MANCUSO, MICHELANGELO Statistiche
MANCUSO, MICHELANGELO
DIPARTIMENTO DI MEDICINA CLINICA E SPERIMENTALE
A mitochondrial tRNAPhe mutation causes MERRF syndrome [Sindrome MERRF associata a mutazione del tRNAPhe]
2005-01-01 Pizzanelli, C; Galli, Renato; Mancuso, Michelangelo; Virgili, Mp; Geri, G; Chiari, A; Jensen, S; Iudice, Alfonso; Siciliano, Gabriele; Murri, Luigi
A new truncating MPZ mutation associated with a very mild CMT1 B phenotype
2010-01-01 Piazza, S; Baldinotti, F; Fogli, A; Conidi, Me; Michelucci, A; CALDARAZZO IENCO, Elena; Mancuso, Michelangelo; Simi, P; Siciliano, Gabriele
A non-syndromic hearing loss caused by very low levels of the mtDNA A3243G mutation
2004-01-01 Mancuso, Michelangelo; Filosto, M; Forli, Francesca; Rocchi, A; Berrettini, Stefano; Siciliano, Gabriele; Murri, Luigi
A novel mitochondrial tRNA(Ile) point mutation associated with chronic progressive external ophthalmoplegia and hyperCKemia.
2011-01-01 Souilem, S; Chebel, S; Mancuso, Michelangelo; Petrozzi, Lucia; Siciliano, Gabriele; Frihayed, M; Hentati, F; Amouri, R.
A novel mitochondrial tRNAPhe mutation causes MERRF syndrome
2004-01-01 Mancuso, Michelangelo; Filosto, M; Mootha, Vk; Rocchi, A; Pistolesi, S; Murri, Luigi; Dimauro, S; Siciliano, Gabriele
A screening for superoxide dismutase-1 d90a mutation in italian patients with sporadic amyotrophic lateral sclerosis
2002-01-01 Mancuso, Michelangelo; Filosto, M; Naini, A; Rocchi, A; DEL CORONA, A; Sartucci, Ferdinando; Siciliano, Gabriele; Murri, L.
A SER326CYS POLYMORPHISM IN THE DNA REPAIR GENE HOGG1 IS NOT ASSOCIATED WITH SPORADIC ALZHEIMER'S DISEASE
2007-01-01 Coppede', Fabio; Mancuso, Michelangelo; LO GERFO, A; Manca, MARIA LAURA; Petrozzi, L; Migliore, Lucia; Siciliano, Gabriele; Murri, Luigi
Abnormal H-Tfam in a patient harboring a single mtDNA deletion.
2000-01-01 Tessa, A; Manca, MARIA LAURA; Mancuso, Michelangelo; Renna, Mr; Murri, Luigi; Martini, B; Santorelli, Fm; Siciliano, Gabriele
Abnormal levels of human mitochondrial transcription factor A in skeletal muscle in mitochondrial encephalomyopathies.
2000-01-01 Siciliano, Gabriele; Mancuso, Michelangelo; Pasquali, Livia; Manca, MARIA LAURA; Tessa, A; Iudice, Alfonso
Absence of angiogenic genes modification in Italian ALS patients
2008-01-01 DEL BO, R; Scarlato, M; Ghezzi, S; MARTINELLI BONESCHI, F; Corti, S; Locatelli, F; Santoro, D; Prelle, A; Briani, C; Nardini, M; Siciliano, Gabriele; Mancuso, Michelangelo; Murri, Luigi; Bresolin, N; Comi, Gp
Acute encephalopathy of the temporal lobes leading to m.3243A>G. When MELAS is not always MELAS
2016-01-01 CALDARAZZO IENCO, Elena; Orsucci, Daniele; Simoncini, Costanza; Montano, Vincenzo; LO GERFO, Annalisa; Siciliano, Gabriele; Bonuccelli, Ubaldo; Mancuso, Michelangelo
Adult-onset mitochondrial movement disorders: a national picture from the Italian Network
2021-01-01 Montano, V; Orsucci, D; Carelli, V; La Morgia, C; Valentino, M L; Lamperti, C; Marchet, S; Musumeci, O; Toscano, A; Primiano, G; Santorelli, F M; Ticci, C; Filosto, M; Rubegni, A; Mongini, T; Tonin, P; Servidei, S; Ceravolo, R; Siciliano, G; Mancuso, Michelangelo
Aging with Cerebral Small Vessel Disease and Dizziness: The Importance of Undiagnosed Peripheral Vestibular Disorders
2017-01-01 Cerchiai, Niccolo'; Mancuso, Michelangelo; Navari, Elena; Giannini, Nicola; Casani, AUGUSTO PIETRO
