(Q81329635)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18500496%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

title

A novel KIF5A/SPG10 mutation in spastic paraplegia associated with axonal neuropathy (English)

1 reference

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7 January 2020

1 reference

2

1 reference

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7 January 2020

Marcella Masciullo

6

1 reference

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7 January 2020

Mariarosa A.B. Melone

9

1 reference

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7 January 2020

Antonio Federico

10

1 reference

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7 January 2020

Filippo Maria Santorelli

12

object named as

Filippo M Santorelli

1 reference

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7 January 2020

1

Alessandra Tessa

1 reference

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7 January 2020

8

Carlo Casali

1 reference

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7 January 2020

7

M Teresa Dotti

1 reference

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7 January 2020

author name string

Maria Fulvia de Leva

3

1 reference

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7 January 2020

Anna Modoni

4

1 reference

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7 January 2020

Paola S Denora

5

1 reference

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7 January 2020

Alessandro Filla

11

1 reference

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7 January 2020

publication date

2 June 2008

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7 January 2020

1 reference

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7 January 2020

volume

255

1 reference

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7 January 2020

issue

7

1 reference

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7 January 2020

page(s)

1090-1092

1 reference

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https://scigraph.springernature.com/pub.10.1007/s00415-008-0840-8

7 January 2020

exact match

0 references

cites work

Exon deletions of SPG4 are a frequent cause of hereditary spastic paraplegia

1 reference

12 December 2020

Evidence of kinesin heavy chain (KIF5A) involvement in pure hereditary spastic paraplegia

1 reference

12 December 2020

Abnormal neurofilament transport caused by targeted disruption of neuronal kinesin heavy chain KIF5A.

1 reference

12 December 2020

Mutation in KIF5A can also cause adult-onset hereditary spastic paraplegia

1 reference

12 December 2020

NIPA1 (SPG6) mutations are a rare cause of autosomal dominant spastic paraplegia in Europe

1 reference

12 December 2020

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

1 reference

12 December 2020

Autosomal dominant hereditary spastic paraplegia: DHPLC-based mutation analysis of SPG4 reveals eleven novel mutations

1 reference

12 December 2020

A Missense Mutation in the Coiled-Coil Domain of the KIF5A Gene and Late-Onset Hereditary Spastic Paraplegia

1 reference

12 December 2020

SPG3A is the most frequent cause of hereditary spastic paraplegia with onset before age 10 years

1 reference

12 December 2020

Hereditary spastic paraplegia

1 reference

12 December 2020

Kinesin molecular motors: transport pathways, receptors, and human disease

1 reference

12 December 2020