(Q36621524)

29 June 2018

title

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

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29 June 2018

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2

Paul A Romitti

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29 June 2018

Katherine D Mathews

5

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author name string

Lisa A Miller

1

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29 June 2018

Christopher Cunniff

3

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29 June 2018

Charlotte Druschel

4

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29 June 2018

F John Meaney

6

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29 June 2018

Dennis Matthews

7

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29 June 2018

Jiji Kantamneni

8

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29 June 2018

Zhen-Fang Feng

9

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29 June 2018

Nancy Zemblidge

10

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29 June 2018

Timothy M Miller

11

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29 June 2018

Jennifer Andrews

12

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29 June 2018

Deborah Fox

13

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29 June 2018

Emma Ciafaloni

14

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29 June 2018

Shree Pandya

15

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29 June 2018

April Montgomery

16

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29 June 2018

Aileen Kenneson

17

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29 June 2018

publication date

1 November 2006

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29 June 2018

Birth Defects Research Part A: Clinical and Molecular Teratology

published in

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29 June 2018

volume

76

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29 June 2018

issue

11

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29 June 2018

page(s)

793-797

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29 June 2018

Public health monitoring of developmental disabilities with a focus on the autism spectrum disorders

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5863910

Delayed diagnosis of Duchenne muscular dystrophy

2 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5863910

Experience with screening newborns for Duchenne muscular dystrophy in Wales

2 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5863910

Neonatal screening for muscular dystrophy. Consensus recommendation of the 14th workshop sponsored by the European Neuromuscular Center (ENMC).

2 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5863910

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

2 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5863910

Three years' experience with neonatal screening for Duchenne/Becker muscular dystrophy: gene analysis, gene expression, and phenotype prediction

2 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5863910

A multiple source methodology for the surveillance of fetal alcohol syndrome--The Fetal Alcohol Syndrome Surveillance Network (FASSNet).

2 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5863910

Genetic epidemiology of Duchenne and Becker muscular dystrophy in Slovenia

20 September 2018

1 reference

12 December 2020

Neonatal screening for Duchenne muscular dystrophy: a novel semiquantitative application of the bioluminescence test for creatine kinase in a pilot national program in Cyprus

1 reference

12 December 2020

The incidence of Duchenne muscular dystrophy in eastern Austria. The controversy regarding CK screening

1 reference

12 December 2020

Duchenne and Becker muscular dystrophy prevalence in South Africa and molecular findings in 128 persons affected

1 reference

12 December 2020

Decreased incidence of Duchenne muscular dystrophy in western Japan 1956-1980

1 reference

12 December 2020

Prevalence of Neuromuscular Diseases in Chinese Children: A Study in Southern China

1 reference

12 December 2020

Reappraisal of the incidence rate of Duchenne and Becker muscular dystrophies on the basis of molecular diagnosis

1 reference

12 December 2020

Neuromuscular disorders in childhood: a descriptive epidemiological study from western Sweden

1 reference

12 December 2020

Identifiers

DOI

10.1002/BDRA.20279

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29 June 2018

PMC publication ID

5863910

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29 June 2018

PubMed publication ID

17036307

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29 June 2018