Multicentric Study on the Diagnostic of Neuromuscular Diseases in Children with High Creatinine Phos...
Multicentric Study on the Diagnostic of Neuromuscular Diseases in Children with High Creatinine Phosphokinase Levels
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Publisher
Switzerland: MDPI AG
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Language
English
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Publisher
Switzerland: MDPI AG
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Contents
Neuromuscular diseases (NMDs) are rare, predominantly hereditary, with progressive course disorders. Furthermore, diagnosis can be delayed by years after symptoms emerge, resulting in missed opportunities for modifying disease progression, specific therapeutic approaches, and counseling. Some NMDs have high levels of creatine phosphokinase (CK). Th...
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Full title
Multicentric Study on the Diagnostic of Neuromuscular Diseases in Children with High Creatinine Phosphokinase Levels
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TN_cdi_doaj_primary_oai_doaj_org_article_7f44914b6dc64b1fa01ee1e9ca2387b4
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_7f44914b6dc64b1fa01ee1e9ca2387b4
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ISSN
2227-9067
E-ISSN
2227-9067
DOI
10.3390/children11121462
