(Q36907553)

English

Muscular Dystrophy Surveillance Tracking and Research Network (MD STARnet): case definition in surveillance for childhood-onset Duchenne/Becker muscular dystrophy

scientific article published on September 2010

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Muscular Dystrophy Surveillance Tracking and Research Network (MD STARnet): case definition in surveillance for childhood-onset Duchenne/Becker muscular dystrophy (English)

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

muscular dystrophy

1 reference

based on heuristic

inferred from title

12

object named as

Paul A Romitti

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Katherine Mathews

object named as

Katherine D Mathews

1

0 references

author name string

Chris Cunniff

2

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Jiji R Kantamneni

3

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Emma Ciafaloni

4

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Timothy Miller

5

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Dennis Matthews

6

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Valerie Cwik

7

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Charlotte Druschel

8

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Lisa Miller

9

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

F John Meaney

10

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

John Sladky

11

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

publication date

1 September 2010

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Journal of Child Neurology

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

25

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

9

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

1098-1102

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Delayed diagnosis in duchenne muscular dystrophy: data from the Muscular Dystrophy Surveillance, Tracking, and Research Network (MD STARnet).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3674568

29 September 2017

The muscular Dystrophy Surveillance Tracking and Research Network (MD STARnet): surveillance methodology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3674568

29 September 2017

Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3674568

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3674568

29 September 2017

Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3674568

29 September 2017

Prevalence of Duchenne/Becker muscular dystrophy among males aged 5-24 years - four states, 2007.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3674568

27 June 2018

Duchenne muscular dystrophy: deficiency of dystrophin at the muscle cell surface

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3674568

27 June 2018

Mutation analysis in a population-based cohort of boys with Duchenne or Becker muscular dystrophy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3674568

4 September 2018

LGMD2I presenting with a characteristic Duchenne or Becker muscular dystrophy phenotype.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3674568

4 September 2018

Diagnosis of Duchenne dystrophy by enhanced detection of small mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/20817884

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Improved molecular diagnosis of dystrophinopathies in an unselected clinical cohort

1 reference

https://pubmed.ncbi.nlm.nih.gov/20817884

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnostic criteria for Duchenne and Becker muscular dystrophy and myotonic dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/20817884

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1177/0883073810371001

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

ResearchGate publication ID

0 references

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