Zobrazeno 1 - 10
of 179
pro vyhledávání: '"V. Gabutti"'
Autor:
C. Borgna-Pignatti, V. Gabutti
Publikováno v:
Baillière's Clinical Haematology. 7:919-940
Summary Long-term blood transfusions lead to the accumulation of iron that in the absence of chelation therapy causes complications such as liver cirrhosis, growth failure, hypogonadism, hypothyroidism, hypoparathyroidism, diabetes and myocardiopathy
Autor:
V. Gabutti
Publikováno v:
Annals of the New York Academy of Sciences. 612:268-274
Care and life quality of thalassemic patients in Italy have greatly improved over the last years thanks to cooperation between many clinical centers. The achievement of the following points played an important role: 1. A national treatment protocol w
Autor:
F, Timeus, N, Crescenzio, D, Marranca, M, Dall'Aglio, L, Fazio, M, Di Marco, P, Saracco, M, Ricotti, V, Gabutti
Publikováno v:
Bone marrow transplantation. 22
We investigated the expression of different cell adhesion molecules on cord blood (CB) and bone marrow (BM) CD34+/CD38+ and CD34+/CD38- cells. CD11a and CD62L were more expressed in CB than in BM CD34+/CD38- subset, suggesting a possible advantage in
Autor:
V, Gabutti, C, Borgna-Pignatti
Publikováno v:
Bailliere's clinical haematology. 7(4)
Long-term blood transfusions lead to the accumulation of iron that in the absence of chelation therapy causes complications such as liver cirrhosis, growth failure, hypogonadism, hypothyroidism, hypoparathyroidism, diabetes and myocardiopathy. The la
Autor:
V Gabutti, Paolo Fortina, Eric F. Rappaport, E. S. Mansfield, Elias Schwartz, M. Sartore, C Camaschella, E Gottardi, T Parrella, Kathleen Delgrosso
The clinical diversity of thalassemia depends on interaction of diverse genetic defects. We have characterized a severe form of alpha thalassemia caused by coinheritance of a rare alpha-globin gene deletion and a nondeletional defect in a southern It
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75fced3c9190a2750eb950ffa2ca81a7
http://hdl.handle.net/11573/502778
http://hdl.handle.net/11573/502778
Autor:
V, Gabutti, F, Timeus, U, Ramenghi, P, Saracco, D, Fassio, M C, Giubellino, R, Miniero, E, Madon
The high number of cord blood (CB) hematopoietic progenitors made possible CB transplantation in children with hematologic diseases. We collected and cryopreserved CB from siblings of 11 hematologic pediatric patients for possible transplant. The num
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::5bea99519399847025d566aa45a37dd6
http://hdl.handle.net/2318/123008
http://hdl.handle.net/2318/123008
Publikováno v:
European Journal of Cancer (1965). 5:343-348
Resume Dans cinq cas de leucemie lymphoblastique aigue (tires d'un materiel plus vaste de leucemies lymphoblastiques aigues), l'indice de marquage par thymidine- 3 H des elements blastiques circulants s'est revele superieur a celui des elements blast
Publikováno v:
Acta Haematologica. 41:215-224
Publikováno v:
Acta Haematologica. 38:193-199
Publikováno v:
European Journal of Cancer (1965). 6:33-38
In vivo pulse-labelling with 3 H-thymidine was employed to obtain red cell kinetics data in 3 untreated cases of acute myeloblastic leukaemia (AML). The K out of the proliferating into the non-proliferating compartment was below the sum of the indivi