Coexistent central and peripheral nervous system involvement in a Charcot-Marie-Tooth syndrome X-linked patient.
about
Gap junctions in inherited human disorders of the central nervous system.Clinical and Genetic Features of Chinese X-linked Charcot-Marie-Tooth Type 1 Disease.Early disruption of glial communication via connexin gap junction in multiple sclerosis, Baló's disease and neuromyelitis optica.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.Loss of Coupling Distinguishes GJB1 Mutations Associated with CNS Manifestations of CMT1X from Those Without CNS Manifestations.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.Hereditary neuropathy with liability to pressure palsy (HNPP): report of a family with a new point mutation in PMP22 gene.CNS involvement in CMTX1 caused by a novel connexin 32 mutation: a 6-year follow-up in neuroimaging and nerve conduction.
P2860
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P2860
Coexistent central and peripheral nervous system involvement in a Charcot-Marie-Tooth syndrome X-linked patient.
description
2010 nî lūn-bûn
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2010年の論文
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2010年学术文章
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name
Coexistent central and periphe ...... oth syndrome X-linked patient.
@en
Coexistent central and periphe ...... oth syndrome X-linked patient.
@nl
type
label
Coexistent central and periphe ...... oth syndrome X-linked patient.
@en
Coexistent central and periphe ...... oth syndrome X-linked patient.
@nl
prefLabel
Coexistent central and periphe ...... oth syndrome X-linked patient.
@en
Coexistent central and periphe ...... oth syndrome X-linked patient.
@nl
P2093
P2860
P356
P1476
Coexistent central and periphe ...... oth syndrome X-linked patient.
@en
P2093
Alessandra Ferlini
Carlo Fusco
Elvio Della Giustina
Federica Spaggiari
Francesco Pisani
P2860
P304
P356
10.1177/0883073809344119
P577
2010-04-09T00:00:00Z