(Q27011968)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26155064%20AND%20SRC:MED&resulttype=core&format=json

18 February 2020

review article

1 reference

title

Clinical features of patients with dystrophinopathy sharing the 45-55 exon deletion of DMD gene (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26155064%20AND%20SRC:MED&resulttype=core&format=json

18 February 2020

11

Gerardo Nigro

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26155064%20AND%20SRC:MED&resulttype=core&format=json

18 February 2020

12

Luisa Politano

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26155064%20AND%20SRC:MED&resulttype=core&format=json

18 February 2020

10

Alberto Palladino

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26155064%20AND%20SRC:MED&resulttype=core&format=json

18 February 2020

author name string

Antonella Taglia

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26155064%20AND%20SRC:MED&resulttype=core&format=json

18 February 2020

Roberta Petillo

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26155064%20AND%20SRC:MED&resulttype=core&format=json

18 February 2020

Paola D'Ambrosio

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26155064%20AND%20SRC:MED&resulttype=core&format=json

18 February 2020

Esther Picillo

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26155064%20AND%20SRC:MED&resulttype=core&format=json

18 February 2020

Annalaura Torella

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26155064%20AND%20SRC:MED&resulttype=core&format=json

18 February 2020

Chiara Orsini

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26155064%20AND%20SRC:MED&resulttype=core&format=json

18 February 2020

Manuela Ergoli

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26155064%20AND%20SRC:MED&resulttype=core&format=json

18 February 2020

Marianna Scutifero

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26155064%20AND%20SRC:MED&resulttype=core&format=json

18 February 2020

Luigia Passamano

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26155064%20AND%20SRC:MED&resulttype=core&format=json

18 February 2020

language of work or name

1 reference

1 May 2015

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26155064%20AND%20SRC:MED&resulttype=core&format=json

18 February 2020

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26155064%20AND%20SRC:MED&resulttype=core&format=json

18 February 2020

volume

34

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26155064%20AND%20SRC:MED&resulttype=core&format=json

18 February 2020

issue

1

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26155064%20AND%20SRC:MED&resulttype=core&format=json

18 February 2020

page(s)

9-13

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26155064%20AND%20SRC:MED&resulttype=core&format=json

Syntrophin binds to an alternatively spliced exon of dystrophin

18 February 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4478772

Identification and characterization of the dystrophin anchoring site on beta-dystroglycan

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4478772

The structure of the N-terminal actin-binding domain of human dystrophin and how mutations in this domain may cause Duchenne or Becker muscular dystrophy

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4478772

The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4478772

Identification of alpha-syntrophin binding to syntrophin triplet, dystrophin, and utrophin

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4478772

Dystrophin quantification and clinical correlations in Becker muscular dystrophy: implications for clinical trials

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4478772

Dystrophin: more than just the sum of its parts

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4478772

Analysis of dystrophin deletion mutations predicts age of cardiomyopathy onset in becker muscular dystrophy

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4478772

Recognition and elimination of nonsense mRNA.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4478772

Characteristics and outcomes of cardiomyopathy in children with Duchenne or Becker muscular dystrophy: a comparative study from the Pediatric Cardiomyopathy Registry

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4478772

Follow-up of three patients with a large in-frame deletion of exons 45-55 in the Duchenne muscular dystrophy (DMD) gene

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4478772

Dystrophin and mutations: one gene, several proteins, multiple phenotypes

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4478772

Molecular pathophysiology of myofiber injury in deficiencies of the dystrophin-glycoprotein complex

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4478772

Function and genetics of dystrophin and dystrophin-related proteins in muscle

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4478772

The dystrophin-glycoprotein complex, cellular signaling, and the regulation of cell survival in the muscular dystrophies

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4478772

The limb-girdle muscular dystrophies-multiple genes, multiple mechanisms

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4478772

Dystrophin and its isoforms

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4478772

Searching for the 1 in 2,400,000: a review of dystrophin gene point mutations

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4478772

Frameshift deletions of exons 3-7 and revertant fibers in Duchenne muscular dystrophy: mechanisms of dystrophin production

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4478772

Dystrophin and utrophin: the missing links!

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4478772

Exploring the molecular basis for variability among patients with Becker muscular dystrophy: dystrophin gene and protein studies

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4478772

Preservation of the C-terminus of dystrophin molecule in the skeletal muscle from Becker muscular dystrophy

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4478772

Characterization of deletion breakpoints in patients with dystrophinopathy carrying a deletion of exons 45-55 of the Duchenne muscular dystrophy (DMD) gene

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4478772

A preliminary randomized study of growth hormone administration in Becker and Duchenne muscular dystrophies

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4478772

Is the value of QT dispersion a valid method to foresee the risk of sudden death? A study in Becker patients.

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4478772

Dystrophies and heart disease.

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4478772

An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4478772

Familial X-linked myalgia and cramps: a nonprogressive myopathy associated with a deletion in the dystrophin gene

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4478772

Association of dystrophin and an integral membrane glycoprotein.

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4478772

Asymptomatic Becker muscular dystrophy in a family with a multiexon deletion

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4478772

Large in-frame deletions of the rod-shaped domain of the dystrophin gene resulting in severe phenotype.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4478772

Elevation of serum creatine kinase as the only manifestation of an intragenic deletion of the dystrophin gene in three unrelated families

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4478772

Clinical variability in Becker muscular dystrophy. Genetic, biochemical and immunohistochemical correlates

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4478772

Evaluation of the cardiomyopathy in becker muscular dystrophy

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4478772

Mutation of dystrophin gene and cardiomyopathy

28 November 2018

1 reference

12 December 2020

Cardiac dysfunction with Becker muscular dystrophy

1 reference

12 December 2020

Prognostic factors in mild dystrophinopathies

1 reference

12 December 2020

Myocardial involvement is very frequent among patients affected with subclinical Becker's muscular dystrophy

1 reference

12 December 2020

Left ventricular function and perfusion in Becker's muscular dystrophy

1 reference

12 December 2020

Autonomic nervous system imbalance and left ventricular systolic dysfunction as potential candidates for arrhythmogenesis in Becker muscular dystrophy

1 reference

12 December 2020

Circular dystrophin RNAs consisting of exons that were skipped by alternative splicing

1 reference

12 December 2020

Multiexon skipping leading to an artificial DMD protein lacking amino acids from exons 45 through 55 could rescue up to 63% of patients with Duchenne muscular dystrophy

1 reference

12 December 2020

Genotype and phenotype characterization in a large dystrophinopathic cohort with extended follow-up

1 reference

12 December 2020

Becker muscular dystrophy severity is linked to the structure of dystrophin

1 reference

12 December 2020

Pulsed Doppler tissue imaging in dystrophinopathic cardiomyopathy

1 reference

12 December 2020

Identifiers

1429332

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

2 references

1429332

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26155064%20AND%20SRC:MED&resulttype=core&format=json

18 February 2020

PubMed publication ID

26155064

2 references

Consolidated OpenCitations Corpus – April 2017

1429332