myalgia/atrophy

Lyen an sove nan clipboard la

Chwazi kalite sòt

Paj 1 soti nan 344 rezilta yo

Decreased grip strength, muscle pain, and atrophy occur in rats following long-term exposure to excessive repetitive motion.

Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo

Work-related musculoskeletal disorders (WMSD) are caused by the overuse of muscles in the workplace. Performing repetitive tasks is a primary risk factor for the development of WMSD. Many workers in highly repetitive jobs exhibit muscle pain and decline in handgrip strength, yet the mechanisms

Only some patients with bulbar and spinal muscular atrophy may develop cardiac disease.

Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo

UNASSIGNED According to recent publications, some patients with spinal and bulbar muscular atrophy (BSMA) develop cardiac disease, manifesting as ST-segment abnormalities, Brugada-syndrome, dilative cardiomyopathy, or sudden cardiac death. Here we present neurological and cardiac data of a BSMA

Only some patients with bulbar and spinal muscular atrophy may develop cardiac disease.

Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo

Muscle pain in neuromuscular disorders and primary fibromyalgia.

Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo

Muscle fiber degeneration and regeneration, inflammation in the intramuscular connective tissue and hypoxia in resting muscle are not necessarily associated with pain. However, when sustained or dynamic muscle contractions are performed in an ischaemic muscle, severe pain develops. In the chronic

Muscle pain in neuromuscular disorders and primary fibromyalgia.

Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo

Muscle fibre degeneration and regeneration, inflammation in intramuscular connective tissue and hypoxia in resting muscle are not necessarily associated with pain. However, when sustained or dynamic muscle contractions are performed in an ischaemic muscle, severe pain develops. In the chronic muscle

Eosinophilia-myalgia syndrome: findings at MR imaging and proton spectroscopy of the lower leg.

Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo

Five magnetic resonance (MR) studies of the lower leg were performed in three patients with eosinophilia-myalgia syndrome (EMS). The 1H spectroscopic and imaging findings were compared with seven examinations of age-matched healthy controls. Standard imaging with proton density-, T1-, and

Chronic relapsing myalgia (? Post viral): clinical, histological, and biochemical studies.

Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo

Two patients with persistent myalgia characterised by onset after an ill-defined systemic illness, marked fluctuations in the severity of the symptoms, and normal neuromuscular examination with the exception of variable muscle tenderness on deep palpation, may have a forme fruste of myalgic

Effects of Light-Emitting Diode Therapy on Muscle Hypertrophy, Gene Expression, Performance, Damage, and Delayed-Onset Muscle Soreness: Case-control Study with a Pair of Identical Twins.

Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo

The aim of this study was to verify how a pair of monozygotic twins would respond to light-emitting diode therapy (LEDT) or placebo combined with a strength-training program during 12 weeks. This case-control study enrolled a pair of male monozygotic twins, allocated randomly to LEDT or placebo

Cardiac abnormalities in the toxic oil syndrome, with comparative observations on the eosinophilia-myalgia syndrome.

Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo

Early in the course of studies of the Spanish toxic oil syndrome it was recognized that vascular lesions were a major problem, most logically attributable to endothelial damage by the toxic oil. However, most clinical attention has been directed to the pulmonary complications and the evolution into

L-tryptophan and the eosinophilia-myalgia syndrome: pathologic findings in eight patients.

Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo

Pathologic findings in eight patients with the eosinophilia-myalgia syndrome, secondary to L-tryptophan ingestion, are reported. Tissue was obtained by biopsy alone in six patients, by biopsy and autopsy in the seventh patient, and by autopsy alone in the eighth patient. Muscle biopsies in five

[A case of Becker type congenital myotonia with myalgia].

Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo

We reported a case of Becker type congenital myotonia with myalgia. A 28 year-old woman admitted to our hospital because of right anterior chest pain and back pain. She was diagnosed as myotonic dystrophy by other university hospital when she was 16 years old. Physical examination revealed only

Role of muscle spindle in weightlessness-induced amyotrophia and muscle pain.

Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo

To date, the medium and long-term space flight is urgent in need and has become a major task of our manned space flight program. There is no doubt that medium and long-term space flight has serious damaging impact upon human physiological systems. For instance, atrophy of the lower limb anti-gravity

Magnetic resonance imaging of muscle injury and atrophy in glycolytic myopathies.

Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo

Exertional muscle pain, contractures, recurrent rhabdomyolysis, and pigmenturia are common in certain muscle glycolytic disorders. However, the frequency, distribution, and long-term significance of these findings are poorly understood. First we performed magnetic resonance imaging (MRI) of the

Late postpoliomyelitis muscular atrophy: clinical, virologic, and immunologic studies.

Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo

Seventeen relatively young patients, ages 31-65 years (average, 45) with prior poliomyelitis, who after a number of years of stability had experienced new neuromuscular symptoms, were studied. Seven patients had deterioration of functional capacity and then stabilization without new muscular

[Postpolio late progressive muscular atrophy--clinical and epidemiologic analyses in 4 Japanese cases].

Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo

Four Japanese cases of postpolio progressive muscular atrophy (PPMA) of late onset were clinically studied to characterize their clinical features and discussed upon the epidemiologic viewpoint. Four male patients were included with mean age of 43.5 (30-59) years on examination, diagnosed as PPMA

Antre nan paj
facebook nou an

Herbal & Natural Medicine

Baz done ki pi konplè remèd fèy medsin te apiye nan syans

Travay nan 55 lang
Geri èrbal te apiye nan syans
Remèd fèy rekonesans pa imaj
Kat entèaktif GPS - tag zèb sou kote (vini byento)
Li piblikasyon syantifik ki gen rapò ak rechèch ou an
Search remèd fèy medsin pa efè yo
Izeganize enterè ou yo ak rete kanpe fè dat ak rechèch la nouvèl, esè klinik ak rive

Tape yon sentòm oswa yon maladi epi li sou remèd fèy ki ta ka ede, tape yon zèb ak wè maladi ak sentòm li itilize kont.
* Tout enfòmasyon baze sou rechèch syantifik pibliye