Výsledky vyhledávání - Fulvia Brugnoletti
- Zobrazuji výsledky 1 - 3 z 3
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1
Burkitt lymphoma as fourth neoplasia in a patient affected by Cowden Syndrome with a novel PTEN germline pathogenic variant Autor Eugenio Galli, Francesco D’Alò, Annarosa Cuccaro, Eleonora Alma, Elena Maiolo, Fulvia Brugnoletti, Luigi Maria Larocca, Marcella Zollino, Andrea Bacigalupo, Stefan Hohaus
Vydáno 2020Artigo -
2
TP53 mutations are frequent in adult acute lymphoblastic leukemia cases negative for recurrent fusion genes and correlate with poor response to induction therapy Autor Sabina Chiaretti, Fulvia Brugnoletti, Simona Tavolaro, Silvia Bonina, Francesca Paoloni, M Marinelli, Nancy Patten, Massimiliano Bonifacio, Mariagrazia Kropp, Simona Sica, Anna Guarini, Robin Foà
Vydáno 2013Carta -
3
Exome-based cancer predisposition gene testing can provide a genetic diagnosis for individuals with heterogeneous tumor phenotypes Autor Snežana Hinić, Arjen R. Mensenkamp, Janneke Schuurs-Hoeijmakers, Fulvia Brugnoletti, Lilian Vreede, Elke M. van Veen, Barend Mijzen, Rachel S. van der Post, Maurizio Genuardi, Marjolijn J. L. Ligtenberg, Nicoline Hoogerbrugge, Richarda M. de Voer
Vydáno 2025Artigo
Vyhledávací nástroje:
Související témata
Biology
Gene
Genetics
Mutation
Apoptosis
Cancer research
Germline
Germline mutation
Internal medicine
Medicine
Oncology
PI3K/AKT/mTOR pathway
PTEN
Acute lymphocytic leukemia
Bioinformatics
CHEK2
Cancer
Candidate gene
Chemotherapy
Complete response
Cowden syndrome
Dermatology
Disease
Exome
Exome sequencing
Folliculin
Fusion gene
Genetic predisposition
Genetic testing
Immunology