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Coexistent hereditary and inflammatory neuropathy
L Ginsberg
, O Malik
, AR Kenton
, D Sharp
, JR Muddle
, M Davis
, John Winer
, R Orrell
, RHM King
Birmingham Medical School
Research output
:
Contribution to journal
›
Article
123
Citations (Scopus)
Overview
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Keyphrases
Asymptomatic Period
16%
Charcot-Marie-Tooth Disease
66%
Chromosome 17p11.2
16%
Chronic Inflammatory Demyelinating Polyneuropathy
16%
Clinical Conditions
16%
CMT Disease
16%
CMT1B
16%
Disease Experience
16%
Disease Pattern
16%
Distal Hereditary Motor Neuropathy (dHMN)
33%
Duplication
16%
Epidemiological Study
16%
Family History
16%
Genetic Defects
16%
Genetic Parameters
16%
GJB1
16%
Hereditary Neuropathy
100%
Immunoglobulin
16%
Immunosuppressive Therapy
16%
Inflammatory Neuropathy
100%
Intravenous Immunoglobulin (IVIg)
16%
Lymphocyte Infiltration
16%
Nerve Biopsy
33%
Neuropathic Pain
16%
Neuropathology
16%
Patient Assessment
16%
Patient Management
16%
Positive Responses
16%
Sensory Symptoms
16%
Stable Period
16%
X-linked Disorder
16%
Medicine and Dentistry
Chronic Inflammatory Demyelinating Polyneuropathy
14%
DeJerine-Sottas Disease
71%
Deterioration
42%
Diseases
14%
Family History
14%
Genetic Disorder
14%
Immunoglobulin
28%
Lymphocytic Infiltration
14%
Nerve Biopsy
28%
Neuropathic Pain
14%
Neuropathy
100%
Polyneuropathy
14%
Prevalence
14%
X Chromosome Linked Disorder
14%
Neuroscience
Charcot-Marie-Tooth Disease
50%
Intravenous Immunoglobulin
25%
Neuropathic Pain
12%
Neuropathy
100%
Polyneuropathy
25%