Results 161 to 170 of about 40,558 (343)
Status quo and future developments in the diagnosis and treatment of hereditary angioedema
Summary Hereditary angioedema (HAE) is a rare hereditary disease characterized by edema, which can be life‐threatening in case of swelling in the larynx. The most common form of HAE is caused by a mutation of the SERPING1 gene and is characterized by a deficiency (type I) or loss of function (type II) of the C1 inhibitor (C1‐INH), leading to excessive ...
Andreas Recke
wiley +1 more source
Recurrent laryngeal nerve pathology in spasmodic dysphonia.
Joseph V. Bocchino, Harvey M. Tucker
openalex +1 more source
Voice care knowledge, attitude and behavior [PDF]
Thesis (B.Sc)--University of Hong Kong, 2009."A dissertation submitted in partial fulfilment of the requirements for the Bachelor of Science (Speech and Hearing Sciences), The University of Hong Kong, June 30, 2009."Includes bibliographical references (p.
Mo, Lai-nga, Moly, 巫麗雅
core
Abstract Aim To describe the real‐world effects of trofinetide in individuals with Rett syndrome (RTT) using the 18‐month follow‐up analysis of the LOTUS study. Method Caregivers of any patients who were prescribed trofinetide under routine clinical care were eligible to participate.
Louise Cosand +3 more
wiley +1 more source
Vocal Load of University Professors: Preliminary Results
Purpose. To describe the acoustic characteristics of a classroom, voice quality, fatigue, and vocal load of university professors. Methods. Exploratory, observational, longitudinal, and descriptive study with a single group of participants, including ...
Cristiane Lemos Carvalho de Oliveira +4 more
doaj +1 more source
Incapacidad vocal en docentes de la provincia de Huelva Voice handicap in Huelva's teachers
Introducción: La prevalencia de trastornos de la voz en docentes en nuestro entorno se sitúa entre el 34% y 57%. Desde el año 2006 la patología por nódulos de las cuerdas vocales se considera enfermedad profesional.
Francisco Javier Barbero-Díaz +4 more
doaj
Diagnosis of degenerative myelopathy in a Boston terrier–French bulldog mixed breed
Canine degenerative myelopathy (DM) has been associated with mutations in the superoxide dismutase 1 gene (SOD1). Although the SOD1:c.118G>A mutation has been identified in Boston terriers and French bulldogs, no histological‐confirmed degenerative myelopathy has been reported in either breed.
A. M. K. Chan +4 more
wiley +1 more source
Fundamental Frequency and Sound Pressure Level of Voice in Dysphonia Patients.
Machiko Fujita
openalex +2 more sources

