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Research outputs

Pure myopathy with enlarged mitochondria associated to a new mutation in MTND2 gene [2017]

Zanolini, Alice; Potic, Ana D; Carrara, Franco; Lamantea, Eleonora; Diodato, Daria; Blasevich, Flavia; Marchet, Silvia; Marina, Mora; Pallotti, Francesco; Morandi, Lucia;

Zeviani, Massimo; Lamperti, Costanza;

Glycogen storage disease type IX: Long-term follow-up of 52 patients from three European countries [2026]

Magner, Martin; ...; Petkovic-Ramadza, Danijela; ...; Ilic, Nikola A; ...; (broj, koautora 18)

Untreated PKU patients without intellectual disability: SHANK gene family as a candidate modifier [2021]

Klaassen, Kristel ; Đorđević, M.; Skakić, Anita ; Kecman, B.; Drmanac, R.; Pavlović, Sonja ; Stojiljković, Maja

Pure myopathy with enlarged mitochondria associated to a new mutation in MTND2 gene [2017]

Glycogen storage disease type IX: Long-term follow-up of 52 patients from three European countries [2026]

Untreated PKU patients without intellectual disability: SHANK gene family as a candidate modifier [2021]

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