Resultados de búsqueda - Michaela Calvillo

Similar favorable outcome of pegfilgrastim overdose in patients with different age and underlying disease por Carlo Dufour, Barbara Cappelli, Michaela Calvillo, Francesca Fioredda, Rossella Tonelli, Roberto Crocchiolo

Enlace del recurso

Novel HAX1 gene mutations associated to neurodevelopment abnormalities in two Italian patients with severe congenital neutropenia por Marina Lanciotti, Stefania Indaco, Sonia Bonanomi, Tiziana Coliva, Elena Mastrodicasa, Gianluca Caridi, Michaela Calvillo, Carlo Dufour

Enlace del recurso

Severe Lactic Acidosis Caused by Thiamine Deficiency in a Child with Relapsing Acute Lymphoblastic Leukemia: A Case Report por Francesco Baldo, Enrico Drago, Daniela Nisticò, Silvia Buratti, Michaela Calvillo, Concetta Micalizzi, Maria Cristina Schiaffino, Mohamad Maghnie

Enlace del recurso

Hypomorphic FANCA mutations correlate with mild mitochondrial and clinical phenotype in Fanconi anemia por Roberta Bottega, Elena Nicchia, Enrico Cappelli, Silvia Ravera, Daniela De Rocco, Michela Faleschini, Fabio Corsolini, Filomena Pierri, Michaela Calvillo, Giovanna Russo, Gabriella Casazza, Ugo Ramenghi, Piero Farruggia, Carlo Dufour, Anna Savoia

Enlace del recurso

Autoimmune Lymphoproliferative Syndrome (ALPS) Disease and ALPS Phenotype: Are They Two Distinct Entities? por Elena Palmisani, Maurizio Miano, Alice Grossi, Marina Lanciotti, Michela Lupia, Paola Terranova, Isabella Ceccherini, Eugenia Montanari, Michaela Calvillo, Filomena Pierri, Concetta Micalizzi, Rosario Maggiore, Daniela Guardo, Sabrina Zanardi, Elena Facchini, Angela Maggio, Elena Mastrodicasa, Paola Corti, Giovanna Russo, Marta Pillon, Piero Farruggia, Simone Cesaro, Angelica Barone, Francesca Tosetti, Ugo Ramenghi, Nicoletta Crescenzio, Jack Bleesing, Carlo Dufour, Francesca Fioredda

Enlace del recurso