Tools for standardized data collection: Speech, Language, and Hearing measurement protocols in the PhenX Toolkit

CC Morton, ML Marazita, B Peter… - Annals of human …, 2022 - Wiley Online Library
Abstract The PhenX Toolkit (https://www. phenxtoolkit. org/) is an online catalog of
recommended measurement protocols to facilitate cross‐study analyses for biomedical …

Epidemiology of Peripheral Nerve Sheath Tumors

AS Jack, CJ Huie, LG Jacques - Diagnostic Assessment and Treatment of …, 2021 - Springer
Peripheral nerve sheath tumors (PNSTs) were first reported over 200 years ago. Since that
time, our understanding of their epidemiological characteristics, in addition to their …

Análisis agregado de variantes en el exoma de pacientes con enfermedad de Meniere familiar e inicio precoz

P Román-Naranjo Varela - 2020 - digibug.ugr.es
Introduction: Meniere's disease (MD) is a rare inner ear disorder characterized by
sensorineural hearing loss, episodic vertigo and tinnitus. Although most of MD patients are …

Rare Variants in the OTOG Gene Are a Frequent Cause of Familial Meniere's Disease

P Roman-Naranjo, A Gallego-Martinez, A Soto-Varela… - bioRxiv, 2019 - biorxiv.org
Objectives Meniere's disease (MD) is a rare inner ear disorder characterized by
sensorineural hearing loss, episodic vertigo and tinnitus. Familial MD has been reported in 6 …

Vestibuläre Migräne

HA Rambold - Nervenheilkunde, 2022 - thieme-connect.com
Eine Sonderform der Migräne ist die vestibuläre Migräne (VM), die die häufigste
Drehschwindelerkrankung und die zweithäufigste Form des Schwindels ist. Diese …

[PDF][PDF] GISELLE BIANCO BORTOLETTO

DE MÉNIÈRE - repositorio.unicamp.br
ABSTRACT Ménière's Disease (MD) is an inner ear complex disorder characterized by
recurrent episodes of spontaneous vertigo, tinnitus, fluctuating sensorineural hearing loss …

[HTML][HTML] Update on Genetic Study of Vestibular Disorder

JH Choi - Research in Vestibular Science, 2021 - e-rvs.org
The wide availability of next-generation sequencing has enabled a rapid progress in the
discovery of genetic variants associated with many disorders. However, the contribution of …

[HTML][HTML] 전정질환에서유전학연구의최신지견

JH Choi - Research in Vestibular Science, 2021 - e-rvs.org
The wide availability of next-generation sequencing has enabled a rapid progress in the
discovery of genetic variants associated with many disorders. However, the contribution of …