Results 31 to 40 of about 121,621 (353)
Speech signal analysis and pattern recognition in diagnosis of dysarthria
Annals of Indian Academy of Neurology, 2017 Background: Dysarthria refers to a group of disorders resulting from disturbances in muscular control over the speech mechanism due to damage of central or peripheral nervous system.
Minu George Thoppil +3 more
doaj +1 more source
Journal of Neurorestoratology, 2021 Brain-derived paralysis is a disease dominated by limb paralysis caused by various brain diseases. The damage of upper motor neurons can lead to spastic paralysis of the limbs in different parts.
HaiLong Zhang +3 more
doaj +1 more source
Rescue axonal defects by targeting mitochondrial dynamics in hereditary spastic paraplegias
Neural Regeneration Research, 2019 Impaired axonal development and degeneration underlie debilitating neurodegenerative diseases including hereditary spastic paraplegia, a large group of inherited diseases.
Yongchao Mou, Xue-Jun Li
doaj +1 more source
Targeted high throughput sequencing in hereditary ataxia and spastic paraplegia
PLoS ONE, 2017 Hereditary ataxia and spastic paraplegia are heterogeneous monogenic neurodegenerative disorders. To date, a large number of individuals with such disorders remain undiagnosed.
Z. Iqbal +8 more
semanticscholar +1 more source
Demographic and Clinical Characteristics of Patients with Cerebral Palsy
İstanbul Medical Journal, 2018 Introduction: The purpose of this study was to identify the demographic and clinical characteristics of patients with cerebral palsy (SP) who applied to the Physical Therapy and Rehabilitation Center and to increase the awareness of physicians and ...
Hamza Sucuoğlu
doaj +1 more source
Journal of Rehabilitation Medicine, 2017 OBJECTIVE To present interdisciplinary practical guidance for the assessment and treatment of spastic equinovarus foot after stroke. RESULTS Clinical examination and diagnostic nerve block with anaesthetics determine the relative role of the factors ...
T. Deltombe +4 more
semanticscholar +1 more source
Mitochondrial DNA disorders in neuromuscular diseases in diverse populations
Annals of Clinical and Translational Neurology, EarlyView.Abstract Neuromuscular features are common in mitochondrial DNA (mtDNA) disorders. The genetic architecture of mtDNA disorders in diverse populations is poorly understood. We analysed mtDNA variants from whole‐exome sequencing data in neuromuscular patients from South Africa, Brazil, India, Turkey and Zambia. In 998 individuals, there were two definite
Fei Gao +34 more
wiley +1 more source
HPDL Variant Type Correlates With Clinical Disease Onset and Severity
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Recently, a mitochondrial encephalopathy due to biallelic HPDL variants was described, associated with a broad range of clinical manifestations ranging from severe, infantile‐onset neurodegeneration to adolescence‐onset hereditary spastic paraplegia. HPDL converts 4‐hydroxyphenylpyruvate acid (4‐HPPA) into 4‐hydroxymandelate (4‐HMA),
Eun Hye Lee +19 more
wiley +1 more source
Travmatologiâ i Ortopediâ Rossii, 2016 Specific upper limb disorders accompanying spastic cerebral palsy substantially restrict self-care, writing abilities, hinder movements with external support aids and limit work capability.
A. A. Andreev +2 more
doaj +1 more source