Perrotta S - Search Results

1

Characterization of red cell membrane proteins as a function of red cell density: annexin VII in different forms of hereditary spherocytosis.

Caterino M, Ruoppolo M, Orrù S, Savoia M, Perrotta S, Del Vecchio L, Salvatore F, Stewart GW, Iolascon A. Caterino M, et al. Among authors: perrotta s. FEBS Lett. 2006 Dec 11;580(28-29):6527-32. doi: 10.1016/j.febslet.2006.10.070. Epub 2006 Nov 7. FEBS Lett. 2006. PMID: 17112522 Free article.

2

Hereditary spherocytosis (HS) due to loss of anion exchange transporter.

Iolascon A, Miraglia del Giudice E, Perrotta S, Pinto L, Fiorelli G, Cappellini DM, Vasseur C, Bursaux E, Cutillo S. Iolascon A, et al. Among authors: perrotta s. Haematologica. 1992 Nov-Dec;77(6):450-6. Haematologica. 1992. PMID: 1289181

3

Alpha I/65 hereditary elliptocytosis in southern Italy: evidence for an African origin.

del Giudice EM, Ducluzeau MT, Alloisio N, Wilmotte R, Delaunay J, Perrotta S, Cutillo S, Iolascon A. del Giudice EM, et al. Among authors: perrotta s. Hum Genet. 1992 Jul;89(5):553-6. doi: 10.1007/BF00219183. Hum Genet. 1992. PMID: 1353056

4

Hereditary spherocytosis characterized by increased spectrin/band 3 ratio.

Miraglia del Giudice E, Perrotta S, Pinto L, Cappellini MD, Fiorelli G, Cutillo S, Iolascon A. Miraglia del Giudice E, et al. Among authors: perrotta s. Br J Haematol. 1992 Jan;80(1):133-4. doi: 10.1111/j.1365-2141.1992.tb06417.x. Br J Haematol. 1992. PMID: 1536803 No abstract available.

5

Ankyrin deficiency in dominant hereditary spherocytosis: report of three cases.

Iolascon A, Miraglia del Giudice E, Camaschella C, Pinto L, Nobili B, Perrotta S, Cutillo S. Iolascon A, et al. Among authors: perrotta s. Br J Haematol. 1991 Aug;78(4):551-4. doi: 10.1111/j.1365-2141.1991.tb04487.x. Br J Haematol. 1991. PMID: 1832935

6

Congenital dyserythropoietic anemia type II associated with G6PD Seattle in a Sicilian child.

Gangarossa S, Romano V, Miraglia del Giudice E, Perrotta S, Iolascon A, Schiliro G. Gangarossa S, et al. Among authors: perrotta s. Acta Haematol. 1995;93(1):36-9. doi: 10.1159/000204087. Acta Haematol. 1995. PMID: 7725848

7

Increased membrane-protein methylation in hereditary spherocytosis. A marker of cytoskeletal disarray.

Ingrosso D, D'Angelo S, Perna AF, Iolascon A, Miraglia del Giudice E, Perrotta S, Zappia V, Galletti P. Ingrosso D, et al. Among authors: perrotta s. Eur J Biochem. 1995 Mar 15;228(3):894-8. doi: 10.1111/j.1432-1033.1995.tb20337.x. Eur J Biochem. 1995. PMID: 7737191 Free article.

8

Spectrin Anastasia (alpha I/78): a new spectrin variant (alpha 45 Arg-->Thr) with moderate elliptocytogenic potential.

Perrotta S, Iolascon A, De Angelis F, Pagano L, Colonna G, Cutillo S, Miraglia del Giudice E. Perrotta S, et al. Br J Haematol. 1995 Apr;89(4):933-6. Br J Haematol. 1995. PMID: 7772539

9

Erythrocyte membrane protein alterations underlying clinical heterogeneity in hereditary spherocytosis.

Miraglia del Giudice E, Iolascon A, Pinto L, Nobili B, Perrotta S. Miraglia del Giudice E, et al. Among authors: perrotta s. Br J Haematol. 1994 Sep;88(1):52-5. doi: 10.1111/j.1365-2141.1994.tb04976.x. Br J Haematol. 1994. PMID: 7803256

10

Molecular heterogeneity of hereditary elliptocytosis in Italy.

Miraglia del Giudice E, Perrotta S, Sannino E, De Angelis F, Nobili B, Iolascon A. Miraglia del Giudice E, et al. Among authors: perrotta s. Haematologica. 1994 Sep-Oct;79(5):400-5. Haematologica. 1994. PMID: 7843625

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