Results 91 to 100 of about 2,651 (192)

Shared molecular framework and bidirectional effects of osteoporosis on periodontal disease and dental implant therapy in the elderly

open access: yesPeriodontology 2000, EarlyView.
Abstract Objectives This review synthesizes evidence regarding the prevalence, epidemiological associations, and mechanistic pathways between osteoporosis, periodontal disease, and dental implant therapy. Materials and Methods A literature review was conducted to identify studies focused on: osteoporosis, periodontal disease, and dental implants ...
Samin Sirous   +4 more
wiley   +1 more source

Surgical considerations based on oral and periodontal vascularization

open access: yesPeriodontology 2000, EarlyView.
Abstract Objectives To synthesize current evidence on vascular and anastomotic patterns, emphasizing their operative implications for optimizing flap perfusion, neovascularization, and wound healing in periodontal and implant surgery, while accounting for anatomical variability and collateral circulation. Materials and Methods A comprehensive review of
Arvin Shahbazi   +5 more
wiley   +1 more source

Implantological treatment in patients with atrophic maxillas

open access: yesRevista Electrónica Dr. Zoilo E. Marinello Vidaurreta, 2017
Background: the rehabilitation of patients with atrophic maxillas is almost impossible as the retention of the conventional prostheses is not fulfilled, so the implant-supported ones are the solution for this problem.Objective: to describe the results of the implantological treatment in patients with atrophic maxillas and retention problems with the ...
Disney Tablada Peralta   +4 more
openaire   +1 more source

A 57‐Year‐Old Male With Behavioral Variant Frontotemporal Dementia and MATR3 and NOS3 Mutations

open access: yesAnnals of Clinical and Translational Neurology, Volume 13, Issue 8, Page 1726-1732, August 2026.
ABSTRACT This report presents a case of behavioral variant frontotemporal dementia caused by mutations in the MATR3 and NOS3 genes, aiming to analyze its clinical manifestations and genetic characteristics. For a case presenting with personality changes and gait abnormalities as the initial symptoms, this study conducted a comprehensive analysis of its
Feifei Lin, Saie Huang
wiley   +1 more source

Phenotype Expansion of Malan Syndrome: New Cases and a Review of the Literature

open access: yesAmerican Journal of Medical Genetics Part A, Volume 200, Issue 8, Page 1783-1798, August 2026.
ABSTRACT Malan syndrome is an ultra‐rare overgrowth syndrome caused by pathogenic variants or deletions in nuclear factor one X (NFIX) located at 19p13.2. Here, we report a comprehensive literature review and phenotyping of known patients with Malan syndrome and present a novel cohort of eight patients.
Alex F. Nisbet   +10 more
wiley   +1 more source

Endoscopic Management of a Rare Pediatric Fronto‐Ethmoidal Mucocele With Orbital Involvement: Navigating Surgical Challenges

open access: yesClinical Case Reports, Volume 14, Issue 8, August 2026.
ABSTRACT Paranasal mucoceles are benign lesions causing bone erosion with orbital and intracranial extension. An 11‐year‐old male presented with right orbital proptosis with restricted movement. Computed tomography and Magnetic Resonance Imaging revealed a fronto‐ethmoidal mucocele involving orbit.
Sushil Raj Shrestha   +8 more
wiley   +1 more source

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