BONATO, SARA

BONATO, SARA  

Universita' degli Studi di MILANO  

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Risultati 1 - 20 di 33 (tempo di esecuzione: 0.004 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
A novel homozygous PLA2G6 mutation causes dystonia-parkinsonism 1-mar-2015 E. MonfriniG. FrancoL. BorelliniI. TrezziG. Monzio CompagnoniD. RonchiS. BonatoN. BresolinS. CortiG.P. Comi + Article (author) -
A novel missense mutation of IGHMBP2 gene in an Italian infant with spinal muscular atrophy with respiratory distress type 1 1-gen-2005 R. Del BoS. BonatoROSSETTI, GIORGIAS. CortiN. BresolinV. CarnelliG.P. Comi + Article (author) -
Bioengineering and muscular dystrophy 1-gen-2009 M.G. D’AngeloS. GandossiniS. BonatoG.P. ComiN. Bresolin. + Conference Object -
Clinical evaluation of muscular dystrophies: new tools from BioEngineering. 1-giu-2009 M.G. D’AngeloS. GandossiniS. BonatoG.P. ComiN. Bresolin + Conference Object -
Clinical features and disease course of patients with acute ischaemic stroke just before the Italian index case: Was COVID-19 already there? 1-ago-2021 Pietroboni, Anna MLanfranconi, SilviaCarandini, TizianaArighi, AndreaAbati, ElenaBrusa, RobertaCostamagna, GianlucaLazzeri, GiuliaMauri, EleonoraPozzato, MattiaValcamonica, GloriaVilla, DavideBonato, SaraComi, Giacomo PBresolin, NereoGalimberti, DanielaScarpini, Elio + Article (author) -
Clinical trial using nitric oxide releasing drug and nonsteroidal antiinflammatory drugs in muscular dystrophy: Design of a study. 1-gen-2009 S. GandossiniM.G. d’AngeloS. BonatoG.P. ComiF. MagriN. BresolinE. Clementi + Conference Object -
Consumption of complement in a 26-year-old woman with severe thrombotic thrombocytopenia after ChAdOx1 nCov-19 vaccination 1-nov-2021 Cugno M.Griffini S.Valenti L.Bonato S.Comi G.Artoni A.Meroni P. L.Peyvandi F. + Article (author) -
Dystonia-ataxia syndrome with permanent torsional nystagmus caused by ECHS1 deficiency 1-gen-2020 Ronchi, DarioMonfrini, EdoardoBonato, SaraCinnante, ClaudiaSalani, SabrinaBordoni, AndreinaFortunato, FrancescoCorti, StefaniaBresolin, NereoComi, Giacomo P + Article (author) -
Expanding the genotypic and phenotypic spectrum of Beta-propeller-associated neurodegeneration (BPAN) 1-gen-2021 Monfrini, EdoardoBonato, SaraFrattini, EmanueleFranco, GiuliaCorti, StefaniaComi, Giacomo PietroBresolin, Nereo + 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) -
Intrafamilial variable presentation of CMT2, spastic paraparesis and cognitive impairment caused by a novel autosomal dominant MFN2 mutation 1-gen-2007 R. Del BoS. BonatoM.G. D’AngeloN. BresolinG.P. Comi + Conference Object -
La bioingegneria nella valutazione del respiro nelle distrofie muscolari 1-giu-2009 M.G. D'AngeloS. BonatoG.P. ComiN. Bresolin + Conference Object -
La pletismografia optoelettrica per la valutazione della funzionalità respiratoria nella distrofia muscolare di Duchenne 1-giu-2009 M.G. D'AngeloS. GandossiniS. BonatoG.P. ComiN. Bresolin + Conference Object -
Loss of the nucleoporin Aladin in central nervous system and fibroblasts of Allgrove Syndrome 1-gen-2019 Ronchi, DarioBonato, SaraPittaro, AlessandraCompagnoni, Giacomo MonzioBordoni, AndreinaSalani, SabrinaFrattini, EmanueleLopez, GianlucaCorti, StefaniaComi, Giacomo PBresolin, Nereo + Article (author) -
Low abdominal contribution to breathing as daytime predictor of nocturnal desaturation in adolescents and young adults with Duchenne muscular dystrophy 1-gen-2012 M.G. D'AngeloS. GandossiniS. BonatoE. BrighinaG.P. ComiN. Bresolin + Article (author) -
Massive cerebral venous thrombosis due to vaccine-induced immune thrombotic thrombocytopenia 1-gen-2021 Bonato, SaraArtoni, AndreaLa Marca, SilviaClerici, MarigraziaComi, Giacomo PietroTripodi, ArmandoPeyvandi, Flora + Article (author) -
Mitochondrial DNA G8363A mutation in the tRNA Lys gene : clinical features of a new family 1-giu-2008 R. VirgilioD. RonchiA. BordoniE. FassoneS. BonatoG. ContiS. CortiN. BresolinG.P. Comi + Article (author) -
Mitochondrial DNA G8363A mutation in the tRNA Lys gene: clinical, biochemical and pathological study 15-giu-2009 R. VirgilioD. RonchiA. BordoniE. FassoneS. BonatoS. CortiN. BresolinG.P. Comi + Article (author) -
Molecular epidemiology and clinical features of a large Italian cohort of 291 dystrophinopathic patients. 1-giu-2009 F. MagriM.G. D’AngeloR. Del BoR. VirgilioS. BonatoS. GandossiniA. BordoniS. CortiV. CrugnolaC. LampertiN. BresolinG.P. Comi. + Conference Object -
Mutational analysis of COQ2 in patients with MSA in Italy 1-set-2016 D. RonchiG. FrancoR. Del BoF. FortunatoL. BorelliniI. TrezziG. Monzio CompagnoniE. MonfriniE. FrattiniS. BonatoA. PrioriN. BresolinS. CortiG.P. Comi + Article (author) -