Mitochondrial Medicine in the COVID-19 Era

por Daniele Orsucci
Publicado 2021

Mutational Analysis and mtDNA Haplogroup Characterization in Three Serbian Cases of Mitochondrial Encephalomyopathies and Literature Review

por Phepy G. A. Dawod, Jasna Jancic, Ana Marjanovic, Marija Brankovic, Milena Jankovic, Janko Samardzic, Ayman Gamil Anwar Dawod, Ivana Novakovic, Fayda I. Abdel Motaleb, Vladimir Radlovic, Vladimir S. Kostic, Dejan Nikolic
Publicado 2021

Point Prevalence and Associated Factors of Hip Displacement in Pediatric Patients With Mitochondrial Disease

por Sungmin Kim, Young-Mock Lee, Kun-Bo Park, Minsu Lee, Hoon Park
Publicado 2021

Mutations in SURF1 are important genetic causes of Leigh syndrome in Slovak patients

por Danis Daniel, Brennerova Katarina, Skopkova Martina, Kurdiova Timea, Ukropec Jozef, Stanik Juraj, Kolnikova Miriam, Gasperikova Daniela
Publicado 2018