Results 91 to 100 of about 14,551 (210)

Anti-Neurofascin–Associated Nephrotic-Range Proteinuria in Chronic Inflammatory Demyelinating Polyneuropathy

open access: yesKidney Medicine, 2020
There are few case reports of concomitant chronic inflammatory demyelinating polyneuropathy (CIDP) and focal segmental glomerulosclerosis. A rare autoantibody to a neuronal and podocyte structural component, neurofascin, may be contributory.
Syed Bukhari   +5 more
doaj   +1 more source

Pathological classification of equine recurrent laryngeal neuropathy [PDF]

open access: yes, 2018
Recurrent Laryngeal Neuropathy (RLN) is a highly prevalent and predominantly left‐sided, degenerative disorder of the recurrent laryngeal nerves (RLn) of tall horses, that causes inspiratory stridor at exercise because of intrinsic laryngeal muscle ...
Draper, A C E, Piercy, R J
core   +2 more sources

Clinical and diagnostic role of autoantibodies to gangliosides of peripheral nerves: literature review and own expirience

open access: yesНервно-мышечные болезни, 2015
The study of anti-glycolipid antibodies has become available to general practice in Russia. Indications for determining antibodies to gangliosidesare Guillain–Barré syndrome, Miller Fisher syndrome, Bickerstaff’s encephalitis, chronic inflammatory ...
N. A. Suponeva
doaj   +1 more source

Presence of both anti-contactin 1 and anti-neurofascin 140 antibodies in a case of chronic inflammatory demyelinating polyneuropathy

open access: yeseNeurologicalSci, 2018
Chronic inflammatory demyelinating polyneuropathy (CIDP) is an acquired disorder of peripheral nerves and nerve roots. Its cause is unknown, but recently antibodies to nodal and paranodal proteins have been discovered in a small subset of CIDP patients ...
Hsin-Pin Lin   +2 more
doaj   +1 more source

Changes in lymphocyte subsets in patients with Guillain-Barré syndrome treated with immunoglobulin [PDF]

open access: yes, 2014
BACKGROUND: Guillain-Barré syndrome (GBS) is an autoimmune condition characterized by peripheral neuropathy. The pathogenesis of GBS is not fully understood, and the mechanism of how intravenous immunoglobulin (IVIG) cures GBS is ambiguous.
Hui Qing Hou   +5 more
core   +1 more source

Predicting the Response to Intravenous Immunoglobulins in an Animal Model of Chronic Neuritis [PDF]

open access: yes, 2016
Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) is a disabling autoimmune disorder of the peripheral nervous system (PNS). Intravenous immunoglobulins (IVIg) are effective in CIDP, but the treatment response varies greatly between ...
Bendszus, Martin   +8 more
core   +2 more sources

Neurofascin antibodies in autoimmune, genetic, and idiopathic neuropathies [PDF]

open access: yes, 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

CHRONIC INFLAMMATORY DEMYELINATING POLYNEUROPATHY IN CHILDREN: DIAGNOSIS AND TREATMENT

open access: yesВопросы современной педиатрии, 2014
Chronic inflammatory demyelinating polyneuropathy (CIDP) in children is a rare autoimmune disease of the peripheral nervous system. The article analyzes current international diagnostic criteria and clinical presentation features of the disease in ...
А.L. Kurenkov   +3 more
doaj   +1 more source

Distal motor latency and residuallatency as sensitive markersof anti-MAG polyneuropathy [PDF]

open access: yes, 2018
.: There is debate whether the terminal latency index (TLI) is a sensitive marker for polyneuropathy with anti-myelinassociated-glycoprotein antibodies (anti-MAGP).
Fuhr, P.   +3 more
core  

Can plasma exchange therapy induce regulatory T lymphocytes in multiple sclerosis patients? [PDF]

open access: yes, 2012
Plasma exchange is used increasingly as an individual therapeutic decision for treating of severe, steroid-resistant relapses of multiple sclerosis (MS).
Gharagozloo, M., Jamshidian, A.
core   +1 more source

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