(Q33586962)

28 July 2017

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1084423

20 August 2022

1 reference

https://api.crossref.org/works/10.1136/JMG.13.3.217

6 September 2023

author name string

M. Zatz

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1084423

20 August 2022

C. Penha-Serrano

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1084423

20 August 2022

P. A. Otto

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1084423

20 August 2022

language of work or name

English

0 references

publication date

1 June 1976

1 reference

full work available at URL

28 July 2017

http://jmg.bmjjournals.com/cgi/content/abstract/13/3/217

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%3A1084423

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/1084423/pdf/?tool=EBI

20 August 2022

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%3A1084423

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/1084423/?tool=EBI

20 August 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1084423

https://europepmc.org/articles/PMC1013396

20 August 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1084423

https://europepmc.org/articles/PMC1013396?pdf=render

20 August 2022

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%3A1084423

https://syndication.highwire.org/content/doi/10.1136/jmg.13.3.217

20 August 2022

1 reference

https://api.crossref.org/works/10.1136/JMG.13.3.217

Journal of Medical Genetics

6 September 2023

published in

1 reference

28 July 2017

13

1 reference

28 July 2017

217-222

1 reference

28 July 2017

3

1 reference

Hereditary spastic paraplegia with amyotrophy and pes cavus

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013396

A sex-linked recessive form of spastic paraplegia

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013396

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013396

Sequential tests for the detection of linkage

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013396

Distribution and heredity of erythrocyte G6PD activity and electrophoretic variants among different racial groups at Sao Paulo, Brazil

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013396

Genetic linkage between the loci for colour blindness and Duchenne type muscular dystrophy.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013396

New linkage data for the X-linked types of muscular dystrophy and G6PD variants, colour blindness, and Xg blood groups

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013396

Linkage between the loci for benign (Becker-type) X-borne muscular dystrophy and deutan colour blindness

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013396

Hereditary cerebral palsy; a preliminary report

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013396

DIAGNOSTIC AND PROGNOSTIC SIGNIFICANCE OF SERUM ENZYMES. II. NEUROLOGIC DISEASES OTHER THAN MUSCULAR DYSTROPHY

31 October 2018

1 reference

12 December 2020

SERUM CREATINE PHOSPHOKINASE (CPK) ACTIVITY IN DISORDERS OF HEART AND SKELETAL MUSCLE

1 reference

12 December 2020

Hereditary spastic paraplegia. A family with ten injured

1 reference

12 December 2020

Hereditary spastic paraplegia

1 reference

12 December 2020

Hereditary (familial) spastic paraplegia

1 reference

12 December 2020

[Genetic study of familial spasmodic paraplegia]

1 reference

12 December 2020

[Spasmodic familial paraplegia of the Strumpell-Lorrain type.]

1 reference

12 December 2020

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

1 reference

12 December 2020

The linkage relations of the loci for benign (Becker type) X-borne muscular dystrophy, colour blindness and the Xg blood groups

1 reference

12 December 2020

X-linked hereditary spastic paraplegia

1 reference

12 December 2020

A malignant form of neurogenic muscular atrophy in adults, with dominant inheritance

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.13.3.217

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1084423

20 August 2022

1 reference

28 July 2017

1 reference