Publications by authors named "Valeria Lucchini"

Claim this Profile
P
Purkinje cell COX deficiency and mtDNA depletion in an animal model of spinocerebellar ataxia type 1.
Michela Ripolone, Valeria Lucchini, Dario Ronchi, Gigliola Fagiolari, Andreina Bordoni

J Neurosci Res· September 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mitochondrial changes in platelets are not related to those in skeletal muscle during human septic shock.
Alessandro Protti, Francesco Fortunato, Maria L Caspani, Mauro Pluderi, Valeria Lucchini

PLoS One· June 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Impaired Muscle Mitochondrial Biogenesis and Myogenesis in Spinal Muscular Atrophy.
Michela Ripolone, Dario Ronchi, Raffaella Violano, Dionis Vallejo, Gigliola Fagiolari, Valeria Lucchini

JAMA Neurol· June 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Prevalence of asymptomatic vertebral fractures in late-onset Pompe disease.
Francesco Bertoldo, Francesca Zappini, Martina Brigo, Maurizio Moggio, Valeria Lucchini

J Clin Endocrinol Metab· February 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Prevalence of Asymptomatic Vertebral Fractures in Late-Onset Pompe Disease.
Francesco Bertoldo, Francesca Zappini, Martina Brigo, Maurizio Moggio, Valeria Lucchini

J Neuromuscul Dis· January 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Novel CLN3 mutation causing autophagic vacuolar myopathy.
Andrea Cortese, Arianna Tucci, Giovanni Piccolo, Carlo A Galimberti, Pietro Fratta, Valeria Lucchini

Neurology· June 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Null ABCA3 in humans: large homozygous ABCA3 deletion, correlation to clinical-pathological findings.
Paola Carrera, Maurizio Ferrari, Silvia Presi, Luisa Ventura, Barbara Vergani, Valeria Lucchini

Pediatr Pulmonol· March 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
POLG1 mutations and stroke like episodes: a distinct clinical entity rather than an atypical MELAS syndrome.
Antonella Cheldi, Dario Ronchi, Andreina Bordoni, Bianca Bordo, Silvia Lanfranconi, Valeria Lucchini

BMC Neurol· January 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Frequency and characterisation of anoctamin 5 mutations in a cohort of Italian limb-girdle muscular dystrophy patients.
Francesca Magri, Roberto Del Bo, Maria Grazia D'Angelo, Monica Sciacco, Sandra Gandossini, Valeria Lucchini

Neuromuscul Disord· November 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genotype and phenotype characterization in a large dystrophinopathic cohort with extended follow-up.
Francesca Magri, Alessandra Govoni, Maria Grazia D'Angelo, Roberto Del Bo, Serena Ghezzi, Valeria Lucchini

J Neurol· September 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
Two novel mutations in PEO1 (twinkle) gene associated with chronic external ophthalmoplegia.
Dario Ronchi, Elisa Fassone, Andreina Bordoni, Monica Sciacco, Valeria Lucchini

J Neurol Sci· September 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
U
Unusual adult-onset Leigh syndrome presentation due to the mitochondrial m.9176T>C mutation.
Dario Ronchi, Andreina Bordoni, Alessandra Cosi, Mafalda Rizzuti, Elisa Fassone, Valeria Lucchini

Biochem Biophys Res Commun· August 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Clinical and molecular characterization of a cohort of patients with novel nucleotide alterations of the Dystrophin gene detected by direct sequencing.
Francesca Magri, Roberto Del Bo, Maria G D'Angelo, Alessandra Govoni, Serena Ghezzi, Valeria Lucchini

BMC Med Genet· March 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mitochondrial respiratory chain dysfunction in muscle from patients with amyotrophic lateral sclerosis.
Veronica Crugnola, Costanza Lamperti, Valeria Lucchini, Dario Ronchi, Lorenzo Peverelli

Arch Neurol· July 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Muscular dystrophy: central nervous system alpha-dystroglycan glycosylation defects and brain malformation.
Gigliola Fagiolari, Anna Cappellini, Rachele Cagliani, Alessandro Prelle, Valeria Lucchini

J Child Neurol· March 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Chromosome territories, X;Y translocation and Premature Ovarian Failure: is there a relationship?
Sara Lissoni, Simona Baronchelli, Nicoletta Villa, Valeria Lucchini, Enrico Betri

Mol Cytogenet· September 2009

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Amyotrophic lateral sclerosis linked to a novel SOD1 mutation with muscle mitochondrial dysfunction.
Stefania Corti, Chiara Donadoni, Dario Ronchi, Andreina Bordoni, Francesco Fortunato, Valeria Lucchini

J Neurol Sci· January 2009

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Identifying the causes of stillbirth: a comparison of four classification systems.
Patrizia Vergani, Sabrina Cozzolino, Elisa Pozzi, Maria Serena Cuttin, Massimiliano Greco, Valeria Lucchini

Am J Obstet Gynecol· September 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Follow-up of a large population of asymptomatic/oligosymptomatic hyperckemic subjects.
Elisabetta D'Adda, Monica Sciacco, Maria Elisa Fruguglietti, Veronica Crugnola, Valeria Lucchini

J Neurol· November 2006

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Muscle coenzyme Q10 level in statin-related myopathy.
Costanza Lamperti, Ali B Naini, Valeria Lucchini, Alessandro Prelle, Nereo Bresolin

Arch Neurol· November 2005

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis