Results 91 to 100 of about 11,788 (205)
Neurological Peculiarities of POEMS Syndrome: Experience From a Brazilian University Center
Muscle &Nerve, Volume 73, Issue 3, Page 421-426, March 2026.ABSTRACT Aim Polyneuropathy, organomegaly, endocrinopathy, monoclonal protein, and skin changes (POEMS) syndrome is a rare paraneoplastic syndrome associated with significant neurologic morbidity. Better understanding of the manifestations of this disease is crucial to early diagnosis and improvement of prognosis.
Renan Fabri Rosenstein +5 more
wiley +1 more source
European Journal of Inflammation, 2020 Inflammatory polyradiculoneuropathies are heterogeneous disorders characterized by immune-mediated leukocyte infiltration of peripheral nerves and nerve roots leading to demyelination or axonal degeneration or both.
Vincenzo Di Stefano +6 more
doaj +1 more source
An unusual presentation of gbs: case report and literature review [PDF]
, 2016 Guillain-Barre syndrome (GBS), also known as Landry paralysis is an acute idiopathic polyneuritis, believed to be immunologically mediated. It usually presents as a demyelinating neuropathy with ascending weakness, however, many clinical variants have ...
Badshah, Mazhar +3 more
core +1 more source
Toxic and drug-induced peripheral neuropathies: updates on causes, mechanisms and management. [PDF]
, 2013 PURPOSE OF REVIEW: This review discusses publications highlighting current research on toxic, chemotherapy-induced peripheral neuropathies (CIPNs), and drug-induced peripheral neuropathies (DIPNs).
Buclin, T., Diezi, M., Kuntzer, T.
core +1 more source
Journal of the Peripheral Nervous System, Volume 31, Issue 1, March 2026.ABSTRACT Background and Aims Differentiating hereditary axonal polyneuropathies caused by distinct gene variants remains a clinical challenge. This comparative case study of DNAJB2‐ and HINT1‐related neuropathies aimed to broaden the phenotypic spectrum associated with these genes and to explore non‐motor symptoms and quality of life (QoL) in affected ...
Bogdan Bjelica +8 more
wiley +1 more source
Diagnosis of Guillain–Barré syndrome in children and validation of the Brighton criteria [PDF]
, 2017 To describe the key diagnostic features of pediatric Guillain–Barré syndrome (GBS) and validate the Brighton criteria. Retrospective cohort study of all children (
Berg, B. (Bianca) van den +6 more
core +1 more source
Neurofascin antibodies in autoimmune, genetic, and idiopathic neuropathies [PDF]
, 2017 OBJECTIVE: To measure the frequency, persistence, isoform specificity, and clinical correlates of neurofascin antibodies in patients with peripheral neuropathies.
Burnor, E +8 more
core +1 more source
Conduction block in acute motor axonal neuropathy [PDF]
, 2017 Guillain-Barré syndrome is divided into two major subtypes, acute inflammatory demyelinating polyneuropathy and acute motor axonal neuropathy. The characteristic electrophysiological features of acute motor axonal neuropathy are reduced amplitude or ...
Hirata, Koichi +5 more
core
Changes in the severity and subtype of Guillain-Barré syndrome admitted to a specialist Neuromedical ICU over a 25 year period [PDF]
, 2017 We report a retrospective review of 110 patients with acute Guillain-Barré syndrome (GBS) admitted to a specialised intensive care unit (ICU) in a tertiary referral centre over a 25 year period, the start of which coincided with the widespread ...
Hirsch, NP +3 more
core +2 more sources
Neurosarcoidose: orientações para o neurologista geral [PDF]
, 2012 Neurosarcoidosis (NS) more commonly occurs in the setting of systemic disease. The diagnosis is based on a clinical history suggestive of NS, presence of noncaseating granulomas, and supportive evidence of sarcoid pathology, laboratory, and imaging ...
Abrahão, Agessandro +5 more
core +2 more sources