Structural and immunocytochemical features of olivopontocerebellar atrophy caused by the spinocerebellar ataxia type 1 (SCA-1) mutation define a unique phenotype (Q71043039)

From Wikidata

Jump to navigation Jump to search

scientific article published on 01 January 1995

Language	Label	Description	Also known as
English	Structural and immunocytochemical features of olivopontocerebellar atrophy caused by the spinocerebellar ataxia type 1 (SCA-1) mutation define a unique phenotype	scientific article published on 01 January 1995

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8615077%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

Structural and immunocytochemical features of olivopontocerebellar atrophy caused by the spinocerebellar ataxia type 1 (SCA-1) mutation define a unique phenotype (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8615077%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

spinocerebellar ataxia type 1

1 reference

based on heuristic

inferred from title

olivopontocerebellar atrophy

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

author name string

Y Robitaille

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8615077%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

L Schut

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8615077%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

S J Kish

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8615077%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

publication date

1 January 1995

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8615077%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

Acta Neuropathologica

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8615077%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

90

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8615077%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8615077%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

572-581

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8615077%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

On an autosomal dominant form of retinal-cerebellar degeneration: an autopsy study of five patients in one family

1 reference

https://pubmed.ncbi.nlm.nih.gov/8615077

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Linkage study of hereditary spinocerebellar ataxia, and probable correlation for the loci to the disease phenotypes]

1 reference

https://pubmed.ncbi.nlm.nih.gov/8615077

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glial cytoplasmic inclusions in the CNS of patients with multiple system atrophy (striatonigral degeneration, olivopontocerebellar atrophy and Shy-Drager syndrome).

1 reference

https://pubmed.ncbi.nlm.nih.gov/8615077

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The olivopontocerebellar atrophies: a review

1 reference

https://pubmed.ncbi.nlm.nih.gov/8615077

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Epidemiology and clinical aspects of Machado-Joseph disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8615077

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Confirmation of the SCA-2 locus as an alternative locus for dominantly inherited spinocerebellar ataxias and refinement of the candidate region

1 reference

https://pubmed.ncbi.nlm.nih.gov/8615077

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The gene for Machado-Joseph disease maps to human chromosome 14q

1 reference

https://pubmed.ncbi.nlm.nih.gov/8615077

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[An autopsied case of type 2 Machado-Joseph's disease or spino-pontine degeneration]

1 reference

https://pubmed.ncbi.nlm.nih.gov/8615077

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal dominant cerebellar ataxia: clinical analysis of 263 patients from a homogeneous population in Holguín, Cuba

1 reference

https://pubmed.ncbi.nlm.nih.gov/8615077

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Olivopontocerebellar atrophy. A review of 117 cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/8615077

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal dominant cerebellar ataxia with retinal degeneration: clinical, neuropathologic, and genetic analysis of a large kindred

1 reference

https://pubmed.ncbi.nlm.nih.gov/8615077

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dominantly inherited olivopontocerebellar atrophy from eastern Cuba. Clinical, neuropathological, and biochemical findings.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8615077

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1

1 reference

https://pubmed.ncbi.nlm.nih.gov/8615077

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Study on argyrophilic inclusions of multisystem atrophy (Oppenheimer)

1 reference

https://pubmed.ncbi.nlm.nih.gov/8615077

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mapping of mutation causing Friedreich's ataxia to human chromosome 9

1 reference

https://pubmed.ncbi.nlm.nih.gov/8615077

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neurofibrillary axonal swellings and amyotrophic lateral sclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/8615077

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The distribution of oligodendroglial inclusions in multiple system atrophy and its relevance to clinical symptomatology

1 reference

https://pubmed.ncbi.nlm.nih.gov/8615077

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Neuropathological study of autosomal dominant ataxia linked to loci on chromosome 6p (SCA 1)]

1 reference

https://pubmed.ncbi.nlm.nih.gov/8615077

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal-dominant dentatorubropallidoluysian atrophy in the United Kingdom

1 reference

https://pubmed.ncbi.nlm.nih.gov/8615077

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Selective delayed alternation deficits in dominantly inherited olivopontocerebellar atrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8615077

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oligodendroglial and neuronal inclusions in multiple system atrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8615077

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8615077

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spinocerebellar degenerations in Japan: a nationwide epidemiological and clinical study

1 reference

https://pubmed.ncbi.nlm.nih.gov/8615077

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary ataxia: a pathologic study of five cases of common ancestry

1 reference

https://pubmed.ncbi.nlm.nih.gov/8615077

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cerebral cortical pathology of sporadic olivopontocerebellar atrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8615077

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cognitive deficits in olivopontocerebellar atrophy: implications for the cholinergic hypothesis of Alzheimer's dementia

1 reference

https://pubmed.ncbi.nlm.nih.gov/8615077

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An autopsied case of dentatorubropallidoluysian atrophy with atypical pathological features

1 reference

https://pubmed.ncbi.nlm.nih.gov/8615077

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8615077

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00318569

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8615077%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8615077%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q71043039&oldid=2234263154"