X-linked disorders with cerebellar dysgenesis

Por Zanni, Ginevra, Bertini, Enrico S
Publicado em 2011

The Potential of iPSCs for the Treatment of Premature Aging Disorders

Por Compagnucci, Claudia, Bertini, Enrico
Publicado no Int J Mol Sci (2017)

Mitochondria fingerprint longevity in iPSCs

Por Masotti, Andrea, Bertini, Enrico, Compagnucci, Claudia
Publicado no Oncotarget (2015)

Microtubule Dysfunction: A Common Feature of Neurodegenerative Diseases

Por Sferra, Antonella, Nicita, Francesco, Bertini, Enrico
Publicado no Int J Mol Sci (2020)

Renal involvement in mitochondrial cytopathies

Por Emma, Francesco, Bertini, Enrico, Salviati, Leonardo, Montini, Giovanni
Publicado em 2011

A new phenotypic variant in cleidocranial dysplasia (CCD) associated with mutation c.391C>T of the RUNX2 gene

Por Callea, Michele, Fattori, Fabiana, Yavuz, Izzet, Bertini, Enrico
Publicado no BMJ Case Rep (2012)

The NRF2 Signaling Network Defines Clinical Biomarkers and Therapeutic Opportunity in Friedreich’s Ataxia

Por La Rosa, Piergiorgio, Bertini, Enrico Silvio, Piemonte, Fiorella
Publicado no Int J Mol Sci (2020)

Congenital Muscular Dystrophies: A Brief Review

Por Bertini, Enrico, D'Amico, Adele, Gualandi, Francesca, Petrini, Stefania
Publicado em 2011

Spinal muscular atrophy

Por D'Amico, Adele, Mercuri, Eugenio, Tiziano, Francesco D, Bertini, Enrico
Publicado em 2011

The cytoskeletal arrangements necessary to neurogenesis

Por Compagnucci, Claudia, Piemonte, Fiorella, Sferra, Antonella, Piermarini, Emanuela, Bertini, Enrico
Publicado no Oncotarget (2016)

Oxidative Stress in DNA Repeat Expansion Disorders: A Focus on NRF2 Signaling Involvement

Por La Rosa, Piergiorgio, Petrillo, Sara, Bertini, Enrico Silvio, Piemonte, Fiorella
Publicado no Biomolecules (2020)

Mitochondrial Abnormalities in Induced Pluripotent Stem Cells-Derived Motor Neurons from Patients with Riboflavin Transporter Deficiency

Por Colasuonno, Fiorella, Bertini, Enrico, Tartaglia, Marco, Compagnucci, Claudia, Moreno, Sandra
Publicado no Antioxidants (Basel) (2020)

Friedreich ataxia in COVID-19 time: current impact and future possibilities

Por Schirinzi, Tommaso, Sancesario, Andrea, Castelli, Enrico, Bertini, Enrico, Vasco, Gessica
Publicado no Cerebellum Ataxias (2021)

Aged iPSCs display an uncommon mitochondrial appearance and fail to undergo in vitro neurogenesis

Por Masotti, Andrea, Celluzzi, Antonella, Petrini, Stefania, Bertini, Enrico, Zanni, Ginevra, Compagnucci, Claudia
Publicado no Aging (Albany NY) (2014)

Targeting NRF2 for the Treatment of Friedreich’s Ataxia: A Comparison among Drugs

Por Petrillo, Sara, D’Amico, Jessica, La Rosa, Piergiorgio, Bertini, Enrico Silvio, Piemonte, Fiorella
Publicado no Int J Mol Sci (2019)

Ferroptosis in Friedreich’s Ataxia: A Metal-Induced Neurodegenerative Disease

Por La Rosa, Piergiorgio, Petrillo, Sara, Fiorenza, Maria Teresa, Bertini, Enrico Silvio, Piemonte, Fiorella
Publicado no Biomolecules (2020)

Mitochondrial Dynamics: Molecular Mechanisms, Related Primary Mitochondrial Disorders and Therapeutic Approaches

Por Di Nottia, Michela, Verrigni, Daniela, Torraco, Alessandra, Rizza, Teresa, Bertini, Enrico, Carrozzo, Rosalba
Publicado no Genes (Basel) (2021)

ASTROCYTES: EMERGING STARS IN LEUKODYSTROPHY PATHOGENESIS

Por Lanciotti, Angela, Brignone, Maria Stefania, Bertini, Enrico, Petrucci, Tamara C., Aloisi, Francesca, Ambrosini, Elena
Publicado em 2013

P016. Congenital ataxia, hemiplegic migraine due to a novel mutation of CACNA1A: a case report

Por Frusciante, Roberto, Capuano, Alessandro, Travaglini, Lorena, Zanni, Ginevra, Vigevano, Federico, Bertini, Enrico, Valeriani, Massimiliano
Publicado no J Headache Pain (2015)

miRNAs as serum biomarkers for Duchenne muscular dystrophy

Por Cacchiarelli, Davide, Legnini, Ivano, Martone, Julie, Cazzella, Valentina, D'Amico, Adele, Bertini, Enrico, Bozzoni, Irene
Publicado em 2011