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Veronica Crugnola

Mitochondrial Respiratory Chain Dysfunction in Muscle From Patients With Amyotrophic Lateral Sclerosis
2010 · Veronica Crugnola, Costanza Lamperti, et al. · Archives of Neurology · 146
Gait pattern in myotonic dystrophy (Steinert disease): A kinematic, kinetic and EMG evaluation using 3D gait analysis
2011 · Manuela Galli, Veronica Cimolin, et al. · Journal of the Neurological Sciences · 47
Amyotrophic lateral sclerosis linked to a novel SOD1 mutation with muscle mitochondrial dysfunction
2008 · Stefania Corti, Chiara Donadoni, et al. · Journal of the Neurological Sciences · 41
Follow-up of a large population of asymptomatic/oligosymptomatic hyperckemic subjects
2006 · Elisabetta D’Adda, Monica Sciacco, et al. · Journal of Neurology · 29
Neuropathological study of skeletal muscle, heart, liver, and brain in a neonatal form of glycogen storage disease type IV associated with a new mutation in GBE1 gene
2009 · C. Lamperti, S. Salani, et al. · Journal of Inherited Metabolic Disease · 26
IgD Multiple Myeloma Paraproteinemia as a Cause of Myositis
2010 · I. Colombo, M. E. Fruguglietti, et al. · Neurology Research International · 5
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Muscular Dystrophy: Central Nervous System α-Dystroglycan Glycosylation Defects and Brain Malformation
2009 · Gigliola Fagiolari, Anna Cappellini, et al. · Journal of Child Neurology · 4
Juvenile and adult forms of type II glycogenosis: Clinical aspects
2012 · Costanza Lamperti, V. Crugnola, et al. · 2
Adult form type II Glycogen Storage Disease in a Northern Italy population :_phenotype, charatcerization, early diagnosis and prognostic determinants
2008 · Gauthier Remiche, Dario Ronchi, et al. · 2
Familial amyotrophic lateral sclerosis with a novel Q23R mutation in the copper/zinc superoxide dismutase gene associated with muscle mitochondrial dysfunction
2007 · Stefania Corti, Andreina Bordoni, et al. · 1
Intrafamilial phenotype-genotype variability in FSHD
2011 · Michela Ripolone, C. Lamperti, et al.
G.P.9.06 Infantile inflammatory myopathy presenting as SMARD 1
2009 · V. Crugnola, I. Colombo, et al. · Neuromuscular Disorders
Reading frame nelle distrofinopatie: le regole delle eccezioni
2009 · F. Magri, Amy L. Govoni, et al.
Miopatia infiammatoria associata a grave insufficienza neonatale
2009 · V. Crugnola, I. Colombo, et al.
Molecular epidemiology and clinical features of a large Italian cohort of 291 dystrophinopathic patients.
2009 · Flavia Magri, Alessandra Govoni, et al.
D.P.1.08 Morphological pattern of muscle biopsy in a large cohort of FSHD patients
2008 · V. Crugnola, V. Ghiaroni, et al. · Neuromuscular Disorders
G.P.7.05 Becker muscular dystrophy with a stop codon mutation in the 5′ of the dystrophin gene
2008 · F. Magri, R. Del Bo, et al. · Neuromuscular Disorders
A Late Role of ANT-1 Overexpression in the Pathogenesis of FSHD
2008 · C. Lamperti, V. Crugnola, et al.
Descrizione di un caso clinico con inusuale affaticabilità muscolare e miopatia metabolica
2008 · G. Ricci, L. Volpi, et al.
A stop codon mutation in the 5’ of the dystrophin gene associated to a Becker muscular dystrophy phenotype
2008 · Francesca Magri, R. Virgilio, et al.
Becker muscular dystrophy with a stop codon mutation in the 5′ of the dystrophin gene
2008 · Francesca Magri, Roberto Del Bo, et al.
Muscle mitochondrial oxidative defects in Amyotrophic Lateral Scelosis
2007 · V. Crugnola, Valeria Lucchini, et al.
Purkinje cell mitochondrial oxidative defect in the animal model of spinocerebellarataxia type 1Clinical and pathological aspects of an Italian patient with inclusion body myopathy and frontotemporal dementia carrying a novel mutation in valosin-containing protein gene.
2007 · Valeria Lucchini, Gigliola Fagiolari, et al.
New twinkle gene mutations in PEO patients with multiple mitochondrial DNA deletions
2006 · R. Virgilio, Andreina Bordoni, et al.
Neuropathological study of skeletal muscle, heart, liver, and brain in a neonatal form of Andersen disease associated with a new mutation in GBE gene
2006 · C. Lamperti, Sabrina Salani, et al. · Basic and applied myology
Works count: 29
Citation count: 303
H-index: 5
I10-index: 5
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