Results 191 to 200 of about 5,144,883 (382)
STUDY AIM: Undiagnosed and therefore untreated permanent paediatric hearing loss can have a detrimental impact on a child’s speech, language, social and educational development, and quality of life.
Samuel P. Hofmann+2 more
doaj +1 more source
Frequency-following response in subjects with complete unilateral hearing loss: evidence for two generators [PDF]
David Daly+2 more
openalex +1 more source
Hearing loss and COVID-19: A note
W. Sriwijitalai, V. Wiwanitkit
semanticscholar +1 more source
Stress, Health, and Injury Among Illinois Farmers
ABSTRACT Objectives The goal of this cross‐sectional study was to characterize stress, injury, and chronic health conditions among agricultural producers in Illinois. The objectives were to: (1) describe the prevalence and nature of work‐related injuries; (2) describe chronic health conditions, stress, and symptoms of mental health conditions; and (3 ...
Josie M. Rudolphi+3 more
wiley +1 more source
Background Children with special needs often manifest multiple developmental, linguistic, cognitive, and behavioral symptoms. Hearing difficulties could be sometimes misdiagnosed, aggravating the behavioral manifestations and possibly affecting their ...
Heba Tallah Sherif Abd El Hady+1 more
doaj +1 more source
Loss (Hysterical) of Speech and Hearing successfully treated by the Inhalation of Ether [PDF]
James Hutchinson
openalex +1 more source
Measurements of the distortion tone 2f1−f2 in normal‐hearing and high‐frequency‐hearing‐loss subjects [PDF]
R. M. Sachs, F. L. Wightman
openalex +1 more source
ABSTRACT Genitopatellar syndrome (GPS) and Say‐Barber‐Biesecker‐Young‐Simpson Syndrome (SBBYSS) are clinically distinct neurodevelopmental disorders caused by monoallelic pathogenic variants in KAT6B. In some cases, GPS and SBBYSS features can overlap, determining an intermediate phenotype.
Vittorio Maglione+12 more
wiley +1 more source
Allergy in ménière's disease related fluctuating hearing loss preliminary findings in a double‐blind crossover clinical study [PDF]
James N. Endicott, Fred J. Stucker
openalex +1 more source
Worth the Effort: Lessons for Discovery and Care From an Unusual Case of Gorlin Syndrome
ABSTRACT Gorlin‐Goltz Syndrome (GGS) is a rare autosomal dominant genetic disorder encompassing a diverse range of clinical manifestations, including congenital anomalies and predisposition to cancer. Pathogenic variants in PTCH1 and SUFU account for up to 79% and 6% of cases, respectively. Currently, an estimated 15%–27% of individuals with a clinical
V. Taliercio+13 more
wiley +1 more source