Close to unraveling the secrets of congenital dyserythropoietic anemia types I and II

Por Iolascon, Achille, Delaunay, Jean
Publicado em 2009

Steatosis as a co-factor in chronic liver diseases

Por Persico, Marcello, Iolascon, Achille
Publicado em 2010

Red cells in post-genomic era: impact of personalized medicine in the treatment of anemias

Por Iolascon, Achille, Andolfo, Immacolata, Russo, Roberta
Publicado no Haematologica (2015)

Next generation research and therapy in red blood cell diseases

Por Russo, Roberta, Andolfo, Immacolata, Iolascon, Achille
Publicado no Haematologica (2016)

Molecular basis of inherited microcytic anemia due to defects in iron acquisition or heme synthesis

Por Iolascon, Achille, De Falco, Luigia, Beaumont, Carole
Publicado em 2009

Clinical aspects and pathogenesis of congenital dyserythropoietic anemias: from morphology to molecular approach

Por Iolascon, Achille, Esposito, Maria Rosaria, Russo, Roberta
Publicado em 2012

Congenital dyserythropoietic anemias: molecular insights and diagnostic approach

Por Iolascon, Achille, Heimpel, Hermann, Wahlin, Anders, Tamary, Hannah
Publicado em 2013

Molecular and Genetic Basis of Inherited Nephrotic Syndrome

Por Gigante, Maddalena, Piemontese, Matteo, Gesualdo, Loreto, Iolascon, Achille, Aucella, Filippo
Publicado em 2011

Inhibition of hypoxia inducible factors combined with all-trans retinoic acid treatment enhances glial transdifferentiation of neuroblastoma cells

Por Cimmino, Flora, Pezone, Lucia, Avitabile, Marianna, Acierno, Giovanni, Andolfo, Immacolata, Capasso, Mario, Iolascon, Achille
Publicado no Sci Rep (2015)

An Autosomal Dominant Thrombocytopenia Gene Maps to Chromosomal Region 10p

Por Savoia, Anna, Del Vecchio, Maria, Totaro, Antonio, Perrotta, Silverio, Amendola, Giovanni, Moretti, Arcangela, Zelante, Leopoldo, Iolascon, Achille
Publicado em 1999

Regulation of divalent metal transporter 1 (DMT1) non-IRE isoform by the microRNA Let-7d in erythroid cells

Por Andolfo, Immacolata, De Falco, Luigia, Asci, Roberta, Russo, Roberta, Colucci, Simona, Gorrese, Marisa, Zollo, Massimo, Iolascon, Achille
Publicado em 2010

Congenital dyserythropoietic anaemias: new acquisitions

Por Iolascon, Achille, Russo, Roberta, Esposito, Maria Rosaria, Piscopo, Carmelo, Asci, Roberta, De Falco, Luigia, Di Noce, Francesca
Publicado em 2011

The role of Matriptase-2 during the early postnatal development in humans

Por De Falco, Luigia, Bruno, Mariasole, Yilmaz-Keskin, Ebru, Sal, Ertan, Büyükavci, Mustafa, Kaya, Zühre, Girelli, Domenico, Iolascon, Achille
Publicado no Haematologica (2016)

Hypomorphic mutations of SEC23B gene account for mild phenotypes of congenital dyserythropoietic anemia type II

Por Russo, Roberta, Langella, Concetta, Esposito, Maria Rosaria, Gambale, Antonella, Vitiello, Francesco, Vallefuoco, Fara, Ek, Torben, Yang, Elizabeth, Iolascon, Achille
Publicado em 2013

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

Por Iolascon, Achille, Russo, Roberta, Esposito, Maria Rosaria, Asci, Roberta, Piscopo, Carmelo, Perrotta, Silverio, Fénéant-Thibault, Madeleine, Garçon, Loïc, Delaunay, Jean
Publicado em 2010

Iron refractory iron deficiency anemia

Por De Falco, Luigia, Sanchez, Mayka, Silvestri, Laura, Kannengiesser, Caroline, Muckenthaler, Martina U., Iolascon, Achille, Gouya, Laurent, Camaschella, Clara, Beaumont, Carole
Publicado em 2013

Impact of Interleukin-6 –174 G>C Gene Promoter Polymorphism on Neuroblastoma

Por Totaro, Francesca, Cimmino, Flora, Pignataro, Piero, Acierno, Giovanni, De Mariano, Marilena, Longo, Luca, Tonini, Gian Paolo, Iolascon, Achille, Capasso, Mario
Publicado em 2013

Galectin-1 and Its Involvement in Hepatocellular Carcinoma Aggressiveness

Por Spano, Daniela, Russo, Roberta, Di Maso, Vittorio, Rosso, Natalia, Terracciano, Luigi M, Roncalli, Massimo, Tornillo, Luigi, Capasso, Mario, Tiribelli, Claudio, Iolascon, Achille
Publicado em 2010

Mutational spectrum in congenital dyserythropoietic anemia type II: Identification of 19 novel variants in SEC23B gene

Por Russo, Roberta, Esposito, Maria Rosaria, Asci, Roberta, Gambale, Antonella, Perrotta, Silverio, Ramenghi, Ugo, Forni, Gian Luca, Uygun, Vedat, Delaunay, Jean, Iolascon, Achille
Publicado em 2010

Oxidative stress modulates heme synthesis and induces peroxiredoxin-2 as a novel cytoprotective response in β-thalassemic erythropoiesis

Por De Franceschi, Lucia, Bertoldi, Mariarita, De Falco, Luigia, Santos Franco, Sara, Ronzoni, Luisa, Turrini, Franco, Colancecco, Alessandra, Camaschella, Clara, Cappellini, Maria Domenica, Iolascon, Achille
Publicado em 2011