A review of all myopathic patients treated at the Neurologic Clinic of the Medical School of the University of São Paulo during the past 15 years is reported. A total of 466 cases were examined and distributed as follows: 56% of progressive muscular dystrophy; 31% of myasthenia gravis; 6% of polymyositis; 4% of myotonic dystrophy; and the remainder of several different diseases (central core disease, Kearns-syndrome, myotonia congenita, adynamia episodica hereditaria, diabetic myopathy and Eaton-Lambert syndrome). Enzymatic dosages, electromyography, muscle biopsy, electrocardiography and genetic counselling are also reported.Os autores fazem uma revisão de todos os casos de miopatias tratados na Clínica Neurológica da F.M.U.S.P. durante os...
Diseases of muscle may be congenital or acquired. They cause muscle weakness without sensory loss. T...
Muscle diseases are an expanding field, mainly due to the progress in genetics and biochemistry. Eva...
Myopathy is a typical clinical finding among patients with the 3243A>G mutation in mitochondrial ...
A review of all myopathic patients treated at the Neurologic Clinic of the Medical School of the Uni...
Primary muscle disorders (myopathies) are rare, even within a neurology clinic. It has been estimate...
The percentage and cause of neuromuscular (NM) diseases have been analysed during a 15-year period o...
As miopatias genéticas são um grupo complexo de doenças neuromusculares. A crescente descrição de no...
Patients with muscle disorders can present a diagnostic challenge to physicians because of the diffe...
Myotonic Dystrophies (DM, Dystrophia Myotonia) are autosomal dominant inherited myopathies with a hi...
Myopathies are rare diseases. They may be genetic (muscular dystrophies, metabolic or congenital myo...
Une fonction musculaire efficiente repose sur l’intégrité fonctionnelle des systèmes nerveux et musc...
In myotonic dystrophy (MD), disease severity has been correlated with expansion of CTG repeats in ch...
We determined the prevalence of genetically determined neuromuscular diseases in adult Norwegian pat...
Symposium C2: Theme: Neurology 2 - Neuromuscular Disoder, the Treatment, the Multidisciplinary Care ...
Various pathological processes, some genetically determined and others acquired, may affect the func...
Diseases of muscle may be congenital or acquired. They cause muscle weakness without sensory loss. T...
Muscle diseases are an expanding field, mainly due to the progress in genetics and biochemistry. Eva...
Myopathy is a typical clinical finding among patients with the 3243A>G mutation in mitochondrial ...
A review of all myopathic patients treated at the Neurologic Clinic of the Medical School of the Uni...
Primary muscle disorders (myopathies) are rare, even within a neurology clinic. It has been estimate...
The percentage and cause of neuromuscular (NM) diseases have been analysed during a 15-year period o...
As miopatias genéticas são um grupo complexo de doenças neuromusculares. A crescente descrição de no...
Patients with muscle disorders can present a diagnostic challenge to physicians because of the diffe...
Myotonic Dystrophies (DM, Dystrophia Myotonia) are autosomal dominant inherited myopathies with a hi...
Myopathies are rare diseases. They may be genetic (muscular dystrophies, metabolic or congenital myo...
Une fonction musculaire efficiente repose sur l’intégrité fonctionnelle des systèmes nerveux et musc...
In myotonic dystrophy (MD), disease severity has been correlated with expansion of CTG repeats in ch...
We determined the prevalence of genetically determined neuromuscular diseases in adult Norwegian pat...
Symposium C2: Theme: Neurology 2 - Neuromuscular Disoder, the Treatment, the Multidisciplinary Care ...
Various pathological processes, some genetically determined and others acquired, may affect the func...
Diseases of muscle may be congenital or acquired. They cause muscle weakness without sensory loss. T...
Muscle diseases are an expanding field, mainly due to the progress in genetics and biochemistry. Eva...
Myopathy is a typical clinical finding among patients with the 3243A>G mutation in mitochondrial ...