Comprehensive clinical and genetic work-up of patients carrying single mtDNA deletions is warranted

অনুরূপ উপাদানগুলি

• Mitochondrial Ophthalmoplegia Is Not Only due to mtDNA Deletions
  অনুযায়ী: Finsterer, Josef
  প্রকাশিত: (2019)
• Broad Phenotypic Heterogeneity and Multisystem Involvement in Single mtDNA Deletion-associated Pearson Syndrome
  অনুযায়ী: Finsterer, Josef, অন্যান্য
  প্রকাশিত: (2018)
• Unmasking fibromyalgia as a mitochondrial disorder requires search for more than a single variant or single mtDNA deletions
  অনুযায়ী: Finsterer, Josef
  প্রকাশিত: (2020)
• Comprehensive work-up is warranted for patients with severe COVID-19 and muscle weakness including respiratory muscles
  অনুযায়ী: Finsterer, Josef
  প্রকাশিত: (2021)
• Comment on “CPEO and Mitochondrial Myopathy in a Patient with DGUOK Compound Heterozygous Pathogenetic Variant and mtDNA Multiple Deletions”
  অনুযায়ী: Finsterer, Josef
  প্রকাশিত: (2020)