Barbara Pasini (B Pasini)

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 16

Top Topics

Amyotrophic Lateral Sclerosis

Top Venues

Journal of endocrinological investigation

Journal of clinical medicine

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

Publications

Martina Tetti, Jacopo Burrello, Marguerite Hureaux, Clarisse Billon, Eric Clauser, Franco Veglio, Franco Rabbia, Barbara Pasini, Annalisa Crisetti, Xavier Jeunemaitre, Paolo Mulatero, Silvia Monticone
Prevalence of Hyperkalemia and Familial Hyperkalemic Hypertension in 5100 Patients Referred to a Tertiary Hypertension Unit. Hypertension (Dallas, Tex. : 1979) (2024)
Carlo Smirne, Greta Maria Giacomini, Alessandro Maria Berton, Barbara Pasini, F Mercalli, Flavia Prodam, Marina Caputo, Lodewijk A A Brosens, E L M Mollero, R Pitino, Mario Pirisi, Gianluca Aimaretti, Ezio Ghigo
A novel likely pathogenetic variant p.(Cys235Arg) of the MEN1 gene in multiple endocrine neoplasia type 1 with multifocal glucagonomas. Journal of endocrinological investigation 47 (7) (2024)
Carlo Smirne, Greta Maria Giacomini, Alessandro Maria Berton, Barbara Pasini, F Mercalli, Flavia Prodam, Marina Caputo, Lodewijk A A Brosens, E L M Mollero, R Pitino, Mario Pirisi, Gianluca Aimaretti, Ezio Ghigo
A novel likely pathogenetic variant p.(Cys235Arg) of the MEN1 gene in multiple endocrine neoplasia type 1 with multifocal glucagonomas. Journal of endocrinological investigation (2024)
Carlo Smirne, Greta Maria Giacomini, Alessandro Maria Berton, Barbara Pasini, F Mercalli, Flavia Prodam, Marina Caputo, Lodewijk A A Brosens, E L M Mollero, R Pitino, Mario Pirisi, Gianluca Aimaretti, Ezio Ghigo
A novel likely pathogenetic variant p.(Cys235Arg) of the MEN1 gene in multiple endocrine neoplasia type 1 with multifocal glucagonomas. Journal of endocrinological investigation 47 (7) (2024)
Carlo Smirne, Greta Maria Giacomini, Alessandro Maria Berton, Barbara Pasini, F Mercalli, Flavia Prodam, Marina Caputo, Lodewijk A A Brosens, E L M Mollero, R Pitino, Mario Pirisi, Gianluca Aimaretti, Ezio Ghigo
A novel likely pathogenetic variant p.(Cys235Arg) of the MEN1 gene in multiple endocrine neoplasia type 1 with multifocal glucagonomas. Journal of endocrinological investigation 47 (7) (2024)
Carlo Smirne, Greta Maria Giacomini, Alessandro Maria Berton, Barbara Pasini, F Mercalli, Flavia Prodam, Marina Caputo, Lodewijk A A Brosens, E L M Mollero, R Pitino, Mario Pirisi, Gianluca Aimaretti, Ezio Ghigo
A novel likely pathogenetic variant p.(Cys235Arg) of the MEN1 gene in multiple endocrine neoplasia type 1 with multifocal glucagonomas. Journal of endocrinological investigation 47 (7) (2024)
Carlo Smirne, Greta Maria Giacomini, Alessandro Maria Berton, Barbara Pasini, F Mercalli, Flavia Prodam, Marina Caputo, Lodewijk A A Brosens, E L M Mollero, R Pitino, Mario Pirisi, Gianluca Aimaretti, Ezio Ghigo
A novel likely pathogenetic variant p.(Cys235Arg) of the MEN1 gene in multiple endocrine neoplasia type 1 with multifocal glucagonomas. Journal of endocrinological investigation 47 (7) (2024)
Lenka Stolarova, Petra Kleiblova, Petra Zemankova, Barbora Stastna, Marketa Janatova, Jana Soukupova, Maria Isabel Waddington Achatz, Christine B Ambrosone, Paraskevi Apostolou, Banu K Arun, Paul L Auer, Mollie E Barnard, Birgitte Bertelsen, null null, Marinus J Blok, Nicholas J Boddicker, Joan Brunet, Elizabeth S Burnside, Mariarosaria Calvello, Ian G Campbell, Sock Hoai Chan, Fei Chen, Jian Bang Chiang, Anna Coppa, Laura Cortesi, Ana Crujeiras-González, null null, Kim De Leeneer, Robin de Putter, Allison DePersia, Lisa Devereux, Susan M Domchek, Anna Efremidis, Christoph Engel, Corinna Ernst, Dafydd Gareth Evans, Lidia Feliubadaló, Florentia Fostira, Olivia Fuentes-Ríos, Encarna B Gómez-García, Sara González, Christopher A Haiman, Thomas Van Overeem Hansen, Jan Hauke, James M Hodge, Chunling Hu, Hongyan Huang, Nur Diana Binte Ishak, Yusuke Iwasaki, Irene Konstantopoulou, Peter Kraft, James V Lacey, Conxi Lazaro Garcia, Na Li, Weng Khong Lim, Sara Lindström, Adriana Lori, María Elena Martínez, Alexandra Martins, Koichi Matsuda, Giuseppe Matullo, Simone McInerny, Kyriaki Michailidou, Marco Montagna, Alvaro N A Monteiro, Luigi Mori, Katherine L Nathanson, Susan L Neuhausen, Heli Nevanlinna, Janet E Olson, Julie R Palmer, Barbara Pasini, Alpa V Patel, Maria Piane, Bruce Poppe, Paolo Radice, Alessandra Renieri, Nicoletta Resta, Marcy E Richardson, Toon Rosseel, Kathryn J Ruddy, Marta Santamariña, Elizabeth Santana Dos Santos, Lauren R Teras, Amanda Ewart Toland, Amy Trentham-Dietz, Celine M Vachon, Alexander E Volk, Nana Weber-Lassalle, Jeffrey N Weitzel, Lisa Wiesmuller, Stacey J Winham, Siddhartha Yadav, Drakoulis Yannoukakos, Song Yao, Valentina Zampiga, Magnus Zethoven, Ze Wen Zhang, Tomáš Zima, Amanda B Spurdle, Ana Vega, Maria Rossing, Jesús Del Valle, Arcangela De Nicolo, Eric Hahnen, Kathleen B M Claes, Joanne Ngeow Yuen Yie, Yukihide Momozawa, Paul A James, Fergus J Couch, Libor Macůrek, Zdenek Kleibl
ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk. Clinical cancer research : an official journal of the American Association for Cancer Research (2023)
Gabriele Roccuzzo, Silvia Giordano, Thomas Granato, Francesco Cavallo, Luca Mastorino, Gianluca Avallone, Barbara Pasini, Pietro Quaglino, Simone Ribero
Phenotypic and Dermoscopic Patterns of Familial Melanocytic Lesions: A Pilot Study in a Third-Level Center. Cancers 15 (15) (2023)
Chiara Giovenino, Slavica Trajkova, Lisa Pavinato, Simona Cardaropoli, Verdiana Pullano, Enza Ferrero, Elena Sukarova-Angelovska, Silvia Carestiato, Paola Salmin, Antonina Rinninella, Anthony Battaglia, Luca Bertoli, Antonio Fadda, Flavia Palermo, Diana Carli, Alessandro Mussa, Paola Dimartino, Alessandro Bruselles, Tawfiq Froukh, Giorgia Mandrile, Barbara Pasini, Silvia De Rubeis, Joseph D Buxbaum, Tommaso Pippucci, Tartaglia Marco, Marzia Rossato, Massimo Delledonne, Giovanni Battista Ferrero, Alfredo Brusco
Skewed X-chromosome inactivation in unsolved neurodevelopmental disease cases can guide re-evaluation For X-linked genes. European journal of human genetics : EJHG (2023)
Valentina Elisabetta Bounous, Elisabetta Robba, Stefania Perotto, Barbara Pasini, Nicoletta Tomasi Cont, Maria Teresa Ricci, Antonino Ditto, Vitellaro Marco, Francesco Raspagliesi, Nicoletta Biglia
Gynecological Cancers in Lynch Syndrome: A Comparison of the Histological Features with Sporadic Cases of the General Population. Journal of clinical medicine 11 (13) (2022)
Enrico Berrino, Roberto Filippi, Clara Visintin, Serena Peirone, Elisabetta Fenocchio, Giovanni Farinea, Franco Veglio, Massimo Aglietta, Anna Sapino, Matteo Cereda, Rosella Visintin, Barbara Pasini, Caterina Marchio
Collision of germline POLE and PMS2 variants in a young patient treated with immune checkpoint inhibitors. NPJ precision oncology 6 (1) (2022)
Mirko Parasiliti Caprino, Fabio Bioletto, Chiara Lopez, Martina Bollati, Francesca Maletta, Marina Caputo, Valentina Gasco, Antonio La Grotta, Paolo Limone, Giorgio Borretta, Marco Volante, Mauro Papotti, Anna Pia, Massimo Terzolo, Mario Morino, Barbara Pasini, Franco Veglio, Ezio Ghigo, Emanuela Arvat, Mauro Maccario
From SGAP-Model to SGAP-Score: A Simplified Predictive Tool for Post-Surgical Recurrence of Pheochromocytoma. Biomedicines 10 (6) (2022)
Yael Laitman, Tara M Friebel, Drakoulis Yannoukakos, Florentia Fostira, Irene Konstantopoulou, Gisella Figlioli, Bernardo Bonanni, Siranoush Manoukian, Monica Zuradelli, Carlo Alberto Tondini, Barbara Pasini, Paolo Peterlongo, Dijana Plaseska-Karanfilska, Milena Jakimovska Özdemir, Keivan Majidzadeh-A, Shiva Zarinfam, Maria A Loizidou, Andreas Hadjisavvas, Kyriaki Michailidou, Kyriacos Kyriacou, Doron M Behar, Rinat Bernstein Molho, Patricia A Ganz, Paul A James, Michael T Parsons, Aminah Sallam, Olufunmilayo I Olopade, Arun Seth, Georgia Chenevix-Trench, Goska Leslie, Lesley McGuffog, Makia J Marafi, Andre Megarbane, Fahd Al-Mulla, Timothy R Rebbeck, Eitan Friedman
The spectrum of BRCA1 and BRCA2 pathogenic sequence variants in Middle Eastern, North African, and South European countries. Human mutation 40 (11) (2019)
Simona Osella-Abate, Luca Bertero, Rebecca Senetta, Sara Mariani, Francesco Lisa, Vittoria Coppola, Jasna Metovic, Barbara Pasini, Susana Puig S, Maria Teresa Fierro, Esperanza Manrique-Silva, Rajiv Kumar, Eduardo Nagore, Paola Cassoni, Simone Ribero
TERT Promoter Mutations are Associated with Visceral Spreading in Melanoma of the Trunk. Cancers 11 (4) (2019)
Martina Tetti, Silvia Monticone, Jacopo Burrello, Patrizia Matarazzo, Franco Veglio, Barbara Pasini, Xavier Jeunemaitre, Paolo Mulatero
Liddle Syndrome: Review of the Literature and Description of a New Case. International journal of molecular sciences 19 (3) (2018)