Zobrazeno 1 - 10
of 83
pro vyhledávání: '"Laura Breda"'
Autor:
Silvia Pires Lourenco, Danuta Jarocha, Valentina Ghiaccio, Amaliris Guerra, Osheiza Abdulmalik, Ping La, Alexandra Zezulin, Kim Smith-Whitley, Janet L. Kwiatkowski, Virginia Guzikowski, Yukio Nakamura, Tobias Raabe, Laura Breda, Stefano Rivella
Publikováno v:
Haematologica, Vol 106, Iss 10 (2021)
Externí odkaz:
https://doaj.org/article/af3ad5908f5d468bbcfda257356590f8
Autor:
Alisa Dong, Valentina Ghiaccio, Irene Motta, Shuling Guo, Raechel Peralta, Susan M. Freier, Andy Watt, Sagar Damle, Yasuhiro Ikawa, Danuta Jarocha, Maxwell Chappell, Coralea Stephanou, Paola Delbini, Connie Chen, Soteroula Christou, Marina Kleanthous, Kim Smith-Whitley, Deepa Manwani, Carla Casu, Osheiza Abdulmalik, Maria Domenica Cappellini, Stefano Rivella, Laura Breda
Publikováno v:
Haematologica, Vol 106, Iss 5 (2020)
β-thalassemia is a disorder caused by altered hemoglobin protein synthesis and affects individuals worldwide. Severe forms of the disease, left untreated, can result in death before the age of 3 years (1). The standard of care consists of chronic an
Externí odkaz:
https://doaj.org/article/0a9af0f8d129480daf7391c3232c9430
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 11, Iss 1 (2019)
Inherited hemoglobin disorders, including beta-thalassemia (BT) and sickle-cell disease (SCD) are the most common monogenic diseases worldwide, with a global carrier frequency of over 5%. With migration they are becoming more common worldwide, making
Externí odkaz:
https://doaj.org/article/3e52e66b8dae44d5bfa76cce64763a0f
Autor:
Laura Breda, Carla Casu, Sara Gardenghi, Nicoletta Bianchi, Luca Cartegni, Mohandas Narla, Karina Yazdanbakhsh, Marco Musso, Deepa Manwani, Jane Little, Lawrence B Gardner, Dorothy A Kleinert, Eugenia Prus, Eitan Fibach, Robert W Grady, Patricia J Giardina, Roberto Gambari, Stefano Rivella
Publikováno v:
PLoS ONE, Vol 7, Iss 3, p e32345 (2012)
Preclinical and clinical studies demonstrate the feasibility of treating β-thalassemia and Sickle Cell Disease (SCD) by lentiviral-mediated transfer of the human β-globin gene. However, previous studies have not addressed whether the ability of len
Externí odkaz:
https://doaj.org/article/472254d68557495b9619e90809e22289
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 1, Iss 1, Pp e2009008-e2009008 (2009)
Sickle cell disease (SCD) and ß-thalassemia represent the most common hemoglobinopathies caused, respectively, by the alteration of structural features or deficient production of the ß-chain of the Hb molecule. Other hemoglobinopathies are characte
Externí odkaz:
https://doaj.org/article/f2898a125082434197f3a3e3d859f249
Autor:
Maxwell Chappell, Laura Breda, Danuta Jadwiga Jarocha, Michael Triebwasser, Tyler E Papp, Valentina Ghiaccio, Megan T Fedorky, Amaliris Guerra, Kandace Gollomp, Osheiza Y. Abdulmalik, Nattiya Teawtrakul, Stavros Glentis, Antonis Kattamis, Hamideh Parhiz, Stefano Rivella
Publikováno v:
Blood. 140:300-302
Publikováno v:
International Journal of Paleopathology. 33:25-29
Objective This study presents evidence of a probable case of holoprosencephaly with cyclopia, which has been rarely reported in the paleopathological literature. Materials The skeletal remains of a male fetus between 36 and 40 gestational weeks from
Autor:
Danuta Jarocha, Janet L. Kwiatkowski, Tobias Raabe, Virginia Guzikowski, Silvia Pires Lourenco, Stefano Rivella, Yukio Nakamura, Amaliris Guerra, Kim Smith-Whitley, Alexandra Zezulin, Laura Breda, Ping La, Valentina Ghiaccio, Osheiza Abdulmalik
Publikováno v:
Haematologica. 106:2740-2745
Autor:
Laura Breda, Tyler E Papp, Michael Triebwasser, Amir Yadegari, Megan T Fedorky, Naoto Tanaka, Houping Ni, Drew Weissman, Stefano Rivella, Hamideh Parhiz
Publikováno v:
Blood. 140:305-306
Autor:
Amaliris Guerra, Perry Demsko, Ariel Rivera, Carlo Castruccio Castracani, Laura Breda, Naoto Tanaka, Shuling Guo, Stefano Rivella
Publikováno v:
Blood. 140:1944-1945