mancuso, michelangelo: search on Z-Library

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1

Drugs and mitochondrial diseases: 40 queries and answers

Mancuso, Michelangelo, Orsucci, Daniele, Filosto, Massimiliano, Simoncini, Costanza, Siciliano, Gabriele

Journal:

Expert Opinion on Pharmacotherapy

Year:

2012

Language:

english

File:

PDF, 398 KB

english, 2012

2

Diagnosis and Management of Mitochondrial Disorders || Mitochondrial Myopathies, Chronic Progressive External Ophthalmoparesis, and Kearns-Sayre Syndrome

Mancuso, Michelangelo, Klopstock, Thomas

Year:

2019

File:

PDF, 297 KB

2019

3

G41S SOD1 mutation: A common ancestor for six ALS Italian families with an aggressive phenotype

Battistini, Stefania, Ricci, Claudia, Giannini, Fabio, Calzavara, Silvia, Greco, Giuseppe, Del Corona, Alberto, Mancuso, Michelangelo, Battistini, Noè, Siciliano, Gabriele, Carrera, Paola

Journal:

Amyotrophic Lateral Sclerosis

Year:

2010

Language:

english

File:

PDF, 157 KB

english, 2010

4

Novel Mitochondrial DNA ND5 Mutation in a Patient With Clinical Features of MELAS and MERRF

Naini, Ali B., Lu, Jiesheng, Kaufmann, Petra, Bernstein, Richard A., Mancuso, Michelangelo, Bonilla, Eduardo, Hirano, Michio, DiMauro, Salvatore

Journal:

Archives of Neurology

Year:

2005

Language:

english

File:

PDF, 130 KB

english, 2005

5

Current Options in the Treatment of Mitochondrial Diseases

Scarpelli, Mauro, Sofia Cotelli, Maria, Mancuso, Michelangelo, Tomelleri, Giuliano, Tonin, Paola, Baronchelli, Carla, Vielmi, Valentina, Gregorelli, Valeria, Todeschini, Alice, Padovani, Alessandro, F

Journal:

Recent Patents on CNS Drug Discovery

Year:

2010

Language:

english

File:

PDF, 107 KB

english, 2010

6

The mtDNA A8344G “MERRF” mutation is not a common cause of sporadic Parkinson disease in Italian population

Michelangelo Mancuso, Claudia Nesti, Lucia Petrozzi, Daniele Orsucci, Daniela Frosini, Lorenzo Kiferle, Ubaldo Bonuccelli, Roberto Ceravolo, Luigi Murri, Gabriele Siciliano

Journal:

Parkinsonism & Related Disorders

Year:

2008

Language:

english

File:

PDF, 73 KB

english, 2008

7

Association study between XRCC1 gene polymorphisms and sporadic amyotrophic lateral sclerosis

Coppedè, Fabio, Migheli, Francesca, Lo Gerfo, Annalisa, Fabbrizi, Maria Rita, Carlesi, Cecilia, Mancuso, Michelangelo, Corti, Stefania, Mezzina, Nicoletta, del Bo, Roberto, Comi, Giacomo P., Siciliano

Journal:

Amyotrophic Lateral Sclerosis

Year:

2010

Language:

english

File:

PDF, 72 KB

english, 2010

8

ERGOREFLEX OVERACTIVITY: A POTENTIAL CAUSE OF EXERCISE LIMITATION AND DYSAUTONOMIA IN PATIENTS WITH MITOCHONDRIAL MYOPATHY

Aimo, Alberto, Giannoni, Alberto, Piepoli, Massimo, Mancuso, Michelangelo, Siciliano, Gabriele, Passino, Claudio, Emdin, Michele

Journal:

Journal of the American College of Cardiology

Year:

2016

Language:

english

File:

PDF, 351 KB

english, 2016

9

Lack of Association between Nuclear Factor Erythroid-Derived 2-Like 2 Promoter Gene Polymorphisms and Oxidative Stress Biomarkers in Amyotrophic Lateral Sclerosis Patients

LoGerfo, Annalisa, Chico, Lucia, Borgia, Loredana, Petrozzi, Lucia, Rocchi, Anna, D'Amelio, Antonia, Carlesi, Cecilia, Caldarazzo Ienco, Elena, Mancuso, Michelangelo, Siciliano, Gabriele

