Results 141 to 150 of about 7,575 (221)

22q11.2 Deletion Syndrome, Oral-Maxillo-Facial Manifestations and Cognitive Functioning: Three Illustrative Case Reports. [PDF]

Children (Basel)
Sardella D, De Giacomo A, Ricci A, Limongelli L, Corsalini M.   +4 more
europepmc   +1 more source

Developmental Disturbances of Teeth in Children with Autism Spectrum Disorder and Attention-deficit Hyperactivity Disorder: A Cross-sectional Study. [PDF]

Int J Clin Pediatr Dent
Shan S, Swaminathan K, Vivek K, Haridoss S.   +3 more
europepmc   +1 more source

Prevalence and severity of molar incisor hypomineralization among children in Madinah, Saudi Arabia: A school-based cross-sectional study. [PDF]

BMC Oral Health
Alqadi SF, Algarni AA, Tarawah RA, Sharbib SH, Alhazmi RT, Alaydaa RM, Baghlaf K, Sabbagh HJ.   +7 more
europepmc   +1 more source

Expert consensus on the diagnosis and management of tooth developmental anomalies. [PDF]

Int J Oral Sci
Zhu J, Wan M, Duan X, Fan Z, Sun Y, Wang X, Zheng S, Zheng L, Zhu Q, Chen D, Dai J, Han D, He M, Huang C, Jiang Y, Jia Z, Pan Y, Pan Y, Wang T, Wang W, Xu B, Yin W, Zhang T, Zhang Y, Zhao Z, Bian Z, Song Y.   +26 more
europepmc   +1 more source

Prenatal vitamin D and enamel hypoplasia in human primary maxillary central incisors: a pilot study. [PDF]

Pediatr Dent J, 2017
Reed SG, Voronca D, Wingate JS, Murali M, Lawson AB, Hulsey TC, Ebeling MD, Hollis BW, Wagner CL.   +8 more
europepmc   +1 more source

Clinical management of severe molar-incisor hypomineralisation using CAD/CAM fabricated PMMA crowns: a case report. [PDF]

Biomater Investig Dent
Ravi V, Sharma M.
europepmc   +1 more source

Stone-Dominant Renal Phenotype Without Nephrocalcinosis in <i>FAM20A</i>-Related Enamel Renal Syndrome. [PDF]

Kidney Int Rep
Koç NS.
europepmc   +1 more source

Regional odontodysplasia: a report of unusual case with in-depth analysis. [PDF]

J Oral Biol Craniofac Res
Béhot C, Cuisinier O, Serraf É, Friedlander L, Vi-Fane B, Garrec P, Nassif A.   +6 more
europepmc   +1 more source

Expanding the phenotypic and immunological landscape of Alazami syndrome: Evidence from seven new patients with LARP7 gene variants. [PDF]

Eur J Pediatr
Sharaf-Eldin W, Ghorab RM, Rafat K, Mahmoud H, Hassib N, Alahlafi A, Maroofian R, Gleeson JG, Essawi M, Zaki MS.   +9 more
europepmc   +1 more source

Ask-Upmark Kidney Disease: Case Report of a Rare Congenital Malformation. [PDF]

Case Rep Pathol
Maia RM, Andrade GA, Guimarães HL, Manzi FR, da Silva LCP, de Abreu Lima IL.   +5 more
europepmc   +1 more source