How do we diagnose Miyoshi Muscular Dystrophy in the absence of symptoms?-Reference-Cited by-同舟云学术

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How do we diagnose Miyoshi Muscular Dystrophy in the absence of symptoms?

Published:2024-07 Issue: Volume: Page:
ISSN:0953-6205
Container-title:European Journal of Internal Medicine
language:en
Short-container-title:European Journal of Internal Medicine

Author:

Sönmez Özge,Kimyon Uğur^ORCID,Çopur Mehmet^ORCID,Ataş İbrahim,Bavunoğlu Işıl

Publisher

Elsevier BV

Reference10 articles.

1. Elevated Liver Enzymes in Asymptomatic Patients – What Should I Do?;Malakouti;J Clin Transl Hepatol,2017

2. Incidental hypertransaminasemia in children: Potential delay in diagnosis of muscle disease;Ghobrial;Gaz Egypt Paediatr Assoc,2018

3. Value of muscle enzyme measurement in evaluating different neuromuscular diseases;Zhang;Clin Chim Acta,2012

4. Serum transaminases are frequently elevated at time of diagnosis of idiopathic inflammatory myopathy and normalize with creatine kinase;Mathur;J Clin Rheumatol,2014

5. Miyoshi Muscular Dystrophy Type 1 with Mutated DYSF Gene Misdiagnosed as Becker Muscular Dystrophy: A Case Report and Literature Review;Park;Genes (Basel),2023

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