(Q36317445)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9408105%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

title

Two families with autosomal recessive spastic paraplegia, pigmented maculopathy, and dementia (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9408105%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

0 references

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9408105%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

author name string

S Webb

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9408105%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

V Patterson

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9408105%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

language of work or name

English

0 references

publication date

1 November 1997

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9408105%20AND%20SRC:MED&resulttype=core&format=json

Journal of Neurology, Neurosurgery and Psychiatry

8 November 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9408105%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

volume

63

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9408105%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

page(s)

628-632

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9408105%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9408105%20AND%20SRC:MED&resulttype=core&format=json

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

8 November 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169835

CAMDEX. A standardised instrument for the diagnosis of mental disorder in the elderly with special reference to the early detection of dementia.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169835

Homocarnosinosis. 2. A familial metabolic disorder associated with spastic paraplegia, progressive mental deficiency, and retinal pigmentation

29 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169835

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

29 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169835

Familial spastic paraplegia with retinal degeneration

22 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9408105

12 December 2020

inferred from PubMed ID database lookup

Fleck retina in Kjellin's syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9408105

12 December 2020

inferred from PubMed ID database lookup

[Cerebellar and spastic heredodegeneration with macular degeneration]

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9408105

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1136/JNNP.63.5.628

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9408105%20AND%20SRC:MED&resulttype=core&format=json

release_jzpjiobobrhmjmzwjsb5oul52m

8 November 2019

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/jzpjiobobrhmjmzwjsb5oul52m

24 November 2022

mapped directly with Wikidata item

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9408105%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

1 reference