LUCCHINI, VALERIA

LUCCHINI, VALERIA  

Universita' degli Studi di MILANO  

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Risultati 1 - 20 di 37 (tempo di esecuzione: 0.013 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
A mouse model of facioscapulohumeral muscular dystrophy 1-gen-2005 C. LampertiV. LucchiniC. ZeccaN. Bresolin + Book Part (author) -
Amyotrophic lateral sclerosis linked to a novel SOD1 mutation with muscle mitochondrial dysfunction 15-gen-2009 S. CortiD. RonchiA. BordoniF. FortunatoD. SantoroR. Del BoV. LucchiniV. CrugnolaD. PapadimitriouS. SalaniN. BresolinG.P. Comi + Article (author) -
Bank of DNA, cell lines and nerve-muscle-cardiac tissues 1-gen-2005 C. LampertiC. ZeccaM.E. FrugugliettiV. LucchiniG.P. ComiA. BordoniF. FortunatoY. Torrente + Book Part (author) -
Caratterizzazione clinica e molecolare della mutazione MERRF A8344G in una famiglia senza coinvolgimento del SNC 1-gen-2010 V. LucchiniD. RonchiM. G. D'AngeloA. BordoniL. PeverelliN. BresolinG.P. Comi + Conference Object -
Clinical and genetical heterogeneity in a cohort of pediatric patients affected with mitochondrial disorders 1-mag-2011 M. RanieriD. RonchiA. BordoniV. LucchiniF. FortunatoE. FassoneD. TondutiM. RipoloneS. CortiP. VeggiottiG.P. Comi + Article (author) -
Clinical and molecular characterization of a cohort of patients with novel nucleotide alterations of the Dystrophin gene detected by direct sequencing 11-mar-2011 F.M.B. MagriR. Del BoM.G.N. D'AngeloA. GovoniS. GandossiniA. BordoniS. TedeschiF.R. FortunatoV. LucchiniM. CeredaS.P CortiN. BresolinG.P. Comi + Article (author) -
Clinical features of an adult-onset Leigh syndrome caused by the T9176C mutation in the mitochondrial DNA ATPase 6 gene 1-giu-2008 D. RonchiA. BordoniR. VirgilioE. FassoneA. DiFonzoM. ServidaV. LucchiniM. MatteoliN. BresolinG.P. Comi + Article (author) -
CNS involvement in a cohort of pediatric patients affected with mitochondrial disorders caused by heterogeneous biochemical and genetic defects 1-gen-2011 D. RonchiA. CosiA. BordoniV. LucchiniF. FortunatoE. FassoneD. TondutiM. RanieriM. RipoloneS. CortiP. VeggiottiG.P. Comi + Conference Object -
Congenital myopathy with ptosis, ophthalmoplegia and muscle dystrophic changes: a possible sporadic case of myosin heavy chain type IIa myopathy. 1-giu-2009 V. LucchiniV. CrugnolaM. ServidaA. BordoniD. RonchiN. BresolinG.P. ComiY. Torrente + Conference Object -
COQ 10 deficiency in statin related Myopathy. 1-gen-2005 C. LampertiV. LucchiniCRUGNOLA, VERONICAN. Bresolin + Article (author) -
Familial amyotrophic lateral sclerosis with a novel Q23R mutation in the copper/zinc superoxide dismutase gene associated with muscle mitochondrial dysfunction 1-gen-2007 S. CortiA. BordoniD. RonchiD. SantoroD. PapadimitriouC. LampertiV. LucchiniF. MagriM. GuglieriV. CrugnolaN. BresolinG.P. Comi + Article (author) -
Follow-up of a large population of asymptomatic / oligosymptomatic hyperckemic subjects. 1-gen-2006 M.E. FrugugliettiV.CrugnolaV.LucchiniC.ZeccaC.LampertiG.P.ComiN.Bresolin + Article (author) -
Frequency and characterisation of anoctamin 5 mutations in a cohort of Italian limb-girdle muscular dystrophy patients 1-nov-2012 F. MagriR. Del BoA. GovoniA. BordoniV. LucchiniS. CortiN. BresolinG.P. Comi + Article (author) -
Genotype and phenotype characterization in a large dystrophinopathic cohort with extended follow-up 1-set-2011 F. MagriA. GovoniM.G. D'AngeloR. Del BoA. BordoniTEDESCHI, SABRINAF. FortunatoV. LucchiniS. BonatoC. LampertiY. TorrenteS. CortiN. BresolinG.P. Comi + Article (author) -
IL DIFETTO OSSIDATIVO E LE ALTERAZIONI DEL DNA MITOCONDRIALE IN TOPI TRANSGENICI MODELLO ANIMALE DELLA ATASSIA SPINOCEREBELLARE DI TIPO 1 8-feb-2012 V. Lucchini Doctoral Thesis -
Impaired muscle mitochondrial biogenesis and myogenesis in spinal muscular atrophy 1-gen-2015 M. RipoloneD. RonchiV. LucchiniI. ColomboL. VillaA. BordoniF. FortunatoS. CortiG.P. Comi + Article (author) -
Incidental Mitochondrial Myopathy 1-gen-2010 V. CrugnolaV. LucchiniD. RonchiM.G. D'AngeloA. BordoniL. PeverelliN. BresolinG.P. Comi + Conference Object -
Miopatia mitocondriale con fenotipo clinico “limb-girdle”: studio morfologico e biomolecolare 1-gen-2010 V. LucchiniD. RonchiM. G. D'AngeloA. BordoniL. PeverelliN. BresolinG. P. Comi + Conference Object -
Miopatia progressiva con ptosi, oftalmoplagia e aspetti distrofici alla biopsia muscolare 1-giu-2009 V. LucchiniV. CrugnolaA. , BordoniD. RonchiN. BresolinG. P. ComiY. Torrente + Conference Object -
Mitochondrial changes in platelets are not related to those in skeletal muscle during human septic shock 1-mag-2014 A. ProttiF. FortunatoM. PluderiV. LucchiniG.P. ComiL. Gattinoni + Article (author) -