نتایج جستجو برای: sensory neuropathy

تعداد نتایج: 132521  

Journal: :Journal of Neurology, Neurosurgery & Psychiatry 2014

Journal: :Journal of Neurology, Neurosurgery & Psychiatry 1985

2013
M Dorchin R Masoumi Dehshiri S Soleiman M Manashi

BACK GROUND Vincristine (VCR), is a chemotherapy drug, useful in the treatment of leukemia, lymphoma and solid tumor and it is a potent neurotoxin and sensory neuropathy drug which a common behavioral toxicity of this drug. Neuropathy is common squeal of intensive chemotherapy protocols that contain vincristine and corticosteroids. MATERIALS AND METHODS This study was a retrospective and desc...

Journal: :The Journal of the Association of Physicians of India 2015
Vikram A Londhey

SLE (systemic lupus erythematosus) is a multisystem autoimmune disorder of unknown aetiology which can present with myriad clinical presentation. The neurological manifestations of SLE consist of central nervous system (CNS) and peripheral nervous system manifestations (PNS). The CNS manifestations are aseptic meningitis, cerebrovascular accidents (stroke), demyelinating disorders, headache, in...

Journal: :Acta neurologica Belgica 2009
B Kocer G Sucak R Kuruoglu Z Aki R Haznedar N Ince Erdogmus

BACKGROUND Whether thalidomide induces a sensory ganglionopathy or a length-dependent axonal neuropathy is disputed. Moreover no agreement exists concerning the effects of thalidomide dosage on the clinical and electrophysiological findings. OBJECTIVE We examined the effect of age, gender disease duration, total cumulative dose on the clinical and electrophysiologic parameters. METHODS Fift...

Journal: :Brain : a journal of neurology 2006
Henry Houlden Rosalind King Julian Blake Mike Groves Seth Love Cathy Woodward Simon Hammans James Nicoll Graham Lennox Dominic G O'Donovan Carolyn Gabriel P K Thomas Mary M Reilly

Hereditary sensory and autonomic neuropathy type I (HSAN I) is the most frequent type of hereditary neuropathy that primarily affects sensory neurons. The genetic locus for HSAN I has been mapped to chromosome 9q22.1-22.3 and recently the gene was identified as SPTLC1, encoding serine palmitoyltransferase, long chain base subunit-1. Sequencing in HSAN I families have previously identified mutat...

Journal: :Journal of neurology, neurosurgery, and psychiatry 2011
Masafumi Ito Kenjiro Matsuno Yasuhiko Sakumoto Koichi Hirata Nobuhiro Yuki

BACKGROUND Ataxic Guillain-Barré syndrome is characterised by profound ataxia with negative Romberg sign and no ophthalmoplegia. Its nosological relationship to acute sensory ataxic neuropathy has yet to be discussed. METHODS Medical records were reviewed of patients suffering acute ataxia and reduced muscle stretch reflexes but without external ophthalmoplegia. Clinical features and laborato...

Journal: :Journal of neurology, neurosurgery, and psychiatry 1995
T Phan J G McLeod J D Pollard O Peiris A Rohan J P Halpern

Four patients are described who developed sensorimotor neuropathy while being treated with simvastatin and had complete or partial resolution of clinical abnormalities after withdrawal of treatment. In one case onset was within days of commencing treatment, but in two cases symptoms did not develop for two years. The electrophysiological and pathological features of the neuropathy were those of...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2006
Sanjay C Keswani Christelene Jack Chunhua Zhou Ahmet Höke

Human immunodeficiency virus (HIV)-associated sensory neuropathy (SN) is the most common neurological complication of HIV infection in the current highly active antiretroviral therapy era. The painful sensory neuropathy is associated with the use of dideoxynucleoside antiretrovirals, and its development limits the choice of antiretroviral drugs in affected patients. There are presently no effec...

Journal: :Annals of oncology : official journal of the European Society for Medical Oncology 2000
T J Postma J J Heimans

Peripheral neuropathy can be defined as a derangement in structure and function of peripheral motor, sensory, and autonomic neurons [1], causing peripheral neuropathic symptoms and signs. In routine clinical practice settings, neuropathic symptoms are evaluated by a more or less standardized neurological history taking. Assessment of neuropathic signs is usually performed with bed-side clinical...

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