All papers authored by Marco Spinazzi
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Charles-Antoine Assenmacher,
Jillian Verrelle,
Esha Banerjee,
Florence Manero,
Salim Khiati,
Anais Girona,
Guillermo Lopez-Lluch,
Placido Navas,
Marco Spinazzi
Mitochondrial defects caused by PARL deficiency lead to arrested spermatogenesis and ferroptosis
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Olivier Baris ,
Guy Lenaers ,
Pascal Reynier ,
Marco Spinazzi
Secondary coenzyme q deficiency in neurological disorders
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Patrick Savickas,
Lorna Omodho,
Marco Spinazzi ,
Enrico Radaelli
Spontaneous Incidental Brain Lesions in C57BL/6J Mice
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Enrico Radaelli,
Katrien Horré,
Amaia M. Arranz,
Natalia V. Gounko,
Patrizia Agostinis,
Teresa Mendes Maia,
Francis Impens ,
Vanessa Alexandra Morais,
Guillermo Lopez-Lluch ,
Lutgarde Serneels,
Placido Navas ,
Bart De Strooper
PARL deficiency in mouse causes Complex III defects, coenzyme Q depletion, and Leigh-like syndrome
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Maria Andrea Desbats,
Leonardo Salviati,
Aaron P. Russell,
Giovanni Miotto ,
Laura Tosatto,
Elena Pegoraro,
Gianni Sorarù,
Maria Pennuto,
Lodovica Vergani
Increased mitophagy in the skeletal muscle of spinal and bulbar muscular atrophy patients
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Marco Spinazzi ,
Patrick Laurette,
Mark Fiers,
Jasper Wouters,
Enrico Radaelli,
Sven Eyckerman,
Carina Leonelli,
Katrien Vanderheyden,
Aljosja Rogiers,
Els Hermans,
Pieter Baatsen,
Stein Aerts,
Frederic Amant
and 9 other authors
Melanoma addiction to the long non-coding RNA SAMMSON
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Giacomo Pietro Comi,
Antonio Federico,
Carlo Minetti ,
Maurizio Moggio,
Tiziana Mongini,
Paola Tonin,
Antonio Toscano,
Claudio Bruno,
Elena Caldarazzo Ienco
and 13 other authors
“Mitochondrial neuropathies”: a survey from the large cohort of the Italian Network
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Giada Lunardi,
Alberto Casarin,
Mara Doimo,
Marco Spinazzi ,
Corrado Angelini,
Giovanna Cenacchi,
Alberto Burlina,
Maria Angeles Rodriguez Hernandez,
Maria Angeles Rodriguez Hernandez,
Rodriguez Hernandez Ma,
Lino Chiandetti
and 5 other authors
Primary coenzyme Q10 deficiency presenting as fatal neonatal multiorgan failure
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Melanie Neumann,
Sébastien S. Hébert,
Asli Silahtaroglu,
Adrian Liston,
Rudi D'Hooge
and 3 other authors
Deficiency of the miR-29a/b-1 cluster leads to ataxic features and cerebellar alterations in mice
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Angelo Sghirlanzoni,
Leonardo Salviati,
Corrado Angelini
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Giacomo Pietro Comi ,
Comi Gp,
Carlo Minetti ,
Maurizio Moggio,
Tiziana Mongini,
Serenella Servidei,
Paola Tonin,
Antonio Toscano,
Graziella Uziel,
Claudio Bruno
and 21 other authors
Phenotypic heterogeneity of the 8344A>G mtDNA "MERRF" mutation.
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Alberto Casarin,
Vanessa Pertegato,
Leonardo Salviati,
Corrado Angelini
Assessment of mitochondrial respiratory chain enzymatic activities on tissues and cultured cells
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Alberto Casarin,
Vanessa Pertegato,
Mario Ermani,
Leonardo Salviati,
Corrado Angelini
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Corrado Angelini,
Cesare Patrini
Subacute sensory ataxia and optic neuropathy with thiamine deficiency
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C. Ferrati
Mitochondrial disorders of the nuclear genome
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Anna Rosa Del Mistro,
Renzo Manara,
Bruno Tavolato,
Domenico Marco Bonifati
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