Foucault, the Iranian Uprising and the Constitution of a Collective Subjectivity
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Published in Foucault studies (22.10.2018)
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Deep sequencing reveals double mutations in cis of MPL exon 10 in myeloproliferative neoplasms
PIETRA, Daniela, BRISCI, Angela, CREMONESI, Laura, CAZZOLA, Mario, RUMI, Elisa, BOGGI, Sabrina, ELENA, Chiara, PIETRELLI, Alessandro, BORDONI, Roberta, FERRARI, Maurizio, PASSAMONTI, Francesco, DE BELLIS, Gianluca
Published in Haematologica (Roma) (01.04.2011)
Published in Haematologica (Roma) (01.04.2011)
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A new microarray substrate for ultra-sensitive genotyping of KRAS and BRAF gene variants in colorectal cancer
Galbiati, Silvia, Damin, Francesco, Pinzani, Pamela, Mancini, Irene, Vinci, Serena, Chiari, Marcella, Orlando, Claudio, Cremonesi, Laura, Ferrari, Maurizio
Published in PloS one (25.03.2013)
Published in PloS one (25.03.2013)
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Advancing the education in molecular diagnostics: The IFCC-Initiative “Clinical Molecular Biology Curriculum” (C-CMBC); A ten-year experience
Lianidou, Evi, Ahmad-Nejad, Parviz, Ferreira-Gonzalez, Andrea, Izuhara, Kenji, Cremonesi, Laura, Schroeder, Maria-Eugenia, Richter, Karin, Ferrari, Maurizio, Neumaier, Michael
Published in Clinica chimica acta (25.09.2014)
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Over-expression of mitochondrial ferritin affects the JAK2/STAT5 pathway in K562 cells and causes mitochondrial iron accumulation
SANTAMBROGIO, Paolo, ERBA, Benedetta Gaia, CAMPANELLA, Alessandro, COZZI, Anna, CAUSARANO, Vincenza, CREMONESI, Laura, GALLI, Anna, PORTA, Matteo Giovanni Della, INVERNIZZI, Rosangela, LEVI, Sonia
Published in Haematologica (Roma) (01.10.2011)
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Study of FTMT and ABCA4 genes in a patient affected by age-related macular degeneration: identification and analysis of new mutations
Stenirri, Stefania, Santambrogio, Paolo, Setaccioli, Marco, Erba, Benedetta Gaia, Pia Manitto, Maria, Rovida, Ermanna, Ferrari, Maurizio, Levi, Sonia, Cremonesi, Laura
Published in Clinical chemistry and laboratory medicine (01.06.2012)
Published in Clinical chemistry and laboratory medicine (01.06.2012)
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Peptide-nucleic acid-mediated enriched polymerase chain reaction as a key point for non-invasive prenatal diagnosis of β-thalassemia
GALBIATI, Silvia, FOGLIENI, Barbara, CREMONESI, Laura, TRAVI, Maurizio, CURCIO, Cristina, RESTAGNO, Gabriella, SBAIZ, Luca, SMID, Maddalena, PASI, Federica, FERRARI, Augusto, FERRARI, Maurizio
Published in Haematologica (Roma) (01.04.2008)
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Relative contribution of iron genes, dysmetabolism and hepatitis C virus (HCV) in the pathogenesis of altered iron regulation in HCV chronic hepatitis
Valenti, Luca, Pulixi, Edoardo A, Arosio, Paolo, Cremonesi, Laura, Biasiotto, Giorgio, Dongiovanni, Paola, Maggioni, Marco, Fargion, Silvia, Fracanzani, Anna Ludovica
Published in Haematologica (Roma) (01.08.2007)
Published in Haematologica (Roma) (01.08.2007)
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Evaluation of human gene variant detection in amplicon pools by the GS-FLX parallel Pyrosequencer
Bordoni, Roberta, Bonnal, Raoul, Rizzi, Ermanno, Carrera, Paola, Benedetti, Sara, Cremonesi, Laura, Stenirri, Stefania, Colombo, Alessio, Montrasio, Cristina, Bonalumi, Sara, Albertini, Alberto, Bernardi, Luigi Rossi, Ferrari, Maurizio, De Bellis, Gianluca