Journal:

Oxidative Medicine & Cellular Longevity

Year:

2014

Language:

english

File:

PDF, 2.17 MB

english, 2014

10

Diagnosis and Management of Mitochondrial Disorders || Mitochondrial Optic Neuropathies

Mancuso, Michelangelo, Klopstock, Thomas

Year:

2019

Language:

english

File:

PDF, 722 KB

english, 2019

11

Bilateral striatal necrosis, dystonia and multiple mitochondrial DNA deletions: Case study and effect of deep brain stimulation

Maria Stella Aniello, Davide Martino, Vittoria Petruzzella, Roberto Eleopra, Michelangelo Mancuso, Rosa Dell'Aglio, Michele Cavallo, Gabriele Siciliano, Giovanni Defazio

Journal:

Movement Disorders

Year:

2008

Language:

english

File:

PDF, 144 KB

english, 2008

12

Genes and the Environment in Neurodegeneration

Fabio Coppedè, Michelangelo Mancuso, Gabriele Siciliano, Lucia Migliore, Luigi Murri

Journal:

Bioscience Reports

Year:

2006

Language:

english

File:

PDF, 286 KB

english, 2006

13

Electron transfer mediators and other metabolites and cofactors in the treatment of mitochondrial dysfunction

Daniele Orsucci, Massimiliano Filosto, Gabriele Siciliano, Michelangelo Mancuso

Journal:

Nutrition Reviews

Year:

2009

Language:

english

File:

PDF, 278 KB

english, 2009

14

Mitochondrial Encephalomyopathies: Diagnostic Approach

SALVATORE DIMAURO, STACEY TAY, MICHELANGELO MANCUSO

Journal:

Annals of the New York Academy of Sciences

Year:

2004

Language:

english

File:

PDF, 3.73 MB

english, 2004

15

Autonomic, functional, skeletal muscle, and cardiac abnormalities are associated with increased ergoreflex sensitivity in mitochondrial disease

Giannoni, Alberto, Aimo, Alberto, Mancuso, Michelangelo, Piepoli, Massimo Francesco, Orsucci, Daniele, Aquaro, Giovanni Donato, Barison, Andrea, De Marchi, Daniele, Taddei, Claudia, Cameli, Matteo, Ra

Journal:

European Journal of Heart Failure

Year:

2017

Language:

english

File:

PDF, 605 KB

english, 2017

16

Diagnosis and Management of Mitochondrial Disorders || Mitochondrial Optic Neuropathies

Mancuso, Michelangelo, Klopstock, Thomas

Year:

2019

File:

PDF, 722 KB

2019

17

Creutzfeldt–Jakob disease with E200KPRNPmutation: a case report and revision of the literature

Michelangelo Mancuso, Gabriele Siciliano, Sabina Capellari, Daniele Orsucci, Policarpo Moretti, Giuseppe Di Fede, Silvia Suardi, Rosaria Strammiello, Piero Parchi, Fabrizio Tagliavini, Luigi Murri

Journal:

Neurological Sciences

Year:

2009

Language:

english

File:

PDF, 256 KB

english, 2009

18

Mitochondrial Encephalomyopathies: Therapeutic Approach

SALVATORE DIMAURO, MICHELANGELO MANCUSO, ALI NAINI

Journal:

Annals of the New York Academy of Sciences

Year:

2004

Language:

english

File:

PDF, 1.24 MB

english, 2004

19

Neurology residency training in Europe: an Italian perspective

Maurizio Facheris, Michelangelo Mancuso, Tomaso Scaravilli, Domenico Marco Bonifati

Journal:

The Lancet Neurology

Year:

2005

Language:

english

File:

PDF, 76 KB

english, 2005

20

Erratum to: Redefining phenotypes associated with mitochondrial DNA single deletion

Mancuso, Michelangelo, Orsucci, Daniele, Angelini, Corrado, Bertini, Enrico, Carelli, Valerio, Comi, Giacomo Pietro, Donati, Maria Alice, Federico, Antonio, Minetti, Carlo, Moggio, Maurizio, Mongini,

Journal:

Journal of Neurology

Year:

2015

File:

