Consequences of epigenetic derepression in facioscapulohumeral muscular dystrophy-Reference-Cited by-同舟云学术

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Consequences of epigenetic derepression in facioscapulohumeral muscular dystrophy

Published:2020-03-04 Issue:6 Volume:97 Page:799-814
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Greco Anna¹²,Goossens Remko³^ORCID,Engelen Baziel¹^ORCID,Maarel Silvère M.³^ORCID

Affiliation:

1. Department of Neurology, Donders Institute for Brain, Cognition and BehaviourRadboud University Medical Center Nijmegen The Netherlands

2. Department of Experimental Internal MedicineRadboud University Medical Center Nijmegen The Netherlands

3. Department of Human GeneticsLeiden University Medical Center Leiden The Netherlands

Funder

National Institute of Neurological Disorders and Stroke

Prinses Beatrix Spierfonds

Stichting Spieren voor Spieren

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cge.13726

Reference205 articles.

1. Population-based incidence and prevalence of facioscapulohumeral dystrophy

2. 171st ENMC International Workshop: Standards of care and management of facioscapulohumeral muscular dystrophy

3. Early onset as a marker for disease severity in facioscapulohumeral muscular dystrophy

4. Coats syndrome in facioscapulohumeral dystrophy type 1: Frequency and D4Z4 contraction size

5. Evidence-based guideline summary: Evaluation, diagnosis, and management of facioscapulohumeral muscular dystrophy

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1. Safety and efficacy of losmapimod in facioscapulohumeral muscular dystrophy (ReDUX4): a randomised, double-blind, placebo-controlled phase 2b trial;The Lancet Neurology;2024-05

2. Best practice guidelines on genetic diagnostics of facioscapulohumeral muscular dystrophy: Update of the 2012 guidelines;Clinical Genetics;2024-04-29

3. IL-6 and TNF are Potential Inflammatory Biomarkers in Facioscapulohumeral Muscular Dystrophy;Journal of Neuromuscular Diseases;2024-03-05

4. Muscle eosinophilia is a hallmark of chronic disease in facioscapulohumeral muscular dystrophy;Human Molecular Genetics;2024-02-10

5. FSHD muscle shows perturbation in fibroadipogenic progenitor cells, mitochondrial function and alternative splicing independently of inflammation;Human Molecular Genetics;2023-10-19

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