Sfoglia per Autore
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
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
Highly sensitive chemiluminescent method for the detection of maternal cell contamination in human cord blood stored for allotransplantation : the experience of the Milano cord blood bank
1997 F. Poli, L. Crespiatico, L. Lecchi, G. Sirchia, M. Scalamogna, S.M. Sirchia, I. Garagiola, L. Pedranzini
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
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
Trisomic zygote rescue revealed by DNA polymorphism analysis in confined placental mosaicism
1998 S.M. Sirchia, I. Garagiola, G. Colucci, S. Guerneri, F. Lalatta, M.G. Grimoldi, G. Simoni
Highly sensitive chemiluminescent method for the detection of cell contamination
1998 S.M. Sirchia, I. Garagiola, C. De Andreis, L. Pedranzini, F. Poli, F.R. Grati, B. Diomelli, G. Simoni
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
Losses of heterozygosity in oral and oropharyngeal epithelial carcinomas
2000 F.R. Grati, S.M. Sirchia, I. Garagiola, E. Sironi, S. Galioto, F. Rossella, P. Serafini, F. Dulcetti, A. Bozzetti, R. Brusati, G. Simoni
Losses of heterozygosity in endometrial adenocarcinomas : positive correlations with histopathological parameters
2000 S.M. Sirchia, E. Sironi, F.R. Grati, P. Serafini, I. Garagiola, F. Rossella, F. Dulcetti, G. Pardi, S. Garsia, G. Simoni
Pitfalls in molecular diagnosis in a family with severe factor VII (FVII) deficiency-misdiagnosis by direct sequence analysis using a PCR product
2003 I. Garagiola, R. Palla, F. Peyvandi
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
International Registry of rare bleeding disorders (RBD)
2004 F. Peyvandi, M. Spreafico, M. Menegatti, I.M. Garagiola, L. Tagliabue, P.M. Mannucci
The P303T mutation in the human factor VII (FVII) gene alters the conformational state of the enzyme and causes a severe functional deficiency
2004 F. Peyvandi, R. De Cristofaro, I. Garagiola, R. Palla, S. Akhavan, R. Landolfi, P.M. Mannucci
The First Deletion Mutation in the TSP1-6 Repeat Domain of ADAMTS13 Leads to a Secretion Defect
2005 F. Peyvandi, S. Lavoretano, R. Palla, I. Garagiola, C. Valsecchi, R. Lombardi, M.T. Canciani, P.M. Mannucci
Localization and Function of Platelet ADAMTS-13
2005 F. Peyvandi, I. Garagiola, A. Artoni, R. Lombardi, R. Palla, R. De Cristofaro, P.M. Mannucci, S. Lavoretano, C. Valsecchi
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
International Rare Bleeding Disorders Database
2005 F. Peyvandi, R. Palla, M. Menegatti, I. Garagiola, S.M. Siboni, P.M. Mannucci, M. Spreafico, L. Tagliabue, S. Lavoretano, A. Cairo
Mutations in the MCFD2 gene and a novel mutation in the LMAN1 gene in Indian families with combined deficiency of factor V and VIII
2005 D. Mohanty, K. Ghosh, S. Shetty, M. Spreafico, I. Garagiola, F. Peyvandi
Role of the 2 adenine (g.11293_11294insAA) insertion polymorphism in the 3' untranslated region of the factor VII (FVII) gene : molecular characterization of a patient with severe FVII deficiency
2005 F. Peyvandi, I. Garagiola, R. Palla, N. Marziliano, P.M. Mannucci
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