Results 51 to 60 of about 161,259 (397)

Change in Oral Health-Related Quality of Life Following Minimally Invasive Aesthetic Treatment for Children with Molar Incisor Hypomineralisation: A Prospective Study

open access: yesDental journal, 2018
Molar incisor hypomineralisation (MIH) is a common enamel condition, presenting with incisor opacities, which may be of psychosocial concern to children.
N. Hasmun   +5 more
semanticscholar   +1 more source

Degree of severity of molar incisor hypomineralization and its relation to dental caries

open access: yesScientific Reports, 2018
Molar incisor hypomineralization is a developmental defect of dental enamel associated with rapid caries progression. In order to discover whether molar incisor hypomineralization predisposes to dental caries, a cross-sectional cohort study was conducted
A. Negre-Barber   +3 more
semanticscholar   +1 more source

Multiscale 3D Whole Joint Cellular and Molecular Mapping Reveals Disease‐Specific Neurovascular Plasticity Underlying the Structure‐Pain Relationship

open access: yesAdvanced Science, EarlyView.
This study presents MUSIC, a novel immunostaining and clearing method coupled with large‐field light sheet microscopy, enabling 3D high‐resolution cellular and molecular mapping of intact musculoskeletal joints across species and joint types. Using joint degenerative and injury models, disease‐specific neurovascular alterations are uncovered, revealing
Peng Chen   +18 more
wiley   +1 more source

Moving an incisor across the midline: A treatment alternative in an adolescent patient [PDF]

open access: yes, 2011
A 13-year-old sought treatment for a severely compromised maxillary left central incisor and an impacted fully developed left canine. Extraction of both teeth became necessary.
Bosio, Jose A   +2 more
core   +1 more source

Traumatic lingual ulceration in a newborn: Riga-Fede disease

open access: yesItalian Journal of Pediatrics, 2012
Riga Fede disease is a reactive mucosal disease as a result of repetitive trauma of the tongue by the anterior primary teeth during forward and backward movement. Although the aspect of the lesion might be impressive, its nature is relatively benign. The
van der Meij Erik H   +3 more
doaj   +1 more source

Correlation of pulp-to-tooth area ratio with age and gender using CBCT of maxillary central incisor and canine: A comparative study

open access: yesJournal of Indian Academy of Oral Medicine and Radiology, 2022
Introduction: Dental age estimation of living or deceased individuals through radiographic methods are popular, among which pulp-tooth ratio is a sensitive indicator.
Vineet Bansal   +5 more
doaj   +1 more source

Molar and Incisor Hypomineralization

open access: yesJournal of Nepal Medical Association, 2021
Molar and incisor hypomineralization is a developmental defect that is systemic in origin that affects one or more than one permanent first molars, and is often associated with permanent incisors. It is usually characterized by well demarcated opacities and qualitative enamel defects caused by decreased inorganic enamel components, and reduced ...
openaire   +4 more sources

Osteoclast‐Derived SLIT3 Mediates Osteoarthritis Pain and Degenerative Changes

open access: yesAdvanced Science, EarlyView.
In TMJ‐OA, osteoclasts play a significant role in promoting the growth of sensory nerves at the osteochondral interface. In early OA, TRAP+ osteoclast‐derived SLIT3 induces sensory nerve growth into the condylar cartilage. This nerve growth facilitates the development of pain associated with OA.
Weiwei Zhu   +13 more
wiley   +1 more source

Quantification of the Individual Characteristics of the Human Dentition [PDF]

open access: yes, 2009
The considerations for admissibility suggested by the Daubert trilogy challenge forensic experts to provide scientific support for opinion testimony. The defense bar has questioned the reliability of bitemark analysis. Under an award from the U.
Johnson, L Thomas   +6 more
core   +1 more source

Nance‐Horan Syndrome: Further Delineation of the Affected Male and the Female Carrier Phenotypes

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Nance‐Horan syndrome (NHS; OMIM 302350) is a rare, X‐linked syndrome characterized by bilateral congenital cataracts leading to profound vision loss, specific dental anomalies including characteristic screwdriver blade‐shaped incisors, facial anomalies, and intellectual disability.
Maria K. Haanpää   +14 more
wiley   +1 more source

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