Results 41 to 50 of about 84,661 (166)
ABSTRACT Objective This study evaluated the efficacy of different manual toothbrush designs in removing extrinsic stains around orthodontic brackets using surface‐specific and time‐dependent assessments. Methods Fifty extracted premolars bonded with brackets and archwires were stained and randomly allocated to five toothbrush groups: conventional (CTB),
Shea Lee Lim +3 more
wiley +1 more source
Hypophosphataemia in adults: approach to diagnosis and management
Abstract Hypophosphataemia is a common electrolyte disorder which can have clinically significant consequences for bone, muscle, neurological and haematological function. Its causes range from transient transcellular shifts in hospitalised patients to chronic renal phosphate‐wasting disorders mediated by fibroblast growth factor 23 (FGF23).
Kajanan Parameshwaran +2 more
wiley +1 more source
Aim: The aim was to assess the prevalence of enamel hypoplasia and its correlation with dental caries in 12 and 15 years old school children in Shimla city, Himachal Pradesh, India.
Shailee Fotedar, G M Sogi, K R Sharma
doaj +1 more source
Excavation at University College London revealed more than 8700 human skeletal fragments representing at least 38 individuals, alongside over 800 animal remains. Features consistent with dissection, specimen preparation and curation provide evidence for the use of human and animal material in nineteenth‐century anatomical education, offering rare ...
Wendy Birch, Tania Kausmally
wiley +1 more source
Supplementary Material for: Genetic Analyses of Enamel Hypoplasia in Multiethnic Cohorts
Enamel hypoplasia causes reduction in the thickness of affected enamel and is one of the most common dental anomalies. This defect is caused by environmental and/or genetic factors that interfere with tooth formation, emphasizing the importance of ...
MorenoUribe L.M. (12093992) +20 more
core +1 more source
CHARGE Syndrome: A Narrative Review and Update on Diagnosis, Assessment and Management
ABSTRACT Background CHARGE syndrome (CS) is a rare multisystemic genetic condition caused by a pathogenic variant in the DNA‐binding protein‐7 CHD7 gene. The condition affects the development of neural crest cells, which give rise to craniofacial structures, cranial nerves, ears, eyes and the heart, resulting in diverse and complex clinical features ...
Eleni M. van Gelder +7 more
wiley +1 more source
Cell Therapy for Periodontal, Soft‐Tissue, and Craniofacial Regeneration
The clinical translation of mesenchymal stem/stromal cells (MSCs) represents a major advancement in dentistry, especially for periodontal, soft‐tissue, and craniofacial regeneration. However, several challenges remain to be addressed, including the absence of standardised protocols, limited scalability, regulatory hurdles, a lack of well‐controlled ...
Kamal Mustafa +5 more
wiley +1 more source
Supplemental material, sj-docx-1-jdr-10.1177_00220345231182355 for Tmem2 Deficiency Leads to Enamel Hypoplasia and Soft Enamel in Mouse by P. Nag, T. Inubushi, J.I. Sasaki, T. Murotani, S. Kusano, Y. Nakanishi, Y. Shiraishi, H. Kurosaka, S.
P. Nag (14186536) +10 more
core +1 more source
application/pdfFrom observation of frequency and measurement of the lengths and widths of enamel hypoplasia on the maxillary and mandibular deciduous canines, extracted from 50 Indians' skulls, the following results were obtained.
峯村, 隆一 +5 more
core +1 more source
Consensus Guidelines for Diagnosis and Management of Pyruvate Dehydrogenase Complex Deficiency
ABSTRACT Primary pyruvate dehydrogenase complex deficiency (PDCD) comprises a group of monogenic disorders caused by pathogenic variants in genes encoding subunits of, or regulatory components affecting, the pyruvate dehydrogenase complex. The clinical phenotype spans a broad continuum, ranging from early onset congenital lactic acidosis to infantile ...
Nandaki Keshavan +23 more
wiley +1 more source

