Results 181 to 190 of about 345,281 (349)

Medical Comorbidities and Behavioral Health in Adolescents With Voice Disorders. [PDF]

JAMA Otolaryngol Head Neck Surg
Fujiki RB, Thibeault SL.
europepmc   +1 more source

Laryngoscopic Examination During the COVID-19 Pandemic: Turkish Voice Speech and Swallowing Disorders Society and Turkish Professional Voice Society Recommendations

, 2020
Bengü Çobanoğlu, Necati Enver, Sevtap Akbulut, E. Ozlem Atmis, Hakan Bırkent, Zahide Çiler Büyükatalay, Erhan Demirhan, İlter Denizoğlu, Ramil Hasimli, Müge Özçelik Korkmaz, Selmin Karataylı Özgürsoy, Kayhan Öztürk, Ceki Paltura, Seher Şirin, Emel Çadallı Tatar, Arzu Tüzüner, Kürşat Yelken, Hakan Çoşkun, Haldun Oğuz, Ferhan Öz, Haldun Oguz, Ferhan Oz   +21 more
openalex   +1 more source

Treatment of Neurogenic Voice Disorders. [PDF]

World J Otorhinolaryngol Head Neck Surg
Syamal M.
europepmc   +1 more source

The Voice of Cantú: Lower Voice Pitch Is a New Phenotypic Feature of Cantú Syndrome

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Cantú syndrome (CS) is a rare genetic condition caused by pathogenic variants in either ABCC9 or KCNJ8, leading to gain‐of‐function of KATP‐channels. The main clinical features are hypertrichosis and cardiovascular abnormalities. This study investigates the voice characteristics in individuals with CS, an aspect that has received little ...
Lotte Kleinendorst, Melanie N. S. Molegraaf, Dorothy K. Grange, Rico N. P. M. Rinkel, Mieke M. van Haelst   +4 more
wiley   +1 more source

Laryngeal Morphology in Voice Disorders: a Review of Imaging and Endoscopic Findings. [PDF]

Maedica (Bucur)
Shrikrishna BH, Deepa G.
europepmc   +1 more source

Gender-related differences in the prevalence of voice disorders and awareness of dysphonia. [PDF]

Acta Otorhinolaryngol Ital, 2022
Marchese MR, Longobardi Y, Di Cesare T, Mari G, Terruso V, Galli J, D'Alatri L.   +6 more
europepmc   +1 more source

Cytosolic Phosphoenoylpyruvate Carboxykinase Deficiency: Clinical, Biochemical, and Genetic Features of Five Non‐Finnish Patients

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Cytosolic phosphoenoylpyruvate carboxykinase (PEPCK‐C) is an essential, rate‐limiting enzyme in the gluconeogenesis pathway. PEPCK‐C deficiency presents with hypoglycaemia, hyperlactataemia and hepatopathy, and was first reported in association with bi‐allelic PCK1 variants in 2014.
Isaac Bernhardt, Polona Le Quesne Stabej, Claire Hart, Mark De Hora, Sarah Hulley, Mark Anderson, Harry G. Leitch, Hugh Lemonde, Bryony Ryder, James Davison   +9 more
wiley   +1 more source

Convergent evidence for a pitch deficit in hyperfunctional voice disorders. [PDF]

JASA Express Lett
Best V, Duque T, Abur D, Stepp CE.
europepmc   +1 more source

Mutual Support Phenomenon: Voices of Students With Written Language Disorders

Ieva Grigienė, Alvyra Galkienė
openalex   +2 more sources

Multi-Class Voice Disorder Classification Using OpenL3-SVM

, 2022
Xiangyu Peng, Huoyao Xu, Jie Liu, Junlang Wang, Chaoming He   +4 more
openalex   +1 more source