TDP-43 pathology in a case of hereditary spastic paraplegia with a NIPA1/SPG6 mutation
about
Molecular Pathological Classification of Neurodegenerative Diseases: Turning towards Precision MedicineNeuropathology of Amyotrophic Lateral Sclerosis and Its Variants.Hereditary spastic paraplegia: clinico-pathologic features and emerging molecular mechanisms.Frontotemporal lobar degeneration: defining phenotypic diversity through personalized medicine.Motor neuron degeneration in spastic paraplegia 11 mimics amyotrophic lateral sclerosis lesions.Hereditary spastic paraplegia is not associated with C9ORF72 repeat expansions in a Danish cohort.
P2860
TDP-43 pathology in a case of hereditary spastic paraplegia with a NIPA1/SPG6 mutation
description
2012 nî lūn-bûn
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2012年の論文
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2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
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2012年论文
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name
TDP-43 pathology in a case of hereditary spastic paraplegia with a NIPA1/SPG6 mutation
@ast
TDP-43 pathology in a case of hereditary spastic paraplegia with a NIPA1/SPG6 mutation
@en
type
label
TDP-43 pathology in a case of hereditary spastic paraplegia with a NIPA1/SPG6 mutation
@ast
TDP-43 pathology in a case of hereditary spastic paraplegia with a NIPA1/SPG6 mutation
@en
prefLabel
TDP-43 pathology in a case of hereditary spastic paraplegia with a NIPA1/SPG6 mutation
@ast
TDP-43 pathology in a case of hereditary spastic paraplegia with a NIPA1/SPG6 mutation
@en
P2093
P2860
P1476
TDP-43 pathology in a case of hereditary spastic paraplegia with a NIPA1/SPG6 mutation
@en
P2093
Dana Falcone
Laura Molina-Porcel
Leo McCluskey
Maria Martinez-Lage
Virginia M-Y Lee
Vivianna M Van Deerlin
P2860
P2888
P304
P356
10.1007/S00401-012-0947-Y
P577
2012-08-01T00:00:00Z