Zobrazeno 1 - 10
of 187
pro vyhledávání: '"B Sharf"'
Publikováno v:
Developmental Medicine & Child Neurology. 22:781-783
SUMMARY An eight-year-old girl with symptoms and signs of myopathy subsequently was found to suffer from coeliac disease. The myopathy disappeared on a gluten-free diet. It is suggested that the acquired myopathy may be related to deficiency in fat-s
Publikováno v:
European Neurology. 33:264-266
Tardive dyskinesia (TD) is an iatrogenic syndrome caused by long-term treatment with neuroleptics and is characterized by abnormal involuntary movements in the orofacial region, lingual dyskinesia and in some cases dyskinesia also in the extremities,
Publikováno v:
Harefuah. 134(4)
Cerebrovascular events have high mortality and morbidity, especially in the elderly. Ischemia is the main cause and 30% of the ischemic events are embolic and of cardiac origin. The clinical picture is not always typical of the type of stroke, but di
Publikováno v:
Journal of psychiatryneuroscience : JPN. 24(4)
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 53:800-802
The abnormal involuntary movements in tardive dyskinesia can be reduced by the dopamine antagonist drugs, phenothiazines and butyrophenones, but most cause an increase in Parkinsonian signs. Sulpiride, a benzamide derivative, and selective antagonist
Autor:
B Sharf, M Rochas, I. Tal, I Eldar, D Attias, N Toubi, M Schwartz, D Golan, A Sheinkman, B Weller
Publikováno v:
The Journal of clinical psychiatry. 59(1)
Background: Lupus anticoagulant (LA) and anticardiolipin antibodies (aCL) are autoantibodies that can be detected in plasma or serum of patients with autoimmune-related diseases. The presence of these autoantibodies has been associated with recurrent
Publikováno v:
Harefuah. 127(1-2)
Idiopathic intracranial hypertension (IIH, pseudotumor cerebri) was diagnosed in 4 patients who had been treated with tetracycline. The main symptom was headache, and in all there was papilledema. Symptoms and signs improved after tetracycline was di
Publikováno v:
Harefuah. 124(2)
Wilson's disease is an inherited, autosomal recessive disease characterized by progressive hepatic and neurological symptoms. Clinical features usually start between the ages of 10 and 40. Psychiatric disturbances are present in almost all patients.
Publikováno v:
The Journal of laryngology and otology. 104(3)
Fifteen Minor Head Trauma patients were investigated by Brainstem Auditory Evoked Potentials at 10/s and 55/s stimulus rate. The results were compared with those of the same patients at a second examination, two months later, as well as with a matche