LOTTA, LUCA ANDREA

LOTTA, LUCA ANDREA  

Universita' degli Studi di MILANO  

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Titolo Data di pubblicazione Autori Tipo File Abstract
Corrigendum to ‘An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs’ [J Hepatol 2021;75(3):572–581] (Journal of Hepatology (2021) 75(3) (572–581), (S0168827821003342), (10.1016/j.jhep.2021.04.055)) 2022 Asselta R.Zhang J.Battezzati P. M.Casella G.Colli A.Cristoferi L.Lampertico P.Malinverno F.Mancuso C.Marra F.Massironi S.Miele L.O'Donnell S.Ronca V.Valenti L.Zuin M.Tanaka T.Lotta L. A.Levi S.Bell A. + Article (author) -
Complications of whole-exome sequencing for causal gene discovery in primary platelet secretion defects 2019 Gorski, Marcin MFemia, Eti ALa Marca, SilviaPappalardo, EmanuelaLotta, Luca AArtoni, AndreaPeyvandi, Flora + Article (author) -
Targeted sequencing to identify novel genetic risk factors for deep vein thrombosis: a study of 734 genes 2018 Lotta, L. A.Gorski, M. M.Bucciarelli, P.Payvandi, F. + Article (author) -
Next-generation DNA sequencing to identify novel genetic risk factors for cerebral vein thrombosis 2018 Gorski, Marcin M.Mancini, IlariaLotta, Luca A.Bucciarelli, PaoloPassamonti, Serena M.Pappalardo, EmanuelaPeyvandi, Flora + Article (author) -
Whole-exome sequencing to identify genetic risk variants underlying inhibitor development in severe hemophilia A patients 2016 M.M. GorskiL.A. LottaE. PappalardoI. GaragiolaI. ManciniM.E. MancusoM.R. FasuloF. Peyvandi + Article (author) -
Next-generation sequencing and in vitro expression study of ADAMTS13 single nucleotide variants in deep vein thrombosis 2016 Pagliari M. T.Lotta L. A.Valsecchi C.Passamonti S. M.Peyvandi F. + Article (author) -
A novel CD46 mutation in a patient with microangiopathy clinically resembling thrombotic thrombocytopenic purpura and normal ADAMTS13 activity 2015 R. RossioL.A. LottaI. GaragiolaM. CugnoF. Peyvandi + Article (author) -
FRETS-VWF73 rather than CBA assay reflects ADAMTS13 proteolytic activity in acquired thrombotic thrombocytopenic purpura patients 2014 I. ManciniC. ValsecchiL.A. LottaR. PallaF. Peyvandi + Article (author) -
Measurement and prevalence of circulating ADAMTS13-specific immune complexes in autoimmune thrombotic thrombocytopenic purpura 2014 L.A. LottaC. ValsecchiI. ManciniA. ArtoniF. Peyvandi + Article (author) -
Raised haematocrit concentration and the risk of death and vascular complications after major surgery 2013 L.A. LottaF. Peyvandi + Article (author) -
Preoperative hematocrit concentration and the risk of stroke in patients undergoing isolated coronary-artery bypass grafting 2013 L.A. LottaF. Peyvandi + Article (author) -
Treatment of chronic hepatitis C with pegylated interferon-α in a patient with recurrent autoimmune thrombotic thrombocytopenic purpura 2013 L.A. LottaE. DegasperiA. AghemoB. FerrariF. PeyvandiM. Colombo Article (author) -
Association between thrombin generation and bleeding severity in 41 patients with coagulation factor VII deficiency 2013 L.A. LottaS.M. SiboniM. ClericiM. MenegattiF. Peyvandi + Article (author) -
Next-generation sequencing study finds an excess of rare, coding single-nucleotide variants of ADAMTS13 in patients with deep vein thrombosis 2013 L.A. LottaWANG, MIAOHANS.M. PassamontiE. PappalardoC. ValsecchiG. RandiF. Peyvandi + Article (author) -
Drop of residual plasmatic activity of ADAMTS13 to undetectable levels during acute disease in a patient with adult-onset congenital thrombotic thrombocytopenic purpura 2013 L.A. LottaF. Peyvandi + Article (author) -
Prevalence of disease and relationships between laboratory phenotype and bleeding severity in platelet primary secretion defects 2013 L.A. LottaA. MainoR. RossioA. ArtoniF. Peyvandi + Article (author) -
Association of a single nucleotide polymorphism of the NPR3 gene promoter with early onset ischemic stroke in an Italian cohort 2013 L.A. LottaF. PeyvandiP.M. Mannucci + Article (author) -
STUDIES ON THE GENETIC PREDISPOSITION TO COMMON THROMBOTIC DISEASES 2012 L.A. Lotta Doctoral Thesis -
Residual plasmatic activity of ADAMTS13 correlates with phenotype severity in congenital thrombotic thrombocytopenic purpura 2012 L.A. LottaG. RemuzziI.M. GaragiolaF. Peyvandi + Article (author) -
Case report : use of thienopyridines in a patient with acquired idiopathic thrombotic thrombocytopenic purpura 2012 L.A. LottaI. ManciniF. Peyvandi + Article (author) -