Results 51 to 60 of about 6,234 (200)

Targeting Myostatin for Sustainable Meat Production: Insights From Multiple Species

Animal Genetics, Volume 57, Issue 3, June 2026.
ABSTRACT Myostatin gene (MSTN), a TGF‐β superfamily member, negatively regulates skeletal muscle growth, positioning it as a prime genetic target for enhancing livestock meat production. This review synthesizes evidence from 1979 to 2025 on MSTN mutations across cattle, pigs, poultry, sheep, goats, and rabbits, emphasising impacts on yield, quality ...
Chiara Santomassimo, Francesco Perini, Daniele Colombi, Stefano Bettini, Maria Federica Trombetta, Marina Pasquini, Simone Ceccobelli, Ishaku L. Haruna, Ketan Patel, Emiliano Lasagna   +9 more
wiley   +1 more source

Macroglossia : Multifactorial etiology, multiple management. [PDF]

, 2013
La macroglosia designa una condición donde la lengua en posición de reposo protruye más allá del reborde alveolar.La lengua es una estructura importante en funciones vitales como la deglución, la fonación y la respiración.
Martínez, Laura Pilar
core  

Duas formas de apresentação da amiloidose em ORL

Revista Portuguesa Otorrinolaringologia e Cirurgia de Cabeça e Pescoço, 2012
Objectivo: Apresentação de dois casos clínicos de amiloidose com apresentação em ORL, assim como uma revisão teórica sobre esta patologia, nomeadamente a forma de apresentação clínica, diagnóstico e opções terapêuticas.
Maria Inês Silva, Hugo Rodrigues, Sara Tavares, Carla André, Maria Helena Rosa, Mário Santos, Luís Antunes   +6 more
doaj   +1 more source

Real‐World Diagnostic Workup of Patients Suspected for Light Chain Amyloidosis and Wild‐Type Transthyretin Amyloid Cardiomyopathy: A Retrospective Cohort Study Using US Electronic Health Records

eJHaem, Volume 7, Issue 3, June 2026.
ABSTRACT Introduction Light chain (AL) amyloidosis and transthyretin amyloid cardiomyopathy (ATTR‐CM) are the most common types of cardiac amyloidosis. Despite similar manifestations, prognosis and treatments are distinct, emphasizing the importance of accurate and timely diagnosis. This retrospective cohort study assessed real‐world diagnostic workups
Muhamed Baljevic, Haechung Chung, Jose Alvir, Patrick Feron, Aaron Crowley, Darrin Benjumea, Yong Chen, Cindi Pankratova   +7 more
wiley   +1 more source

MANAGEMENT AND ROUTING OF CHILDREN WITH SYNDROMAL MACROGLOSSIA

Український стоматологічний альманах
The issue of management problems and substantiation of a multidisciplinary approach to the rehabilita-tion of patients with macroglossia by involving specialists of various profiles in all periods of development re-quires careful analysis and ...
A.O. Melnyk, O.А. Kaniura, N.V. Bidenko, V.V. Filonenko, V.P. Iefimenko   +4 more
doaj   +1 more source

Identify Patients at Risk of Moderate or Severe OSAHS During ENT Examination

Laryngoscope Investigative Otolaryngology, Volume 11, Issue 3, June 2026.
ABSTRACT Objectives To identify anatomical factors predictive of moderate/severe obstructive sleep apnea‐hypopnea syndrome (OSAHS) during routine ENT examinations in awake patients. Methods A total of 110 patients who snore or are suspected to have OSAHS were prospectively included and underwent a standardized ENT examination coupled with recorded ...
Nicolas Lenay, Bruno Toussaint, Phi Linh Nguyen‐Thi, Nicolas Carpentier, Duc Trung Nguyen   +4 more
wiley   +1 more source

The diagnosis of Beckwith-Wiedemann syndrome in a child and psychological implications to parents – A case report

Rwanda Medical Journal, 2023
INTRODUCTION: While Beckwith-Wiedemann syndrome is among rare genomic imprinting disorders, its diagnosis still presents challenges in clinical settings.
B. Tuyishimire, H. Irere, N. Dukuze, B. Iradukunda, C. Muhizi, O. R. Karangwa, F. Rutagarama, C. Nsanzabaganwa, L. Mutesa   +8 more
doaj   +1 more source

Differential Transcriptome Analysis of Intrauterine UPD6pat Fetuses With Distinct Phenotypes

Molecular Genetics &Genomic Medicine, Volume 14, Issue 6, June 2026.
Paternal uniparental disomy of chromosome 6 (UPD6pat) is associated with transient neonatal diabetes mellitus and multisystem developmental anomalies, but the mechanisms underlying its phenotypic variability remain unclear. This study integrates amniotic fluid cfRNA transcriptome analysis and molecular diagnostics, identifying 372 differentially ...
Jiahui Yu, Yan Zhang, Wenlong Shen, Jun Ying, Huanzheng Li, Xiaohua Tang, Xujun He   +6 more
wiley   +1 more source

[Treatment of macroglossia due to acromegaly]. [PDF]

, 2010
Contains fulltext : 87343.pdf (Publisher’s version ) (Open Access)A 61-years-old woman had macroglossia due to acromegaly with complaints of dyspneu at a lying sleeping position and complaints of speech and dysphagia.
Alons, K., Meijer, G.J., Rieu, P.N.M.A., Berge, S.J.   +3 more
core  

Anterior tongue reduction surgery for paediatric macroglossia

, 2011
Objective:Anterior tongue reduction is indicated when macroglossia causes problems with oral hygiene, airway compromise, deglutition, articulation or orthognathic complications.
R Hewitt, B Hartley, M Soma, H Chau, S Massey   +4 more
core   +1 more source