Roberta Russo
Roberta Russo
Dipartimento di Medicina Molecolare e Biotecnologie Mediche
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Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II
K Schwarz, A Iolascon, F Verissimo, NS Trede, W Horsley, W Chen, ...
Nature genetics 41 (8), 936-940, 2009
Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1
I Andolfo, SL Alper, L De Franceschi, C Auriemma, R Russo, L De Falco, ...
Blood 121 (19), 3925-3935, 2013
Suppressor of cytokine signaling 3 (SOCS3) expression and hepatitis C virus–related chronic hepatitis: insulin resistance and response to antiviral therapy
M Persico, M Capasso, E Persico, M Svelto, R Russo, D Spano, L Croce, ...
Hepatology 46 (4), 1009-1015, 2007
Replication of GWAS-identified neuroblastoma risk loci strengthens the role of BARD1 and affirms the cumulative effect of genetic variations on …
M Capasso, SJ Diskin, F Totaro, L Longo, MD Mariano, R Russo, ...
Carcinogenesis 34 (3), 605-611, 2013
Elevated expression and polymorphisms of SOCS3 influence patient response to antiviral therapy in chronic hepatitis C
M Persico, M Capasso, R Russo, E Persico, L Croce, C Tiribelli, ...
Gut 57 (4), 507-515, 2008
Galectin-1 and its involvement in hepatocellular carcinoma aggressiveness
D Spano, R Russo, V Di Maso, N Rosso, LM Terracciano, M Roncalli, ...
Molecular medicine 16 (3-4), 102-115, 2010
Regulation of divalent metal transporter 1 (DMT1) non-IRE isoform by the microRNA Let-7d in erythroid cells
I Andolfo, L De Falco, R Asci, R Russo, S Colucci, M Gorrese, M Zollo, ...
Haematologica 95 (8), 1244-1252, 2010
New insights on hereditary erythrocyte membrane defects
I Andolfo, R Russo, A Gambale, A Iolascon
Haematologica 101 (11), 1284-1294, 2016
Clinical aspects and pathogenesis of congenital dyserythropoietic anemias: from morphology to molecular approach
A Iolascon, MR Esposito, R Russo
Haematologica 97 (12), 1786-1794, 2012
Missense mutations in the ABCB6 transporter cause dominant familialpseudohyperkalemia
I Andolfo, SL Alper, J Delaunay, C Auriemma, R Russo, R Asci, ...
American journal of hematology 88 (1), 66-72, 2013
Recommendations regarding splenectomy in hereditary hemolytic anemias
A Iolascon, I Andolfo, W Barcellini, F Corcione, L Garçon, L De Franceschi, ...
haematologica 102 (8), 1304-1313, 2017
Novel Gardos channel mutations linked to dehydrated hereditary stomatocytosis (xerocytosis)
I Andolfo, R Russo, F Manna, BE Shmukler, A Gambale, G Vitiello, ...
American journal of hematology 90 (10), 921-926, 2015
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
A Iolascon, R Russo, MR Esposito, R Asci, C Piscopo, S Perrotta, ...
Haematologica 95 (5), 708-715, 2010
Diagnosis and management of congenital dyserythropoietic anemias
A Gambale, A Iolascon, I Andolfo, R Russo
Expert review of hematology 9 (3), 283-296, 2016
Multi‐gene panel testing improves diagnosis and management of patients with hereditary anemias
R Russo, I Andolfo, F Manna, A Gambale, R Marra, BE Rosato, P Caforio, ...
American Journal of Hematology 93 (5), 672-682, 2018
Retrospective cohort study of 205 cases with congenital dyserythropoietic anemia type II: definition of clinical and molecular spectrum and identification of new diagnostic scores
R Russo, A Gambale, C Langella, I Andolfo, S Unal, A Iolascon
American journal of hematology 89 (10), E169-E175, 2014
SOCS3 and IRS-1 gene expression differs between genotype 1 and genotype 2 hepatitis C virus-infected HepG2 cells
M Persico, R Russo, E Persico, M Svelto, D Spano, I Andolfo, V La Mura, ...
Clinical Chemistry and Laboratory Medicine (CCLM) 47 (10), 1217-1225, 2009
Mutational spectrum in congenital dyserythropoietic anemia type II: Identification of 19 novel variants in SEC23B gene
R Russo, MR Esposito, R Asci, A Gambale, S Perrotta, U Ramenghi, ...
American journal of hematology 85 (12), 915-920, 2010
Congenital dyserythropoietic anemias
A Iolascon, R Russo, J Delaunay
Current opinion in hematology 18 (3), 146-151, 2011
A predicted functional single-nucleotide polymorphism of bone morphogenetic protein-4 gene affects mRNA expression and shows a significant association with cutaneous melanoma …
M Capasso, F Ayala, R Russo, RA Avvisati, R Asci, A Iolascon
Journal of cancer research and clinical oncology 135 (12), 1799-1807, 2009
Il sistema al momento non può eseguire l'operazione. Riprova più tardi.
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