Results 81 to 90 of about 4,047 (184)

Pituitary adenoma-associated with Schöpf-Schulz-Passarge syndrome. [PDF]

BMJ Case Rep
Brady RT, Allinson K, René C.
europepmc   +1 more source

X-Linked Anhidrotic Ectodermal Dysplasia in A 19-Year-Old Male: A Classic Phenotype. [PDF]

Clin Case Rep
Chapagain L, Dahal A, Gupta P, Pudasaini P, Paudel U.   +4 more
europepmc   +1 more source

Effect of mandibular second premolar hypodontia on trabecular bone structure: a fractal analysis approach. [PDF]

BMC Med Imaging
Gokkurt Yilmaz BN, Yilmaz BE, Ozbey F.
europepmc   +1 more source

Preliminary Insights into Association of Growth Factors with Hypodontia: A Clinical Study. [PDF]

Clin Cosmet Investig Dent
Alenzi RH, Alshammari AF, Abdullah ML, Aldukhyeel SM, Aldosari MN, Aljameel YI.   +5 more
europepmc   +1 more source

Prevalence and Patterns of Five Dental Anomalies in Athletes in Qatar: A Panoramic Radiographic Study. [PDF]

Int J Dent
Hashem A, Almasri D, Chamari K, Tabben M, AlMabrd N, Alsaey M.   +5 more
europepmc   +1 more source

Delayed Dental Development in Children With Non-Syndromic Hypodontia: A Cross-Sectional Study Using a Machine Learning Approach to Dental Age Estimation. [PDF]

Orthod Craniofac Res
Crosnier M, Decaup PH, Santos F, Cavare A.   +3 more
europepmc   +1 more source

Case Report: Novel pathogenic variant in autosomal recessive <i>WNT10A</i>-related odonto-onycho-dermal dysplasia. [PDF]

Front Genet
Kalaszi M, Moore C, Koniari C, Mavridis T.   +3 more
europepmc   +1 more source

Multiple Talon Cusps and Dens Evaginatus in the Maxillary Dentition With Coexisting Single-Tooth Hypodontia: A Case Report. [PDF]

Cureus
Giannakopoulos K, Digka A, Kathopoulis M, Sater C, Karayiannis E.   +4 more
europepmc   +1 more source

Multistage orthodontic-implantology-prosthetic treatment of a patient diagnosed with hypohidrosis ectodermal dysplasia syndrome with EDAR mutation: a case report. [PDF]

BMC Oral Health
Huang C, Yan Y, Algahefi A, Al-Tayar B, Zheng B.   +4 more
europepmc   +1 more source

Familial Tooth Agenesis in Lebanese Patients: Clinical Characterization and Whole-Exome Identification of Rare CACNA2D2 and TRIO Variants. [PDF]

Cureus
Nabbout F, El Hajj J, Badran B, Ghassibe M.   +3 more
europepmc   +1 more source