesSari Pediatri, 2016
Seorang bayi laki-laki berusia 4 bulan menderita displasia ektodermal hipohidrotik (DEH), merupakan kelainan genetik yang sebagian besar diturunkan secara x-linked recessive.
Eveline PN   +2 more
doaj   +1 more source

Perkembangan Gonad Dan Musim Pemijahan Kerang Sepetang (Pharella Acutidens) Di Ekosistem Mangrove Dumai, Riau [PDF]

open access: yes, 2012
This research aims to study the gonadal development and spawning seasonof “sepetang” clam (Pharella acutidens).The study was carried out over 12 month period from November 2010 to October 2011 at Dumai mangrove ecosystem.“Sepetang” clam samples were ...
Affandi, R. (Ridwan)   +2 more
core  

An evaluation of clinical, radiological and three-dimensional dental tomography findings in ectodermal dysplasia cases [PDF]

open access: yes, 2015
Background:This study aimed to review the results related to head and jaw disorders in cases of ectodermal dysplasia. The evaluation of ectodermal dysplasia cases was made by clincal examination and examination of the jaw and facial areas radiologically
Akkus, Zeki   +9 more
core   +2 more sources

Whole genome sequencing in families with oligodontia

open access: yesOral Diseases, Volume 30, Issue 6, Page 3935-3950, September 2024.
Abstract Background/Objectives Tooth agenesis (TA) is among the most common malformations in humans. Although several causative mutations have been described, the genetic cause often remains elusive. Here, we test whether whole genome sequencing (WGS) could bridge this diagnostic gap.
Janna Mitscherling   +6 more
wiley   +1 more source

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