Results 61 to 70 of about 7,829,913 (308)

PSYNDEX Tests Review für RCT (3) - READING COMPREHENSION TESTS 3

open access: yes, 1984
This is a PSYNDEX Tests Review of RCT (3) - READING COMPREHENSION TESTS 3. PSYNDEX Tests Reviews are written in German and describe and evaluate psychological and educational tests used in the German-speaking countries.
Proekel, Gerhard
core   +1 more source

Head and trunk movement strategies in quiet stance : from the deficit of vestibular loss to the expertise of tightrope walkers via prosthetic feedback [PDF]

open access: yes, 2013
Is the head more locked to the trunk or stabilised in space during quite stance? Does prosthetic vestibular feedback have a positive impact on movement strategies and muscle synergies of those with vestibular loss?
Honegger, Flurin
core   +1 more source

Transient Sleep Deprivation Induces Persistent Auditory Neuropathy via ROS‐Initiated Neuroinflammation and BK Channel Suppression

open access: yesAdvanced Science, EarlyView.
Sleep disturbance severity closely tracks hearing loss in a clinical cohort, yet the mechanistic link remains unclear. Acute sleep deprivation is shown to trigger transient cochlear oxidative stress that switches into a self‐sustaining neuroinflammatory state, suppressing BK channels and causing irreversible synaptopathy.
Dan Chen   +11 more
wiley   +1 more source

Aplicações dos potenciais evocados miogênicos vestibulares: revisão sistemática de literatura

open access: yesAudiology: Communication Research, 2019
RESUMO Objetivos Revisar a literatura científica sobre as principais técnicas usadas para gerar o potencial evocado miogênico vestibular (VEMP) e suas aplicações clínicas.
Tatiana Rocha Silva   +6 more
doaj   +1 more source

Quantitative Vestibular Function Testing in the Pediatric Population

open access: yesSeminars in Hearing, 2018
AbstractQuantitative tests of vestibular function include the caloric test, cervical and ocular vestibular evoked myogenic potential (VEMP), rotary chair, and head impulse test, either at the bedside or utilizing video head impulse test (vHIT). The purpose of this article is to provide an overview of how to perform these tests in children, including ...
Kristen L, Janky, Amanda I, Rodriguez
openaire   +3 more sources

PSYNDEX Tests Review für FTF-K - FRANKFURTER TESTS FÜR FÜNFJÄHRIGE - KONZENTRATION

open access: yes, 1982
This is a PSYNDEX Tests Review of FTF-K - FRANKFURTER TESTS FÜR FÜNFJÄHRIGE - KONZENTRATION. PSYNDEX Tests Reviews are written in German and describe and evaluate psychological and educational tests used in the German-speaking countries. PSYNDEX Tests is
Raatz, Ulrich
core   +1 more source

Spinal Involvement in Charge Syndrome: Implications for Management

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT CHARGE syndrome (OMIM #214800) is an autosomal dominant disorder caused by mutations in the CHD7 gene in most cases. Although originally defined by the CHARGE acronym (coloboma, heart defects, choanal atresia, growth restriction, genital hypoplasia, and ear anomalies), the recognized phenotype has expanded considerably to include highly ...
Adriana Gomes   +5 more
wiley   +1 more source

PSYNDEX Tests Review für RCT (1) - READING COMPREHENSION TESTS 1

open access: yes, 1984
This is a PSYNDEX Tests Review of RCT (1) - READING COMPREHENSION TESTS 1. PSYNDEX Tests Reviews are written in German and describe and evaluate psychological and educational tests used in the German-speaking countries.
Proekel, Gerhard
core   +1 more source

HSV-1 not only in human vestibular ganglia but also in the vestibular labyrinth [PDF]

open access: yes, 2001
Reactivation of herpes simplex virus type 1 (HSV-1) in the vestibular ganglion (VG) is the suspected cause of vestibular neuritis (VN). Recent studies reported the presence of HSV-1 DNA not only in human VGs but also in vestibular nuclei, a finding that ...
Mascolo, Andrea   +4 more
core   +1 more source

Review of the Molecular and Developmental Basis of Myhre Syndrome, Bench Research

open access: yesAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome (MS) is a connective‐tissue disorder within the acromelic dysplasia spectrum. It is characterized by congenital craniofacial, skeletal, cutaneous anomalies, respiratory, cardiovascular along with intellectual disability, deafness, and progressive fibrosis.
Camille Viaut, Valerie Cormier‐Daire
wiley   +1 more source

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