Author Search Results :: Katalog UB TU-Chemnitz

1

Chromosomal locus 19p13 as potential hotspot for aberrant gene expression in relapsed paediatric acute lymphoblastic leukaemia

by Lanciotti, Marina, D'Apolito, Maria, Paolucci, Paolo, Dufour, Carlo
Published in British Journal of Haematology (2006)

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2

Gilbert syndrome as differential diagnosis of hyperbilirubinemia in acquired aplastic anemia

by Svahn, Johanna, Lanciotti, Marina, Dufour, Carlo, Perrotta, Silverio, Nobili, Bruno
Published in Pediatric Blood & Cancer (2005)

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3

Non-identical twin sisters concordant for Langerhans cell histiocytosis and discordant for secondary acute promyelocytic leukemia

by Dufour, Carlo, Lanciotti, Marina, Micalizzi, Concetta, Valetto, Angelo, Haupt, Riccardo
Published in Medical and Pediatric Oncology (2001)

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4

Negative Staining of Proteins in Polyacrylamide Gels with Methyl Trichloroacetate

by Candiano, Giovanni, Porotto, Matteo, Lanciotti, Marina, Ghiggeri, Gian Marco
Published in Analytical Biochemistry (1996)

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5

Uridine phosphorylase from Escherichia coli B. enzymatic and molecular properties

by Vita, Alberto, Amici, Adolfo, Cacciamani, Tiziana, Lanciotti, Marina, Magni, Giulio
Published in International Journal of Biochemistry (1986)

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6

Cytidine deaminase from Escherichia coli B. Purification and enzymic and molecular properties

by Vita, Alberto, Amici, Adolfo, Cacciamani, Tiziana, Lanciotti, Marina, Magni, Giulio
Published in Biochemistry (1985)

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7

Clinical heterogeneity in a family with DKC1 mutation, dyskeratosis congenita and Hoyeraal-Hreidarsson syndrome in first cousins

by Olivieri, Cristina, Mondino, Anna, Chinello, Matteo, Risso, Alessandra, Finale, Enrico, Lanciotti, Marina, Guala, Andrea
Published in Pediatric Reports (2017)

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8

Gene expression profiling: a possible tool in the prediction of outcome in paediatric acute lymphoblastic leukaemia? : Correspondence: Correspondence

by Lanciotti, Marina, D’Apolito, Maria, Paolucci, Paolo, Indaco, Stefania, Dufour, Carlo
Published in British Journal of Haematology (2011)

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9

Compound heterozygosity for two new TERT mutations in a patient with aplastic anemia

by Aspesi, Anna, Vallero, Stefano, Rocci, Alberto, Pavesi, Elisa, Lanciotti, Marina, Ramenghi, Ugo, Dianzani, Irma
Published in Pediatric Blood & Cancer (2010)

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10

Severe congenital neutropenia: a negative synergistic effect of multiple mutations ofELANE(ELA2) gene

by Lanciotti, Marina, Caridi, Gianluca, Rosano, Camillo, Pigullo, Simona, Lanza, Tiziana, Dufour, Carlo
Published in British Journal of Haematology (2009)

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11

Possible role of toll-like receptor 9 polymorphism in chemotherapy-related invasive mold infections in children with hematological malignancies

by Lanciotti, Marina, Pigullo, Simona, Lanza, Tiziana, Dufour, Carlo, Caviglia, Ilaria, Castagnola, Elio
Published in Pediatric Blood & Cancer (2008)

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12

Association of cytogenetic abnormalities with detection of BCR-ABL fusion transcripts in children with T-lineage lymphoproliferative diseases (T-ALL and T-NHL)

by Lo Nigro, Luca, Sainati, Laura, Mirabile, Elena, Lanciotti, Marina, Poli, Amelia, Leszl, Anna, Basso, Giuseppe
Published in Pediatric Blood & Cancer (2004)

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13

Reversible vincristine-related flaccid paralysis in a child with acute lymphoblastic leukemia

by Fioredda, Francesca, Micalizzi, Concetta, Lanciotti, Marina, Dufour, Carlo, Lamba, Laura Doria, Fiocchi, Isabella
Published in Medical and Pediatric Oncology (2002)

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14

Rapid detection of γT cell receptor gene rearrangements in acute lymphoblastic leukemia by electrophoresis and silver staining: Implications for detection of minimal residual disea...

by Valetto, Angelo, Lanciotti, Marina, Martino, Daniela Di, Anselmi, Giorgia, Bottini, Federico, Mori, Piergiorgio, Candiano, Giovanni
Published in Electrophoresis (1998)

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15

Long-term use of pegfilgrastim in children with severe congenital neutropenia: clinical and pharmacokinetic data

by Fioredda, Francesca, Lanza, Tiziana, Gallicola, Federica, Riccardi, Francesca, Lanciotti, Marina, Mastrodicasa, Elena, Signa, Sara, Zanardi, Sabrina, Calvillo, Michaela, Dufour, Carlo
Published in Blood (2016)

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16

Poikiloderma With Neutropenia : A Case Report and Review of the Literature: A Case Report and Review of the Literature

by Farruggia, Piero, Indaco, Stefania, Dufour, Carlo, Lanza, Tiziana, Mosa, Clara, Macaluso, Alessandra, Milioto, Mirella, D’Angelo, Paolo, Lanciotti, Marina
Published in Journal of Pediatric Hematology/Oncology (2014)

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17

Pegfilgrastim in children with severe congenital neutropenia : Pegfilgrastim in Severe Congenital Neutropenia: Pegfilgrastim in Severe Congenital Neutropenia

by Fioredda, Francesca, Calvillo, Michaela, Lanciotti, Marina, Lanza, Tiziana, Giunti, Laura, Castagnola, Elio, Lorenzi, Ines, Tonelli, Rossella, Ghezzi, Piero, Dufour, Carlo
Published in Pediatric Blood & Cancer (2010)

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18

Human Fanconi A cells are susceptible to TRAIL-induced apoptosis

by Pigullo, Simona, Ferretti, Elisa, Lanciotti, Marina, Bruschi, Maurizio, Candiano, Giovanni, Svahn, Johanna, Haneline, Laura, Dufour, Carlo, Pistoia, Vito, Corcione, Anna
Published in British Journal of Haematology (2007)

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19

Glutathione S-transferase polymorphisms and susceptibility to neuroblastoma

by Lanciotti, Marina, Coco, Simona, Michele, Paola Di, Haupt, Riccardo, Boni, Luca, Pigullo, Simona, Dufour, Carlo, Garaventa, Alberto, Tonini, Gian Paolo
Published in Pharmacogenetics and Genomics (2005)

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20

Targeted NGS Yields Plentiful Ultra-Rare Variants in Inborn Errors of Immunity Patients

by Grossi, Alice, Miano, Maurizio, Lanciotti, Marina, Fioredda, Francesca, Guardo, Daniela, Palmisani, Elena, Terranova, Paola, Santamaria, Giuseppe, Caroli, Francesco, Caorsi, Roberta, Volpi, Stefano, Gattorno, Marco, Dufour, Carlo, Ceccherini, Isabella
Published in Genes (2021)

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