نتایج جستجو برای: acute motor axonal neuropathy

تعداد نتایج: 700825  

Journal: :Journal of South Asian Federation of Obstetrics and Gynaecology 2015

Journal: :Neurologia 2014
O Terry López D Sagarra Mur A M Gutiérrez Álvarez C Jiménez Corral

Guillain-Barré syndrome (GBS) is an autoimmune polyradiculoneuropathy that may follow infection. The syndrome is divided into several subgroups: chronic inflammatory demyelinating polyneuropathy (the most frequent variant), acute pandysautonomia, acute motor axonal neuropathy, acute motor and sensory axonal neuropathy, and MillerFisher syndrome (MFS).1 This last syndrome, a rare variant of GBS,...

Journal: :Medicina 2009
Ricardo Erazo Torricelli

This paper reviews the current knowledge about Guillain-Barré syndrome (GBS). GBS is defined as an acute, areflexic, flaccid paralysis, which is classified into 4 subgroups: acute inflammatory demyelinating polyneuropathy (AIDP), acute motor-sensory axonal neuropathy (AMSAN), acute motor axonal neuropathy (AMAN) and Miller-Fisher syndrome (MFS). AIDP is associated in 30-50% of cases with crania...

Journal: :Neurologia 2014
G Gutiérrez-Gutiérrez L Ibáñez Sanz R Lobato Rodríguez

16. Drake Jr M. Migraine as an organic cause of monocular diplopia. Psychosomatics. 1983;24:1024—7. 17. Headache Classification Subcommittee of the International Headache Society. The International Classification of Headache Disorders. 2nd ed. Cephalalgia. 2004;24 Suppl. 24:1—160. 18. Dichgans M, Mayer M, Uttner I, Brüning M, Muller-Höcker J, Rungger G, et al. The phenotypic spectrum of CADASIL...

Journal: :Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology 2013
Nortina Shahrizaila Khean Jin Goh Suhailah Abdullah Rishikesan Kuppusamy Nobuhiro Yuki

OBJECTIVE Recent studies have advocated the use of serial nerve conduction studies (NCS) in the electrodiagnosis of Guillain-Barré syndrome (GBS). The current study aims to elucidate when and how frequent NCS can be performed to reflect the disease pathophysiology. METHODS A prospective study of GBS patients documenting the initial and final electrodiagnoses following serial NCS performed at ...

Journal: :Journal of neurology, neurosurgery, and psychiatry 1997
M Hadjivassiliou A K Chattopadhyay G A Davies-Jones A Gibson R A Grünewald A J Lobo

OBJECTIVES To describe the range of neuromuscular disorders which may be associated with cryptic coeliac disease. METHODS Nine patients were described with neuromuscular disorders associated with circulating antigliadin antibodies, whose duodenal biopsies later confirmed the diagnosis of coeliac disease. Neurological symptoms antedated the diagnosis of coeliac disease in all, and most had min...

Journal: :Brain : a journal of neurology 2009
Susanna B Park Cindy S-Y Lin Arun V Krishnan David Goldstein Michael L Friedlander Matthew C Kiernan

Administration of oxaliplatin, a platinum-based chemotherapy used extensively in the treatment of colorectal cancer, is complicated by prominent dose-limiting neurotoxicity. Acute neurotoxicity develops following oxaliplatin infusion and resolves within days, while chronic neuropathy develops progressively with higher cumulative doses. To investigate the pathophysiology of oxaliplatin-induced n...

Journal: :Journal of neurology, neurosurgery, and psychiatry 2011
Margherita Capasso Francesca Notturno Claudia Manzoli Antonino Uncini

BACKGROUND Acute motor axonal neuropathy (AMAN) and acute motor and sensory axonal neuropathy (AMSAN) are due to an antiganglioside antibody mediated attack, thought to be restricted to motor fibres in AMAN. Sensory symptoms and minor sensory conduction abnormalities, however, have been reported in some AMAN patients. OBJECTIVE To verify whether sensory fibres are truly spared in AMAN and whe...

2011
Kimberly N. Capers Sinan Turnacioglu Robert T. Leshner John R. Crawford

Guillain-Barré syndrome (GBS) has been reported in HIV-infected patients in association with the immune reconstitution syndrome whose symptoms can be mimicked by highly active antiretroviral therapy (HAART)-mediated mitochondrial toxicity. We report a case of a 17-year-old, HIV-infected patient on HAART with a normal CD4 count and undetectable viral load, presenting with acute lower extremity w...

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