Published in BMC genomics (08.10.2008)
Published in BMC genomics (08.10.2008)
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Analysis of Nucleotide Variations in Genes of Iron Management in Patients of Parkinson’s Disease and Other Movement Disorders
Cremonesi, Laura, Arosio, Paolo, Ferrari, Maurizio, Maccarinelli, Federica, Girelli, Domenico, Forni, Gianluca, Pezzoli, Gianni, Goldwurm, Stefano, Finazzi, Dario, Castiglioni, Emanuela, Poli, Maura
Published in Parkinson's disease (01.01.2011)
Published in Parkinson's disease (01.01.2011)
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Analysis of Clinically Relevant Single-Nucleotide Polymorphisms by Use of Microelectronic Array Technology
Santacroce, Rosa, Ratti, Antonia, Caroli, Francesco, Foglieni, Barbara, Ferraris, Alessandro, Cremonesi, Laura, Margaglione, Maurizio, Seri, Marco, Ravazzolo, Roberto, Restagno, Gabriella, Dallapiccola, Bruno, Rappaport, Eric, Pollak, Eleanor S, Surrey, Saul, Ferrari, Maurizio, Fortina, Paolo
Published in Clinical chemistry (Baltimore, Md.) (01.12.2002)
Published in Clinical chemistry (Baltimore, Md.) (01.12.2002)
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Evaluation of different approaches for fetal DNA analysis from maternal plasma and nucleated blood cells
SMID, M, LAGONA, F, DE BENASSUTI, L, FERRARI, A, FERRARI, M, CREMONESI, L
Published in Clinical chemistry (Baltimore, Md.) (01.09.1999)
Published in Clinical chemistry (Baltimore, Md.) (01.09.1999)
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Conference Proceeding
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Driver somatic mutations identify distinct disease entities within myeloid neoplasms with myelodysplasia
Malcovati, Luca, Papaemmanuil, Elli, Ambaglio, Ilaria, Elena, Chiara, Gallì, Anna, Della Porta, Matteo G., Travaglino, Erica, Pietra, Daniela, Pascutto, Cristiana, Ubezio, Marta, Bono, Elisa, Da Vià, Matteo C., Brisci, Angela, Bruno, Francesca, Cremonesi, Laura, Ferrari, Maurizio, Boveri, Emanuela, Invernizzi, Rosangela, Campbell, Peter J., Cazzola, Mario
Published in Blood (28.08.2014)
Published in Blood (28.08.2014)
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Prospective evaluation of RASSF1A cell-free DNA as a biomarker of pre-eclampsia
Salvianti, Francesca, Inversetti, Annalisa, Smid, Maddalena, Valsecchi, Luca, Candiani, Massimo, Pazzagli, Mario, Cremonesi, Laura, Ferrari, Maurizio, Pinzani, Pamela, Galbiati, Silvia
Published in Placenta (Eastbourne) (01.09.2015)
Published in Placenta (Eastbourne) (01.09.2015)
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Somatic mutations of JAK2 exon 12 in patients with JAK2 (V617F)-negative myeloproliferative disorders
Pietra, Daniela, Li, Sai, Brisci, Angela, Passamonti, Francesco, Rumi, Elisa, Theocharides, Alexandre, Ferrari, Maurizio, Gisslinger, Heinz, Kralovics, Robert, Cremonesi, Laura, Skoda, Radek, Cazzola, Mario
Published in Blood (01.02.2008)
Published in Blood (01.02.2008)
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COLD-PCR and microarray: two independent highly sensitive approaches allowing the identification of fetal paternally inherited mutations in maternal plasma
Galbiati, Silvia, Monguzzi, Alessandra, Damin, Francesco, Soriani, Nadia, Passiu, Marianna, Castellani, Carlo, Natacci, Federica, Curcio, Cristina, Seia, Manuela, Lalatta, Faustina, Chiari, Marcella, Ferrari, Maurizio, Cremonesi, Laura
Published in Journal of medical genetics (01.07.2016)
Published in Journal of medical genetics (01.07.2016)
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