Results 61 to 70 of about 2,013 (164)

Nasal changes after orthognathic surgery for patients with prognathism and Class III malocclusion: Analysis using three-dimensional photogrammetry

open access: yesJournal of the Formosan Medical Association, 2015
Orthognathic surgery alters the position of maxilla and mandible, and consequently changes the nasal shape. The nasal change remains a concern to Asian patients.
Saran Worasakwutiphong   +5 more
doaj   +1 more source

Metabolic Dysfunction‐Associated Steatotic Liver Disease in Adults With Acromegaly: A Meta‐Analysis of Observational Studies

open access: yesDiabetes/Metabolism Research and Reviews, Volume 42, Issue 6, September 2026.
ABSTRACT Aims Acromegaly is a chronic, progressive disease characterised by excess growth hormone secretion and elevated circulating insulin‐like growth factor 1 levels. Data on hepatic fat content and liver stiffness in adults with active or controlled acromegaly remain inconsistent.
Alessandro Mantovani   +8 more
wiley   +1 more source

Surgical correction of prognathism

open access: yes, 1977
PLEASE NOTE: This work is protected by copyright. Downloading is restricted to the BU community: please log in with a valid BU account to access and click Download.
Baigelman, Lee
core   +1 more source

Differential Relapse of Proximal and Distal Segments after Mandibular Setback Surgery

open access: yesApplied Sciences
This study aimed to evaluate the differential positional changes of the proximal and distal segments during mandibular setback surgery relapse. Thirty patients with mandibular prognathism who underwent bilateral sagittal split ramus osteotomy were ...
Jin-Deok Kim   +2 more
doaj   +1 more source

The rs10781468 Genetic Polymorphism of the Gαq (GNAQ) Gene Is Associated With Responsiveness to Opioid Analgesics in Patients With Postoperative and Cancer Pain: An Exploratory Study

open access: yesNeuropsychopharmacology Reports, Volume 46, Issue 3, September 2026.
In our exploratory hypothesis‐generating study using patients with postoperative pain and cancer pain, for rs10781468 in the GNAQ gene, the minor allele was associated with reduced opioid consumption and an increased pain threshold. ABSTRACT Background G protein–coupled receptors, the largest class of cell surface receptors, are ubiquitously expressed ...
Hiroaki Owada   +15 more
wiley   +1 more source

Manhattan plot for maxillary prognathism.

open access: yes, 2014
(A) A genome-wide case-control study showed a significant association of the phenotype maxillary prognathism on the distal end of chromosome ECA 13.
Sylvie Froidevaux (512198)   +7 more
core   +1 more source

Stapled side‐to‐side anastomosis to treat a pelvic flexure stricture in a miniature horse

open access: yesEquine Veterinary Education, Volume 38, Issue 9, Page e603-e608, September 2026.
Summary Fecaliths are a recognised cause of non‐strangulating colon obstruction in horses. Although they more commonly obstruct the small colon, they can also lodge in the pelvic flexure, requiring enterotomy for removal. Stricture at the enterotomy site is an uncommon but surgically significant complication.
M. Baglioni   +5 more
wiley   +1 more source

Repair of mandibular prognathism by vertical osteotomy [PDF]

open access: yes, 1987
Klinik te alt diş orkusunun üst diş arkusuna göre daha önde olması biçiminde görülen, sefalometrik olarak ise SNB açısının normalden büyük olması ile karakterize olan mandibular prognatizm olgularının tedavisinde çeşitli osteotomi yöntemleri ...

core  

Soft-tissue profile changes after orthognathic surgery of mandibular prognathism [PDF]

open access: yes, 2012
During surgical correction of facial deformities, accurate prediction of the resulting facial profile is important for the patient and the surgeon. The purpose of the present study was to investigate profile changes after surgical treatment of mandibular
Steven Lai   +9 more
core   +1 more source

Alpha‐Mannosidosis in a 3.5‐Year‐Old Girl: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 8, August 2026.
ABSTRACT Alpha‐mannosidosis is a rare lysosomal storage disease caused by a deficiency of the enzyme alpha‐mannosidase. It manifests as a continuous spectrum of signs and symptoms characterized by dysmorphic features, skeletal abnormalities, delayed psychomotor and speech development, impaired hearing, and psychiatric involvement. When suspected, alpha‐
Samuel Bonilla Fornes   +4 more
wiley   +1 more source

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