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Francesca Meloni
Francesca Meloni
University of Parma
Biology
Genetics
Mutation
Mitochondrial disease
Diabetes mellitus
5
Papers
166
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Mutations of cytochrome c identified in patients with thrombocytopenia THC4 affect both apoptosis and cellular bioenergetics
2014
Biochimica et Biophysica Acta
Daniela De Rocco
Cristina Cerqua
Paola Goffrini
Giovanna Russo
Annalisa Pastore
Francesca Meloni
Elena Nicchia
Carlos T. Moraes
Alessandro Pecci
Leonardo Salviati
Anna Savoia
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Citations (55)
Recessive germline SDHA and SDHB mutations causing leukodystrophy and isolated mitochondrial complex II deficiency
2012
Journal of Medical Genetics
Charlotte L. Alston
James E. Davison
Francesca Meloni
van, der, Westhuizen, Fh
Langping He
Ht Hornig-Do
Andrew C. Peet
Paul Gissen
Paola Goffrini
Iliana Ferrero
Evangeline Wassmer
Robert McFarland
Robert W. Taylor
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Citations (86)
P4.60 Long-term survival of neonatal mitochondrial complex III deficiency associated with a novel BCS1L gene mutation
2010
Neuromuscular Disorders
Helen A. L. Tuppen
J. Fehmi
Birgit Czermin
Paola Goffrini
Francesca Meloni
Iliana Ferrero
Langping He
Emma L. Blakely
Robert McFarland
Rita Horvath
Douglass M. Turnbull
Robert W. Taylor
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Long-term survival of neonatal mitochondrial complex III deficiency associated with a novel BCS1L gene mutation
2010
Molecular Genetics and Metabolism
Helen A. L. Tuppen
Janev Fehmi
Birgit Czermin
Paola Goffrini
Francesca Meloni
Iliana Ferrero
Langping He
Emma L. Blakely
Robert McFarland
Rita Horvath
Douglass M. Turnbull
Robert W. Taylor
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Citations (25)
Yeast as a model of mitochondrial dysfunctions: neurodegenerative diseases and cancer.
2010
Claudia Donnini
Enrico Baruffini
Cristina Dallabona
Francesca Meloni
Elena Panizza
Jade Quartararo
Marco Tigano
Paola Goffrini
Tiziana Lodi
Iliana Ferrero
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