(Q57970899)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17452950%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

title

[Familial spastic paraplegia with severe amyotrophy of the hands. (Silver syndrome?)] (English)

1 reference

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29 December 2019

5

1 reference

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29 December 2019

Chokri Mhiri

7

1 reference

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29 December 2019

author name string

I Feki

1

1 reference

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29 December 2019

M I Miladi

2

1 reference

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29 December 2019

N Elleuch

3

1 reference

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29 December 2019

A Boukhris

4

1 reference

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29 December 2019

A Brice

6

1 reference

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29 December 2019

publication date

1 April 2007

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29 December 2019

1 reference

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29 December 2019

volume

163

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29 December 2019

issue

4

1 reference

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29 December 2019

page(s)

476-479

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Hereditary motor system diseases (chronic juvenile amyotrophic lateral sclerosis). Conditions combining a bilateral pyramidal syndrome with limb and bulbar amyotrophy

29 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2807%2990424-5

7 January 2021

Autosomal recessive paraparesis with amyotrophy of the hands and feet

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2807%2990424-5

7 January 2021

Amyotrophy of the hands and pyramidal features of predominantly the legs segregating within one large family

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2807%2990424-5

7 January 2021

Advances in the hereditary spastic paraplegias

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2807%2990424-5

7 January 2021

The phenotype of motor neuropathies associated with BSCL2 mutations is broader than Silver syndrome and distal HMN type V.

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2807%2990424-5

7 January 2021

The Silver syndrome variant of hereditary spastic paraplegia maps to chromosome 11q12-q14, with evidence for genetic heterogeneity within this subtype

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2807%2990424-5

7 January 2021

The hereditary spastic paraplegias.

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2807%2990424-5

7 January 2021

BSCL2 mutations in two Dutch families with overlapping Silver syndrome-distal hereditary motor neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2807%2990424-5

7 January 2021

Distal amyotrophy of predominantly the upper limbs with pyramidal features in a large kinship

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2807%2990424-5

7 January 2021

A clinical, genetic and candidate gene study of Silver syndrome, a complicated form of hereditary spastic paraplegia

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2807%2990424-5

7 January 2021

Familial spastic paraplegia with amyotrophy of the hands

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2807%2990424-5

7 January 2021

10.1016/S0035-3787(07)90424-5

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17452950%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

1 reference