Patrizia de Marco (Patrizia De Marco)

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 7

Top Topics

Vascular Smooth Muscle Cells

Subarachnoid Hemorrhage

Top Venues

Molecular genetics & genomic medicine

International journal of molecular sciences

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

Publications

Marzia Ognibene, Patrizia de Marco, Loredana Amoroso, Martina Fragola, Federico Zara, Stefano Parodi, Annalisa Pezzolo
Neuroblastoma Patients' Outcome and Chromosomal Instability. International journal of molecular sciences 24 (21) (2023)
Marzia Ognibene, Marcello Scala, Michele Iacomino, Irene Schiavetti, Francesca Madia, Monica Traverso, Sara Guerrisi, Marco Di Duca, Francesco Caroli, Simona Baldassari, Barbara Tappino, Ferruccio Romano, Paolo Uva, Diego Vozzi, Cristina Chelleri, Gianluca Piatelli, Maria Cristina Diana, Federico Zara, Valeria Capra, Marco Pavanello, Patrizia de Marco
Moyamoya Vasculopathy in Neurofibromatosis Type 1 Pediatric Patients: The Role of Rare Variants of RNF213 . Cancers 15 (6) (2023)
Marzia Ognibene, Marcello Scala, Michele Iacomino, Irene Schiavetti, Francesca Madia, Monica Traverso, Sara Guerrisi, Marco Di Duca, Francesco Caroli, Simona Baldassari, Barbara Tappino, Ferruccio Romano, Paolo Uva, Diego Vozzi, Cristina Chelleri, Gianluca Piatelli, Maria Cristina Diana, Federico Zara, Valeria Capra, Marco Pavanello, Patrizia de Marco
Moyamoya Vasculopathy in Neurofibromatosis Type 1 Pediatric Patients: The Role of Rare Variants of RNF213 . Cancers 15 (6) (2023)
Marzia Ognibene, Patrizia de Marco, Loredana Amoroso, Davide Cangelosi, Federico Zara, Stefano Parodi, Annalisa Pezzolo
Multiple Genes with Potential Tumor Suppressive Activity Are Present on Chromosome 10q Loss in Neuroblastoma and Are Associated with Poor Prognosis. Cancers 15 (7) (2023)
Ana Filipa Geraldo, César Augusto Pinheiro Ferreira Alves, Aysha Luis, Domenico Tortora, Joana Guimarães, Daisy Abreu, Sofia Reimão, Marco Pavanello, Patrizia de Marco, Marcello Scala, Valeria Capra, Rui Vaz, Andrea Rossi, Erin Simon Schwartz, Kshitij Mankad, Mariasavina Severino
Natural history of familial cerebral cavernous malformation syndrome in children: a multicenter cohort study. Neuroradiology (2022)
Giulia Romanisio, Cristina Chelleri, Marcello Scala, Gianluca Piccolo, Barbara Carlini, Laura Gatti, Valeria Capra, Federico Zara, Anna Bersano, Marco Pavanello, Patrizia de Marco, Maria Cristina Diana
RNF213 variant in a patient with Legius syndrome associated with moyamoya syndrome. Molecular genetics & genomic medicine 9 (6) (2021)
Philippe Lemay, Patrizia de Marco, Monica Traverso, Elisa Merello, Alexandre Dionne-Laporte, Dan Spiegelman, Édouard Henrion, Ousmane Diallo, François Audibert, Jacques L Michaud, Armando Cama, Guy A Rouleau, Zoha Kibar, Valeria Capra
Whole exome sequencing identifies novel predisposing genes in neural tube defects. Molecular genetics & genomic medicine 7 (1) (2018)