Results 81 to 90 of about 594,005 (300)

Peripheral facial nerve palsy associated with COVID-19

open access: yesJournal of Neurovirology, 2020
COVID-19 pandemic revealed several neurological syndromes related to this infection. We describe the clinical, laboratory, and radiological features of eight patients with COVID-19 who developed peripheral facial palsy during infection. In three patients,
M. Lima   +8 more
semanticscholar   +1 more source

The psychosocial toll of Dublin III on asylum seekers in the Netherlands

open access: yesAmerican Journal of Community Psychology, EarlyView.
Abstract The Dublin III Regulation determines which EU Member State is responsible for examining asylum claims, but its implementation carries significant consequences for those subjected to it. This study examines how Dublin III, as implemented in the Netherlands, affects asylum seekers' psychosocial wellbeing using Silove′s Adaptation and Development
Imen El Amouri
wiley   +1 more source

A Smartphone-Based Automatic Diagnosis System for Facial Nerve Palsy

open access: yesSensors, 2015
Facial nerve palsy induces a weakness or loss of facial expression through damage of the facial nerve. A quantitative and reliable assessment system for facial nerve palsy is required for both patients and clinicians.
Hyun Seok Kim   +3 more
doaj   +1 more source

Patient‐perceived severity of synkinesis reduces quality of life in facial palsy: A cross‐sectional analysis in 92 patients

open access: yesClinical Otolaryngology, 2019
KEY POINTS Synkinesis can decrease quality of life in facial palsy patients. Patient-perceived severity of synkinesis may be of additional value in predicting facial palsy related-quality of life.
M. V. van Veen   +7 more
semanticscholar   +1 more source

The Homozygous p.(Arg215Ter) Variant in XRCC2 Is Associated With Atypical Fanconi Anemia Without Major Hematological Abnormalities in Childhood

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Fanconi Anemia (FA) is the most frequent inherited bone marrow failure syndrome. A role for the XRCC2 gene in FA was suspected in 2012 and confirmed in 2016, but only two affected individuals have been described thus far, and no long‐term follow‐up is available.
Sabina Cenciarelli   +11 more
wiley   +1 more source

Delayed facial palsy after microvascular decompression for hemifacial spasm: multivariate Logistic regression analysis of influencing factors

open access: yesChinese Journal of Contemporary Neurology and Neurosurgery, 2020
Objective To explore the influencing factors for delayed facial palsy after microvascular decompression for hemifacial spasm. Methods We retrospectively analyzed 306 cases of hemifacial spasm undergoing microvascular decompression. The cases were divided
Yu⁃hua GUAN   +3 more
doaj  

Musculoskeletal Phenotypes of 19 Patients With X‐Linked HNRNPH2‐Related Neurodevelopmental Disorder: A Prospective Case Series

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Detailed clinical phenotypes have been previously reported for 33 individuals with X‐linked HNRNPH2‐related neurodevelopmental disorder. Of these, 75% self‐reported a musculoskeletal abnormality, including hip dysplasia, scoliosis, kyphosis, lordosis, pes planus, arthritis, and missing spinous processes.
Ambar Garcia   +6 more
wiley   +1 more source

Patient and Family Reported Clinical Picture of IRF2BPL‐Related Disorders

open access: yesAmerican Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT IRF2BPL‐related disorder is a neurodevelopmental disorder caused by heterozygous variants in the IRF2BPL (Interferon Regulatory Factor 2 Binding Protein‐Like) gene. The few reports available in the literature suggest that common symptoms include developmental delay, intellectual disability, and developmental regression.
Zoe Goldstone‐Joubert   +4 more
wiley   +1 more source

Facial Palsy

open access: yes
Facial ...
John M. Graham, Pedro A. Sanchez-Lara
  +5 more sources

Facial Palsy [PDF]

open access: yesBMJ, 1956
T, CAWTHORNE, D R, HAYNES
openaire   +2 more sources

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