An “all-wheel drive” proposal to accelerate clinical research in common and rare neurological diseases
2019-01-01 Salvetti, Marco; Battaglia, Mario A.; Di Filippo, Massimiliano; Mancardi, Gian Luigi; Mancuso, Michelangelo; Patti, Francesco; Sormani, Maria Pia; Zaratin, Paola
Alzheimer's pathogenesis and its link to the mitochondrion
2015-01-01 Simoncini, C.; Orsucci, Daniele; CALDARAZZO IENCO, Elena; Siciliano, Gabriele; Bonuccelli, Ubaldo; Mancuso, Michelangelo
Alzheimer's pathogenesis and its link to the mitochondrion
2015-01-01 Simoncini, C.; Orsucci, Daniele; CALDARAZZO IENCO, Elena; Siciliano, Gabriele; Bonuccelli, Ubaldo; Mancuso, Michelangelo
Amyotrophic Lateral Sclerosis and Oxidative Stress: a Double-Blind Therapeutic Trial After Curcumin Supplementation
2018-01-01 Chico, Lucia; Ienco, Elena Caldarazzo; Bisordi, Costanza; Lo Gerfo, Annalisa; Petrozzi, Lucia; Petrucci, Antonio; Mancuso, Michelangelo; Siciliano, Gabriele
Amyotrophic Lateral Sclerosis: A Genetic Point Of View
2014-01-01 Carlesi, Cecilia; CALDARAZZO IENCO, Elena; Mancuso, Michelangelo; Siciliano, Gabriele
An atypical presentation of sporadic adult-onset centronuclear myopathy
2007-01-01 Pistolesi, S; Masini, M; Ali', Greta; Nuti, S; D'Agostino, Jd; Mancuso, Michelangelo; Volpi, L; Galli, Renato; Siciliano, Gabriele; Fontanini, Gabriella
Anti-Ri-associated paraneoplastic cerebellar degeneration. Report of a case and revision of the literature.
2011-01-01 Mancuso, Michelangelo; Orsucci, Daniele; Bacci, Andrea; CALDARAZZO IENCO, Elena; Siciliano, Gabriele
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
A mitochondrial tRNAPhe mutation causes MERRF syndrome [Sindrome MERRF associata a mutazione del tRNAPhe] | 1-gen-2005 | Pizzanelli, C; Galli, Renato; Mancuso, Michelangelo; Virgili, Mp; Geri, G; Chiari, A; Jensen, S; Iudice, Alfonso; Siciliano, Gabriele; Murri, Luigi | |
A new truncating MPZ mutation associated with a very mild CMT1 B phenotype | 1-gen-2010 | Piazza, S; Baldinotti, F; Fogli, A; Conidi, Me; Michelucci, A; CALDARAZZO IENCO, Elena; Mancuso, Michelangelo; Simi, P; Siciliano, Gabriele | |
A non-syndromic hearing loss caused by very low levels of the mtDNA A3243G mutation | 1-gen-2004 | Mancuso, Michelangelo; Filosto, M; Forli, Francesca; Rocchi, A; Berrettini, Stefano; Siciliano, Gabriele; Murri, Luigi | |
A novel mitochondrial tRNA(Ile) point mutation associated with chronic progressive external ophthalmoplegia and hyperCKemia. | 1-gen-2011 | Souilem, S; Chebel, S; Mancuso, Michelangelo; Petrozzi, Lucia; Siciliano, Gabriele; Frihayed, M; Hentati, F; Amouri, R. | |
A novel mitochondrial tRNAPhe mutation causes MERRF syndrome | 1-gen-2004 | Mancuso, Michelangelo; Filosto, M; Mootha, Vk; Rocchi, A; Pistolesi, S; Murri, Luigi; Dimauro, S; Siciliano, Gabriele | |
A screening for superoxide dismutase-1 d90a mutation in italian patients with sporadic amyotrophic lateral sclerosis | 1-gen-2002 | Mancuso, Michelangelo; Filosto, M; Naini, A; Rocchi, A; DEL CORONA, A; Sartucci, Ferdinando; Siciliano, Gabriele; Murri, L. | |
A SER326CYS POLYMORPHISM IN THE DNA REPAIR GENE HOGG1 IS NOT ASSOCIATED WITH SPORADIC ALZHEIMER'S DISEASE | 1-gen-2007 | Coppede', Fabio; Mancuso, Michelangelo; LO GERFO, A; Manca, MARIA LAURA; Petrozzi, L; Migliore, Lucia; Siciliano, Gabriele; Murri, Luigi | |
