LOTTA, LUCA ANDREA

LOTTA, LUCA ANDREA  

Universita' degli Studi di MILANO  

Risultati 1 - 15 di 15 (tempo di esecuzione: 0.128 secondi).
Titolo Data di pubblicazione Autore(i) Tipo File Abstract
Complications of whole-exome sequencing for causal gene discovery in primary platelet secretion defects 30-set-2019 Gorski, Marcin MFemia, Eti ALa Marca, SilviaPappalardo, EmanuelaLotta, Luca AArtoni, AndreaPeyvandi, Flora + Article (author) -
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)) 1-feb-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.Mori A.Tanaka T.Lotta L. A.Levi S.Bell A. + Article (author) -
Early-onset ischaemic stroke : analysis of 58 polymorphisms in 17 genes involved in methionine metabolism 1-ago-2010 F. PeyvandiL.A. LottaP.M. Mannucci + Article (author) -
Measurement and prevalence of circulating ADAMTS13-specific immune complexes in autoimmune thrombotic thrombocytopenic purpura 1-gen-2014 L.A. LottaC. ValsecchiI. ManciniA. ArtoniF. Peyvandi + Article (author) -
Next-generation sequencing study finds an excess of rare, coding single-nucleotide variants of ADAMTS13 in patients with deep vein thrombosis 1-lug-2013 L.A. LottaWANG, MIAOHANS.M. PassamontiE. PappalardoC. ValsecchiG. RandiF. Peyvandi + Article (author) -
A novel CD46 mutation in a patient with microangiopathy clinically resembling thrombotic thrombocytopenic purpura and normal ADAMTS13 activity 1-gen-2015 R. RossioL.A. LottaI. GaragiolaM. CugnoF. Peyvandi + Article (author) -
Platelet reactive conformation and multimeric pattern of von Willebrand factor in acquired thrombotic thrombocytopenic purpura during acute disease and remission 1-set-2011 L.A. LottaP.M. MannucciF. Peyvandi + Article (author) -
Preoperative hematocrit concentration and the risk of stroke in patients undergoing isolated coronary-artery bypass grafting 1-gen-2013 L.A. LottaF. Peyvandi + Article (author) -
Prevalence of disease and relationships between laboratory phenotype and bleeding severity in platelet primary secretion defects 1-apr-2013 L.A. LottaA. MainoR. RossioA. ArtoniF. Peyvandi + Article (author) -
Raised haematocrit concentration and the risk of death and vascular complications after major surgery 1-lug-2013 L.A. LottaF. Peyvandi + Article (author) -
Residual plasmatic activity of ADAMTS13 correlates with phenotype severity in congenital thrombotic thrombocytopenic purpura 12-lug-2012 L.A. LottaG. RemuzziI.M. GaragiolaF. Peyvandi + Article (author) -
Targeted sequencing to identify novel genetic risk factors for deep vein thrombosis: a study of 734 genes 1-dic-2018 Lotta, L. A.Gorski, M. M.Bucciarelli, P.Payvandi, F. + Article (author) -
Thrombotic Thrombocytopenic Purpura (TTP) Database 1-feb-2007 F. PeyvandiI. GaragiolaA. MainoS. LavoretanoG. MeratiR. PallaC. ValsecchiP.M. MannucciL.A. LottaI. ManciniB. FerrariA. ArtoniG. Bettoni + Multimedia Object (author) -
Treatment of chronic hepatitis C with pegylated interferon-α in a patient with recurrent autoimmune thrombotic thrombocytopenic purpura 1-feb-2013 L.A. LottaE. DegasperiA. AghemoB. FerrariF. PeyvandiM. Colombo Article (author) -
Whole-exome sequencing to identify genetic risk variants underlying inhibitor development in severe hemophilia A patients 9-giu-2016 M.M. GorskiL.A. LottaE. PappalardoI. GaragiolaI. ManciniM.E. MancusoM.R. FasuloF. Peyvandi + Article (author) -