PDF, 291 KB

2015

21

Clinical and Genetic Heterogeneity in Progressive External Ophthalmoplegia Due to Mutations in Polymerase γ

Filosto, Massimiliano, Mancuso, Michelangelo, Nishigaki, Yutaka, Pancrudo, Jacklyn, Harati, Yadollah, Gooch, Clifton, Mankodi, Ami, Bayne, Lydia, Bonilla, Eduardo, Shanske, Sara, Hirano, Michio, DiMau

Journal:

Archives of Neurology

Year:

2003

Language:

english

File:

PDF, 124 KB

english, 2003

22

Studies of COX16, COX19, and PET191 in Human Cytochrome-c Oxidase Deficiency

Tay, Stacey K. H., Nesti, Claudia, Mancuso, Michelangelo, Schon, Eric A., Shanske, Sara, Bonilla, Eduardo, Davidson, Mercy M., DiMauro, Salvatore

Journal:

Archives of Neurology

Year:

2004

Language:

english

File:

PDF, 74 KB

english, 2004

23

Neurohormonal modulation for treatment of cardiac involvement in dystrophinopathies and mitochondrial disease

Aimo, Alberto, Giannoni, Alberto, Castiglione, Vincenzo, Mancuso, Michelangelo, Siciliano, Gabriele, Piepoli, Massimo F, Passino, Claudio, Emdin, Michele

Journal:

European Journal of Preventive Cardiology

Year:

2017

Language:

english

File:

PDF, 314 KB

english, 2017

24

Diagnosis and Management of Mitochondrial Disorders || Mitochondrial Medicine: A Historical Point of View

Mancuso, Michelangelo, Klopstock, Thomas

Year:

2019

Language:

english

File:

PDF, 1.06 MB

english, 2019

25

Mitochondrial DNA depletion and dGK gene mutations

Leonardo Salviati, Sabrina Sacconi, Michelangelo Mancuso, David Otaegui, Pilar Camaño, Alberto Marina, Simon Rabinowitz, Rebecca Shiffman, Karen Thompson, Claire M. Wilson, Annette Feigenbaum, Ali B.

Journal:

Annals of Neurology

Year:

2002

Language:

english

File:

PDF, 1.04 MB

english, 2002

26

Congenital or late-onset myopathy in patients with the T14709C mtDNA mutation

Michelangelo Mancuso, Silvio Ferraris, Yutaka Nishigaki, Gaetano Azan, Alessandro Mauro, Piero Sammarco, Sindu Krishna, Stacey K.H. Tay, Eduardo Bonilla, Stephen G. Romansky, Michio Hirano, Salvatore

Journal:

Journal of the Neurological Sciences

Year:

2005

Language:

english

File:

PDF, 134 KB

english, 2005

27

A high-dose bortezomib neuropathy with sensory ataxia and myelin involvement

Massimiliano Filosto, Giuseppe Rossi, Anna Maria Pelizzari, Serena Buzio, Marta Tentorio, Laura Broglio, Michelangelo Mancuso, Marianna Rinaldi, Mauro Scarpelli, Alessandro Padovani

Journal:

Journal of the Neurological Sciences

Year:

2007

Language:

english

File:

PDF, 100 KB

english, 2007

28

Coenzyme Q10 and Neurological Diseases: An Update

Mancuso, Michelangelo, Choub, Anna, Filosto, Massimiliano, Petrozzi, Lucia, Cafforio, Gianfranco, Siciliano, Gabriele, Murri, Luigi

Journal:

Letters in Drug Design & Discovery

Year:

2006

Language:

english

File:

PDF, 96 KB

english, 2006

29

“Cardioembolic Profile” in Patients with Ischemic Stroke: Data from the Analysis of 1037 Cases

Chiti, Alberto, Giannini, Nicola, Terni, Eva, Massimetti, Gabriele, Gialdini, Gino, Mancuso, Michelangelo, Bonuccelli, Ubaldo, Orlandi, Giovanni

Journal:

Journal of Stroke and Cerebrovascular Diseases

Year:

2015

Language:

english

File:

PDF, 87 KB

english, 2015

30

Diagnosis and Management of Mitochondrial Disorders || Leigh Syndrome

Mancuso, Michelangelo, Klopstock, Thomas

Year:

