Limb-girdle and congenital muscular dystrophies: current diagnostics, management, and emerging technologies (Q33837536)

29 July 2017

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title

Limb-girdle and congenital muscular dystrophies: current diagnostics, management, and emerging technologies (English)

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29 July 2017

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Carolina Tesi Rocha

1

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29 July 2017

Eric P Hoffman

series ordinal

2

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29 July 2017

language of work or name

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1 July 2010

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Current Neurology and Neuroscience Reports

29 July 2017

published in

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29 July 2017

volume

10

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29 July 2017

issue

4

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29 July 2017

page(s)

267-276

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Diagnosis and management of Duchenne muscular dystrophy, part 2: implementation of multidisciplinary care

29 July 2017

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4 July 2018

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Congenital muscular dystrophy. Part II: a review of pathogenesis and therapeutic perspectives

4 July 2018

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Congenital muscular dystrophy. Part I: a review of phenotypical and diagnostic aspects

4 July 2018

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4 July 2018

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Muscular dystrophies due to glycosylation defects

4 July 2018

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Cyclosporine A treatment for Ullrich congenital muscular dystrophy: a cellular study of mitochondrial dysfunction and its rescue

4 July 2018

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Inhibition of extracellular signal-regulated kinase signaling to prevent cardiomyopathy caused by mutation in the gene encoding A-type lamins.

4 July 2018

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Dysferlin deficiency shows compensatory induction of Rab27A/Slp2a that may contribute to inflammatory onset.

4 July 2018

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Dysferlin deficiency enhances monocyte phagocytosis: a model for the inflammatory onset of limb-girdle muscular dystrophy 2B.

4 July 2018

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PTC124 targets genetic disorders caused by nonsense mutations

4 July 2018

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Phenotypic clustering of lamin A/C mutations in neuromuscular patients.

4 July 2018

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Fukutin gene mutations in steroid-responsive limb girdle muscular dystrophy

4 July 2018

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Nuclear envelope dystrophies show a transcriptional fingerprint suggesting disruption of Rb-MyoD pathways in muscle regeneration

4 July 2018

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Loss of emerin at the nuclear envelope disrupts the Rb1/E2F and MyoD pathways during muscle regeneration.

4 July 2018

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Dystroglycan: important player in skeletal muscle and beyond

4 July 2018

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117th ENMC workshop: ventilatory support in congenital neuromuscular disorders -- congenital myopathies, congenital muscular dystrophies, congenital myotonic dystrophy and SMA (II) 4-6 April 2003, Naarden, The Netherlands

4 July 2018

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Glycosylation defects: a new mechanism for muscular dystrophy?

4 July 2018

1 reference

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108th ENMC International Workshop, 3rd Workshop of the MYO-CLUSTER project: EUROMEN, 7th International Emery-Dreifuss Muscular Dystrophy (EDMD) Workshop, 13-15 September 2002, Naarden, The Netherlands

4 July 2018

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Mutations of the selenoprotein N gene, which is implicated in rigid spine muscular dystrophy, cause the classical phenotype of multiminicore disease: reassessing the nosology of early-onset myopathies

4 July 2018

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Tibial muscular dystrophy is a titinopathy caused by mutations in TTN, the gene encoding the giant skeletal-muscle protein titin

4 July 2018

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Myotilin is mutated in limb girdle muscular dystrophy 1A

4 July 2018

1 reference

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4 July 2018

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Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy

4 July 2018

1 reference

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Homozygous alpha-sarcoglycan mutation in two siblings: one asymptomatic and one steroid-responsive mild limb-girdle muscular dystrophy patient

4 July 2018

1 reference

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Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4079458

Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4079458

Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4079458

Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4079458

Beta-sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex

4 July 2018

1 reference

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β–sarcoglycan: characterization and role in limb–girdle muscular dystrophy linked to 4q12

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4079458

Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophy

4 July 2018

1 reference

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Efficacy of systemic morpholino exon-skipping in Duchenne dystrophy dogs

4 July 2018

1 reference

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Caveolin-3 T78M and T78K missense mutations lead to different phenotypes in vivo and in vitro

29 October 2018

1 reference

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Heart transplantation in patients with Emery-Dreifuss muscular dystrophy: case reports

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4079458

Distal anterior compartment myopathy with early ankle contractures

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4079458

Reliable surrogate outcome measures in multicenter clinical trials of Duchenne muscular dystrophy.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4079458

Phenotypic spectrum associated with mutations in the fukutin-related protein gene

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4079458

82nd ENMC international workshop, 5th international Emery-Dreifuss muscular dystrophy (EDMD) workshop, 1st Workshop of the MYO-CLUSTER project EUROMEN (European muscle envelope nucleopathies), 15-16 September 2000, Naarden, The Netherlands.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4079458

Calpainopathy-a survey of mutations and polymorphisms

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4079458

Towards harmonisation of outcome measures for DMD and SMA within TREAT-NMD; Report of three expert workshops: TREAT-NMD/ENMC Workshop on outcome measures, 12th–13th May 2007, Naarden, The Netherlands; TREAT-NMD Workshop on outcome measures in exper

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4079458

Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C

29 October 2018

1 reference

12 December 2020

Dysferlin mutations in LGMD2B, Miyoshi myopathy, and atypical dysferlinopathies

1 reference

12 December 2020

Inflammation and response to steroid treatment in limb-girdle muscular dystrophy 2I

1 reference

12 December 2020

EMG and nerve conduction studies in children with congenital muscular dystrophy

1 reference

12 December 2020

Calpain III mutation analysis of a heterogeneous limb-girdle muscular dystrophy population

1 reference

12 December 2020

10.1007/S11910-010-0119-1

Identifiers

DOI

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Dimensions Publication ID

29 July 2017

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29 July 2017

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