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Rosario Notaro

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Articles 64
Citations 1585
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Recent Articles
11.
Notaro R, Luzzatto L
N Engl J Med . 2022 Jul; 387(2):160-166. PMID: 35830642
No abstract available.
12.
Kulasekararaj A, Risitano A, Maciejewski J, Notaro R, Browett P, Lee J, et al.
Blood . 2021 Jul; 138(20):1928-1938. PMID: 34314483
Paroxysmal nocturnal hemoglobinuria (PNH) is characterized by uncontrolled terminal complement activation and subsequent intravascular hemolysis (IVH). C5 inhibitors prevent membrane attack complex formation, but patients may experience extravascular hemolysis (EVH)...
13.
Debureaux P, Kulasekararaj A, Cacace F, Silva B, Calado R, Barone F, et al.
Bone Marrow Transplant . 2021 Jul; 56(10):2600-2602. PMID: 34226670
No abstract available.
14.
Luzzatto L, Risitano A, Notaro R
N Engl J Med . 2021 Jun; 384(22):2164. PMID: 34077653
No abstract available.
15.
Barcellini W, Fattizzo B, Giannotta J, Quattrocchi L, Aydin S, Barone F, et al.
Br J Haematol . 2021 May; 194(5):854-856. PMID: 34036575
No abstract available.
16.
Risitano A, Kulasekararaj A, Lee J, Maciejewski J, Notaro R, Brodsky R, et al.
Haematologica . 2020 Oct; 106(12):3188-3197. PMID: 33121236
Paroxysmal nocturnal hemoglobinuria (PNH) is characterised by complement-mediated intravascular hemolysis (IVH) due to absence of complement regulators CD55 and CD59 on affected erythrocytes. Danicopan is a first-in-class oral proximal, complement...
17.
Sica M, Pellecchia A, De Angioletti M, Caocci G, Nannelli C, La Nasa G, et al.
Blood . 2020 Aug; 136(26):3082-3085. PMID: 32845970
No abstract available.
18.
Cosi I, Pellecchia A, De Lorenzo E, Torre E, Sica M, Nesi G, et al.
J Hematol Oncol . 2020 Aug; 13(1):112. PMID: 32791988
Background: ETV4 is one of the ETS proteins overexpressed in prostate cancer (PC) as a result of recurrent chromosomal translocations. In human prostate cell lines, ETV4 promotes migration, invasion, and...
19.
Luzzatto L, Ally M, Notaro R
Blood . 2020 Jul; 136(11):1225-1240. PMID: 32702756
Glucose 6-phosphate dehydrogenase (G6PD) deficiency is 1 of the commonest human enzymopathies, caused by inherited mutations of the X-linked gene G6PD. G6PD deficiency makes red cells highly vulnerable to oxidative...
20.
Risitano A, Marotta S, Ricci P, Marano L, Frieri C, Cacace F, et al.
Front Immunol . 2019 Jul; 10:1157. PMID: 31258525
The treatment of paroxysmal nocturnal hemoglobinuria has been revolutionized by the introduction of the anti-C5 agent eculizumab; however, eculizumab is not the cure for Paroxysmal nocturnal hemoglobinuria (PNH), and room...