IRIS

RUSSO, ROBERTA

RUSSO, ROBERTA  

DIPARTIMENTO DI MEDICINA MOLECOLARE E BIOTECNOLOGIE MEDICHE  

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Hypomorphic mutations of SEC23B gene account for mild phenotypes of congenital dyserythropoietic anemia type II 1.1 Articolo in rivista 2013 Russo, Roberta; Langella, C; Esposito, Mr; Gambale, A; Vitiello, F; Vallefuoco, F; Ek, T; Yang, E; Iolascon, Achille
Regulation of divalent metal transporter 1 (DMT1) non-IRE isoform by the microRNA Let-7d in erythroid cells. 1.1 Articolo in rivista 2010 Andolfo, I; De Falco, L; Asci, R; Russo, Roberta; Colucci, S; Gorrese, M; Zollo, Massimo; Iolascon, Achille
Comparative proteomic expression profile in all-trans retinoic acid differentiated neuroblastoma cellline. 1.1 Articolo in rivista 2007 Cimmino, F; Spano, D; Capasso, Mario; Zambrano, Nicola; Russo, Roberta; Zollo, Massimo; Iolascon, Achille
Regulation of divalent metal transporter 1 (DMT1) non-IRE isoform by the microRNA Let-7d inerythroid cells. 1.1 Articolo in rivista 2010 Andolfo, I; De Falco, L; Asci, R; Russo, R; Colucci, S; Gorrese, M; Zollo, Massimo; Iolascon, Achille
Congenital dyserythropoietic anaemias: new acquisitions. 1.1 Articolo in rivista 2011 Iolascon, Achille; Russo, Roberta; Esposito, Mr; Piscopo, C; Asci, R; De Falco, L; Di Noce, F.
Congenital dyserythropoietic anemias. 1.1 Articolo in rivista 2011 Iolascon, Achille; Russo, Roberta; Delaunay, J.
Replication of GWAS-identified neuroblastoma risk loci strengthens the role of BARD1 and affirms the cumulative effect of genetic variations on disease susceptibility 1.1 Articolo in rivista 2013 Capasso, Mario; Diskin, Sj; Totaro, F; Longo, L; Mariano, Md; Russo, Roberta; Cimmino, F; Hakonarson, H; Tonini, Gp; Devoto, M; Maris, Jm; Iolascon, Achille
Retrospective cohort study of 205 cases with congenital dyserythropoietic anemia type II: Definition of clinical and molecular spectrum and identification of new diagnostic scores 1.1 Articolo in rivista 2014 Russo, Roberta; Gambale, Antonella; Langella, Concetta; Andolfo, Immacolata; Unal, Sule; Iolascon, Achille
Two founder mutations in the SEC23B gene account for the relatively high frequency of CDA II in the Italian population. 1.1 Articolo in rivista 2011 Russo, Roberta; Gambale, A; Esposito, Mr; Serra, Ml; Troiano, A; De Maggio, I; Capasso, Mario; Luzzatto, L; Delaunay, J; Tamary, H; Iolascon, Achille
Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1 1.1 Articolo in rivista 2013 Andolfo, I; Alper, Sl; De Franceschi, L; Auriemma, C; Russo, Roberta; De Falco, L; Vallefuoco, F; Esposito, Mr; Vandorpe, Dh; Shmukler, Be; Narayan, R; Montanaro, D; D'Armiento, Maria; Vetro, A; Limongelli, I; Zuffardi, O; Glader, Be; Schrier, Sl; Brugnara, C; Stewart, Gw; Delaunay, J; Iolascon, Achille
Successful hematopoietic stem cell transplantation in a patient with congenital dyserythropoietic anemia type II 1.1 Articolo in rivista 2014 Sule, Unal; Russo, Roberta; Fatma, Gumruk; Baris, Kuskonmaz; Mualla, Cetin; Tulin, Sayli; Betul, Tavil; Concetta, Langella; Iolascon, Achille; Duygu Uckan, Cetinkaya
Inherited hematological disorders due to defects in coat protein (COP)II complex. 1.1 Articolo in rivista 2013 Russo, Roberta; Esposito, Mr; Iolascon, Achille
Missense mutations in the ABCB6 transporter cause dominant familial pseudohyperkalemia 1.1 Articolo in rivista 2013 Andolfo, I; Alper, Sl; Delaunay, J; Auriemma, C; Russo, Roberta; Asci, R; Esposito, Mr; Sharma, Ak; Shmukler, Be; Brugnara, C; De Franceschi, L; Iolascon, Achille
Integration of Pharmacogenetics and Pharmacogenomics in Drug Development: Implications for Regulatory and Medical Decision Making in Pediatric Diseases. 1.1 Articolo in rivista 2011 Piana, C; Surh, L; Furst Recktenwald, S; Iolascon, Achille; Jacqz Aigrain, Em; Jonker, I; Russo, Roberta; van Schaik, Rh; Wessels, J; Della Pasqua, O. E.
Clinical aspects and pathogenesis of congenital dyserythropoietic anemias: from morphology to molecular approach. 1.1 Articolo in rivista 2012 Iolascon, Achille; Esposito, Mr; Russo, Roberta
Diagnosis and management of congenital dyserythropoietic anemias 1.1 Articolo in rivista 2016 Gambale, Antonella; Iolascon, Achille; Andolfo, Immacolata; Russo, Roberta
Suppressor of cytokine signaling 3 (SOCS3) expression and hepatitis C virus-related chronic hepatitis:Insulin resistance and response to antiviral therapy 1.1 Articolo in rivista 2007 Persico, M; Capasso, Mario; Persico, E; Svelto, Maria; Russo, Roberta; Spano, D; Crocè, L; La Mura, V; Moschella, F; Masutti, F; Torella, R; Tiribelli, C; Iolascon, Achille
Pediatric pharmacogenetic and pharmacogenomic studies: the current state and future perspectives. 1.1 Articolo in rivista 2011 Russo, Roberta; Capasso, Mario; Paolucci, P; Iolascon, Achille
Functional characterization of novel ABCB6 mutations and their clinical implications in familial pseudohyperkalemia 1.1 Articolo in rivista 2016 Andolfo, Immacolata; Russo, Roberta; Manna, Francesco; De Rosa, Gianluca; Gambale, Antonella; Zouwail, Soha; Detta, Nicola; Pardo, Catia Lo; Alper, Seth L; Brugnara, Carlo; Sharma, Alok K; De Franceschi, Lucia; Iolascon, Achille
Novel Gardos channel mutations linked to dehydrated hereditary stomatocytosis (xerocytosis) 1.1 Articolo in rivista 2015 Andolfo, Immacolata; Russo, Roberta; Manna, Francesco; Shmukler, Boris E; Gambale, Antonella; Vitiello, Giuseppina; DE ROSA, Gianluca; Brugnara, Carlo; Alper, Seth L; Snyder, L. Michael; Iolascon, Achille