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2012
Fagioli F, Zecca M, Rognoni C, Lanino E, Balduzzi A, Berger M, Messina C, Favre C, Rabusin M, Nigro LLo, Masetti R, Prete A, Locatelli F. Allogeneic hematopoietic stem cell transplantation for Philadelphia-positive acute lymphoblastic leukemia in children and adolescents: a retrospective multicenter study of the Italian Association of Pediatric Hematology and Oncology (AIEOP). Biol Blood Marrow Transplant 2012;18(6):852-60.
Fagioli F, Zecca M, Rognoni C, Lanino E, Balduzzi A, Berger M, Messina C, Favre C, Rabusin M, Nigro LLo, Masetti R, Prete A, Locatelli F. Allogeneic hematopoietic stem cell transplantation for Philadelphia-positive acute lymphoblastic leukemia in children and adolescents: a retrospective multicenter study of the Italian Association of Pediatric Hematology and Oncology (AIEOP). Biol Blood Marrow Transplant 2012;18(6):852-60.
Pecci A, Biino G, Fierro T, Bozzi V, Mezzasoma A, Noris P, Ramenghi U, Loffredo G, Fabris F, Momi S, Magrini U, Pirastu M, Savoia A, Balduini C, Gresele P. Alteration of liver enzymes is a feature of the MYH9-related disease syndrome. PLoS One 2012;7(4):e35986.
Pecci A, Biino G, Fierro T, Bozzi V, Mezzasoma A, Noris P, Ramenghi U, Loffredo G, Fabris F, Momi S, Magrini U, Pirastu M, Savoia A, Balduini C, Gresele P. Alteration of liver enzymes is a feature of the MYH9-related disease syndrome. PLoS One 2012;7(4):e35986.
Filho CB, Rodrigues FF, Segat L, Fonseca AM, Araujo J, Arahata C, Pontes L, Vilar L, Filho JL de Lima, Crovella S. Association of MBL2 gene exon 1 variants with autoimmune thyroid disease in Brazilian patients. Int J Immunogenet 2012;39(4):357-61.
Filho CB, Rodrigues FF, Segat L, Fonseca AM, Araujo J, Arahata C, Pontes L, Vilar L, Filho JL de Lima, Crovella S. Association of MBL2 gene exon 1 variants with autoimmune thyroid disease in Brazilian patients. Int J Immunogenet 2012;39(4):357-61.
Filho CB, Rodrigues FF, Segat L, Fonseca AM, Araujo J, Arahata C, Pontes L, Vilar L, Filho JL de Lima, Crovella S. Association of MBL2 gene exon 1 variants with autoimmune thyroid disease in Brazilian patients. Int J Immunogenet 2012;39(4):357-61.
Copertino M, Barbi E, Poli F, Zennaro F, Ferrari M, Carrera P, Ventura A. A child with severe pneumomediastinum and ABCA3 gene mutation: a puzzling connection. Arch Bronconeumol 2012;48(4):139-40.
Cuttini M, Ferrante P, Mirante N, Chiandotto V, Fertz M, Dall'Oglio AMaria, Coletti MFranca, Johnson S. Cognitive assessment of very preterm infants at 2-year corrected age: performance of the Italian version of the PARCA-R parent questionnaire. Early Hum Dev 2012;88(3):159-63.
Cuttini M, Ferrante P, Mirante N, Chiandotto V, Fertz M, Dall'Oglio AMaria, Coletti MFranca, Johnson S. Cognitive assessment of very preterm infants at 2-year corrected age: performance of the Italian version of the PARCA-R parent questionnaire. Early Hum Dev 2012;88(3):159-63.
Rocca MSanta, Fabretto A, Faletra F, Carlet O, Skabar A, Gasparini P, Pecile V. Contribution of SNP arrays in diagnosis of deletion 2p11.2-p12. Gene 2012;492(1):315-8.
Rocca MSanta, Fabretto A, Faletra F, Carlet O, Skabar A, Gasparini P, Pecile V. Contribution of SNP arrays in diagnosis of deletion 2p11.2-p12. Gene 2012;492(1):315-8.

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