Evidence for neuroaxonal injury in patients with proteolipid protein gene mutations.
about
Pelizaeus-Merzbacher disease and spastic paraplegia type 2: two faces of myelin loss from mutations in the same geneInsertion of mutant proteolipid protein results in missorting of myelin proteins.Protecting axons in multiple sclerosis.Patients lacking the major CNS myelin protein, proteolipid protein 1, develop length-dependent axonal degeneration in the absence of demyelination and inflammation.A PLP splicing abnormality is associated with an unusual presentation of PMD.Hearing profile and MRI myelination of auditory pathway in Pelizaeus-Merzbacher disease.
P2860
Evidence for neuroaxonal injury in patients with proteolipid protein gene mutations.
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年学术文章
@wuu
2001年学术文章
@zh-cn
2001年学术文章
@zh-hans
2001年学术文章
@zh-my
2001年学术文章
@zh-sg
2001年學術文章
@yue
2001年學術文章
@zh
2001年學術文章
@zh-hant
name
Evidence for neuroaxonal injury in patients with proteolipid protein gene mutations.
@en
Evidence for neuroaxonal injury in patients with proteolipid protein gene mutations.
@nl
type
label
Evidence for neuroaxonal injury in patients with proteolipid protein gene mutations.
@en
Evidence for neuroaxonal injury in patients with proteolipid protein gene mutations.
@nl
prefLabel
Evidence for neuroaxonal injury in patients with proteolipid protein gene mutations.
@en
Evidence for neuroaxonal injury in patients with proteolipid protein gene mutations.
@nl
P2093
P356
P1433
P1476
Evidence for neuroaxonal injury in patients with proteolipid protein gene mutations.
@en
P2093
Boespflüg-Tanguy O
Bonavita S
Patronas MD N
Schiffmann R
Tedeschi G
P304
P356
10.1212/WNL.56.6.785
P407
P577
2001-03-01T00:00:00Z