Results 81 to 90 of about 14,731 (217)
Chlorpyrifos-Induced Delayed Neurotoxicity with A Rare Presentation of Flaccid Quadriplegia: A Diagnostic Challenge [PDF]
, 2017 Chlorpyrifos is an organophosphate compound recognized as causing acute toxicity. However, organophosphate-induced delayed polyneuropathy (OPIDP), although rare, has also been described.
Afonso Mendes, Patrícia +3 more
core +3 more sources
Endovascular and surgical treatment of spinal dural arteriovenous fistulas [PDF]
, 2018 Introduction: The aim of this retrospective study was to evaluate the clinical outcome of patients with spinal dural arteriovenous fistulas (SDAVFs) that were treated with surgery, catheter embolization, or surgery after incomplete embolization. Methods:
Andres, Robert +7 more
core
Mutations in the SPAST gene causing hereditary spastic paraplegia arerelated to global topological alterations in brain functional networks [PDF]
, 2019 Aim: Our aim was to describe the rearrangements of the brain activity related to genetic mutations in the SPAST gene. Methods: Ten SPG4 patients and ten controls underwent a 5 min resting state magnetoencephalography recording and neurological ...
Antenora, A +10 more
core +3 more sources
Synaptic Plasticity and Neurological Disorders in Neurotropic Viral Infections [PDF]
, 2015 Based on the type of cells or tissues they tend to harbor or attack, many of the viruses are characterized. But, in case of neurotropic viruses, it is not possible to classify them based on their tropism because many of them are not primarily neurotropic.
Atluri, Venkata +4 more
core +2 more sources
Revista do Instituto de Medicina Tropical de São Paulo, 2014 Here a young patient (< 21 years of age) with a history of infective dermatitis is described. The patient was diagnosed with myelopathy associated with HTLV-1/tropical spastic paraparesis and treated with interferon beta-1a.
Graça Maria de Castro Viana +5 more
doaj +1 more source
Esclerose lateral amiotrófica: considerações sobre critérios diagnósticos [PDF]
, 2010 Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder, compromising the motor neuron, characterized by progressive muscle weakness, with reserved prognosis. The diagnosis is based on inclusion and exclusion clinical criteria, since there is
Chieia, Marco A. +3 more
core +3 more sources
Fluorosis Masquerading as Compressive Myelopathy
National Board of Examinations Journal of Medical SciencesA 60-year-old woman from Cuddalore presented with restricted neck movements, progressive difficulty in walking, and lower limb weakness, leading to bed confinement.
Jayaram Saibaba, Gopinath Karuppiah
doaj +1 more source
Revista da Sociedade Brasileira de Medicina Tropical, 2006 O presente estudo avaliou a ocorrência da infecção pelo HTLV-1 e seus subtipos em amostras de sangue de pacientes com diagnóstico clínico de paraparesia espástica tropical/mielopatia associada ao Htlv-1.
Lucinda A. Souza +7 more
doaj +1 more source
Revista da Sociedade Brasileira de Medicina Tropical, 2015 INTRODUCTION: This study aimed to evaluate spasticity in human T-lymphotropic virus type 1-associated myelopathy/tropical spastic paraparesis (HAM/TSP) patients before and after physical therapy using the International Classification of Functioning ...
Luana Rego Rodrigues +5 more
doaj +1 more source
Clinical phenotype and genetic associations in autosomal dominant familial Alzheimer's disease: a case series [PDF]
, 2016 Background - The causes of phenotypic heterogeneity in familial Alzheimer’s disease with autosomal dominant inheritance are not well understood. We aimed to characterise clinical phenotypes and genetic associations with APP and PSEN1 mutations in ...
Adamson, G +15 more
core