(Q36803129)

English

Characteristics of Japanese Duchenne and Becker muscular dystrophy patients in a novel Japanese national registry of muscular dystrophy (Remudy).

scientific article published on 19 April 2013

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Characteristics of Japanese Duchenne and Becker muscular dystrophy patients in a novel Japanese national registry of muscular dystrophy (Remudy). (English)

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Becker muscular dystrophy

1 reference

based on heuristic

inferred from title

object named as

En Kimura

2

0 references

object named as

Ichizo Nishino

8

0 references

Madoka Mori-Yoshimura

3

object named as

Madoka Mori-Yoshimura

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Harumasa Nakamura

1

object named as

Harumasa Nakamura

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Shin'ichi Takeda

9

object named as

Shin'ichi Takeda

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Hirofumi Komaki

4

object named as

Hirofumi Komaki

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

author name string

Yu Matsuda

5

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Kanako Goto

6

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Yukiko K Hayashi

7

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Mitsuru Kawai

10

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

publication date

19 April 2013

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Orphanet Journal of Rare Diseases

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

8

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

60

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Systemic administration of PRO051 in Duchenne's muscular dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3639029

29 September 2017

Molecular treatments in Duchenne muscular dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3639029

29 September 2017

PTC124 targets genetic disorders caused by nonsense mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3639029

29 September 2017

Entries in the Leiden Duchenne muscular dystrophy mutation database: an overview of mutation types and paradoxical cases that confirm the reading-frame rule

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3639029

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3639029

29 September 2017

Advances in Duchenne muscular dystrophy gene therapy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3639029

29 September 2017

Mild and severe muscular dystrophy associated with deletions in Xp21 of the human X chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3639029

29 September 2017

Duchenne muscular dystrophy: survival by cardio-respiratory interventions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3639029

5 September 2018

Mutation spectrum of the dystrophin gene in 442 Duchenne/Becker muscular dystrophy cases from one Japanese referral center.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3639029

5 September 2018

Patient Registries and Trial Readiness in Myotonic Dystrophy--TREAT-NMD/Marigold International Workshop Report.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3639029

5 September 2018

[Database for patients with Duchenne muscular dystrophy]

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3639029

5 September 2018

The muscular dystrophies

1 reference

https://pubmed.ncbi.nlm.nih.gov/23601510

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

China's first rare-disease registry is under development

1 reference

https://pubmed.ncbi.nlm.nih.gov/23601510

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Local dystrophin restoration with antisense oligonucleotide PRO051

1 reference

https://pubmed.ncbi.nlm.nih.gov/23601510

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/1750-1172-8-60

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Dimensions Publication ID

0 references

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

ResearchGate publication ID

0 references

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