Silvia Bresolin

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 6

Top Topics

Intellectual Disability

Top Venues

British journal of haematology

American journal of hematology

This page only lists publications with an associated author ORCID identifier.

Publications

Antonio Marzollo, Stefania Zampieri, Serena Barozzi, Muhammad Abrar Yousaf, Jade Quartararo, Daniela De Rocco, Michela Faleschini, Caterina Marconi, Camilla Ceccatelli Berti, Valeria Bozzi, Giovanna Russo, Paola Giordano, Paola Goffrini, Silvia Bresolin, Annalisa Pastore, Anna Savoia, Alessandro Pecci
Thrombocytopenia 4 (THC4): Six novel families with mutations of the cytochrome c gene. British journal of haematology 205 (1) (2024)
Antonio Marzollo, Stefania Zampieri, Serena Barozzi, Muhammad Abrar Yousaf, Jade Quartararo, Daniela De Rocco, Michela Faleschini, Caterina Marconi, Camilla Ceccatelli Berti, Valeria Bozzi, Giovanna Russo, Paola Giordano, Paola Goffrini, Silvia Bresolin, Annalisa Pastore, Anna Savoia, Alessandro Pecci
Thrombocytopenia 4 (THC4): Six novel families with mutations of the cytochrome c gene. British journal of haematology (2024)
Antonio Marzollo, Stefania Zampieri, Serena Barozzi, Muhammad Abrar Yousaf, Jade Quartararo, Daniela De Rocco, Michela Faleschini, Caterina Marconi, Camilla Ceccatelli Berti, Valeria Bozzi, Giovanna Russo, Paola Giordano, Paola Goffrini, Silvia Bresolin, Annalisa Pastore, Anna Savoia, Alessandro Pecci
Thrombocytopenia 4 (THC4): Six novel families with mutations of the cytochrome c gene. British journal of haematology (2024)
Daniele Ammeti, Antonio Marzollo, Maria Gabelli, Melania Eva Zanchetta, Caterina Tretti-Parenzan, Roberta Bottega, Valeria Capaci, Alessandra Biffi, Anna Savoia, Silvia Bresolin, Michela Faleschini
A novel mutation in MECOM affects MPL regulation in vitro and results in thrombocytopenia and bone marrow failure. British journal of haematology (2023)
Antonio Marzollo, Giacomo Maestrini, Roberta La Starza, Loredana Elia, Francesco Malfona, Tiziana Pierini, Caterina Tretti Parenzan, Alessandro Coppe, Stefania Bortoluzzi, Alessandra Biffi, Cristina Mecucci, Silvia Bresolin, Anna Maria Testi
A novel germline variant in PIK3R1 results in SHORT syndrome associated with TAL/LMO T-cell acute lymphoblastic leukemia. American journal of hematology 95 (12) (2020)
Alessandro Coppe, Leonardo Nogara, Matteo Samuele Pizzuto, Alice Cani, Simone Cesaro, Riccardo Masetti, Franco Locatelli, Geertruy Te Kronnie, Giuseppe Basso, Stefania Bortoluzzi, Silvia Bresolin
Somatic mutations activating Wiskott-Aldrich syndrome protein concomitant with RAS pathway mutations in juvenile myelomonocytic leukemia patients. Human mutation 39 (4) (2018)