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Hereditary spastic paraplegia
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
12432827
retrieved
5 August 2017
review article
1 reference
stated in
Europe PubMed Central
title
Hereditary spastic paraplegia.
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
12432827
retrieved
5 August 2017
author name string
John K Fink
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
12432827
retrieved
5 August 2017
publication date
1 August 2002
1 reference
stated in
Europe PubMed Central
PubMed ID
12432827
retrieved
5 August 2017
published in
Neurologic Clinics
1 reference
stated in
Europe PubMed Central
PubMed ID
12432827
retrieved
5 August 2017
volume
20
1 reference
stated in
Europe PubMed Central
PubMed ID
12432827
retrieved
5 August 2017
issue
3
1 reference
stated in
Europe PubMed Central
PubMed ID
12432827
retrieved
5 August 2017
page(s)
711-726
1 reference
stated in
Europe PubMed Central
PubMed ID
12432827
retrieved
5 August 2017
cites work
Hereditary spastic paraplegia: advances in genetic research. Hereditary Spastic Paraplegia Working group
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Crossref
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7 January 2021
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Hereditary spastic paraplegia: genetic heterogeneity and genotype-phenotype correlation
1 reference
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Crossref
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7 January 2021
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Mapping of a complicated familial spastic paraplegia to locus SPG4 on chromosome 2p.
1 reference
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Crossref
reference URL
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7 January 2021
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Association of late onset spastic paraparesis and dementia: probably an autosomal dominant form of complicated paraplegia
1 reference
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Crossref
reference URL
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7 January 2021
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inferred from DOI database lookup
Autosomal dominant hereditary spastic paraparesis with cognitive loss linked to chromosome 2p.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
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7 January 2021
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Linkage of AD HSP and cognitive impairment to chromosome 2p: haplotype and phenotype analysis indicates variable expression and low or delayed penetrance
1 reference
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Crossref
reference URL
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7 January 2021
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Subclinical cognitive impairment in autosomal dominant "pure" hereditary spastic paraplegia
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7 January 2021
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Multisystem involvement of the central nervous system in Strümpell's disease. A neurophysiological and neuropsychological study
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Crossref
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Progressive spastic paraparesis: hereditary spastic paraplegia and its relation to primary and amyotrophic lateral sclerosis
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
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7 January 2021
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The Troyer syndrome. A recessive form of spastic paraplegia with distal muscle wasting
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
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7 January 2021
based on heuristic
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Troyer Syndrome: report of the first "non-Amish" sibship and review
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
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7 January 2021
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Familial spastic paraplegia with amyotrophy of the hands
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
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7 January 2021
based on heuristic
inferred from DOI database lookup
Familial spastic paraplegia with neuropathy and poikiloderma. A new syndrome?
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
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7 January 2021
based on heuristic
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Autosomal recessive hereditary sensory neuropathy with spastic paraplegia
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
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7 January 2021
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Hereditary sensory neuropathy with spastic paraplegia
1 reference
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Crossref
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7 January 2021
based on heuristic
inferred from DOI database lookup
Familial spastic paraplegia, peroneal neuropathy, and crural hypopigmentation: a new neurocutaneous syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
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7 January 2021
based on heuristic
inferred from DOI database lookup
A new locus for autosomal recessive spastic paraplegia associated with mental retardation and distal motor neuropathy, SPG14, maps to chromosome 3q27-q28.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
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7 January 2021
based on heuristic
inferred from DOI database lookup
Familial spastic paraplegia with peroneal amyotrophy. A family with hypersensitivity to pyrexia
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
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7 January 2021
based on heuristic
inferred from DOI database lookup
Familial spastic paraplegia with distal muscle wasting in the Old Order Amish; atypical Troyer syndrome or “new” syndrome*
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
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7 January 2021
based on heuristic
inferred from DOI database lookup
The phenotype of "pure" autosomal dominant spastic paraplegia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
MRI of autosomal dominant pure spastic paraplegia.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
