Hereditary diffuse leukoencephalopathy with spheroids: ultrastructural and immunoelectron microscopic studies.

about

The pallidopyramidal syndromes: nosology, aetiology and pathogenesis.Hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS): a misdiagnosed disease entity.

P2860

Q34336776-2DAACF42-D29A-447F-A7C4-106F21FF6C84 Q35745338-A2A630FB-C095-4E73-8D4C-BDE6B8A15C51

P2860

Hereditary diffuse leukoencephalopathy with spheroids: ultrastructural and immunoelectron microscopic studies.

Item

http://www.wikidata.org/entity/Q42130117

description

2010 nî lūn-bûn

@nan

2010年の論文

@ja

2010年論文

@yue

2010年論文

@zh-hant

2010年論文

@zh-hk

2010年論文

@zh-mo

2010年論文

@zh-tw

2010年论文

@wuu

2010年论文

@zh

2010年论文

@zh-cn

name

Hereditary diffuse leukoenceph ...... oelectron microscopic studies.

@en

Hereditary diffuse leukoenceph ...... oelectron microscopic studies.

@nl

type

Item

label

Hereditary diffuse leukoenceph ...... oelectron microscopic studies.

@en

Hereditary diffuse leukoenceph ...... oelectron microscopic studies.

@nl

prefLabel

Hereditary diffuse leukoenceph ...... oelectron microscopic studies.

@en

Hereditary diffuse leukoenceph ...... oelectron microscopic studies.

@nl

P1476

Hereditary diffuse leukoenceph ...... oelectron microscopic studies.

@en

P2093

Dennis W Dickson

http://www.w3.org/2001/XMLSchema#string

Wen-Lang Lin

http://www.w3.org/2001/XMLSchema#string

P2860

The life and death of oligodendrocytes in vanishing white matter disease

Developmental and pathogenic mechanisms of basement membrane assembly

Subunits of the translation initiation factor eIF2B are mutant in leukoencephalopathy with vanishing white matter

Mutations in each of the five subunits of translation initiation factor eIF2B can cause leukoencephalopathy with vanishing white matter

Axonal transection in the lesions of multiple sclerosis

Adult onset leukodystrophy with neuroaxonal spheroids and pigmented glia: report of a family, historical perspective, and review of the literature.

Hereditary diffuse leucoencephalopathy with spheroids.

Filamentous tau in oligodendrocytes and astrocytes of transgenic mice expressing the human tau isoform with the P301L mutation.

Oligodendrocyte apoptosis and primary demyelination induced by local TNF/p55TNF receptor signaling in the central nervous system of transgenic mice: models for multiple sclerosis with primary oligodendrogliopathy.

Increased expression of fibronectin and the alpha 5 beta 1 integrin in angiogenic cerebral blood vessels of mice subject to hypobaric hypoxia.

P304

665-674

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Zbigniew K Wszolek

P577

2010-07-26T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

20830237

http://www.w3.org/2001/XMLSchema#string

P921

Hereditary diffuse leukoencephalopathy with spheroids

P932

2933386

http://www.w3.org/2001/XMLSchema#string

Hereditary diffuse leukoencephalopathy with spheroids: ultrastructural and immunoelectron microscopic studies.

about

P2860

P2860

Hereditary diffuse leukoencephalopathy with spheroids: ultrastructural and immunoelectron microscopic studies.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P433

P478

P50

P577

P698

P921

P932

P1433

P1476

P2093

P2860

P304

P31

P433

P478

P50

P577

P698

P921

P932