GARAGIOLA, ISABELLA MARIA

GARAGIOLA, ISABELLA MARIA  

Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti  

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Risultati 1 - 20 di 73 (tempo di esecuzione: 0.004 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
A novel mutation of alpha2-plasmin inhibitor gene causes an inherited deficiency and a bleeding tendency 1-gen-2008 A. MainoI. GaragiolaA. ArtoniF. Peyvandi + Article (author) -
A rare inherited coagulation disorder : combined homozygous factor VII and factor X deficiency 1-set-2004 M. MenegattiI.M. GaragiolaP.M. MannucciF. Peyvandi + Article (author) -
Absence of detectable maternal DNA and identification of proviral HIV in the cord blood of two infants who became HIV-infected 1-lug-1997 G. SimoniSACCHI, LAURAS.M. SirchiaI.M. GaragiolaT. PersicoG. PardiA.E. Semprini + Article (author) -
ADAMTS-13 Binds Platelets in a Specific, Divalent Cation and Activation Dependent Manner 1-gen-2005 A. ArtoniI. GaragiolaF. PeyvandiP.M. Mannucci + Article (author) -
ADAMTS13 mutations and polymorphisms in congenital thrombotic thrombocytopenic purpura 1-gen-2010 L.A. LottaI. GaragiolaR. PallaF. Peyvandi + Article (author) -
Advances in the treatment of bleeding disorders 1-gen-2016 Peyvandi F.Garagiola I. + Article (author) -
Characterization of four microsatellites in an Italian population and their application to paternity testing 1-apr-1996 S.M. SirchiaI. Garagiola + Article (author) -
Clinical advances in gene therapy updates on clinical trials of gene therapy in haemophilia 1-set-2019 Peyvandi F.Garagiola I. Article (author) -
Clustered F8 missense mutations cause hemophilia A by combined alteration of splicing and protein biosynthesis and activity 1-feb-2018 Garagiola, IsabellaMortarino, MimosaPeyvandi, Flora + Article (author) -
Cytogenetic abnormalities and microsatellite instability in endometrial adenocarcinoma 1-apr-1997 S.M. SirchiaF. RossellaI. GaragiolaG. BulfamanteG. Simoni + Article (author) -
Dalla diagnosi di portatrice di emofilia alla diagnosi prenatale 1-gen-2007 F. PeyvandiL. TagliabueM. MenegattiI. M. Garagiola + Working Paper -
Database on rare bleeding disorder (RBDS) : phenotype and genotype analysis on 400 affected patients 1-ago-2007 M. SpreaficoM. MenegattiI. GaragiolaR. PallaL. TagliabueR. AsseltaS. DugaP.M. MannucciF. Peyvandi + Article (author) -
Degradation of two novel congenital TTP ADAMTS13 mutants by the cell proteasome prevents ADAMTS13 secretion 1-gen-2016 Peyvandi F.Garagiola I. + Article (author) -
Detection of maternal DNA in cord blood at birth after elective caesarean section or vaginal delivery 31-mar-2000 A. E. SempriniI. GaragiolaS. M. SirchiaV. SavasiG. Simoni + Article (author) -
Detection of maternal DNA in human cord blood stored for allotransplantation by a highly sensitive chemiluminescent method 1-dic-1997 S.M. SirchiaI. GaragiolaL. Pedranzini + Article (author) -
Development of a specific monoclonal antibody to detect male cells expressing the rps4y1 protein 1-feb-2021 Spena S.Garagiola I.Peyvandi F. + Article (author) -
The EHA research roadmap: Blood coagulation and hemostatic disorders 1-ott-2021 Cattaneo M.Garagiola I.Peyvandi F. + Article (author) -
The First Deletion Mutation in the TSP1-6 Repeat Domain of ADAMTS13 Leads to a Secretion Defect 1-gen-2005 F. PeyvandiS. LavoretanoR. PallaI. GaragiolaC. ValsecchiP.M. Mannucci + Article (author) -
Future of coagulation factor replacement therapy 1-giu-2013 F. PeyvandiI. GaragiolaS. Seregni Article (author) -
Genetic diagnosis of haemophilia and other inherited bleeding disorders 1-lug-2006 F. PeyvandiI. GaragiolaS. LavoretanoM. MenegattiR. PallaM. SpreaficoL. TagliabueR. AsseltaS. DugaP.M. Mannucci + Article (author) -