Slowing of central conduction in X-linked Charcot-Marie-Tooth neuropathy shown by brain stem auditory evoked responses.
about
Gap junctions couple astrocytes and oligodendrocytesGap junctions in inherited human disorders of the central nervous system.Systemic inflammation disrupts oligodendrocyte gap junctions and induces ER stress in a model of CNS manifestations of X-linked Charcot-Marie-Tooth disease.Cx32 and Cx47 mediate oligodendrocyte:astrocyte and oligodendrocyte:oligodendrocyte gap junction coupling.Connexin32 mutations cause loss of function in Schwann cells and oligodendrocytes leading to PNS and CNS myelination defectsCentral visual, acoustic, and motor pathway involvement in a Charcot-Marie-Tooth family with an Asn205Ser mutation in the connexin 32 gene.A unique point mutation in the PMP22 gene is associated with Charcot-Marie-Tooth disease and deafness.Early stages of building a rare disease registry, methods and 2010 data from the Belgian Neuromuscular Disease Registry (BNMDR).Charcot-marie-tooth disease and related neuropathies: molecular basis for distinction and diagnosis.Electrophysiological features of inherited demyelinating neuropathies: A reappraisal in the era of molecular diagnosis.The central nervous system phenotype of X-linked Charcot-Marie-Tooth disease: a transient disorder of children and young adults.A new mutation in GJC2 associated with subclinical leukodystrophy.Connexinopathies: a structural and functional glimpseHow do mutations in GJB1 cause X-linked Charcot-Marie-Tooth disease?Clinical and electrophysiological aspects of Charcot-Marie-Tooth disease.Molecular genetics of X-linked Charcot-Marie-Tooth disease.Molecular diagnostics of Charcot-Marie-Tooth disease and related peripheral neuropathies.X-linked Charcot-Marie-Tooth disease.GJB1-associated X-linked Charcot-Marie-Tooth disease, a disorder affecting the central and peripheral nervous systems.A Review of X-linked Charcot-Marie-Tooth Disease.Temperature-dependent auditory neuropathy: is it an acoustic Uhthoff-like phenomenon? A case report.Coexistent central and peripheral nervous system involvement in a Charcot-Marie-Tooth syndrome X-linked patient.Connexin32-null mice develop demyelinating peripheral neuropathy.Transient central nervous system white matter abnormality in X-linked Charcot-Marie-Tooth disease.X-linked Charcot-Marie-Tooth type 1: stroke-like presentation of a novel GJB1 mutation.Vestibular function in auditory neuropathy.Myelination defects and neuronal hyperexcitability in the neocortex of connexin 32-deficient mice.
P2860
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P2860
Slowing of central conduction in X-linked Charcot-Marie-Tooth neuropathy shown by brain stem auditory evoked responses.
description
1996 nî lūn-bûn
@nan
1996 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1996 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
name
Slowing of central conduction ...... tem auditory evoked responses.
@ast
Slowing of central conduction ...... tem auditory evoked responses.
@en
type
label
Slowing of central conduction ...... tem auditory evoked responses.
@ast
Slowing of central conduction ...... tem auditory evoked responses.
@en
prefLabel
Slowing of central conduction ...... tem auditory evoked responses.
@ast
Slowing of central conduction ...... tem auditory evoked responses.
@en
P2860
P356
P1476
Slowing of central conduction ...... tem auditory evoked responses.
@en
P2093
Nicholson G
P2860
P356
10.1136/JNNP.61.1.43
P407
P577
1996-07-01T00:00:00Z