Chronic inflammatory demyelinating polyradiculoneuropathy: from pathology to phenotype

EK Mathey, SB Park, RAC Hughes… - Journal of Neurology …, 2015 - jnnp.bmj.com
Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) is an inflammatory
neuropathy, classically characterised by a slowly progressive onset and symmetrical …

The epidemiology of neuromuscular disorders: a comprehensive overview of the literature

JCW Deenen, CGC Horlings… - Journal of …, 2015 - content.iospress.com
Background: In 1991, the first world survey of neuromuscular disorders (NMDs) was
published in the peer reviewed literature. Since then, diagnostics have been greatly …

Incidence and prevalence of chronic inflammatory demyelinating polyradiculoneuropathy: a systematic review and meta-analysis

MC Broers, C Bunschoten, D Nieboer, HF Lingsma… - …, 2019 - karger.com
Background: Prevalence and incidence rates of chronic inflammatory demyelinating
polyradiculoneuropathy (CIDP) are required to determine the impact of CIDP on society. We …

Atypical CIDP: diagnostic criteria, progression and treatment response. Data from the Italian CIDP Database

PE Doneddu, D Cocito, F Manganelli… - Journal of Neurology …, 2019 - jnnp.bmj.com
Objectives A few variants of chronic inflammatory demyelinating polyradiculoneuropathy
(CIDP) have been described, but their frequency and evolution to typical CIDP remain …

Advances in the diagnosis, pathogenesis and treatment of CIDP

MC Dalakas - Nature Reviews Neurology, 2011 - nature.com
Chronic inflammatory demyelinating polyneuropathy (CIDP) is the most common chronic
autoimmune neuropathy. Despite clinical challenges in diagnosis—owing in part to the …

Chronic inflammatory demyelinating polyradiculoneuropathy: diagnostic and therapeutic challenges for a treatable condition

JM Vallat, C Sommer, L Magy - The Lancet Neurology, 2010 - thelancet.com
Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) is a chronic neuropathy
of supposed immune origin. Understanding of its pathophysiology has recently improved …

Focused HLA analysis in Caucasians with myositis identifies significant associations with autoantibody subgroups

S Rothwell, H Chinoy, JA Lamb, FW Miller… - Annals of the …, 2019 - ard.bmj.com
Objectives Idiopathic inflammatory myopathies (IIM) are a spectrum of rare autoimmune
diseases characterised clinically by muscle weakness and heterogeneous systemic organ …

Diagnosis and treatment of chronic acquired demyelinating polyneuropathies

N Latov - Nature Reviews Neurology, 2014 - nature.com
Chronic neuropathies are operationally classified as primarily demyelinating or axonal, on
the basis of electrodiagnostic or pathological criteria. Demyelinating neuropathies are …

Epidemiology of chronic inflammatory neuropathies in southeast E ngland

M Mahdi‐Rogers, RAC Hughes - European journal of …, 2014 - Wiley Online Library
Background and purpose There is little information about the prevalence and disease
burden of chronic inflammatory demyelinating polyradiculoneuropathy (CIDP), multifocal …

A population-based epidemiologic study of adult neuromuscular disease in the Republic of Ireland

S Lefter, O Hardiman, AM Ryan - Neurology, 2017 - AAN Enterprises
Objective: To estimate the prevalence rates (PRs) of acquired and inherited neuromuscular
diseases (NMD) in the adult Irish population, reflecting the burden of these conditions in a …