GARAGIOLA, ISABELLA MARIA
GARAGIOLA, ISABELLA MARIA
Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti
A novel CD46 mutation in a patient with microangiopathy clinically resembling thrombotic thrombocytopenic purpura and normal ADAMTS13 activity
2015 R. Rossio, L.A. Lotta, S. Pontiggia, N. Borsa Ghiringhelli, I. Garagiola, G. Ardissino, D. Mikovic, M. Cugno, F. Peyvandi
A novel mutation of alpha2-plasmin inhibitor gene causes an inherited deficiency and a bleeding tendency
2008 A. Maino, I. Garagiola, A. Artoni, S. Al-Humood, F. Peyvandi
A Randomized Trial of Factor VIII and Neutralizing Antibodies in Hemophilia A
2016 F. Peyvandi, P.M. Mannucci, I. Garagiola, A. El Beshlawy, M. Elalfy, V. Ramanan, P. Eshghi, S. Hanagavadi, R. Varadarajan, M. Karimi, M.V. Manglani, C. Ross, G. Young, T. Seth, S. Apte, D.M. Nayak, E. Santagostino, M.E. Mancuso, A.C. Sandoval Gonzalez, J.N. Mahlangu, S. Bonanad Boix, M. Cerqueira, N.P. Ewing, C. Male, T. Owaidah, V. Soto Arellano, N.L. Kobrinsky, S. Majumdar, R. Perez Garrido, A. Sachdeva, M. Simpson, M. Thomas, E. Zanon, B. Antmen, K. Kavakli, M.J. Manco Johnson, M. Martinez, E. Marzouka, M.G. Mazzucconi, D. Neme, A. Palomo Bravo, R. Paredes Aguilera, A. Prezotti, K. Schmitt, B.M. Wicklund, B. Zulfikar, F.R. Rosendaal
A rare inherited coagulation disorder : combined homozygous factor VII and factor X deficiency
2004 M. Menegatti, M. Karimi, I.M. Garagiola, P.M. Mannucci, F. Peyvandi
A recurrent F8 mutation (c.6046C>T) causing hemophilia A in 8% of northern Italian patients : evidence for a founder effect
2016 I. Garagiola, S. Seregni, M. Mortarino, M.E. Mancuso, M.R. Fasulo, L.D. Notarangelo, F. Peyvandi
Absence of detectable maternal DNA and identification of proviral HIV in the cord blood of two infants who became HIV-infected
1997 C. De Andreis, G. Simoni, C. Castagna, L. Sacchi, S.M. Sirchia, I.M. Garagiola, T. Persico, P. Serafini, G. Pardi, A.E. Semprini
ADAMTS-13 Binds Platelets in a Specific, Divalent Cation and Activation Dependent Manner
2005 A. Artoni, I. Garagiola, R. Lombardi, F. Peyvandi, P.M. Mannucci
ADAMTS13 mutations and polymorphisms in congenital thrombotic thrombocytopenic purpura
2010 L.A. Lotta, I. Garagiola, R. Palla, A. Cairo, F. Peyvandi
Advances in the treatment of bleeding disorders
2016 F. Peyvandi, I. Garagiola, E. Biguzzi
Characterization of four microsatellites in an Italian population and their application to paternity testing
1996 S.M. Sirchia, I. Garagiola, C. De Andreis, I. Gazzoli, M. Gramegna, G. Colucci
Clinical advances in gene therapy updates on clinical trials of gene therapy in haemophilia
2019 F. Peyvandi, I. Garagiola
Clustered F8 missense mutations cause hemophilia A by combined alteration of splicing and protein biosynthesis and activity
2018 I. Donadon, J.H. Mcvey, I. Garagiola, A. Branchini, M. Mortarino, F. Peyvandi, F. Bernardi, M. Pinotti
Cytogenetic abnormalities and microsatellite instability in endometrial adenocarcinoma
1997 S.M. Sirchia, S. Pariani, F. Rossella, I. Garagiola, C. De Andreis, G. Bulfamante, E. Zannoni, U. Radaelli, G. Simoni
Dalla diagnosi di portatrice di emofilia alla diagnosi prenatale
2007 F. Peyvandi, L. Tagliabue, M. Menegatti, I.M. Garagiola, E. Santagostino
Database on rare bleeding disorder (RBDS) : phenotype and genotype analysis on 400 affected patients
2007 M. Spreafico, M. Menegatti, I. Garagiola, R. Palla, L. Tagliabue, M. Karimi, M. Lak, A. Srivastava, R. Saxena, S. Shetty, K. Kavakli, M.B. Dolnicar, S. Aronis Vournas, R. Asselta, S. Duga, P.M. Mannucci, F. Peyvandi
Degradation of two novel congenital TTP ADAMTS13 mutants by the cell proteasome prevents ADAMTS13 secretion
2016 M. Underwood, F. Peyvandi, I. Garagiola, S. Machin, I. Mackie
Detection of maternal DNA in cord blood at birth after elective caesarean section or vaginal delivery
2000 A.E. Semprini, C. De Andreis, S. Fiore, I. Garagiola, S.M. Sirchia, V. Savasi, M.L. Newell, G. Simoni
Detection of maternal DNA in human cord blood stored for allotransplantation by a highly sensitive chemiluminescent method
1997 F. Poli, S.M. Sirchia, M. Scalamogna, I. Garagiola, L. Crespiatico, L. Pedranzini, L. Lecchi, G. Sirchia
Development of a specific monoclonal antibody to detect male cells expressing the rps4y1 protein
2021 S. Spena, C. Cordiglieri, I. Garagiola, F. Peyvandi
Future of coagulation factor replacement therapy
2013 F. Peyvandi, I. Garagiola, S. Seregni