Results 51 to 60 of about 31,200 (259)

Electrophysiological evaluation of Guillain–Barre syndrome subtypes in childhood

open access: yesمجلة كلية الطب, 2017
Background: Guillain-Barre syndrome (GBS) is the most common cause of acute motor paralysis in children where most of electrophysiological findings reveal demyelinating neuropathy. However, an axonal form of Guillain-Barre syndrome had been reported too.
Lamees M. Hussein   +2 more
doaj   +1 more source

Guillain-Barré syndrome (GBS) complicated by rhabdomyolysis (RML): Case reports of 2 children and literature review

open access: yesFrontiers in Pediatrics, 2022
We initially described two children who developed Guillain-Barré syndrome (GBS) complicated by rhabdomyolysis (RML), and reviewed five adult patients from the literature.
Xin-Ying Yang, Tong-Li Han, Jun-Lan Lv
doaj   +1 more source

Neurophysiological profile of peripheral neuropathy associated with childhood mitochondrial disease [PDF]

open access: yes, 2016
INTRODUCTION: Peripheral nerve involvement is common in mitochondrial disease but often unrecognised due to the prominent central nervous system features.
Bhattacharya, K   +13 more
core   +1 more source

Severe Pure Acute Motor Axonal Neuropathy

open access: yesErciyes Tıp Dergisi/Erciyes Medical Journal, 2015
Acute motor axonal neuropathy (AMAN) is a subtype of Guillain-Barre syndrome. Characteristic electrophysiological features of AMAN are reduced amplitude or absence of muscle action potentials. Our patient described progressive weakness in his leg and was not able to independently walk; he had a feeling weakness in his arms within 24 h after the onset ...
Taşdemir, Nebahat   +3 more
openaire   +2 more sources

P08.01 Immune-Related Acute Motor Axonal Neuropathy: A Small Case Series and Review of the Literature

open access: yesNeuro-Oncology, 2021
Immunotherapy have revolutionized cancer treatment in the past decade, with a significant increased survival in patients with solid tumors. However, the use of immune checkpoint inhibitors (ICIs) has been associated with a growing number of ...
Y. Piña   +4 more
semanticscholar   +1 more source

The effects of age and ganglioside composition on the rate of motor nerve terminal regeneration following antibody-mediated injury in mice [PDF]

open access: yes, 2013
Gangliosides are glycosphingolipids highly enriched in neural plasma membranes, where they mediate a diverse range of functions and can act as targets for auto-antibodies present in human immune-mediated neuropathy sera.
Cunningham, Madeleine E.   +4 more
core   +1 more source

Pearls & Oy-sters: Delayed Diagnosis of Acute Motor Axonal Neuropathy With Cardiac Arrest

open access: yesNeurology, 2021
We present the case of a 53-year-old woman who presented with right lower extremity weakness with preceding systemic symptoms including fever and chest pain.
Sina Marzoughi   +3 more
semanticscholar   +1 more source

Epidemiologic and Clinical Characteristics of Guillain-Barré Syndrome in Patients Referred to Sina Hospital in Hamadan in 2018 [PDF]

open access: yesInternational Journal of Epidemiologic Research, 2022
Background and aims: Guillain-Barré syndrome (GBS) has several types, some of which damage myelin and some others cause axonal damage. Detecting the type of GBS is important in determining the type of treatment and its prognosis. This study was conducted
Mojtaba Khazaei   +4 more
doaj   +1 more source

Current status and future directions of botulinum neurotoxins for targeting pain processing. [PDF]

open access: yes, 2015
Current evidence suggests that botulinum neurotoxins (BoNTs) A1 and B1, given locally into peripheral tissues such as skin, muscles, and joints, alter nociceptive processing otherwise initiated by inflammation or nerve injury in animal models and humans.
Pellett, Sabine   +2 more
core   +2 more sources

HIV positive patient with GBS-like syndrome [PDF]

open access: yes, 2017
Introduction. Guillain–Barré Syndrome (GBS) is an acute demyelinating polyneuropathy which can occur post-infection. Criteria of diagnosis of GBS include areflexia with progressive bilateral weakness in arms and legs.
Black, Heather   +3 more
core   +1 more source

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