Multiple sclerosis associated with duplicated CMT1A: a report of two cases.
about
Myelin protein zero mutation His39Pro: hereditary motor and sensory neuropathy with variable onset, hearing loss, restless legs and multiple sclerosis.Central Nervous System Demyelination in a Charcot-Marie-Tooth Type 1A Patient.A rare association between multiple sclerosis and Charcot-Marie-Tooth type 1B.Intractable epilepsy, audio-visual hallucinations and Charcot-Marie-Tooth disease 1A in an African-American boy.Clinical and pathological correlations in Charcot-Marie-Tooth neuropathy type 1A with the 17p11.2p12 duplication: a cross-sectional morphometric and immunohistochemical study in twenty cases.
P2860
Multiple sclerosis associated with duplicated CMT1A: a report of two cases.
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
1997年论文
@zh
1997年论文
@zh-cn
name
Multiple sclerosis associated with duplicated CMT1A: a report of two cases.
@en
Multiple sclerosis associated with duplicated CMT1A: a report of two cases.
@nl
type
label
Multiple sclerosis associated with duplicated CMT1A: a report of two cases.
@en
Multiple sclerosis associated with duplicated CMT1A: a report of two cases.
@nl
prefLabel
Multiple sclerosis associated with duplicated CMT1A: a report of two cases.
@en
Multiple sclerosis associated with duplicated CMT1A: a report of two cases.
@nl
P2093
P356
P1476
Multiple sclerosis associated with duplicated CMT1A: a report of two cases.
@en
P2093
A Di Summa
G M Fabrizi
P304
P356
10.1136/JNNP.63.3.413A
P407
P577
1997-09-01T00:00:00Z