2019

Language:

english

File:

PDF, 409 KB

english, 2019

31

The first Italian family with evidence of pyramidal impairment as phenotypic manifestation of Silver syndrome BSCL2 gene mutation

Gianfranco Cafforio, Rosanna Calabrese, Nicola Morelli, Michelangelo Mancuso, Selina Piazza, Andrea Martinuzzi, Maria Teresa Bassi, Francesco Crippa, Gabriele Siciliano

Journal:

Neurological Sciences

Year:

2008

Language:

english

File:

PDF, 342 KB

english, 2008

32

POLG1-Related and other “Mitochondrial Parkinsonisms”: an Overview

Daniele Orsucci, Elena Caldarazzo Ienco, Michelangelo Mancuso, Gabriele Siciliano

Journal:

Journal of Molecular Neuroscience

Year:

2011

Language:

english

File:

PDF, 240 KB

english, 2011

33

Oxidative stress biomarkers in patients with untreated obstructive sleep apnea syndrome

Michelangelo Mancuso, Enrica Bonanni, Annalisa LoGerfo, Daniele Orsucci, Michelangelo Maestri, Lucia Chico, Elisa DiCoscio, Monica Fabbrini, Gabriele Siciliano, Luigi Murri

Journal:

Year:

2012

Language:

english

File:

PDF, 302 KB

english, 2012

34

An “inflammatory” mitochondrial myopathy. A case report

Mancuso, Michelangelo, Orsucci, Daniele, Ienco, Elena Caldarazzo, Ricci, Giulia, Ali, Greta, Servadio, Adele, Fontanini, Gabriella, Filosto, Massimiliano, Vielmi, Valentina, Rocchi, Anna, Petrozzi, Lu

Journal:

Neuromuscular Disorders

Year:

2013

Language:

english

File:

PDF, 1.04 MB

english, 2013

35

Disulfiram neuropathy: Two cases of distal axonopathy

Filosto, Massimiliano, Tentorio, Marta, Broglio, Laura, Buzio, Serena, Lazzarini, Clara, Pasolini, Maria Pia, Cotelli, Maria Sofia, Scarpelli, Mauro, Mancuso, Michelangelo, Choub, Anna, Padovani, Ales

Journal:

Clinical Toxicology (Informa Healthcare)

Year:

2008

Language:

english

File:

PDF, 62 KB

english, 2008

36

ARE WHITE MATTER ABNORMALITIES A CAUSE OF ‘UNEXPLAINED DIZZINESS’? A RETROSPECTIVE BI–CENTRE STUDY

Ahmad, Hena, Cerchiai, Niccolò, Mancuso, Michelangelo, Casani, Augusto, Bronstein, Adolfo

Journal:

Journal of Neurology Neurosurgery & Psychiatry

Year:

2015

Language:

english

File:

PDF, 56 KB

english, 2015

37

Diagnosis and Management of Mitochondrial Disorders || Coenzyme Q10 Deficiency

Mancuso, Michelangelo, Klopstock, Thomas

Year:

2019

Language:

english

File:

PDF, 475 KB

english, 2019

38

Meet Our Associate Editor

Mancuso, Michelangelo

Journal:

Current Molecular Medicine

Year:

2016

File:

PDF, 80 KB

2016

39

Coenzyme Q10 and Neurological Diseases

Mancuso, Michelangelo, Orsucci, Daniele, Calsolaro, Valeria, Choub, Anna, Siciliano, Gabriele

Journal:

Pharmaceuticals

Year:

2009

Language:

english

File:

PDF, 213 KB

english, 2009

40

Progressive External Ophthalmoplegia and Vision and Hearing Loss in a Patient With Mutations in POLG2 and OPA1

Ferraris, Silvio, Clark, Susanna, Garelli, Emanuela, Davidzon, Guido, Moore, Steven A., Kardon, Randy H., Bienstock, Rachelle J., Longley, Matthew J., Mancuso, Michelangelo, Gutiérrez Ríos, Purificaci

Journal:

Archives of Neurology

Year:

2008

Language:

english

File:

PDF, 391 KB

english, 2008

41

Biomarkers and progress of antioxidant therapy for rare mitochondrial disorders

Chico, Lucia, Orsucci, Daniele, Lo Gerfo, Annalisa, Marconi, Letizia, mancuso, michelangelo, Siciliano, Gabriele

