Results 151 to 160 of about 47,347 (285)
Noise‐induced reduction and early recovery of superior paraolivary nucleus sound‐offset responses
Abstract figure legend Acoustic over‐exposure transiently disrupts auditory temporal processing in mouse superior paraolivary nucleus neurons. In control conditions, neurons exhibit robust sound‐offset (OFF) responses, which are abolished immediately following noise trauma, indicating impaired temporal encoding.
Mihai Stancu +4 more
wiley +1 more source
En la actualidad, los implantes de cochlea se han establecido como una opción efectiva en la rehabilitación y en el tratamiento de individuos con perdidas auditivas profundas.
Múnera, Juan Carlos
core
A Quarter Century of EHD Protein Research: From Endosomal Recycling to Ciliopathies
Human EHD protein subcellular localization. ABSTRACT Eps15 homology domain‐containing proteins comprise a conserved family of membrane‐remodeling ATPases that regulate endocytic trafficking, membrane fission, receptor recycling, primary ciliogenesis and membrane dynamics across eukaryotes. Since the initial identification of EHD1 and its Caenorhabditis
Devin Frisby +3 more
wiley +1 more source
En la actualidad, los implantes de cochlea se han establecido como una opción efectiva en la rehabilitación y en el tratamiento de individuos con perdidas auditivas profundas.
Múnera, Juan Carlos
core
ABSTRACT Purpose Pediatric central nervous system (CNS) tumors often recur despite multimodality therapy. Although re‐irradiation (re‐RT) has historically been limited by concerns for severe late toxicities, modern techniques have renewed interest in this approach. Proton therapy provides dosimetric advantages that may enable curative re‐treatment with
Jin‐Ho Song +15 more
wiley +1 more source
Hearing Loss in Adults With Diabetes and Prediabetes: A Systematic Review and Meta‐Analysis
ABSTRACT Diabetes impairs hearing through microvascular damage and neuropathy, yet the prevalence of moderate‐to‐severe hearing loss (≥ 40 dB HL) remains inadequately explored. Variations by age, diabetes duration, and socioeconomic factors are inadequately characterised. This systematic review quantified the prevalence and comparative risk of moderate‐
Mehwish Nisar +4 more
wiley +1 more source
ABSTRACT Rett syndrome is a neurodevelopmental disorder caused by an X‐linked mutation of the MeCP2 gene. Individuals with Rett syndrome, as well as rodent models of this disorder, demonstrate abnormal cortical responses to sound, which impair auditory discrimination ability.
Isabella K. Myers +6 more
wiley +1 more source
GSP Cochlea: A graph signal processing approach for studying sound encoding. [PDF]
Bonomo ME, Segarra S, Raphael RM.
europepmc +1 more source
Disrupted Vestibular Nuclei Neuron Development in a Chick Model for Congenital Vestibular Disorders
ABSTRACT Children with syndromic, congenital vestibular disorders (CVDs) form a sac‐like inner ear with missing or truncated semicircular canals and experience delayed motor development with lifelong challenges to maintain posture and balance. How the abnormal inner ear affects downstream central vestibular neural circuitry has not been investigated ...
Elizabeth B. Bogin +5 more
wiley +1 more source

