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V Gabutti

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Articles 62
Citations 303
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Recent Articles
1.
Santucci M, Bagnara G, Strippoli P, Bonsi L, Vitale L, Tonelli R, et al.
Exp Hematol . 1999 Jan; 27(1):9-18. PMID: 9923439
The hematopoietic defect of Diamond-Blackfan anemia (DBA) results in selective failure of erythropoiesis. Thus far, it is not known whether this defect originates from an intrinsic impediment of hematopoietic progenitors...
2.
Timeus F, Crescenzio N, Marranca D, Dallaglio M, Fazio L, Di Marco M, et al.
Bone Marrow Transplant . 1998 Aug; 22 Suppl 1:S61-2. PMID: 9715892
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...
3.
Timeus F, Crescenzio N, Basso G, Ramenghi U, Saracco P, Gabutti V
Stem Cells . 1998 Apr; 16(2):120-6. PMID: 9554036
Self-renewal, proliferation, differentiation, homing, and mobilization of hematopoietic progenitor cells (HPCs) are regulated by a complex mechanism that involves the bone marrow (BM) microenvironment. Cell adhesion molecules (CAMs) expressed on...
4.
Dianzani I, Garelli E, Crescenzio N, Timeus F, MORI P, Varotto S, et al.
Exp Hematol . 1997 Nov; 25(12):1270-7. PMID: 9357971
Diamond-Blackfan anemia (DBA) is a congenital pure red blood cell aplasia that often requires lifelong transfusional therapy. Autosomal dominant and recessive inheritance have both been reported, suggesting genetic heterogeneity, but...
5.
Della Ragione F, Borriello A, Mastropietro S, DELLA PIETRA V, Monno F, Gabutti V, et al.
Biochem Biophys Res Commun . 1997 Feb; 231(1):73-6. PMID: 9070222
Characterization of proteins that control the passage through the G1 phase of the cell cycle is of particular interest because virtually all stimuli regulating cell proliferation or differentiation act primarily...
6.
David O, Fiorucci G, Tosi M, Altare F, Valori A, Saracco P, et al.
Pediatr Hematol Oncol . 1996 May; 13(3):271-5. PMID: 8735344
Previous studies have reported erythrocyte macrocytosis in adults and children with Down syndrome (DS), the significance of which remains unclear. We compared hematological parameters of 50 DS children aged 2...
7.
Dianzani I, Garelli E, Dompe C, Crescenzio N, Locatelli F, Schiliro G, et al.
Blood . 1996 Mar; 87(6):2568-72. PMID: 8630424
Diamond-Blackfan anemia (DBA) is an inherited pure red blood cell aplasia that often requires lifelong transfusional support. The origin of the imperfect erythrogenesis is not known. The existence of more...
8.
Gabutti V, Piga A
Acta Haematol . 1996 Jan; 95(1):26-36. PMID: 8604584
The improvement in survival and quality of life of iron-overloaded patients achieved by regular subcutaneous chelation has been extensively documented over the years. A review of the long-term results allows...
9.
Carlson J, Nash G, Gabutti V, Wahlgren M
Blood . 1994 Dec; 84(11):3909-14. PMID: 7949147
Genes for two lethal diseases, thalassemia and sickle cell anemia, are favored by evolution because, in their heterozygous form, they protect against cerebral malaria. Rosette formation, the binding of uninfected...
10.
Gabutti V, Borgna-Pignatti C
Baillieres Clin Haematol . 1994 Dec; 7(4):919-40. PMID: 7881160
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....