Results 71 to 80 of about 74,735 (268)

Sudden hearing loss as an early detector of multiple sclerosis: a systematic review [PDF]

, 2018
To evaluate whether Sudden Sensorineural Hearing Loss (S-SNHL) may be an early symptom of Multiple Sclerosis (MS). A systematic review was conducted using the following keywords: "Multiple sclerosis, hearing loss, sudden hearing loss, vertigo, tinnitus ...
Bernitsas, E, Di Stadio, A, Dipietro, L, Greco, A, Meneghello, F, Minni, A, Ralli, M, Stabile, M R   +7 more
core   +1 more source

Expanding the Phenotype of TUFM‐Related Combined Oxidative Phosphorylation Deficiency 4

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Combined oxidative phosphorylation deficiency 4 (COXPD4) is a rare mitochondrial condition caused by biallelic deleterious variants in the nuclear‐encoded gene TUFM. To date, most individuals with COXPD4 have presented with encephalopathy, hypotonia, and abnormal brain imaging. Many of the reported individuals died in infancy. We aim to expand
Noémie Villeneuve‐Cloutier, Jodi Warman‐Chardon, Danielle K. Bourque   +2 more
wiley   +1 more source

Prevalence Of Sensorineural Hearing Loss Among Stroke

Liaquat Medical Research Journal
This study was designed to determine the prevalence of sensorineural hearing loss among stroke patients. A cross-sectional analytical study was conducted. Medicine department of HMC Peshawar and lady reading hospital (LRH) in Peshawar.
Zarafshan Ahsan, Muhammad Sikander Ghayas Khan, Ayesha Badar, Malik Muhammad Qasim, Ultamish Munir, Hadia Sultan, Tayyaba Usman   +6 more
doaj   +1 more source

Evaluation of hearing and cochlear function by audiometric testing in patients with hyperemesis gravidarum [PDF]

, 2015
INTRODUCTION: The aim of this study was to investigate cochlear functions in patients with hyperemesis gravidarum (HG).METHODS: Twenty-nine HG patients (58 ears) and 31 healthy control subjects (62 ears) were included.
Demirtas, Ömer, Genç, Selahattin, Kale, Ahmet, Selçuk, Adin, Terzi, Hasan, Yavuz, Arzu   +5 more
core   +2 more sources

Descriptive Epidemiology From the Myhre Syndrome Foundation Registry: The Value of Self‐Reported Data

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome is an ultrarare genetic disease characterized by short stature, distinct craniofacial features, cardiovascular and respiratory fibrosis and stenosis, neurodevelopmental delays, autism, intellectual disability, and hearing loss. The natural history of Myhre syndrome is still not fully understood due to a small patient population ...
Mary K. Young, Armelle Pindon, Maggie R. Brand, Kate Wears, Katherine H. Young, Alyssa Mendel, Michael J. Lyons   +6 more
wiley   +1 more source

Rehabilitation with Cochlear Implant in Patient with Harboyan Syndrome

International Archives of Otorhinolaryngology, 2013
Background Harboyan syndrome, defined as congenital corneal dystrophy associated with progressive sensorineural hearing loss, was first described by Harboyan in 1971.
Lauren Medeiros Paniagua, Maria Elza Kazumi Yamaguti Dorfman, Luiz Lavinsky, Pricila Sleifer   +3 more
doaj   +1 more source

Neonatal hearing screening in high-risk patients with otoacoustic emissions: evaluation of results [PDF]

, 2015
Resumen Objetivo: evaluar la efectividad del programa de tamizaje auditivo del Homic en pacientes de alto riesgo de hipoacusia neurosensorial, el cual está basado en la realización de otoemisiones acústicas Diseño: estudio de cohorte retrospectiva, en ...
Diaz Patiño, Diana Patricia, Gonzalez Marin, Nestor, Ordoñez Ordoñez, Leonardo, Paredes, Dunia, Ramirez, Claudia, Rodriguez, Silvia Raquel, Silva Rueda, Ricardo   +6 more
core  

R705H mutation of MYH9 is associated with MYH9-related disease and not only with non-syndromic deafness DFNA17 [PDF]

, 2015
MYH9-related disease (MYH9-RD) is a rare autosomal dominant disease caused by mutation of MYH9, the gene encoding for the heavy chain of non-muscle myosin IIA (NMMHC-IIA).
Barozzi S, De Rocco D, Kunst H, Pecci A, Ryh\ue4nen S, Savoia A, Topsakal V, Verver E   +7 more
core   +1 more source

Statistical shape modeling of the human inner ear through micro‐computed tomography imaging

The Anatomical Record, EarlyView.
In this study, 54 cadaveric temporal bone specimens underwent high‐resolution micro‐CT imaging. Images were semi‐automatically segmented and converted to 3D surface mesh models for morphological measurement and analysis. Statistical shape models were created for the inner ear, cochlea, and vestibular system, as well as for sex‐ and side‐based subgroups.
Carmine Spedaliere, Alexandra Vaupotic, Jaehyun Hwang, Khalil Husein, Mustafa Hafidh, Kyle Rioux, S. Alireza Rohani, Sumit K. Agrawal, Hanif M. Ladak   +8 more
wiley   +1 more source