Gabutti V - Search Results

1

A newly-characterized alpha-thalassaemia-1 deletion removes the entire alpha-like globin gene cluster in an Italian family.

Fortina P, Dianzani I, Serra A, Gottardi E, Saglio G, Farinasso L, Piga A, Gabutti V, Camaschella C. Fortina P, et al. Among authors: gabutti v. Br J Haematol. 1991 Aug;78(4):529-34. doi: 10.1111/j.1365-2141.1991.tb04483.x. Br J Haematol. 1991. PMID: 1911344

2

Interaction of rare illegitimate recombination event and a poly A addition site mutation resulting in a severe form of alpha thalassemia.

Fortina P, Parrella T, Sartore M, Gottardi E, Gabutti V, Delgrosso K, Mansfield E, Rappaport E, Schwartz E, Camaschella C, et al. Fortina P, et al. Among authors: gabutti v. Blood. 1994 Jun 1;83(11):3356-62. Blood. 1994. PMID: 8193372 Free article.

3

Behaviour of myeloid precursors in homozygous beta thalassaemia.

Gabutti V, Miniero R, Piga A, Incarbone E, Sacchetti L, Balegno G. Gabutti V, et al. Br J Haematol. 1980 Aug;45(4):599-605. doi: 10.1111/j.1365-2141.1980.tb07183.x. Br J Haematol. 1980. PMID: 7426439

4

Results of long-term iron-chelating therapy.

Gabutti V, Piga A. Gabutti V, et al. Acta Haematol. 1996;95(1):26-36. doi: 10.1159/000203853. Acta Haematol. 1996. PMID: 8604584 Review.

5

Vitamin E and beta-thalassaemia.

Miniero R, Piga A, Luzzatto L, Gabutti V. Miniero R, et al. Among authors: gabutti v. Haematologica. 1983 Jul-Aug;68(4):562-3. Haematologica. 1983. PMID: 6414910 No abstract available.

6

Correlation between transfusion requirement, blood volume and haemoglobin level in homozygous beta-thalassaemia.

Gabutti V, Piga A, Fortina P, Miniero R, Nicola P. Gabutti V, et al. Acta Haematol. 1980;64(2):103-8. doi: 10.1159/000207218. Acta Haematol. 1980. PMID: 6776764

7

Mutations in the erythropoietin receptor gene are not a common cause of Diamond-Blackfan anemia.

Dianzani I, Garelli E, Dompè C, Crescenzio N, Locatelli F, Schilirò G, Castaman G, Bagnara GP, Olivieri NF, Gabutti V, Ramenghi U. Dianzani I, et al. Among authors: gabutti v. Blood. 1996 Mar 15;87(6):2568-72. Blood. 1996. PMID: 8630424 Free article.

8

High-dose desferrioxamine as a cause of growth failure in thalassemic patients.

Piga A, Luzzatto L, Capalbo P, Gambotto S, Tricta F, Gabutti V. Piga A, et al. Among authors: gabutti v. Eur J Haematol. 1988 Apr;40(4):380-1. doi: 10.1111/j.1600-0609.1988.tb00198.x. Eur J Haematol. 1988. PMID: 3366230 No abstract available.

9

Quality of life and life expectancy in thalassemic patients with complications.

Gabutti V, Piga A, Sacchetti L, Sandri A, Biginelli M, Saracco P, Ferri M. Gabutti V, et al. Prog Clin Biol Res. 1989;309:35-41. Prog Clin Biol Res. 1989. PMID: 2780748 No abstract available.

10

Hearing loss and desferrioxamine in homozygous beta-thalassemia.

Albera R, Pia F, Morra B, Lacilla M, Bianco L, Gabutti V, Piga A. Albera R, et al. Among authors: gabutti v. Audiology. 1988;27(4):207-14. doi: 10.3109/00206098809081591. Audiology. 1988. PMID: 3190562

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