Zobrazeno 1 - 10
of 126
pro vyhledávání: '"D, Cappellini"'
Autor:
M. D. Cappellini, A. T. Taher, J. B. Porter, K. H. Kuo, T. D. Coates, E. Voskaridou, G. L. Forni, S. Perrotta, A. Khelif, A. Lal, A. Kattamis, A. Piga, O. Hermine, N. Holot, F. Lersch, J. K. Shetty, S. Vodala, J. Zhang, D. Miteva, V. Viprakasit
Publikováno v:
HemaSphere, Vol 6, Pp 171-172 (2022)
Externí odkaz:
https://doaj.org/article/fdc14d67f80643488ce4a387ce85d2d7
Autor:
L. Raggi, A. Aprile, S. Bolamperti, I. Villa, M. Storto, G. Morello, S. Marktel, C. Tripodo, M. D. Cappellini, I. Motta, A. Rubinacci, G. Ferrari
Publikováno v:
HemaSphere, Vol 6, Pp 1400-1401 (2022)
Externí odkaz:
https://doaj.org/article/11332f68f1b0479e95263693495da6fd
P1518: LONG-TERM SAFETY RESULTS OF THE BELIEVE STUDY OF LUSPATERCEPT IN ADULTS WITH ΒETA-THALASSEMIA
Autor:
V. Viprakasit, M. D. Cappellini, J. B. Porter, K. H. M. Kuo, T. D. Coates, E. Voskaridou, V. M. Pinto, I. Tartaglione, A. Khelif, A. Lal, A. Kattamis, A. Piga, O. Hermine, N. Holot, F. Lersch, J. K. Shetty, J. Zhang, L. Bueno, A. C. Giuseppi, D. Miteva, A. T. Taher
Publikováno v:
HemaSphere, Vol 6, Pp 1399-1400 (2022)
Externí odkaz:
https://doaj.org/article/ad1d0d1123114d8d9a584574271f5e23
Publikováno v:
HemaSphere, Vol 6, Pp 1404-1405 (2022)
Externí odkaz:
https://doaj.org/article/f4e40edafe664dabbb693e6fa82802f1
Cardiopulmonary testing in adult patients with β-thalassemia major in comparison to healthy subjects
Publikováno v:
Annals of Hematology. 101:2445-2452
β-Thalassemia patients often have a reduced capacity of exercise and abnormal respiratory function parameters, but the reasons are unclear. In order to identify the causes of the exercise limitation, we performed a cardiopulmonary exercise testing (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8164ce31e6553e4ca3b9a99927c8892b
https://doi.org/10.1007/s00277-022-04974-w
https://doi.org/10.1007/s00277-022-04974-w
Publikováno v:
Polish Archives of Internal Medicine.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::163c9fb79e8ab84de776efbd491e3a18
https://doi.org/10.20452/pamw.16430
https://doi.org/10.20452/pamw.16430
Role of T1 mapping as a complementary tool to T2* for non-invasive cardiac iron overload assessment.
Autor:
Camilla Torlasco, Elena Cassinerio, Alberto Roghi, Andrea Faini, Marco Capecchi, Amna Abdel-Gadir, Cristina Giannattasio, Gianfranco Parati, James C Moon, Maria D Cappellini, Patrizia Pedrotti
Publikováno v:
PLoS ONE, Vol 13, Iss 2, p e0192890 (2018)
Iron overload-related heart failure is the principal cause of death in transfusion dependent patients, including those with Thalassemia Major. Linking cardiac siderosis measured by T2* to therapy improves outcomes. T1 mapping can also measure iron; p
Externí odkaz:
https://doaj.org/article/49a3abeb1a784325b28717a769b28614
Autor:
Laura Dell'Arti, Giulio Barteselli, Lorenzo Riva, Elisa Carini, Giovanna Graziadei, Eleonora Benatti, Alessandro Invernizzi, Maria D Cappellini, Francesco Viola
Publikováno v:
PLoS ONE, Vol 13, Iss 3, p e0193582 (2018)
To identify systemic risk factors for sickle cell maculopathy, and to analyze the microstructure of the macula of Sickle Cell Disease (SCD) patients by using automated segmentation of individual retinal layers.Thirty consecutive patients with SCD and
Externí odkaz:
https://doaj.org/article/81203f8d2d5d41a0becd44d46dca562c
Autor:
Giorgio Derchi, Manuela Balocco, Patrizio Bina, Vincenzo Caruso, Domenico G D’Ascola, Roberto Littera, Raffaella Origa, Maria D. Cappellini, Gian L. Forni
Publikováno v:
Haematologica, Vol 99, Iss 2 (2014)
Externí odkaz:
https://doaj.org/article/c5943e7abc9c458a842cecfa00a4bd98
Autor:
Cornelis L. Harteveld, Chiara Refaldi, Antonino Giambona, Claudia A. L. Ruivenkamp, Mariëtte J. V. Hoffer, Jeroen Pijpe, Peter De Knijff, Caterina Borgna-Pignatti, Aurelio Maggio, Maria D. Cappellini, Piero C. Giordano
Publikováno v:
Haematologica, Vol 98, Iss 5 (2013)
Genomic DNA of 3 patients, born as healthy carriers and developing a late-onset severe transfusion-dependent beta-thalassemia major was studied by high-density genome wide SNP array analysis. A mosaic loss of heterozygosity for almost the entire 11p
Externí odkaz:
https://doaj.org/article/f1660300ae484b0b87c193ab19383d51