Martin Abelleyro

PUBLICACIONES CIENTÍFICAS EN REVISTAS INDEXADAS 1. Radic CP - Rossetti LC, Zuccoli JR, Abelleyro MM, Larripa IB, De Brasi CD. Inverse shifting PCR based prenatal diagnosis of hemophilia-causative inversions involving int22h and int1h hotspots from chorionic villus samples. Prenatal Diagnosis 2009, 29(12): 1183-5. 2. Miguel Martín Abelleyro, Liliana Carmen Rossetti, Claudia Pamela Radic, Miguel Candela, Irene Beatriz Larripa, Carlos Daniel De Brasi. Are int22h mediated deletions a common cause of hemophilia?. Ann Hematol 2012, 91(4): 633-6. 3. Rossetti LC, Radic CP, Abelleyro MM, Larripa IB, De Brasi CD. Eighteen Years of Molecular Genotyping the Hemophilia Inversion Hotspot: From Southern Blot to Inverse Shifting-PCR. Int J Mol Sci 2011, 12(10): 7271-85. 4. Radic CP, Rossetti LC, Abelleyro MM, Candela M, Pérez Bianco R, Tezanos Pinto M, Larripa IB, Goodeve A, De Brasi CD. Assessment of the F9 genotype-specific FIX inhibitor risks and characterization of 10 novel severe F9 defects in the first molecular series of Argentine patients with haemophilia B. Thromb Haemost 2013, 109(1): 24-33. 5. Rossetti LC, Szurkalo I, Radic CP, Abelleyro MM, Primiani L, Neme D, Candela M, Bianco RP, de Tezanos Pinto M, Larripa IB, De Brasi CD. Factor VIII genotype characterization of haemophilia A affected patients with transient and permanent inhibitors: a comprehensive Argentine study of inhibitor risks. Haemophilia 2013, 19(4): 511-8