(Q33629324)

28 July 2017

title

Sex-linked recessive congenital ataxia (English)

1 reference

28 July 2017

Young ID

1

1 reference

28 July 2017

Moore JR

series ordinal

2

1 reference

28 July 2017

Tripp JH

series ordinal

3

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 September 1987

1 reference

Journal of Neurology, Neurosurgery and Psychiatry

28 July 2017

published in

1 reference

28 July 2017

volume

50

1 reference

28 July 2017

issue

9

1 reference

28 July 2017

page(s)

1230-1232

1 reference

2 Cases of cerebellar hypoplasia in the same family

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032362

Familial agenesis of the cerebellar vermis. A syndrome of episodic hyperpnea, abnormal eye movements, ataxia, and retardation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032362

Autosomal recessive non-progressive ataxia with an early childhood debut

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032362

Autosomal recessive congenital cerebellar hypoplasia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032362

Congenital hydrocephalus and cerebellar agenesis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032362

A spinocerebellar degeneration with X-linked inheritance

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032362

Early familial cerebellar degeneration; report of 3 cases in one family.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032362

Evaluation of familial biochemically determined mental retardation in children, with special reference to aminoaciduria.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032362

Symmetrical hypogenesis of the cerebellum

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/3668574

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The Dysequilibrium Syndrome – A genetic study

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/3668574

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Unusual form of cerebellar ataxia with sex-linked inheritance

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/3668574

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JNNP.50.9.1230

1 reference

28 July 2017

1 reference

28 July 2017

1 reference