(Q37015214)

17 August 2017

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

1 reference

17 August 2017

A. E. Harding

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7310405

28 April 2024

language of work or name

English

0 references

publication date

1 October 1981

1 reference

PMC publication ID

491171

full work available at URL

17 August 2017

https://jnnp.bmj.com/content/jnnp/44/10/871.full.pdf

file format

Portable Document Format

online access status

open access

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7310405

https://europepmc.org/articles/PMC491171

28 April 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7310405

https://europepmc.org/articles/PMC491171?pdf=render

28 April 2024

file format

Portable Document Format

online access status

open access

content deliverer

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7310405

https://syndication.highwire.org/content/doi/10.1136/jnnp.44.10.871

28 April 2024

1 reference

https://api.crossref.org/works/10.1136/JNNP.44.10.871

Journal of Neurology, Neurosurgery and Psychiatry

28 April 2024

published in

1 reference

17 August 2017

44

1 reference

17 August 2017

10

1 reference

17 August 2017

871-883

1 reference

Hereditary spastic paraplegia with amyotrophy and pes cavus

17 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=491171

A sex-linked recessive form of spastic paraplegia

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=491171

Sporadic and familial varieties of tonic seizures

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=491171

The range of conduction velocity in normal motor nerve fibers to the small muscles of the hand and foot

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=491171

Oligophrenia in combination with congenital ichthyosis and spastic disorders; a clinical and genetic study

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=491171

Further scoring types in sequential linkage tests, with a critical review of autosomal and partial sex linkage in man.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=491171

Hereditary (familial) spastic paraplegia; further clinical and pathologic observations.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=491171

The estimation of intraclass correlation in the analysis of family data

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=491171

Spinal somatosensory evoked potentials in hereditary spastic paraplegia

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=491171

The Troyer syndrome. A recessive form of spastic paraplegia with distal muscle wasting

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=491171

Strümpell's familial spastic paraplegia: genetics and neuropathology

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=491171

X-linked recessive type of pure spastic paraplegia in a large pedigree: absence of detectable linkage with Xg

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=491171

Occurrence of familial spastic paraplegia in only one of monozygous twins

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=491171

Electrophysiological studies in familial spastic paraplegia

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=491171

Strumpell's pure familial spastic paraplegia: case study and review of the literature

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=491171

The late form of pure familial spastic paraplegia

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=491171

Neurotoxicity of halogenated hydroxyquinolines: clinical analysis of cases reported outside Japan

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=491171

Hereditary sensory neuropathy with spastic paraplegia

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=491171

Spastic paraplegia of unknown origin. A follow-up of 32 patients

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=491171

Familial Spastic Paraplegia with Amyotrophy, Oligophrenia, and Central Retinal Degeneration

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=491171

A FAMILY WITH HEREDITARY SPASTIC ATAXIA: AN INVESTIGATION INTO THE EXISTENCE OF THE SO CALLED "FORMES FRUSTES"

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=491171

Familial spastic spinal paralysis

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=491171

Spastic paraparesis associated with optic atrophy in monozygotic twins

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=491171

Familial spastic paraplegia with amyotrophy of the hands

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=491171

Sex-linked spastic paraplegia

20 October 2018

1 reference

12 December 2020

Sphincter involvement in hereditary spastic paraplegia

1 reference

12 December 2020

X-linked hereditary spastic paraplegia

1 reference

12 December 2020

Two kindreds with a sex-linked recessive form of spastic paraplegia

1 reference

12 December 2020

Hereditary spastic paraplegia; report of a family with associated extrapyramidal signs

1 reference

12 December 2020

Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. II. Neurologic, genetic, and electrophysiologic findings in various neuronal degenerations

1 reference

12 December 2020

A case of familial Strumpell-Lorrain disease

1 reference

12 December 2020

Hereditary (familial) spastic paraplegia

1 reference

12 December 2020

Hereditary spastic paraplegia

1 reference

12 December 2020

Spastic paraplegia of middle age; a clinicopathological study

1 reference

12 December 2020

[Spasmodic, familial paraplegia. IV. The Fev... family; a very late form histopathology.]

1 reference

12 December 2020

The sib-sib age of onset correlation among individuals suffering from a hereditary syndrome produced by more than one gene

series ordinal

30

1 reference

https://api.crossref.org/works/10.1136/JNNP.44.10.871

An Essay towards solving a Problem in the Doctrine of Chances

28 April 2024

series ordinal

31

1 reference

https://api.crossref.org/works/10.1136/JNNP.44.10.871

PRIMARY SPASTIC PARALYSIS AND PSEUDOHYPERTROPHIC PARALYSIS IN DIFFERENT MEMBERS OF THE SAME FAMILY, WITH PROBABLE HEREDITY IN BOTH

28 April 2024

series ordinal

45

1 reference

https://api.crossref.org/works/10.1136/JNNP.44.10.871

28 April 2024

Identifiers

1 reference

17 August 2017

1 reference

PMC publication ID

491171

17 August 2017

1 reference

PMC publication ID

491171