Final Program in it's entirety - MyGirlsBlood
Final Program in it's entirety - MyGirlsBlood
Final Program in it's entirety - MyGirlsBlood
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Index of Poster Presenters cont’d<br />
MOLECULAR GENETICS OF BLEEDING<br />
DISORDERS<br />
21P09<br />
Performance of Inverse Shift<strong>in</strong>g-PCR (IS-PCR) to Investigate<br />
F8 Intron 22 Inversions and Potential Rearrangements<br />
Involv<strong>in</strong>g Int22h Recomb<strong>in</strong>ation<br />
Abelleyro M, Radic P, Rossetti L, Zuccoli J, Larripa I, De Brasi C<br />
IIHema, National Academy of Medic<strong>in</strong>e, Buenos Aires,<br />
Argent<strong>in</strong>a<br />
21P10<br />
Factor VIII Gene Mutations and Polymorphisms <strong>in</strong> IL10 and<br />
TNFA Genes <strong>in</strong> Patients with Severe Hemophilia A <strong>in</strong><br />
Venezuela<br />
Albánez S1 , Porco A1 , Ruiz-Sáez A2 , Boadas A2 , De Bosch N2 1Laboratorio de Genética Molecular Humana B, Universidad<br />
Simón Bolívar, and 2Centro Nacional de Hemofilia, Banco<br />
Metropolitano de Sangre, Caracas, Venezuela<br />
21P11<br />
Detection of Factor IX Gene Mutations by High-Resolution<br />
Melt<strong>in</strong>g Analysis<br />
Classen J1 , Pepermans X1 , Hermans C2 , Lannoy N1 1 2 Center of Human Genetics and Departement of<br />
Haematology, Cl<strong>in</strong>iques Universitaires Sa<strong>in</strong>t-Luc, Bruxelles,<br />
Belgium<br />
21P12<br />
Safety Retroviral System To Generate A Human Recomb<strong>in</strong>ant<br />
Factor VIII Producer Cell L<strong>in</strong>e<br />
Crist<strong>in</strong>a Correa De Freitas M, Maria Fontes A, de Castilho<br />
Fernandes A, Maria Russo-Carbolante E, Picanco-Castro V,<br />
Tadeu Covas D<br />
National Institute of Science And Technology <strong>in</strong> Stem Cells,<br />
Sao Paulo, Brazil<br />
21P13<br />
Ex Vivo Genetic Modification of Liver-Derived Mesenchymal<br />
Stem Cells with Human Factor IX as Therapeutic Approach<br />
for Hemophilia B<br />
De Castilho Fernandes A, Maria Fontes A, Ursoli Ferreira<br />
Melo F, Candido Almeida D, Vianna Bon<strong>in</strong>i Palma P, Tadeu<br />
Covas D<br />
National Institute of Science and Technology <strong>in</strong> Stem Cell<br />
and Cell Therapy – FMR, Sao Paulo, Brazil<br />
21P14<br />
Identification of 5 Novel Mutations <strong>in</strong> Tunisian Families with<br />
Hemophilia B Disease<br />
Elmahmoudi H1 , Gouider E2 , Khoudjetelkhil H1 , Ben Amor M1 ,<br />
Meddeb B2 , Elgaaied A1 1 2 Faculté des sciences de Tunis, Tunisia, Centre de Traitement<br />
des Hémophiles, Hopital Aziza Othmana Tunis, Tunisia<br />
21P15<br />
Generation and Characterization of Mur<strong>in</strong>e Model With<br />
Hemophilia A and Severe Comb<strong>in</strong>ed Immunodeficient<br />
Disease (SCID) for Factor VIII Studies<br />
Gonsales Da Rosa N, Maria Fontes A, de Castilho Fernandes<br />
A, Strazza Rodrigues E, Navarro Ueda Yaochite J, Tadeu<br />
Covas D<br />
National Institute of Science and Technology <strong>in</strong> Stem Cell<br />
and Cell Therapy, Sao Paulo, Brazil<br />
21P16<br />
National Center of Genetics Study on Hemophilia: Mexican<br />
Database and Multidiscipl<strong>in</strong>ary Diagnosis <strong>Program</strong><br />
Jaloma Cruz AR1 , Luna Zaizar H2 , López Jiménez JJ2 , Mundo<br />
Ayala JN2 , González Ramos IA2 , Esparza Flores MA3 1Centro de Investigación Biomédica de Occidente, IMSS,<br />
2Centro Universitario de Ciencias de la Salud, de Guadalajara,<br />
3Federación de Hemofilia de la República Mexicana, A.C.<br />
Universidad, Mexico<br />
21P17<br />
Haplotype Analysis to Determ<strong>in</strong>e Founder Effect <strong>in</strong> 150<br />
Belgian Hemophilia A Patients<br />
Lannoy N1 , Soree N1 , Pepermans X1 and Hermans C2 1 2 Centre of Human Genetics and Department of<br />
Haematology, Université Catholique de Louva<strong>in</strong>, Belgium<br />
21P18<br />
Hemophilia A: Genetic Characterization <strong>in</strong> Patients and<br />
Relatives<br />
L<strong>in</strong>ari S1 , Frusconi S2 , Romol<strong>in</strong>i C2 , M<strong>in</strong>uti B2 , Morf<strong>in</strong>i M1 ,<br />
Torricelli F2 1Agency For Haemophilia -A.O.U. Careggi - Florence, Italy,<br />
2Genetic Unit- A.O.U Careggi - Florence, Italy<br />
21P19<br />
Characterisation of Natural FVIII Variants of the B-Doma<strong>in</strong><br />
Regard<strong>in</strong>g Their Biological Activity<br />
Pahl S1 , Schwaab R2 , Oldenburg J3 , Herb<strong>in</strong>iaux U4 ,<br />
Aburubaiha Z5 1 2 Unicl<strong>in</strong>ic Bonn, Institut of Haematology and<br />
Transfusionmedic<strong>in</strong>e, 3Institute of Experimental Haematology<br />
and Transfusion Medic<strong>in</strong>e, 4Department of Molecular<br />
Haemostaseology, 5University Cl<strong>in</strong>ic Bonn, Bonn, Germany<br />
21P20<br />
A Newly Discovered Mutation among Austrian Hemophilia<br />
A Patients: Population Genetic Analysis to Trace Common<br />
Ancestry<br />
Reitter S1 , von Haeseler A2 , Horvath B3 , Freitag R3 , Pab<strong>in</strong>ger-<br />
Fasch<strong>in</strong>g I1 , Mannhalter C3 1Medical University of Vienna, Department of Medic<strong>in</strong>e I,<br />
2 3 Center for Integrative Bio<strong>in</strong>formatics Vienna, Department<br />
of Medical and Chemical Laboratory Diagnostics, Medical<br />
University of Vienna, Austria<br />
75<br />
Posters, Tuesday and Wednesday