Results 71 to 80 of about 10,897 (217)

Chronic inflammatory demyelinating polyneuropathy in an eight year old girl

open access: yes, 2008
Chronic inflammatory demyelinating polyneuropathy is an acquired neuropathy which is rarely seen pediatric patients. It is characterised by chronic progressive or relapsing remitting weakness. The prognosis in childhood is good compared to adult patients.
Yis, ULUÇ, Kurul, S. Hiz, Senocak, O.
core  

Importance of electromiographic examination in diagnostification and monitoring of chronic inflammatory demyelinating polyneuropathy

open access: yes, 2010
Introduction. Polyneuropathies or peripheral neuropathies present a dysfunction or disease of larger number of peripheral nerves or their dysfunction.
Igor Damjan   +2 more
core   +1 more source

Chronic inflammatory demyelinating polyneuropathy. A case description

open access: yesClinical Case Reports
Key Clinical Message Patients affected by chronic inflammatory demyelinating polyradiculoneuropathy require close follow up due to the neuronal demyelination along with axonal degeneration associated with the disease process, giving the opportunity to ...
Garcia‐Castillo María Ariana
doaj   +1 more source

Pediatric Therapeutic Plasma Exchange: Characterization of Practice, Epidemiology, and Safety Profile at a Children's Hospital in the United States

open access: yesJournal of Clinical Apheresis, Volume 41, Issue 3, June 2026.
ABSTRACT There is a need to better understand the indications and safety profiles for therapeutic plasma exchange (TPE) in children. We aimed to assess pediatric TPE practice at a large academic center by retrospective chart review from 2011 to 2022. Patient demographics and clinical information including American Society for Apheresis (ASFA) category ...
Benjamin C. Lee   +4 more
wiley   +1 more source

Biological Drivers of IMiD‐Induced Peripheral Neuropathy in Multiple Myeloma

open access: yeseJHaem, Volume 7, Issue 3, June 2026.
ABSTRACT The introduction of immunomodulatory drugs (IMiDs), such as thalidomide, lenalidomide and pomalidomide, have led to significant improvements in multiple myeloma (MM) treatment. Many patients now live 10 years or longer with their disease, making treatment‐related side effects increasingly important.
Sina A. Beer   +2 more
wiley   +1 more source

Nerve Ultrasound Detects Peripheral Nerve Enlargement in Cerebrotendinous Xanthomatosis

open access: yesMuscle &Nerve, Volume 73, Issue 6, Page 1082-1088, June 2026.
ABSTRACT Introduction/Aims Cerebrotendinous xanthomatosis (CTX) is a rare autosomal recessive disorder caused by variants in the CYP27A1 gene, resulting in cholestanol accumulation in various tissues, including peripheral nerves. Polyneuropathy is common but often under‐recognized in CTX.
Antonio Edvan Camelo‐Filho   +8 more
wiley   +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

Quantitative Neuromuscular MRI in CIDP Patients: Interest of a Multiparametric Approach

open access: yesEuropean Journal of Neurology, Volume 33, Issue 6, June 2026.
Multiparametric quantitative MRI (qMRI) of nerves and muscles identifies distinct structural alterations in CIDP. Nerve volume is increased while magnetization transfer ratio (MTR) is reduced in leg muscle, with MTR showing the strongest correlations with clinical disability and electrophysiological measures.
A. Guérémy   +12 more
wiley   +1 more source

Chronic Inflammatory Demyelinating Polyneuropathy

open access: yes, 2018
This poster focuses on chronic inflammatory demyelinating polyneuropathy (CIDP) and the complex pathophysiological processes associated with the disorder.
Holland, Katherine
core  

Restless Legs Syndrome in Patients With PMP22‐Related Neuropathies

open access: yesJournal of the Peripheral Nervous System, Volume 31, Issue 2, June 2026.
ABSTRACT Background and Aims Restless legs syndrome (RLS) is frequently reported in peripheral neuropathies, but its prevalence and clinical correlates in Charcot–Marie–Tooth disease type 1A (CMT1A) and hereditary neuropathy with liability to pressure palsies (HNPP) remain poorly defined.
Bogdan Bjelica   +7 more
wiley   +1 more source

Home - About - Disclaimer - Privacy