(Q46688548)

24 December 2017

title

Spinal cord magnetic resonance imaging in autosomal dominant hereditary spastic paraplegia (English)

1 reference

24 December 2017

author name string

P Hedera

1

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24 December 2017

O P Eldevik

2

1 reference

24 December 2017

P Maly

3

1 reference

24 December 2017

S Rainier

4

1 reference

24 December 2017

J K Fink

5

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24 December 2017

publication date

6 September 2005

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24 December 2017

published in

Neuroradiology

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24 December 2017

volume

47

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24 December 2017

issue

10

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24 December 2017

page(s)

730-734

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24 December 2017

https://scigraph.springernature.com/pub.10.1007/s00234-005-1415-3

exact match

0 references

cites work

Hereditary spastic paraplegia: advances in genetic research. Hereditary Spastic Paraplegia Working group

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00234-005-1415-3

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

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00234-005-1415-3

Novel mutations in spastin gene and absence of correlation with age at onset of symptoms

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00234-005-1415-3

Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia

21 January 2018

1 reference

12 December 2020

The hereditary spastic paraplegias: nine genes and counting

1 reference

12 December 2020

Novel locus for autosomal dominant hereditary spastic paraplegia, on chromosome 8q

1 reference

12 December 2020

Linkage of autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum to chromosome 15A13-15.

1 reference

12 December 2020

The phenotype of "pure" autosomal dominant spastic paraplegia

1 reference

12 December 2020

Neurological and neuroradiological progression in hereditary spastic paraplegia with a thin corpus callosum.

1 reference

12 December 2020

NIPA1 Gene Mutations Cause Autosomal Dominant Hereditary Spastic Paraplegia (SPG6)

1 reference

12 December 2020

A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10)

1 reference

12 December 2020

Familial spastic paraplegia-clinical and pathologic studies in a large kindred

1 reference

12 December 2020

Hereditary (familial) spastic paraplegia

1 reference

12 December 2020

Hereditary spastic paraplegia SPG13 is associated with a mutation in the gene encoding the mitochondrial chaperonin Hsp60

1 reference

12 December 2020

Phenotypic analysis of autosomal dominant hereditary spastic paraplegia linked to chromosome 8q.

1 reference

12 December 2020

Autosomal dominant, familial spastic paraplegia, type I: clinical and genetic analysis of a large North American family

1 reference

12 December 2020

Multilocus linkage analysis in humans: detection of linkage and estimation of recombination

1 reference

12 December 2020

MRI of autosomal dominant pure spastic paraplegia.

1 reference

12 December 2020

Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia

1 reference

12 December 2020

Analysis of cross-sectional area measurements of the corpus callosum adjusted for brain size in male and female subjects from childhood to adulthood

1 reference

12 December 2020

Autosomal dominant pure spastic paraplegia: a clinical, paraclinical, and genetic study

1 reference

12 December 2020

10.1007/S00234-005-1415-3

Identifiers

DOI

1 reference

24 December 2017

PubMed ID

16143870

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24 December 2017