Results 221 to 230 of about 154,924 (355)

Cone-beam CT evaluation of impacted mandibular third molars and their possible association with mandibular incisor crowding. [PDF]

Med Oral Patol Oral Cir Bucal
Akkitap MP.
europepmc   +1 more source

[Solitary median maxillary central incisor syndrome:a case of report].

Shanghai kou qiang yi xue = Shanghai journal of stomatology, 2014
Li-ying Kang, Xin-qiang Liu
semanticscholar   +1 more source

Impact of a Culturally Adapted Intervention on Early Childhood Caries Among Immigrants—A Cluster‐Randomised Trial

Community Dentistry and Oral Epidemiology, EarlyView.
ABSTRACT Objectives Early Childhood Caries (ECC) is reported to be more common among immigrant children than their native counterparts. There are no community‐based studies that assess the effectiveness of an intervention in reducing the risk of ECC among immigrant children in Norway.
Mariam Reda, Knut Helge M. Jensen, Abhijit Sen, Anne N. Åstrøm, Manal Mustafa   +4 more
wiley   +1 more source

Partial Ceramic Veneers as a Conservative Restorative Strategy: A Narrative Review with Case Report. [PDF]

Dent J (Basel)
Villalobos-Tinoco J, Jurado CA, Antal MA, Rojas-Rueda S, Nurrohman H.   +4 more
europepmc   +1 more source

Functional Data Strengthen Clinical Validation of PhenoScore Phenotype‐Guided AI for ANKRD11 Missense Variants

Clinical Genetics, EarlyView.
PhenoScore, an AI framework integrating facial recognition and clinical phenotype data, accurately identifies pathogenic ANKRD11 missense variants associated with KBG syndrome (AUC 0.95). Validated against functional data, PhenoScore outperforms REVEL and complements AlphaMissense, providing objective phenotypic evidence to reduce variants of uncertain
Evi Andriessen, Elke de Boer, Gholson J. Lyon, Bert B. A. de Vries, Charlotte W. Ockeloen, Alexander J. M. Dingemans   +5 more
wiley   +1 more source

Breastfeeding and interdental spacing in primary dentition: a digital cross-sectional study. [PDF]

Front Dent Med
Boo-Gordillo P, García-Morales MF, Marqués-Martinez L, Borrell-García C, Guinot-Barona C, Aura-Tormos JI, García-Miralles E.   +6 more
europepmc   +1 more source

WDTC1 Haploinsufficiency as a Cause of Neurodevelopmental Phenotypes

Clinical Genetics, EarlyView.
In seven individuals heterozygous for loss‐of‐function or conserved missense variants, we demonstrate that loss of WDTC1 function causes a neurodevelopmental syndrome characterized by developmental delay, intellectual disability, and seizures.
Elyssa Smith, Victor Faundes, Xiaonan Zhao, Bixia Zheng, Gang Zhang, Xiao Mao, Emily Danko, Jason Laufman, Thomas Besnard, Bertrand Isidor, Benjamin Cogné, Brynjar Örn Jensson, Telma S. Sulem, Patrick Sulem, Jill A. Rosenfeld, Daryl A. Scott   +15 more
wiley   +1 more source

Prevalence of Different Etiologies of Excessive Gingival Display: Identifying Diagnostic Patterns. [PDF]

ScientificWorldJournal
Amro LA, Abdalwahab MM, Zazou N, Amr AEH.   +3 more
europepmc   +1 more source

The Diagnostic Odyssey of a Biochemically Confirmed Case of ML II: The First Western Patient With LYSET Deficiency

Clinical Genetics, EarlyView.
We identify a female patient with a homozygous nonsense variant (p.Gln38Ter) in the LYSET gene. This is the first western report of a challenging case of an extensive diagnostic odyssey and demonstrates that the LYSET gene must be considered in the differential diagnosis when M6P‐labeled lysosomal enzymes are altered.
Fernanda Sperb‐Ludwig, Taciane Alegra, Leonardo Martinello da Rosa, Nataniel Floriano Ludwig, Renata Voltolini Velho, Ida Vanessa Doederlein Schwartz   +5 more
wiley   +1 more source

Diode and er: YAG laser therapy versus other desensitizing treatments for dentin hypersensitivity in molar-incisor hypomineralization: a systematic review. [PDF]

Lasers Med Sci
Cappellaro EC, Ribeiro JF, da Silva CL, Cavalheiro CP, Martins MD, Lenzi TL.   +5 more
europepmc   +1 more source