نتایج جستجو برای: myopathies

تعداد نتایج: 2714  

Journal: :iranian journal of neurology 0
farnaz sinaei department of neurology, shariati hospital, tehran university of medical sciences, tehran, iran farzad fatehi department of neurology, shariati hospital, tehran university of medical sciences, tehran, iran

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2011
Jasvinder Chawla

Muscle diseases can constitute a large variety of both acquired and hereditary disorders. Myopathies in systemic disease results from several different disease processes including endocrine, inflammatory, paraneoplastic, infectious, drug- and toxin-induced, critical illness myopathy, metabolic, and myopathies with other systemic disorders. Patients with systemic myopathies often present acutely...

Journal: :iranian journal of pathology 2008
fatemeh mahjoub farrokh tirgari zarrin keyhani nargess tabarzan saghi vaziri

muscle tissue, skeletal muscle as well as cardiac muscle, is commonly affected in mitochondrial disorders. one explanation for this observation is that muscle tissue has a high-energy demand and therefore is more sensitive to a deficiency of mitochondrial energy production than some other tissues. in mitochondrial disorders, skeletal muscle tissue may be affected primarily by defective respirat...

Journal: :Reumatologia clinica 2012
Gerardo Gutiérrez-Gutiérrez Carla Barbosa López Francisco Navacerrada Ambrosio Miralles Martínez

Inflammatory myopathies are a heterogeneous group of myopathies in which there is biopsy-evident inflammation. In its evaluation it is essential to use neurophysiological techniques that provide information on the nature of the process. This paper reviews the electromigram pattern characteristic of inflammatory myopathies, its diagnostic value, limitations, and some clues on the interpretation ...

Journal: :Journal of Neurology, Neurosurgery & Psychiatry 1978

Journal: :European journal of anaesthesiology 2017
Mark Schieren Jerome Defosse Andreas Böhmer Frank Wappler Mark U Gerbershagen

: The anaesthetic management of patients with myopathies is challenging. Considering the low incidence and heterogeneity of these disorders, most anaesthetists are unfamiliar with key symptoms, associated co-morbidities and implications for anaesthesia. The pre-anaesthetic assessment aims at the detection of potentially undiagnosed myopathic patients and, in case of known or suspected muscular ...

Journal: :General physiology and biophysics 1999
Z Lukás

Immunohistochemical reactivity for utrophin has been recorded in 45 biopsies from patients with various neuromuscular diseases. The upregulation of utrophin on the extrajunctional sarcolemma has been found in dystrophinopathies, other muscular dystrophies, congenital myopathies, inflammatory myopathies, neurogenic muscle disorders (diabetic neuropathy, amyotrophic lateral sclerosis and spinal m...

Journal: :The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 1998
D Zochodne

Myopathies that occur in the intensive care unit can be divided into preexisting myopathies or newly acquired myopathies that develop in the intensive care unit. Myotonic dystrophy is an example of a preexisting myopathy that may render patients susceptible to acute respiratory failure following surgical procedures and anaesthesia. A group of myopathies that develop within the intensive care un...

Journal: :Annals of neurology 2011
Kimberly Amburgey Nancy McNamara Lindsey R Bennett M Eileen McCormick Gyula Acsadi James J Dowling

The prevalence of congenital myopathies in the United States has not been examined. To address this, we determined the point prevalence of congenital myopathies in a well-defined pediatric population from Southeastern Michigan. The overall point prevalence was 1:26,000. Mutations in RYR1 were the most common cause of congenital myopathies at 1:90,000. Our data broadly agrees with estimates from...

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