Luisa Ronzoni

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 8

Top Topics

Contrast Enhanced Ultrasound

Gene Expression

Top Venues

Prenatal diagnosis

Liver international : official journal of the International Association for the Study of the Liver

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

Publications

Sarah Shalaby, Luisa Ronzoni, Virginia Hernández-Gea, Luca Vittorio Valenti
The genetics of portal hypertension: Recent developments and the road ahead. Liver international : official journal of the International Association for the Study of the Liver (2023)
Luisa Ronzoni, Matteo Mureddu, Francesco Malvestiti, Vittoria Moretti, Cristiana Bianco, Giulia Periti, Margherita Baldassarri, Francesca Ariani, Anna Carrer, Serena Pelusi, Alessandra Renieri, Daniele Prati, Luca Valenti
Liver Involvement in Patients with Rare MBOAT7 Variants and Intellectual Disability: A Case Report and Literature Review. Genes 14 (8) (2023)
Serena Pelusi, Luisa Ronzoni, Francesco Malvestiti, Cristiana Bianco, Ilaria Marini, Roberta D'Ambrosio, Juri Alessandro Giannotta, Giorgio Soardo, Marco Maggioni, Daniele Prati, Luca Vittorio Valenti
Clinical exome sequencing for diagnosing severe cryptogenic liver disease in adults: A case series. Liver international : official journal of the International Association for the Study of the Liver 42 (4) (2022)
Luca Vittorio Valenti, Luisa Ronzoni
Genetics: A new clinical tool for the hepatologist. Liver international : official journal of the International Association for the Study of the Liver 42 (4) (2022)
Luisa Ronzoni, Simona Boito, Camilla Meossi, Claudia Cesaretti, Berardo Rinaldi, Emanuele Agolini, Tommaso Rizzuti, Laura Pezzoli, Rosamaria Silipigni, Antonio Novelli, Maria Iascone, Nicola Persico, Federica Natacci
Prenatal ultrasound findings associated with PIGW variants: One more piece in the FRYNS syndrome puzzle? PIGW-related prenatal findings. Prenatal diagnosis 42 (12) (2022)
Luisa Ronzoni, Maria Francesca Bedeschi, Gaia Silibello, Veronica Accurti, Marina Di Segni, Valeria Nicotra, Paola Vizziello, Faustina Lalatta
Increased RISK for 47,XXY on cell-free DNA screen: Not always Klinefelter syndrome. Prenatal diagnosis 41 (10) (2021)
Nicola Persico, Simona Boito, Paolo Volpe, Benedetta Ischia, Mattia Gentile, Luisa Ronzoni, Valentina De Robertis, Isabella Fabietti, Claudiana Olivieri, Enrico Periti, Romina Ficarella, Rosamaria Silipigni, Georgios Rembouskos
Incidence of chromosomal abnormalities in fetuses with first trimester ultrasound anomalies and a low-risk cell-free DNA test for common trisomies. Prenatal diagnosis 40 (11) (2020)
Luisa Ronzoni, Gaia Silibello, Donatella Quagliarini, Faustina Lalatta
A comment on "clinical experience with sex chromosome aneuploidies detected by noninvasive prenatal testing (NIPT): Accuracy and patient decision-making". Prenatal diagnosis 38 (13) (2018)