Clinical and hematologic features of 300 patients affected by hereditary spherocytosis grouped according to the type of the membrane protein defect von Mariani, Mariagabriella, Barcellini, Wilma, Vercellati, Cristina, Marcello, Anna Paola, Fermo, Elisa, Pedotti, Paola, Boschetti, Carla, Zanella, Alberto

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P1526: AUTOIMMUNE HEMOLYTIC ANEMIAS: RELATIONSHIP BETWEEN SINGLE NUCLEOTIDE POLYMORPHISMS OF CYTOKINE GENES AND CLINICAL/HEMATOLOGICAL PARAMETERS von Zaninoni, A., Fattizzo, B., Giannotta, J., Fermo, E., Bianchi, P., Cecchi, N., Barcellini, W.

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S278: EVALUATION OF THE MAIN REGULATORS OF SYSTEMIC IRON HOMEOSTASIS IN PYRUVATE KINASE DEFICIENCY von Zaninoni, A., Russo, R., Marra, R., Andolfo, I., Fermo, E., Marcello, A. P., Consonni, D., Eleni Rosato, B., Martone, S., Fattizzo, B., Barcellini, W., Iolascon, A., Bianchi, P.

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Diagnostic power of laboratory tests for hereditary spherocytosis: a comparison study in 150 patients grouped according to molecular and clinical characteristics von BIANCHI, Paola, FERMO, Elisa, VERCELLATI, Cristina, MARCELLO, Anna P, PORRETTI, Laura, CORTELEZZI, Agostino, BARCELLINI, Wilma, ZANELIA, Alberto

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Red cell pyruvate kinase deficiency: molecular and clinical aspects von Zanella, Alberto, Fermo, Elisa, Bianchi, Paola, Valentini, Giovanna

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Missense variant in TPI1 (Arg189Gln) causes neurologic deficits through structural changes in the triosephosphate isomerase catalytic site and reduced enzyme levels in vivo von Roland, Bartholomew P., Richards, Kristen R., Hrizo, Stacy L., Eicher, Samantha, Barile, Zackery J., Chang, Tien-Chien, Savon, Grace, Bianchi, Paola, Fermo, Elisa, Ricerca, Bianca Maria, Tortorolo, Luca, Vockley, Jerry, VanDemark, Andrew P., Palladino, Michael J.

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Imatinib and ruxolitinib association: first experience in two patients von Iurlo, Alessandra, Gianelli, Umberto, Rapezzi, Davide, Cattaneo, Daniele, Fermo, Elisa, Binda, Francesca, Santambrogio, Elisa, Bucelli, Cristina, Cortelezzi, Agostino

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Severe Ankyrin-R deficiency results in impaired surface retention and lysosomal degradation of RhAG in human erythroblasts von Satchwell, Timothy J, Bell, Amanda J, Hawley, Bethan R, Pellegrin, Stephanie, Mordue, Kathryn E, van Deursen, Cees Th B M, Braak, Nicole Heitink-Ter, Huls, Gerwin, Leers, Mathie P G, Overwater, Eline, Tamminga, Rienk Y J, van der Zwaag, Bert, Fermo, Elisa, Bianchi, Paola, van Wijk, Richard, Toye, Ashley M

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Characteristic phenotypes associated with congenital dyserythropoietic anemia (type II) manifest at different stages of erythropoiesis von Satchwell, Timothy J, Pellegrin, Stephanie, Bianchi, Paola, Hawley, Bethan R, Gampel, Alexandra, Mordue, Kathryn E, Budnik, Annika, Fermo, Elisa, Barcellini, Wilma, Stephens, David J, van den Akker, Emile, Toye, Ashley M

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Pyruvate kinase deficiency von Zanella, Alberto, Bianchi, Paola, Fermo, Elisa

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Inaugurazione delle statue di Annibal Caro e Giacomo Leopardi a Fermo il 25 giugno 1876 von Fermo (Italy)

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Reply to "Flow cytometry test for hereditary spherocytosis". Haematologica. 2012;97(12):e47 von Bianchi, P., Fermo, E., Zanella, A.

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Reply to "Testing for hereditary spherocytosis: a French experience". Haematologica. 2012;97(12):e48-9 von Bianchi, P., Fermo, E., Zanella, A.

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Hereditary pyrimidine 5′‐nucleotidase deficiency: from genetics to clinical manifestations von Zanella, Alberto, Bianchi, Paola, Fermo, Elisa, Valentini, Giovanna

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P076 Acquisition of RAS and JAK2 mutations contributes to progression of CMML from the dysplastic to the proliferative variant von Onida, F, Ricci, C, Fermo, E, Miranda, C, Corti, S, Cortelezzi, A, Fariciotti, A, Soligo, D, Lambertenghi Deliliers, G

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VEGF Expression Correlates With Microvessel Density in Philadelphia Chromosome-Negative Chronic Myeloproliferative Disorders von GIANELLI, Umberto, VENER, Claudia, BOSARI, Silvano, COGGI, Guido, LAMBERTENGHI DELILIERS, Giorgio, RAFANIELLO RAVIELE, Paola, SAVI, Federica, SOMALVICO, Francesco, CALORI, Rossella, IURLO, Alessandra, RADAELLI, Franca, FERMO, Elisa, BUCCIARELLI, Paolo

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Regolamento per la Deputazione de' pubblici spettacoli in Fermo von Fermo (Italy). Deputazione de' pubblici spettacoli

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Functional analysis of pyrimidine 5′-nucleotidase mutants causing nonspherocytic hemolytic anemia von Chiarelli, Laurent R., Bianchi, Paola, Fermo, Elisa, Galizzi, Alessandro, Iadarola, Paolo, Mattevi, Andrea, Zanella, Alberto, Valentini, Giovanna

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Red cell pyruvate kinase deficiency: 17 new mutations of the PK‐LR gene von Fermo, Elisa, Bianchi, Paola, Chiarelli, Laurent R., Cotton, Frederic, Vercellati, Cristina, Writzl, Karin, Baker, Kerry, Hann, Ian, Rodwell, Robin, Valentini, Giovanna, Zanella, Alberto

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Molecular characterization of six unrelated Italian patients affected by pyrimidine 5′‐nucleotidase deficiency von Bianchi, Paola, Fermo, Elisa, Alfinito, Fiorella, Vercellati, Cristina, Baserga, Mariangiola, Ferraro, Filomena, Guzzo, Immacolata, Rotoli, Bruno, Zanella, Alberto

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