GRANATA, TIZIANA

GRANATA, TIZIANA  

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Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
Neuromuscular syndrome associated with the 3291T→C mutation of mitochondrial DNA: A second case 2000 Granata T.Mora M.Zeviani M. + NEUROMUSCULAR DISORDERS - -
Epileptic phenotypes associated with mitochondrial disorders 2001 Granata T.Zeviani M. + NEUROLOGY - -
VARS2 and TARS2 Mutations in Patients with Mitochondrial Encephalomyopathies 2014 Granata T.Zeviani M.Ghezzi D. + HUMAN MUTATION - -
Symptomatic and presumed symptomatic focal epilepsies in childhood: An observational, prospective multicentre study 2016 VECCHI, MARILENADE CARLO, DEBORALUNARDI, GIADABONIVER, CLEMENTINAGRANATA, TIZIANADARRA, FRANCESCAPERISSINOTTO, EGLEFRANCIONE, STEFANO + EPILEPSIA - -
Clinical and genetic features of paroxysmal kinesigenic dyskinesia in Italian patients 2016 Zeviani M.Granata T. + EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY - -
Encephalopathies with intracranial calcification in children: Clinical and genetic characterization 2018 Carecchio M.Granata T.CEREDA, CINZIAValente M. L.Fusco C.BERTINI, ELENA SOFIA + ORPHANET JOURNAL OF RARE DISEASES - -
Gait abnormalities in people with Dravet syndrome: A cross-sectional multi-center study 2019 Di Marco R.Bellon G.Granata T.Darra F.Sawacha Z.Scarpa B.Masiero S.Del Felice A. + EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY - -