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Mostrati risultati da 1 a 20 di 77
Titolo Data di pubblicazione Autori Tipo File Abstract
Characterization of four microsatellites in an Italian population and their application to paternity testing 1996 S.M. SirchiaI. Garagiola + Article (author) -
Cytogenetic abnormalities and microsatellite instability in endometrial adenocarcinoma 1997 S.M. SirchiaF. RossellaI. GaragiolaG. BulfamanteG. Simoni + Article (author) -
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 S.M. SirchiaI. Garagiola + Article (author) -
Absence of detectable maternal DNA and identification of proviral HIV in the cord blood of two infants who became HIV-infected 1997 G. SimoniSACCHI, LAURAS.M. SirchiaI.M. GaragiolaT. PersicoG. PardiA.E. Semprini + Article (author) -
Detection of maternal DNA in human cord blood stored for allotransplantation by a highly sensitive chemiluminescent method 1997 S.M. SirchiaI. GaragiolaL. Pedranzini + Article (author) -
Trisomic zygote rescue revealed by DNA polymorphism analysis in confined placental mosaicism 1998 S.M. SirchiaI. GaragiolaM.G. GrimoldiG. Simoni + Article (author) -
Highly sensitive chemiluminescent method for the detection of cell contamination 1998 S.M. SirchiaI. GaragiolaG. Simoni + Article (author) -
Detection of maternal DNA in cord blood at birth after elective caesarean section or vaginal delivery 2000 A. E. SempriniI. GaragiolaS. M. SirchiaV. SavasiG. Simoni + Article (author) -
Losses of heterozygosity in oral and oropharyngeal epithelial carcinomas 2000 F.R. GratiS.M. SirchiaI. GaragiolaE. SironiF. RossellaR. BrusatiG. Simoni + Article (author) -
Losses of heterozygosity in endometrial adenocarcinomas : positive correlations with histopathological parameters 2000 S.M. SirchiaF.R. GratiI. GaragiolaF. RossellaG. PardiG. Simoni + Article (author) -
Pitfalls in molecular diagnosis in a family with severe factor VII (FVII) deficiency-misdiagnosis by direct sequence analysis using a PCR product 2003 I. GaragiolaR. PallaF. Peyvandi Article (author) -
A rare inherited coagulation disorder : combined homozygous factor VII and factor X deficiency 2004 M. MenegattiI.M. GaragiolaP.M. MannucciF. Peyvandi + Article (author) -
International Registry of rare bleeding disorders (RBD) 2004 F. PeyvandiM. SpreaficoM. MenegattiI. M. GaragiolaL. TagliabueP. M. Mannucci Article (author) -
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. PeyvandiI. GaragiolaR. PallaP.M. Mannucci + Article (author) -
The First Deletion Mutation in the TSP1-6 Repeat Domain of ADAMTS13 Leads to a Secretion Defect 2005 F. PeyvandiS. LavoretanoR. PallaI. GaragiolaC. ValsecchiP.M. Mannucci + Article (author) -
Localization and Function of Platelet ADAMTS-13 2005 F. PeyvandiI. GaragiolaR. PallaP.M. MannucciS. LavoretanoC. Valsecchi + Article (author) -
ADAMTS-13 Binds Platelets in a Specific, Divalent Cation and Activation Dependent Manner 2005 A. ArtoniI. GaragiolaF. PeyvandiP.M. Mannucci + Article (author) -
International Rare Bleeding Disorders Database 2005 F. PeyvandiR. PallaM, MenegattiI. GaragiolaS. M. SiboniP. M. MannucciM. SpreaficoL. TagliabueS. Lavoretano + Multimedia Object (author) -
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 M. SpreaficoI. GaragiolaF. Peyvandi + Article (author) -
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. PeyvandiI. GaragiolaR. PallaP.M. Mannucci + Article (author) -
Mostrati risultati da 1 a 20 di 77
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