Примери за използване на Myasthenic на Английски и техните преводи на Български
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Myasthenic syndrome.
Uncommon epilepsy epilepsy myasthenic syndrome.
Rare myasthenic syndrome o.
Symptomatic treatment of Lambert-Eaton myasthenic syndrome(LEMS) in adults.
G73.3 Myasthenic syndromes in other diseases classified elsewhere.
Muscle weakness of the limbs, drooping orfalling of the upper eyelid(myasthenic syndrome).
Convulsion, hypertonia, tremor,somnolence, myasthenic syndrome, dizziness, headache, paraesthesia, dysgeusia.
Myasthenic syndrome, demyelinating lesions of NS, myasthenia is treated with a dose of 20-40 mg, 4 to 5 times a day.
Firdapse is used to treat the symptoms of Lambert-Eaton myasthenic syndrome(LEMS) in adults.
Amnesia Coma Grand mal seizure Myasthenic syndrome Neuroleptic malignant syndrome Status epilepticus Dyspnoea Pneumonia aspiration Respiratory disorder.
FIRDAPSE is used to treat symptoms of a disease of the nerves andthe muscles called Lambert-Eaton myasthenic syndrome or LEMS in adults.
The term“myasthenic crisis” is meant as a weakness attack, appeared suddenly and concentrated in pharyngeal and respiratory muscles(MedlinePlus).
Treatment with atezolizumab must be permanently discontinued for any grade of myasthenic syndrome/ myasthenia gravis or Guillain-Barré syndrome.
A myasthenic crisis occurs when the muscles that control breathing weaken so much that the patient requires emergency ventilation assistance.
Approximately half of all individuals diagnosed with Lambert-Eaton myasthenic syndrome(LEMS) will eventually be found to have a small-cell carcinoma of the lung.
Hard cases of the myasthenic crisis provide the need for carrying out an artificial ventilation of lungs and a plasmapheresis in the conditions of resuscitation departments.
Beta-adrenergic blocking medicinal products have been reported to potentiate muscle weakness consistent with certain myasthenic symptoms(e.g. diplopia, ptosis and generalised weakness).
MG must be distinguished from congenital myasthenic syndromes that can present similar symptoms but offer no response to immunosuppressive treatments.
In future PSURs, the MAH is expected to submit cumulative reviews and discuss the following safety concerns: vasculitis, CNS inflammation, GBS,diabetes type 1, myasthenic syndrome, myositis, sarcoidosis, GBS, pneumonitis and EBV hepatitis.
Myasthenic syndrome/myasthenia gravis or Guillain-Barré syndrome, which may be life threatening, were observed in patients receiving atezolizumab.
A prospective, placebo-controlled, randomised study in 26 patients with Lambert-Eaton myasthenic syndrome(LEMS) reported clinical efficacy for amifampridine at the standard recommended maximum dose of 60 mg/day(Sanders et al 2000).
A myasthenic crisis occurs when the muscles that control breathing weaken so much that you need emergency ventilation assistance to help breath.
A temporary inflammation of the nerves that causes pain, weakness, and paralysis in the extremities(Guillain- Barré syndrome), loss of the protective sheath around nerves(demyelination), a condition in which the muscles become weak andtire easily(myasthenic syndrome).
A myasthenic crisis occurs when weakness affects the muscles that control breathing, creating a medical emergency and requiring a respirator for assisted ventilation.
The following additional clinically significant, immune-related adverse reactions have been reported in clinical trials or in post-marketing experience: uveitis, arthritis, myositis, myocarditis, pancreatitis,Guillain-Barré syndrome, myasthenic syndrome, haemolytic anaemia, sarcoidosis and encephalitis(see sections 4.2 and 4.8).
A myasthenic crisis is a medical emergency that occurs when the muscles that control breathing weaken to the point where individuals require a ventilator to help them breathe.
The following immune-related adverse reactions were reported in less than 1% of patients treated with nivolumab in clinical trials across doses and tumour types: pancreatitis, uveitis, demyelination, autoimmune neuropathy(including facial and abducens nerve paresis), Guillain-Barré syndrome,hypopituitarism, and myasthenic syndrome.
A myasthenic crisis occurs when the muscles that control breathing weaken to the point that ventilation is inadequate, creating a medical emergency and requiring a respirator for assisted ventilation.
Intensive therapy ward performs prolonged artificial pulmonary ventilation, which may continue for months and years in patients with severe neurological diseases and acute respiratory failure(acute inflammatory demyelinating polyneuropathy(Guillain-Barré syndrome),severe myasthenic crises, prolonged epileptic status, progressive muscular dystrophy, etc.).
The myasthenic crisis is a medical emergency that happens when the muscles that are responsible for controlling your breathing will be weakened to the point that individuals will need to use a ventilator to help them in breathing.