Results 81 to 90 of about 137,721 (313)

Prevalence of self-reported swallowing difficulties and associated factors among older Colombians [PDF]

open access: yes
OBJECTIVE: We aimed to determine the prevalence of self-reported swallowing difficulty (dysphagia) among older Colombians and to explore the factors associated with this condition.
Chavarro-Carvajal,Diego Andrés   +7 more
core   +1 more source

The State of Exercise‐Based Dysphagia Intervention in the Literature: A Scoping Review

open access: yesLaryngoscope Investigative Otolaryngology
Introduction Exercise‐based interventions for dysphagia are frequently recommended in the clinical setting. We aim to characterize the state of the dysphagia treatment literature to provide a high‐level overview on four domains: Study characteristics ...
Claire Crossman   +4 more
doaj   +1 more source

The Impact of Goiter and Thyroid Surgery on Goiter Related Esophageal Dysfunction. A Systematic Review

open access: yesFrontiers in Endocrinology, 2018
Background: Patients with goiter referred for thyroidectomy report swallowing difficulties. This might be associated with esophageal compression and deviation as this is present in a significant number of patients.
Jesper Roed Sorensen   +3 more
doaj   +1 more source

The Critical Role of Fractionated Urine Glycosaminoglycans in the Evaluation of Mucopolysaccharidosis Type II in Four Unrelated Families

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Since 2015, Ann and Robert H. Lurie Children's Hospital has performed diagnostic testing for infants who screen positive for mucopolysaccharidosis type II (MPS II) on the Illinois newborn screen. Preliminary diagnostic testing includes measurement of plasma iduronate‐2‐sulfatase enzyme activity and urinary glycosaminoglycan analysis, followed ...
Carly A. Rasmussen   +5 more
wiley   +1 more source

Prevalence of swallowing dysfunction screened in Swedish cohort of COPD patients [PDF]

open access: yes, 2017
Margareta Gonzalez Lindh,1,2 Monica Blom Johansson,1 Margareta Jennische,1 Hirsh Koyi2,3 1Department of Neuroscience, Speech and Language Pathology, Uppsala University, Uppsala, Sweden; 2Centre for Research and Development (CFUG), Uppsala University ...
Jennische M   +3 more
core  

Hard to swallow [PDF]

open access: yesNature, 2007
Madhusudan, Grover   +3 more
openaire   +4 more sources

Clinical, Behavioral and Neuroradiological Phenotype in an Italian Cohort of Patients With Xia Gibbs Syndrome: A Multicenter Cross‐Sectional Study and Systematic Literature Review

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Heterozygous variants in the AHDC1 gene are associated with Xia Gibbs Syndrome (XGS), a genetic disorder with a highly variable phenotype. Cognitive impairment, motor delay, language delay, neonatal hypotonia, and sleep apnea are considered “cardinal” signs of the disease.
Giulia Cinelli   +18 more
wiley   +1 more source

A efetividade da oximetria de pulso na detectabilidade da broncoaspiração [PDF]

open access: yes, 2013
TCC(graduação) - Universidade Federal de Santa Catarina. Centro de Ciências da Saúde. Fonoaudiologia.Introdução: A disfagia é um sintoma de uma doença de base que pode acometer qualquer parte do trato digestivo, desde a boca até o estômago e que pode ...
Silva, Francine Lucia da
core  

Developing the Hungarian version of the MATCH test from the original German language: an evidence-based protocol for the translation, cultural adaptation and validation of paediatric speech audiometry tests from one language into another

open access: yesBMJ Open
Introduction Speech audiometry is widely used in routine clinical settings to assess auditory function in children. Appropriate test materials are available in languages such as English or German; however, formally validated translations do not exist in ...
Laszlo Tamas   +5 more
doaj   +1 more source

Histidine Supplementation Stabilizes Hearing and Vision and Improves Growth in HARS1‐Related Autosomal Recessive Disorder Associated With Usher‐Like Symptoms

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Autosomal recessive HARS1‐related disorder (originally described as Usher syndrome type 3B) caused by a homozygous Y454S variant in the histidyl‐tRNA synthetase gene (HARS1) is characterized by progressive sensorineural hearing and vision loss and respiratory deterioration with risk for sudden death following febrile illnesses.
Victoria Mok Siu   +23 more
wiley   +1 more source

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