Hip flexion weakness is associated with impaired mobility in oculopharyngeal muscular dystrophy: a retrospective study with implications for trial design (Q35164440)

From Wikidata

Jump to navigation Jump to search

scientific article

Language	Label	Description	Also known as
English	Hip flexion weakness is associated with impaired mobility in oculopharyngeal muscular dystrophy: a retrospective study with implications for trial design	scientific article

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Hip flexion weakness is associated with impaired mobility in oculopharyngeal muscular dystrophy: a retrospective study with implications for trial design (English)

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

oculopharyngeal muscular dystrophy

1 reference

based on heuristic

inferred from title

Leslie Morrison

4

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25500011%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

author name string

Sarah Youssof

1

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25500011%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

Ronald Schrader

2

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25500011%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

David Bear

3

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25500011%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

language of work or name

1 reference

based on heuristic

inferred from title

publication date

20 November 2014

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Neuromuscular Disorders

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25500011%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

25

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25500011%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

3

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25500011%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

238-246

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25500011%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

Lithium chloride attenuates cell death in oculopharyngeal muscular dystrophy by perturbing Wnt/β-catenin pathway.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4355309

13 July 2018

The poly(A)-binding protein nuclear 1 suppresses alternative cleavage and polyadenylation sites.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4355309

13 July 2018

Antiprion drugs 6-aminophenanthridine and guanabenz reduce PABPN1 toxicity and aggregation in oculopharyngeal muscular dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4355309

13 July 2018

Prevalence of mild cognitive impairment is higher in men. The Mayo Clinic Study of Aging

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4355309

13 July 2018

Widespread shortening of 3'UTRs by alternative cleavage and polyadenylation activates oncogenes in cancer cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4355309

13 July 2018

The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement: guidelines for reporting observational studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4355309

13 July 2018

The development of a comorbidity index with physical function as the outcome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4355309

13 July 2018

Use of biomarkers and surrogate endpoints in drug development and regulatory decision making: criteria, validation, strategies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4355309

13 July 2018

Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4355309

13 July 2018

Epidemiology and inheritance of oculopharyngeal muscular dystrophy in Israel

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4355309

13 July 2018

Epidemiology of peripheral neuropathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4355309

13 July 2018

Neuropathic findings in oculopharyngeal muscular dystrophy. A report of seven cases and a review of the literature

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4355309

13 July 2018

Clinical features of oculopharyngeal muscular dystrophy among Bukhara Jews

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4355309

13 July 2018

Oculopharyngeal muscular dystrophy. A census of French families and genealogic study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4355309

13 July 2018

Cognitive impairment and reduced life span of oculopharyngeal muscular dystrophy homozygotes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4355309

27 September 2018

Two different PABPN1 expanded alleles in a Mexican population with oculopharyngeal muscular dystrophy arising from independent founder effects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4355309

27 September 2018

Inclusion body myositis functional rating scale: A reliable and valid measure of disease severity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4355309

27 September 2018

Challenges in drug development for muscle disease: a stakeholders' meeting

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4355309

27 September 2018

Oculopharyngeal muscular dystrophy with limb girdle weakness as major complaint

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4355309

27 September 2018

The ALSFRS-R: a revised ALS functional rating scale that incorporates assessments of respiratory function. BDNF ALS Study Group (Phase III).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4355309

27 September 2018

191st ENMC International Workshop: Recent advances in oculopharyngeal muscular dystrophy research: From bench to bedside 8-10 June 2012, Naarden, The Netherlands

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4355309

25 October 2018

Oculopharyngeal muscular dystrophy. A familial disease of late life characterized by dysphagia and progressive ptosis of the evelids

1 reference

https://pubmed.ncbi.nlm.nih.gov/25500011

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Long-term results of cricopharyngeal myotomy in oculopharyngeal muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/25500011

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

GCG genetic expansions in Italian patients with oculopharyngeal muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/25500011

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

GCG repeats and phenotype in oculopharyngeal muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/25500011

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oculopharyngeal muscular dystrophy in Hispanic New Mexicans

1 reference

https://pubmed.ncbi.nlm.nih.gov/25500011

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recent studies on oculopharyngeal muscular dystrophy in Québec

1 reference

https://pubmed.ncbi.nlm.nih.gov/25500011

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oculopharyngeal muscular dystrophy in France

1 reference

https://pubmed.ncbi.nlm.nih.gov/25500011

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oculopharyngeal muscular dystrophy in Uruguay

1 reference

https://pubmed.ncbi.nlm.nih.gov/25500011

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical characterization and blepharoptosis surgery outcomes in Hispanic New Mexicans with oculopharyngeal muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/25500011

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Involvement of the peripheral nerves in oculopharyngeal muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/25500011

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Executive functions are impaired in heterozygote patients with oculopharyngeal muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/25500011

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genotype and phenotype study of 34 Spanish patients diagnosed with oculopharyngeal muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/25500011

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ocular, bulbar, limb, and cardiopulmonary involvement in oculopharyngeal muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/25500011

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/J.NMD.2014.11.010

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25500011%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25500011%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25500011%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

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=Q35164440&oldid=1861564757"