Perrotta S - Search Results

1

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

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

Congenital dyserythropoietic anemia type II: molecular basis and clinical aspects.

Iolascon A, D'Agostaro G, Perrotta S, Izzo P, Tavano R, Miraglia del Giudice B. Iolascon A, et al. Among authors: perrotta s. Haematologica. 1996 Nov-Dec;81(6):543-59. Haematologica. 1996. PMID: 9009444 Review.

4

Abnormalities of erythrocyte glycoconjugates are identical in two families with congenital dyserythropoietic anemia type II with different chromosomal localizations of the disease gene.

Zdebska E, Iolascon A, Spychalska J, Perrotta S, Lanzara C, Smolenska-Sym G, Koscielak J. Zdebska E, et al. Among authors: perrotta s. Haematologica. 2007 Mar;92(3):427-8. doi: 10.3324/haematol.10803. Haematologica. 2007. PMID: 17339199 Free article.

5

Molecular analysis of 42 patients with congenital dyserythropoietic anemia type II: new mutations in the SEC23B gene and a search for a genotype-phenotype relationship.

Iolascon A, Russo R, Esposito MR, Asci R, Piscopo C, Perrotta S, Fénéant-Thibault M, Garçon L, Delaunay J. Iolascon A, et al. Among authors: perrotta s. Haematologica. 2010 May;95(5):708-15. doi: 10.3324/haematol.2009.014985. Epub 2009 Dec 16. Haematologica. 2010. PMID: 20015893 Free PMC article.

6

Apparently normal ankyrin content in unsplenectomized hereditary spherocytosis patients with the inactivation of one ankyrin (ANK1) allele.

Miraglia del Giudice E, Francese M, Polito R, Nobili B, Iolascon A, Perrotta S. Miraglia del Giudice E, et al. Among authors: perrotta s. Haematologica. 1997 May-Jun;82(3):332-3. Haematologica. 1997. PMID: 9234582

7

Exclusion of three candidate genes as determinants of congenital dyserythropoietic anemia type II (CDA-II).

Iolascon A, Miraglia del Giudice E, Perrotta S, Granatiero M, Zelante L, Gasparini P. Iolascon A, et al. Among authors: perrotta s. Blood. 1997 Nov 15;90(10):4197-200. Blood. 1997. PMID: 9354691 Free article.

8

Hereditary spherocytosis: from clinical to molecular defects.

Iolascon A, Miraglia del Giudice E, Perrotta S, Alloisio N, Morlé L, Delaunay J. Iolascon A, et al. Among authors: perrotta s. Haematologica. 1998 Mar;83(3):240-57. Haematologica. 1998. PMID: 9573679 Review.

9

Decision making at the bedside: diagnosis of hereditary spherocytosis in a transfused infant.

Miraglia del Giudice E, Perrotta S, Lombardi C, Iolascon A. Miraglia del Giudice E, et al. Among authors: perrotta s. Haematologica. 1998 Apr;83(4):347-9. Haematologica. 1998. PMID: 9592985

10

Gilbert's syndrome and jaundice in glucose-6-phosphate dehydrogenase deficient neonates.

Iolascon A, Faienza MF, Perrotta S, Meloni GF, Ruggiu G, del Giudice EM. Iolascon A, et al. Among authors: perrotta s. Haematologica. 1999 Feb;84(2):99-102. Haematologica. 1999. PMID: 10091404 Clinical Trial.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

336 results

Search Page

Filters