Phenotype may predict the clinical course of facioscapolohumeral muscular dystrophy-Reference-Cited by-同舟云学术

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Phenotype may predict the clinical course of facioscapolohumeral muscular dystrophy

Published:2019-04-04 Issue:6 Volume:59 Page:711-713
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle Nerve

Author:

Ricci Giulia¹²,Cammish Philip²,Siciliano Gabriele²,Tupler Rossella³,Lochmuller Hanns⁴,Evangelista Teresinha²

Affiliation:

1. John Walton Muscular Dystrophy Research CentreInstitute of Genetic Medicine, Newcastle University Newcastle upon Tyne United Kingdom

2. Department of Clinical and Experimental MedicineUniversity of Pisa Pisa Italy via Roma 67 56126

3. Department of Life SciencesUniversity of Modena and Reggio Emilia Modena Italy

4. Department of Neuropediatrics and Muscle Disorders, Medical Center–University of FreiburgFaculty of Medicine Freiburg Germany

Funder

Muscular Dystrophy UK

Medical Research Council

Rotary Foundation

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Neurology (clinical),Physiology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mus.26474

Reference13 articles.

1. Genetic characterization of a large, historically significant Utah kindred with facioscapulohumeral dystrophy

2. Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north-east Italian population sample

3. Population-based incidence and prevalence of facioscapulohumeral dystrophy

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

5. What's in a name? The clinical features of facioscapulohumeral muscular dystrophy

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1. A human pan-genomic analysis reconfigures the genetic and epigenetic make up of facioscapulohumeral muscular dystrophy;2023-06-20

2. Symptom onset and cellular pathology in facioscapulohumeral muscular dystrophy is accelerated by cigarette smoking;2023-05-24

3. Counseling and prenatal diagnosis in facioscapulohumeral muscular dystrophy: A retrospective study on a 13‐year multidisciplinary approach;Health Science Reports;2022-04-20

4. Pathomechanisms and biomarkers in facioscapulohumeral muscular dystrophy: roles of DUX4 and PAX7;EMBO Molecular Medicine;2021-06-21

5. Elucidation of the Genetic Cause in Dutch Limb Girdle Muscular Dystrophy Families: A 27-Year’s Journey;Journal of Neuromuscular Diseases;2021-03-02

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