Journal:

Expert Opinion on Orphan Drugs

Year:

2016

Language:

english

File:

PDF, 603 KB

english, 2016

42

Diagnosis and Management of Mitochondrial Disorders || Mitochondrial Depletion Syndromes

Mancuso, Michelangelo, Klopstock, Thomas

Year:

2019

Language:

english

File:

PDF, 422 KB

english, 2019

43

Peripheral Benzodiazepine Binding Sites in Platelets of Patients Affected by Mitochondrial Diseases and Large Scale Mitochondrial DNA Rearrangements

Martini, Claudia, Chelli, Beatrice, Betti, Laura, Montali, Marina, Mancuso, Michelangelo, Giannaccini, Gino, Rocchi, Anna, Murri, Luigi, Siciliano, Gabriele

Journal:

Molecular Medicine

Year:

2002

Language:

english

File:

PDF, 81 KB

english, 2002

44

Fibroblast growth factor 21 and grow differentiation factor 15 are sensitive biomarkers of mitochondrial diseases due to mitochondrial transfer-RNA mutations and mitochondrial DNA deletions

Formichi, Patrizia, Cardone, Nastasia, Taglia, Ilaria, Cardaioli, Elena, Salvatore, Simona, Gerfo, Annalisa Lo, Simoncini, Costanza, Montano, Vincenzo, Siciliano, Gabriele, Mancuso, Michelangelo, Mala

Journal:

Neurological Sciences

Year:

2020

File:

PDF, 1.19 MB

2020

45

In vitro and in vivo trans-epidermal water loss evaluation following topical drug delivery systems application for pharmaceutical analysis

Cristiano, Maria Chiara, Froiio, Francesca, Mancuso, Antonia, Iannone, Michelangelo, Fresta, Massimo, Fiorito, Serena, Celia, Christian, Paolino, Donatella

Journal:

Journal of Pharmaceutical and Biomedical Analysis

Year:

2020

File:

PDF, 739 KB

2020

46

A new truncating MPZ mutation associated with a very mild CMT1 B phenotype

Selina Piazza, Fulvia Baldinotti, Antonella Fogli, Maria Elena Conidi, Angela Michelucci, Elena Caldarazzo Ienco, Michelangelo Mancuso, Paolo Simi, Gabriele Siciliano

Journal:

Neuromuscular Disorders

Year:

2010

Language:

english

File:

PDF, 414 KB

english, 2010

47

Twinkle mutation in an Italian family with external progressive ophthalmoplegia and parkinsonism: A case report and an update on the state of art

Kiferle, Lorenzo, Orsucci, Daniele, Mancuso, Michelangelo, Lo Gerfo, Annalisa, Petrozzi, Lucia, Siciliano, Gabriele, Ceravolo, Roberto, Bonuccelli, Ubaldo

Journal:

Neuroscience Letters

Year:

2013

Language:

english

File:

PDF, 799 KB

english, 2013

48

Mitochondria, Mitochondrial DNA and Alzheimers Disease. What Comes First?

Mancuso, Michelangelo, Orsucci, Daniele, Siciliano, Gabiele, Murri, Luigi

Journal:

Current Alzheimer Research

Year:

2008

Language:

english

File:

PDF, 225 KB

english, 2008

49

Cerebral sinus venous thrombosis

Terni, Eva, Giannini, Nicola, Chiti, Alberto, Gialdini, Gino, Orlandi, Giovanni, Montano, Vincenzo, Orsucci, Daniele, Brondi, Marco, Bonuccelli, Ubaldo, Mancuso, Michelangelo

Journal:

Blood Coagulation & Fibrinolysis

Year:

2015

Language:

english

File:

PDF, 106 KB

english, 2015

50

Mitochondrial DNA haplogroups may influence Fabry disease phenotype

Mancuso, Michelangelo, Concolino, Daniela, Sechi, G. P, Feliciani, Claudio, Salviati, Alessandro, Siciliano, Gabriele, Bonuccelli, Ubaldo

Journal:

Molecular Genetics and Metabolism

Year:

2017

Language:

english

File:

PDF, 48 KB

english, 2017

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