CRUGNOLA, VERONICA

CRUGNOLA, VERONICA  

Universita' degli Studi di MILANO  

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Risultati 1 - 20 di 29 (tempo di esecuzione: 0.008 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
Ultrastructural mitochondrial abnormalities in sporadic amyotrophic lateral sclerosis patients 2011 V. CrugnolaC. LampertiV. SilaniN. bresolin + Article (author) -
IgD multiple myeloma paraproteinemia as a cause of myositis 2010 I. ColomboM. FrugugliettiV. CrugnolaN. Bresolin + Article (author) -
Mitochondrial respiratory chain dysfunction in muscle from patients with Amyotrophic Lateral Sclerosis 2010 V. CrugnolaC. LampertiV. LucchiniD. RonchiL. PeverelliA. BordoniE. FassoneF.R. FortunatoS.P. CortiV. SilaniN. BresolinS.I. Di MauroG.P. Comi + Article (author) -
Incidental Mitochondrial Myopathy 2010 V. CrugnolaV. LucchiniD. RonchiM.G. D'AngeloA. BordoniL. PeverelliN. BresolinG.P. Comi + Conference Object -
Muscular Dystrophy : Central Nervous System {alpha}-Dystroglycan Glycosylation Defects and Brain Malformation 2010 R. CaglianiV. LucchiniF. FortunatoF. LocatelliV. CrugnolaG.P. ComiN. BresolinC. Lamperti + Article (author) -
Amyotrophic lateral sclerosis linked to a novel SOD1 mutation with muscle mitochondrial dysfunction 2009 S. CortiD. RonchiA. BordoniF. FortunatoD. SantoroR. Del BoV. LucchiniV. CrugnolaD. PapadimitriouS. SalaniN. BresolinG.P. Comi + Article (author) -
Congenital myopathy with ptosis, ophthalmoplegia and muscle dystrophic changes: a possible sporadic case of myosin heavy chain type IIa myopathy. 2009 V. LucchiniV. CrugnolaM. ServidaA. BordoniD. RonchiN. BresolinG.P. ComiY. Torrente + Conference Object -
Infantile inflammatory myopathy presenting as SMARD 1V 2009 CrugnolaG.P. ComiN. BresolinC. Lamperti + Conference Object -
Molecular epidemiology and clinical features of a large Italian cohort of 291 dystrophinopathic patients. 2009 F. MagriM.G. D’AngeloR. Del BoR. VirgilioS. BonatoS. GandossiniA. BordoniS. CortiV. CrugnolaC. LampertiN. BresolinG.P. Comi. + Conference Object -
Miopatia infiammatoria associata a grave insufficienza neonatale 2009 V. CrugnolaGP ComiN. BresolinC. Lamperti + Conference Object -
Miopatia progressiva con ptosi, oftalmoplagia e aspetti distrofici alla biopsia muscolare 2009 V. LucchiniV. CrugnolaA. , BordoniD. RonchiN. BresolinG. P. ComiY. Torrente + Conference Object -
Reading frame nelle distrofinopatie: le regole delle eccezioni 2009 F. MagriR. Del BoMG D'angeloS. GandossiniF. FortunatoV. CrugnolaN. BresolinG.P. Comi + Conference Object -
Neuropathological study of skeletal muscle, heart, liver, and brainin a neonatal form of glycogen storage disease type IV associated with a newmutation in GBE1 gene 2009 7. C. LampertiS. SalaniS. LucchiariA. BordoniM. RipoloneME FrugugliettiV. CrugnolaN. BresolinG.P. Comi + Article (author) -
A stop codon mutation in the 5’ of the dystrophin gene associated to a Becker muscular dystrophy phenotype 2008 F. MagriR. VirgilioR. Del BoF. FortunatoR. CaglianiM. SironiV. CrugnolaN. BresolinG.P. Comi + Article (author) -
A Late Role of ANT-1 Overexpression in the Pathogenesis of FSHD 2008 C. LampertiV. CrugnolaM. ServidaF. FortunatoA. Di FonzoG. P. ComiN. Bresolin + Article (author) -
Becker muscular dystrophy with a stop codon mutation in the 5′ of the dystrophin gene 2008 F. MagriR. Del BoF. FortunatoR. CaglianiM. SironiV. CrugnolaN. BresolinG.P. Comi + Article (author) -
Descrizione di un caso clinico con inusuale affaticabilità muscolare e miopatia metabolica 2008 V. CrugnolaG.P. Comi + Article (author) -
Morphological pattern of muscle biopsy in a large cohort of FSHD patients 2008 V. CrugnolaM. ServidaN. Bresolin + Conference Object -
Novel Q23R SOD1 mutation associated with muscle mitochondrial dysfunction 2007 D. RonchiS. CortiA. BordoniD. SantoroD. PapadimitriouC. LampertiV. LucchiniM. MagriM. GuglieriV. CrugnolaN. BresolinG.P. Comi + Conference Object -
Purkinje cell mitochondrial oxidative defect in the animal model of spinocerebellar ataxia type 1 Clinical and pathological aspects of an Italian patient with inclusion body myopathy and frontotemporal dementia carrying a novel mutation in valosin-containing protein gene. 2007 V. LucchiniC. LampertiF. FortunatoV. CrugnolaN. BresolinG. P. ComiS. Bonato + Conference Object -