Perrotta S - Search Results

1

The interactome of the N-terminus of band 3 regulates red blood cell metabolism and storage quality.

Issaian A, Hay A, Dzieciatkowska M, Roberti D, Perrotta S, Darula Z, Redzic J, Busch MP, Page GP, Rogers SC, Doctor A, Hansen KC, Eisenmesser EZ, Zimring JC, D'Alessandro A. Issaian A, et al. Among authors: perrotta s. Haematologica. 2021 Nov 1;106(11):2971-2985. doi: 10.3324/haematol.2020.278252. Haematologica. 2021. PMID: 33979990 Free PMC article.

2

CNR2 functional variant (Q63R) influences childhood immune thrombocytopenic purpura.

Rossi F, Mancusi S, Bellini G, Roberti D, Punzo F, Vetrella S, Matarese SM, Nobili B, Maione S, Perrotta S. Rossi F, et al. Among authors: perrotta s. Haematologica. 2011 Dec;96(12):1883-5. doi: 10.3324/haematol.2011.045732. Epub 2011 Aug 9. Haematologica. 2011. PMID: 21828121 Free PMC article. Clinical Trial.

3

HNF-1β mutation affects PKD2 and SOCS3 expression causing renal cysts and diabetes in MODY5 kindred.

Mancusi S, La Manna A, Bellini G, Scianguetta S, Roberti D, Casale M, Rossi F, Della Ragione F, Perrotta S. Mancusi S, et al. Among authors: perrotta s. J Nephrol. 2013 Jan-Feb;26(1):207-12. doi: 10.5301/jn.5000126. J Nephrol. 2013. PMID: 22641569

4

A Novel 12q13.2-q13.3 Microdeletion Syndrome With Combined Features of Diamond Blackfan Anemia, Pierre Robin Sequence and Klippel Feil Deformity.

Roberti D, Conforti R, Giugliano T, Brogna B, Tartaglione I, Casale M, Piluso G, Perrotta S. Roberti D, et al. Among authors: perrotta s. Front Genet. 2018 Nov 19;9:549. doi: 10.3389/fgene.2018.00549. eCollection 2018. Front Genet. 2018. PMID: 30524470 Free PMC article.

5

Effects of Eltrombopag on In Vitro Macrophage Polarization in Pediatric Immune Thrombocytopenia.

Di Paola A, Palumbo G, Merli P, Argenziano M, Tortora C, Strocchio L, Roberti D, Santoro C, Perrotta S, Rossi F. Di Paola A, et al. Among authors: perrotta s. Int J Mol Sci. 2020 Dec 24;22(1):97. doi: 10.3390/ijms22010097. Int J Mol Sci. 2020. PMID: 33374151 Free PMC article.

6

Risk factors for endocrine complications in transfusion-dependent thalassemia patients on chelation therapy with deferasirox: a risk assessment study from a multi-center nation-wide cohort.

Casale M, Forni GL, Cassinerio E, Pasquali D, Origa R, Serra M, Campisi S, Peluso A, Renni R, Cattoni A, De Michele E, Allò M, Poggi M, Ferrara F, Di Concilio R, Sportelli F, Quarta A, Putti MC, Notarangelo LD, Sau A, Ladogana S, Tartaglione I, Picariello S, Marcon A, Sturiale P, Roberti D, Lazzarino AI, Perrotta S. Casale M, et al. Among authors: perrotta s. Haematologica. 2022 Feb 1;107(2):467-477. doi: 10.3324/haematol.2020.272419. Haematologica. 2022. PMID: 33406815 Free PMC article.

7

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

8

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

9

Coexistence of hereditary spherocytosis (HS) due to band 3 deficiency and beta-thalassaemia trait: partial correction of HS phenotype.

Miraglia del Giudice E, Perrotta S, Nobili B, Pinto L, Cutillo L, Iolascon A. Miraglia del Giudice E, et al. Among authors: perrotta s. Br J Haematol. 1993 Nov;85(3):553-7. doi: 10.1111/j.1365-2141.1993.tb03347.x. Br J Haematol. 1993. PMID: 8136278

10

Cytoskeletal behaviour in spectrin and in band 3 deficient spherocytic red cells: evidence for differentiated splenic conditioning role.

Ingrosso D, D'Angelo S, Perrotta S, d'Urzo G, Iolascon A, Perna AF, Galletti P, Zappia V, Miraglia del Giudice E. Ingrosso D, et al. Among authors: perrotta s. Br J Haematol. 1996 Apr;93(1):38-41. doi: 10.1046/j.1365-2141.1996.451990.x. Br J Haematol. 1996. PMID: 8611472

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