(Q57243932)

4

0 references

Bruno Dallapiccola

object named as

Bruno Dallapiccola

7

0 references

Viviana Caputo

3

object named as

Viviana Caputo

0 references

author name string

Francesco Brancati

2

0 references

Clarice Patrono

5

0 references

Danilo Costanti

Hereditary "pure" spastic paraplegia: a clinical and genetic study of 22 families

6

0 references

publication date

23 May 2002

0 references

published in

Annals of Neurology

0 references

volume

51

0 references

issue

6

0 references

page(s)

681-685

0 references

cites work

1 reference

Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14q

21 January 2018

1 reference

Autosomal dominant familial spastic paraplegia: tight linkage to chromosome 15q

21 January 2018

1 reference

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

21 January 2018

1 reference

A new locus for autosomal dominant "pure" hereditary spastic paraplegia mapping to chromosome 12q13, and evidence for further genetic heterogeneity

21 January 2018

1 reference

A locus for autosomal dominant "pure" hereditary spastic paraplegia maps to chromosome 19q13

21 January 2018

1 reference

A new locus for autosomal dominant pure spastic paraplegia, on chromosome 2q24-q34.

21 January 2018

1 reference

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

21 January 2018

1 reference

Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia

21 January 2018

1 reference

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

21 January 2018

1 reference

Linkage of the gene for an autosomal dominant form of juvenile amyotrophic lateral sclerosis to chromosome 9q34.

21 January 2018

1 reference

Advances in hereditary spastic paraplegia.

21 January 2018

1 reference

The phenotype of "pure" autosomal dominant spastic paraplegia

21 January 2018

1 reference

Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markers

21 January 2018

1 reference

Developmental trends of sleep-disordered breathing in Prader-Willi syndrome: the role of obesity

21 January 2018

1 reference

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

21 January 2018

1 reference

Autosomal dominant spastic paraplegia: refined SPG8 locus and additional genetic heterogeneity

21 January 2018

1 reference