Zobrazeno 1 - 10 of 30 pro vyhledávání: '"Raúl Pérez Bianco"'
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Akademický článek
Sixteen novel hemophilia A causative mutations in the first Argentinian series of severe molecular defects
Autor: Liliana C. Rossetti, Claudia Pamela Radic, Miguel Candela, Raúl Pérez Bianco, Miguel de Tezanos Pinto, Anne Goodeve, Irene B. Larripa, Carlos D. De Brasi
Publikováno v: Haematologica, Vol 92, Iss 6 (2007)
Hemophilia A (HA) is caused by heterogeneous mutations in the factor VIII gene (F8). This paper reports 16 novel small F8-mutations and rearrangements in a series of 80 Argentinian families with severe-HA. Using an updated scheme for F8-analysis, we
Externí odkaz: https://doaj.org/article/52936d26ad09443eaddf0690ec512ed0
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2
Severe haemophilia A patients have reduced numbers of peripheral memory B cells
Autor: M. M. E. De Bracco, Raúl Pérez Bianco, L. Primiani, M. B. Irigoyen, M. Candela, N. Galassi, M. Felippo
Publikováno v: Haemophilia. 18:437-443
Summary. The development of inhibitors is a compli-cation of replacement treatment in Haemophilia. Lossof factor VIII-specific memory B cells in the spleen isassociated with down regulation of antibodies in micetreated with high doses of FVIII, but
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5093dd6e4befc6e3fc6739e73ccb7e22
https://doi.org/10.1111/j.1365-2516.2011.02642.x
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3
Elective orthopaedic surgery for haemophilia patients with inhibitors: single centre experience of 40 procedures and review of the literature
Autor: Horacio Caviglia, Raúl Pérez Bianco, N. Moretti, Gustavo Galatro, M. Candela, D. Neme
Publikováno v: Haemophilia. 17:910-919
With the introduction of safe and effective factor VIII/IX-bypassing agents--recombinant activated factor VII (rFVIIa) and plasma-derived activated prothrombin complex concentrates (pd-APCC)--elective orthopaedic surgery (EOS) is a viable option for
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d3995e6263751e37f0ab72a4d2a50633
https://doi.org/10.1111/j.1365-2516.2011.02504.x
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4
Secondary prophylaxis with rFVIIa in hemophilia and inhibitors: Recommendations from an Experts Committee from Argentina
Autor: Raúl, Pérez Bianco, Daniela, Neme, Miguel, Candela, Miguel de, Tezanos Pinto
Publikováno v: Medicina (Buenos Aires), Vol 70, Iss 3, Pp 209-214 (2010)
Secondary prophylaxis with rFVIIa has been the subject of several publications in the past few years. However, there is no general consensus on how this treatment should be put into practice, as publications have been very heterogeneous in the dosing
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::7db758a1162fded2e4681f224dbf7588
http://www.scielo.org.ar/scielo.php?script=sci_arttext&pid=S0025-76802010000300001&lng=en&tlng=en
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6
Evidence of occult HCV genotypes in haemophilic individuals with unapparent HCV mixed infections
Autor: Marcelo Corti, Mariela Bastón, Natalia Aloisi, Raúl Pérez Bianco, Rodolfo Hector Campos, Gabriel García, Beatriz Ruibal Ares, Patricia Baré, Andrés Carlos Alberto Culasso, Cecilia Parodi
Publikováno v: Haemophilia. 14:816-822
Individuals with haemophilia who received non heat-treated factor concentrates were likely to undergo multiple exposures to the hepatitis C virus (HCV). Therefore, HCV mixed-genotype infections might be more frequent in these patients than in the gen
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a89fa932b6dc081fa218a41a270e5a28
https://doi.org/10.1111/j.1365-2516.2008.01773.x
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Randomized, prospective clinical trial of recombinant factor VIIa for secondary prophylaxis in hemophilia patients with inhibitors
Autor: Toshko Lissitchkov, Raúl Pérez Bianco, Margit A. Serban, E. Erhardtsen, Liselotte S. Ebbesen, Barbara A. Konkle, L. Rusen
Publikováno v: Journal of Thrombosis and Haemostasis. 5:1904-1913
Summary. Background: Hemophilic patients with factor VIII (FVIII) and FIX inhibitors suffer from frequent bleeding episodes and reduced quality of life. Objectives: To evaluate whether secondary prophylaxis with activated recombinant factor VII (rFVI
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00c05ce0d142cc47aa90a30f81848ca6
https://doi.org/10.1111/j.1538-7836.2007.02663.x
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9
Sixteen novel hemophilia A causative mutations in the first Argentinian series of severe molecular defects
Autor: Miguel de Tezanos Pinto, Claudia Pamela Radic, Raúl Pérez Bianco, Anne Goodeve, Carlos Daniel de Brasi, M. Candela, Irene Larripa, Liliana Carmen Rossetti
Publikováno v: CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Hemophilia A (HA) is caused by heterogeneous mutations in the factor VIII gene (F8). This paper reports 16 novel small F8-mutations and rearrangements in a series of 80 Argentinian families with severe-HA. Using an updated scheme for F8-analysis, we
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::773eb1c49905ea1c982b14c521899218
https://doi.org/10.3324/haematol.11112
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10
Antibodies to hepatitis C and other viral markersin multi-transfused patients from Argentina
Autor: Ana del Pozo, Silvina Kuperman, María Angélica Marcosa, Gabriela Miguez, Mirta Remesar, Raúl Pérez-Bianco, Alberto Manterola, Cecilia Gamba, Sergio Caldarola
Publikováno v: Journal of Clinical Virology. 34:S20-S26
The knowledge of transfusion-transmitted viral infections in Argentina is scarce. A regional study organized by the Pan American Health Organization let us asses the current status.To estimate the prevalence of HCV, HBV and HIV infection in a populat
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ceaac3408dc51071c6c2dfac26e3ceb
https://doi.org/10.1016/s1386-6532(05)80030-7
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