نتایج جستجو برای: سندرم گیلی باره guillain
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OBJECTIVES To determine the incidence, treatment, and outcome of Guillain-Barré syndrome in south east England. METHODS Patients presenting with confirmed Guillain-Barré syndrome between 1 July 1993 and 30 June 1994 were recruited via a voluntary reporting scheme coordinated by the British Neurological Surveillance Unit, hospital activity data collected from acute admitting hospitals within t...
acute acquired demyelinating polyneuropathy:an initial presentation of diffuse large b cell lymphoma
neurological signs and symptoms are commonly associated with both hodgkin’s and non-hodgkin’s lymphoma and are mostly attributed to either direct lymphomatous involvement of the nervous system, either as a result of extension to the spinal cord or nerves, or due to infiltration by lymphoma cells and drug toxicity. guillain-barre syndrome and its variants have been reported very infrequently in ...
objective the guillain-barre syndrome (gbs) is characterized by the acute onset of rapidlyprogressive, symmetric muscle weakness with absent or decreased deep tendon reflexes. gbs is the most common cause of acute flaccid paralysis in childhood, with an incidence of 0.6-4 per 100 000 population per year. the clinical features are distinct and obtaining patient's history and conducting an exami...
background: anti-ganglioside antibody assays are widely used for diagnosis of autoimmune peripheral neuropathies. objective: this study aimed to determine serum levels of anti-ganglioside antibodies in children with guillain-barre syndrome by immunoblotting technique and compare the results with those obtained by elisa method. method: in this investigation, 50 children with guillain-barre syndr...
guillain barre syndrome (gbs) is an inflammatory, usually demyelinating, polyneuropathy; clinically characterized by acute onset of symmetric progressive muscle weakness with loss of myotatic reflexes. thirty five patients with gbs, defined clinically according to the criteria of asbury and cornblath, were recruited from three hospital affiliated to tehran university of medical sciences.as a co...
BACKGROUND Although infection with Campylobacter jejuni is recognized as a common antecedent of the Guillain-Barré syndrome, the clinical and epidemiologic features of this association are not well understood. METHODS We performed a prospective case-control study in a cohort of patients with Guillain-Barré syndrome (96 patients) or Miller Fisher syndrome (7 patients) who were admitted to hosp...
Objective: To determine the frequency of axonal variants in our patients of Guillain-Barre Syndrome. Study Design: Descriptive study. Place and Duration: Department of Neurology, Military Hospital, Rawalpindi and Armed Forces Institute of Rehabilitation Medicine (AFIRM) from 01 Jan 2009 to 30 Jul 2010. Patients and Methods: Forty adult patients meeting the National Institute of Neurological Dis...
Guillain-Barré syndrome and acute transverse myelitis manifest as demyelinating diseases of the peripheral and central nervous system. Concurrency of these two disorders is rarely documented in literature. A 4-year-old girl presenting with cough, fever, and an impaired walking ability was admitted to hospital. She had no previous complaints in her medical history. A physical examination reveale...
Multiple cranial nerve dysfunction can occur with primary intracranial processes (neoplasm, basilarvertebral insufficiency, congenital defects, aneurysms, dural vein thrombosis, multiple sclerosis), myopathy or neuromuscular junction disorder (myasthenia gravis, botulism, orbital 'myositis', ocular myopathy), and as a manifestation of a more systemic disorder (sarcoidosis, endocrinopathy, conne...
INTRODUCTION Guillain-Barre syndrome, or acute inflammatory demyelinating polyneuropathy, has been described in the presence of malignancies such as lymphoma. Guillain-Barre syndrome/acute inflammatory demyelinating polyneuropathy causes paresthesias and weakness, which can make the treatment of lymphoma with chemotherapy challenging. Given the rarity of this co-presentation it is not known if ...
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