Novel crystalloid oligodendrogliopathy in hereditary spastic paraplegia (Q48627762)

13 February 2018

title

Novel crystalloid oligodendrogliopathy in hereditary spastic paraplegia (English)

1 reference

13 February 2018

author

Herbert Budka

8

1 reference

13 February 2018

Gabor G. Kovacs

9

1 reference

13 February 2018

Adelheid Wöhrer

object named as

Adelheid Woehrer

1

0 references

Claudia Stöllberger

4

object named as

Claudia Stöllberger

1 reference

13 February 2018

author name string

Lajos Laszlo

2

1 reference

13 February 2018

Josef Finsterer

3

1 reference

13 February 2018

Julia Furtner

5

1 reference

13 February 2018

Walter Rinner

6

1 reference

13 February 2018

Kinga Molnar

7

1 reference

13 February 2018

publication date

7 March 2012

1 reference

13 February 2018

published in

Acta Neuropathologica

1 reference

13 February 2018

volume

124

1 reference

13 February 2018

issue

4

1 reference

13 February 2018

page(s)

583-591

1 reference

13 February 2018

Microtubular crystals in mammalian cells

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-0965-9

The neuropathology of hereditary spastic paraparesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-0965-9

Characterization of tubulin in mouse brain myelin

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-0965-9

Crystals in brain and meninges in primary hyperoxaluria and oxalosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-0965-9

Central nervous system crystal-storing histiocytosis: neuroimaging, neuropathology, and literature review

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-0965-9

Protein coding of neurodegenerative dementias: the neuropathological basis of biomarker diagnostics

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-0965-9

Autopsy case of hereditary spastic paraplegia with thin corpus callosum showing severe gliosis in the cerebral white matter.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-0965-9

Dementia in SPG4 hereditary spastic paraplegia: clinical, genetic, and neuropathologic evidence

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-0965-9

Autopsy case of autosomal recessive hereditary spastic paraplegia with reference to the muscular pathology

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-0965-9

Hereditary spastic paraplegia: clinical features and pathogenetic mechanisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-0965-9

Myopathy with tubulin-reactive inclusions in two cats.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-0965-9

Myopathy with tubulin-reactive crystalline inclusions

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-0965-9

Primary progressive multiple sclerosis as a phenotype of a PLP1 gene mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-0965-9

Clinical and pathologic findings in hereditary spastic paraparesis with spastin mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-0965-9

Hereditary spastic paraplegia with frontal lobe dysfunction: a clinicopathologic study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-0965-9

10.1007/S00401-012-0965-9

21 January 2018

Identifiers

DOI

1 reference

13 February 2018

1 reference

13 February 2018