X-linked pure familial spastic paraparesis. Characterization of a large kindred with magnetic resonance imaging studies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic localization of a new locus for recessive familial spastic paraparesis to 15q13-15.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Electrophysiological studies in familial spastic paraplegia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A study of posterior column function in familial spastic paraplegia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A quantitative study of sensory function in hereditary spastic paraplegia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Sensory neuropathy in hereditary spastic paraplegia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Motor and somatosensory evoked potentials in hereditary spastic paraplegia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Visual, auditory and somatosensory pathway involvement in hereditary cerebellar ataxia, Friedreich's ataxia and familial spastic paraplegia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Strümpell's familial spastic paraplegia: an electrophysiological demonstration of selective central distal axonopathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hereditary motor and sensory neuropathies and hereditary spastic paraplegia: a magnetic stimulation study.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
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7 January 2021
based on heuristic
inferred from DOI database lookup
Hereditary "pure" spastic paraplegia: a study of nine families
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Central motor conduction studies in hereditary spastic paraplegia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Phenotypic analysis of autosomal dominant hereditary spastic paraplegia linked to chromosome 8q.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dystonia with marked diurnal variation associated with biopterin deficiency
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autosomal dominant juvenile amyotrophic lateral sclerosis.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial spastic paraparesis: an adrenoleukodystrophy phenotype?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
X-linked adrenoleukodystrophy presenting as neurologically pure familial spastic paraparesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Strümpell's familial spastic paraplegia: genetics and neuropathology
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hereditary spastic paraplegias
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Linkage of a new locus for autosomal dominant familial spastic paraplegia to chromosome 2p
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markers
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A new locus for autosomal dominant pure spastic paraplegia, on chromosome 2q24-q34.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Novel locus for autosomal dominant hereditary spastic paraplegia, on chromosome 8q
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A locus for autosomal dominant "pure" hereditary spastic paraplegia maps to chromosome 19q13
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic mapping to 10q23.3-q24.2, in a large Italian pedigree, of a new syndrome showing bilateral cataracts, gastroesophageal reflux, and spastic paraparesis with amyotrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The Silver syndrome variant of hereditary spastic paraplegia maps to chromosome 11q12-q14, with evidence for genetic heterogeneity within this subtype
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A new locus for autosomal dominant "pure" hereditary spastic paraplegia mapping to chromosome 12q13, and evidence for further genetic heterogeneity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14q
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Quality assessment of whole genome mapping data in the refined familial spastic paraplegia interval on chromosome 14q.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular cloning of microtubule-associated protein 1 (MAP1A) and microtubule-associated protein 5 (MAP1B): identification of distinct genes and their differential expression in developing brain.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
SPG15, a new locus for autosomal recessive complicated HSP on chromosome 14q.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
X-linked spastic paraplegia (SPG1), MASA syndrome and X-linked hydrocephalus result from mutations in the L1 gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The rumpshaker mutation in spastic paraplegia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
X-linked spastic paraplegia and Pelizaeus-Merzbacher disease are allelic disorders at the proteolipid protein locus
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Refined genetic mapping and proteolipid protein mutation analysis in X-linked pure hereditary spastic paraplegia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Evidence of a third locus in X-linked recessive spastic paraplegia.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Segregation of a pure form of spastic paraplegia and NOR insertion into Xq11.2.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Phenotype of autosomal dominant spastic paraplegia linked to chromosome 2.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical and pathologic findings in hereditary spastic paraparesis with spastin mutation.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Intrafamilial variability in hereditary spastic paraplegia associated with an SPG4 gene mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Novel mutations in spastin gene and absence of correlation with age at onset of symptoms
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation analysis of the spastin gene (SPG4) in patients with hereditary spastic paraparesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genomic structure and expression analysis of the spastic paraplegia gene, SPG7
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Different mutations in the same codon of the proteolipid protein gene, PLP, may help in correlating genotype with phenotype in Pelizaeus-Merzbacher disease/X-linked spastic paraplegia (PMD/SPG2).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Assignment of the gene for myelin proteolipid protein to the X chromosome: implications for X-linked myelin disorders
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pelizaeus-Merzbacher disease: identification of Xq22 proteolipid-protein duplications and characterization of breakpoints by interphase FISH.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
X linked complicated spastic paraplegia, MASA syndrome, and X linked hydrocephalus owing to congenital stenosis of the aqueduct of Sylvius: variable expression of the same mutation at Xq28
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial spastic paraparesis syndrome associated with HTLV-I infection.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Effect of intrathecal baclofen on gait control in human hereditary spastic paraparesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Intrathecal baclofen for intractable cerebral spasticity: a prospective placebo-controlled, double-blind study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2802%2900007-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0733-8619(02)00007-5
1 reference
stated in
Europe PubMed Central
PubMed ID
12432827
retrieved
5 August 2017
PubMed ID
12432827
1 reference
stated in
Europe PubMed Central
PubMed ID
12432827
retrieved
5 August 2017
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