Abnormal H-Tfam in a patient harboring a single mtDNA deletion. | 1-gen-2000 | Tessa, A; Manca, MARIA LAURA; Mancuso, Michelangelo; Renna, Mr; Murri, Luigi; Martini, B; Santorelli, Fm; Siciliano, Gabriele | |
Abnormal levels of human mitochondrial transcription factor A in skeletal muscle in mitochondrial encephalomyopathies. | 1-gen-2000 | Siciliano, Gabriele; Mancuso, Michelangelo; Pasquali, Livia; Manca, MARIA LAURA; Tessa, A; Iudice, Alfonso | |
Absence of angiogenic genes modification in Italian ALS patients | 1-gen-2008 | DEL BO, R; Scarlato, M; Ghezzi, S; MARTINELLI BONESCHI, F; Corti, S; Locatelli, F; Santoro, D; Prelle, A; Briani, C; Nardini, M; Siciliano, Gabriele; Mancuso, Michelangelo; Murri, Luigi; Bresolin, N; Comi, Gp | |
Acute encephalopathy of the temporal lobes leading to m.3243A>G. When MELAS is not always MELAS | 1-gen-2016 | CALDARAZZO IENCO, Elena; Orsucci, Daniele; Simoncini, Costanza; Montano, Vincenzo; LO GERFO, Annalisa; Siciliano, Gabriele; Bonuccelli, Ubaldo; Mancuso, Michelangelo | |
Adult-onset mitochondrial movement disorders: a national picture from the Italian Network | 1-gen-2021 | Montano, V; Orsucci, D; Carelli, V; La Morgia, C; Valentino, M L; Lamperti, C; Marchet, S; Musumeci, O; Toscano, A; Primiano, G; Santorelli, F M; Ticci, C; Filosto, M; Rubegni, A; Mongini, T; Tonin, P; Servidei, S; Ceravolo, R; Siciliano, G; Mancuso, Michelangelo | |
Aging with Cerebral Small Vessel Disease and Dizziness: The Importance of Undiagnosed Peripheral Vestibular Disorders | 1-gen-2017 | Cerchiai, Niccolo'; Mancuso, Michelangelo; Navari, Elena; Giannini, Nicola; Casani, AUGUSTO PIETRO | |
An “all-wheel drive” proposal to accelerate clinical research in common and rare neurological diseases | 1-gen-2019 | Salvetti, Marco; Battaglia, Mario A.; Di Filippo, Massimiliano; Mancardi, Gian Luigi; Mancuso, Michelangelo; Patti, Francesco; Sormani, Maria Pia; Zaratin, Paola | |
Alzheimer's pathogenesis and its link to the mitochondrion | 1-gen-2015 | Simoncini, C.; Orsucci, Daniele; CALDARAZZO IENCO, Elena; Siciliano, Gabriele; Bonuccelli, Ubaldo; Mancuso, Michelangelo | |
Alzheimer's pathogenesis and its link to the mitochondrion | 1-gen-2015 | Simoncini, C.; Orsucci, Daniele; CALDARAZZO IENCO, Elena; Siciliano, Gabriele; Bonuccelli, Ubaldo; Mancuso, Michelangelo | |
Amyotrophic Lateral Sclerosis and Oxidative Stress: a Double-Blind Therapeutic Trial After Curcumin Supplementation | 1-gen-2018 | Chico, Lucia; Ienco, Elena Caldarazzo; Bisordi, Costanza; Lo Gerfo, Annalisa; Petrozzi, Lucia; Petrucci, Antonio; Mancuso, Michelangelo; Siciliano, Gabriele | |
Amyotrophic Lateral Sclerosis: A Genetic Point Of View | 1-gen-2014 | Carlesi, Cecilia; CALDARAZZO IENCO, Elena; Mancuso, Michelangelo; Siciliano, Gabriele | |
An atypical presentation of sporadic adult-onset centronuclear myopathy | 1-gen-2007 | Pistolesi, S; Masini, M; Ali', Greta; Nuti, S; D'Agostino, Jd; Mancuso, Michelangelo; Volpi, L; Galli, Renato; Siciliano, Gabriele; Fontanini, Gabriella | |
Anti-Ri-associated paraneoplastic cerebellar degeneration. Report of a case and revision of the literature. | 1-gen-2011 | Mancuso, Michelangelo; Orsucci, Daniele; Bacci, Andrea; CALDARAZZO IENCO, Elena; Siciliano, Gabriele |