Neuromuscular Manifestations
Mostrando 1-12 de 12 artigos, teses e dissertações.
-
1. O que é considerado constipação no lactente e como abordar?
Constipação é definida como dificuldade para evacuar ou a evacuação de fezes duras, de largo calibre e/ou ressecadas, que necessitam muito esforço, com frequência evacuatória de duas ou menos vezes por semana e/ou associação à dor. Quando os sintomas estão presentes por menos de quatro semanas é tida como constipação aguda e além deste per
Núcleo de Telessaúde Rio Grande do Sul. Publicado em: 12/06/2023
-
2. Neuromuscular control strategies of the trunk antagonist muscles during the Biering-Sorensen test in individuals with recurrent low back pain and healthy subjects
Abstract OBJECTIVES To compare the activation pattern of the trunk antagonistic muscles and also the myoelectric manifestations of muscle fatigue between subjects with and without recurrent non-specific low back pain, during the fatigue provocation of the erector spinae. METHODS The study involved 19 subjects with recurrent low back pain with a non-specifi
Motriz: rev. educ. fis.. Publicado em: 2016-12
-
3. Behavioural alterations are independent of sickness behaviour in chronic experimental Chagas disease
The existence of the nervous form of Chagas disease is a matter of discussion since Carlos Chagas described neurological disorders, learning and behavioural alterations in Trypanosoma cruzi-infected individuals. In most patients, the clinical manifestations of the acute phase, including neurological abnormalities, resolve spontaneously without apparent conse
Mem. Inst. Oswaldo Cruz. Publicado em: 11/12/2015
-
4. Alterações das atividades eletromiográficas dos músculos masseter e temporal anterior após desprogramação neuromuscular da mandíbula de acordo com a filosofia de Roth / Changes of the electromyographics activities of the masseter and anterior temporal muscles after the mandibular neuromuscular deprogramming according to Roths philosophy
The electromyographic activity of the muscles masseter and temporal (anterior part) was evaluated in a sample of 37 asymptomatic subjects with Class II malocclusion. They were divided in two groups - experimental and control. The experimental group consisted of 23 subjects, 14 males and 9 females, mean age 23y 7m. This group was neuromuscularly deprogrammed
Publicado em: 2006
-
5. Influência da terapêutica sobre a qualidade de vida do paciente com miastenia gravis / The influence of therapeutics on the quality of life of Myasthenia gravis patients
INTRODUCTION: Myasthenia gravis (MG) is an immune mediated disease with production of antibodies against post-synaptic acetylcholine receptor of neuromuscular junctions (AAChR,Musk) and orders in nervous impulse transmission. The disease´s clinical characteristics include fatigability and fluctuating weakness of voluntary muscles. Acetylcholinesterase inhib
Publicado em: 2006
-
6. ManifestaÃÃes mÃsculo-esquelÃticas nos pacientes em programa de hemodiÃlise
A large diversity of ostearticular complaints has been described in patients in long-term hemodialysis. The aim of this research was to verify the proportion and the type of musculoskeletal manifestations in patients in maintenance hemodialysis, in three centers of metropolitan Recife, and to relate them to the variables: sex, ethnic group, patientâs curren
Publicado em: 2002
-
7. Neuromuscular Manifestations of Systemic Disease
-
8. Joint and Neuromuscular Manifestations of Periarteritis Nodosa
-
9. Chronic juvenile toxic epidemic syndrome.
The clinical manifestations in 21 children with chronic toxic epidemic syndrome (TES) and musculoskeletal manifestations were analysed and compared with those of the adult population. The sex ratio (2.5:1, F/M) was different from the one found in adults (6:1, F/M). The neuromuscular syndrome, the scleroderma-like picture, the pulmonary hypertension, and the
-
10. Scoliosis in a Case of Schinzel–Giedion Syndrome
Schinzel–Giedion syndrome (SGS) is a rare disorder characterized by midface retraction, hypertrichosis, and multiple skeletal anomalies with severe mental retardation. Various skeletal manifestations of the disease have been previously described. We present the first case of SGS developing scoliosis. The patient presented with scoliosis at the age of 8 ye
Springer-Verlag.
-
11. Genetics of congenital nemaline myopathy: a study of 10 families.
In order to investigate the inheritance in congenital nemaline myopathy (CNM), we studied the family histories and pedigrees of 13 patients with CNM from 10 families, and the 20 patients, by physical examination, single fibre electromyography, ultrasonography of muscles, measurement of serum creatine kinase, muscle biopsy, and electrophoresis of muscle prote
-
12. Neurological paraneoplastic syndromes in patients with small cell lung cancer. A prospective survey of 150 patients.
One hundred and fifty patients presenting with small cell lung cancer (SCLC) to chest physicians, were assessed neurologically. Neuromuscular or autonomic deficits were common and occurred in up to 44% of cases. Weakness, dry mouth, and weight loss were not mutually independent and may represent the syndrome formerly described as carcinomatous neuromyopathy.