Neurological Manifestations
Mostrando 1-12 de 148 artigos, teses e dissertações.
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1. Neurological manifestations of tuberous sclerosis complex: the importance of early diagnosis
Arquivos de Neuro-Psiquiatria. Publicado em: 2022
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2. Extrapulmonary manifestations of COVID-19 in children: a comprehensive review and pathophysiological considerations
ABSTRACT Objective: The aim of this review was to summarize the most common extrapulmonary manifestations in pediatric patients with COVID-19, as well as to discuss clinical, epidemiological, and pathophysiological aspects of these clinical presentations in children. Source of data: An extensive search of literature was performed in order to identify pedia
J. Pediatr. (Rio J.). Publicado em: 2021-04
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3. História social e autoritarismo no Brasil: ligações entre passado e presente
ABSTRACT Objective: The aim of this review was to summarize the most common extrapulmonary manifestations in pediatric patients with COVID-19, as well as to discuss clinical, epidemiological, and pathophysiological aspects of these clinical presentations in children. Source of data: An extensive search of literature was performed in order to identify pedia
Estud. av.. Publicado em: 2021-04
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4. Guillain-Barré syndrome associated with SARS-CoV-2 infection: a scoping review
SUMMARY BACKGROUND: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections can affect the nervous system, triggering problems such as the Guillain-Barre Syndrome (GBS), an association that can bring complications to the patient. OBJECTIVE: This scoping review aimed to clarify the clinical features and analyze patients with GBS associated w
Rev. Assoc. Med. Bras.. Publicado em: 2021-02
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5. Is macular lymphocytic arteritis limited to the skin? Long-term follow-up of seven patients,
Abstract Background: Macular lymphocytic arteritis most commonly presents as hyperpigmented macules on the lower limbs. The pathogenesis of this disease is still unclear and there is an ongoing debate regarding whether it represents a new form of cutaneous vasculitis or an indolent form of cutaneous polyarteritis nodosa. Objective: To describe clinical, hi
An. Bras. Dermatol.. Publicado em: 2020-02
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6. Rabies encephalitis and extra-neural manifestations in a patient bitten by a domestic cat
ABSTRACT Rabies encephalitis is a fatal zoonotic viral disease transmitted to humans either by domestic animals like dogs and cats or by wild animals like bats, skunks and raccoons. We present the case of a 25-year-old woman admitted due to behavioral disorders, generalized paresthesiasand acute respiratory deterioration compatible with a respiratory distres
Rev. Inst. Med. trop. S. Paulo. Publicado em: 17/01/2020
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7. SCHISTOSOMAL MYELORADICULOPATHY IN A NON-ENDEMIC AREA
RESUMO Objetivo: Relatar um caso de mielorradiculopatia esquistossomótica em área não endêmica. Descrição do caso: Paciente do sexo masculino, 11 anos, previamente hígido, com história aguda de paresia de membros inferiores, que evoluiu para membros superiores e tronco, associada à alteração de sensibilidade e formação de globo vesical. O exam
Rev. paul. pediatr.. Publicado em: 13/01/2020
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8. HTLV: uma infecção estigmatizante?
Resumo: O HTLV é um vírus que afeta as células T humanas. O Brasil é o país com o maior número absoluto de casos de HTLV no mundo. Estimativas do Ministério da Saúde apontam entre 700 mil e 2 milhões de pessoas infectadas. A maioria são portadores assintomáticos, porém algumas pessoas podem vir a desenvolver quadros neurológicos degenerativos co
Cad. Saúde Pública. Publicado em: 11/11/2019
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9. Polymorphism in the interleukin-10 gene is associated with overactive bladder phenotype associated with HTLV-1 infection
Abstract INTRODUCTION Human T-cell lymphotropic virus type 1 (HTLV-1)-associated inflammatory diseases are not well understood; however, their clinical manifestations may be influenced by the host genetic background. METHODS We genotyped 298 individuals with HTLV-1 and 380 controls for interleukin-10 (IL10) gene variants-rs3024496, rs1800871, rs1800896-a
Rev. Soc. Bras. Med. Trop.. Publicado em: 30/05/2019
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10. Anderson-Fabry Disease: A Rare Disease That Mimics Common Cardiac, Neurological, Renal, and Other Disorders: Approach for the Differential Diagnosis and Follow-Up
Abstract Anderson-Fabry disease (AFD) is a rare inherited X-linked disease, caused by mutations of the gene encoding the α-galactosidase A enzyme, that leads to a deficiency or absence of its activity with consequent accumulation of globotriaosylceramide (Gb3) and other glycosphingolipids in the lysosomes of several cells types in the organism, mainly the e
J. inborn errors metab. screen.. Publicado em: 30/05/2019
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11. Basilar invagination associated with chiari malformation type I: A literature review
Basilar invagination (BI) and Chiari malformation type I (CM-I) are very important anomalies that introduce instability and compression in the occipitocervical transition region and have complex clinical characteristics. These anomalies vary according to the affected structures. The present study revises current knowledge regarding the anatomy, anatomo-physi
Clinics. Publicado em: 08/04/2019
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12. Outcomes of a Physician Survey on the Type, Progression, Assessment, and Treatment of Neurological Disease in Mucopolysaccharidoses
Abstract The mucopolysaccharidosis (MPS) disorders are a group of rare, inherited lysosomal storage disorders. In each of the 11 MPS (sub)types, deficiency in a specific lysosomal enzyme (1 of 11 identified enzymes) leads to accumulation of glycosaminoglycans, resulting in cell, tissue, and multi-organ dysfunction. There is great heterogeneity in the clinica
J. inborn errors metab. screen.. Publicado em: 28/02/2019