Onderzoeker
Thomy de Ravel
- Trefwoorden:Geneeskunde
Affiliaties
- Medische genetica (Departement)
Lid
Vanaf1 nov 2018 → Heden - Observerende Klinische wetenschappen (Departement)
Lid
Vanaf1 dec 2020 → Heden - Observerende Klinische wetenschappen (Departement)
Lid
Vanaf1 dec 2020 → 20 okt 2022
Publicaties
1 - 10 van 39
- Macrocephaly?(2024)
Auteurs: Ellen Rijckmans, Victoria Bordon, Thomy de Ravel, Elien Baert, Anna C Jansen, Katrien Stouffs
Pagina's: 34-36 - Atrial Abnormalities in Brugada Syndrome(2023)
Auteurs: Antonio Bisignani, Luigi Pannone, Alvise Del Monte, Ivan Eltsov, Ida Anna Cappello, Juan Antonio Sieira Rodriguez-Moret, Cinzia Monaco, Gezim Bala, Sahar Mouram, Domenico Giovanni Della Rocca, et al.
Pagina's: 2096-2105 - Genetics in Probands With Idiopathic Ventricular Fibrillation(2023)
Auteurs: Luigi Pannone, Anaïs Gauthey, Giulio Conte, Randy Osei, Daniela Campanale, Enrico Baldi, Paola Berne, Alessandro Vicentini, Pasquale Vergara, Antonio Sorgente, et al.
Pagina's: 1296-1306 - Heart rate variability and microvolt T wave alternans changes during ajmaline test may predict prognosis in Brugada syndrome(2023)
Auteurs: Paul-Adrian Călburean, Luigi Pannone, Antonio Sorgente, Anaïs Gauthey, Cinzia Monaco, Antanas Strazdas, Alexandre Almorad, Antonio Bisignani, Gezim Bala, Robbert Ramak, et al.
Pagina's: 51-62 - Genetic testing in children with Brugada syndrome(2023)
Auteurs: Luigi Pannone, Antonio Bisignani, Randy Osei, Anaïs Gauthey, Antonio Sorgente, Pasquale Vergara, Cinzia Monaco, Domenico Giovanni Della Rocca, Alvise Del Monte, Antanas Strazdas, et al.
- Case report(2022)
Auteurs: Ann Cordenier, Anja Flamez, Thomy de Ravel, Alexander Gheldof, Luigi Pannone, Carlo de Asmundis, Gudrun Pappaert, Véronique Bissay
- Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia(2022)
Auteurs: Maria Solaki, Britta Baumann, Peggy Reuter, Sten Andreasson, Isabelle Audo, Carmen Ayuso, Ghassan Balousha, Francesco Benedicenti, David Birch, Pierre Bitoun, et al.
Pagina's: 832-858 - SCN5A mutation in Brugada syndrome is associated with substrate severity detected by electrocardiographic imaging and high-density electroanatomic mapping(2022)
Auteurs: Luigi Pannone, Cinzia Monaco, Antonio Sorgente, Pasquale Vergara, Anaïs Gauthey, Paul-Adrian Calburean, Antonio Bisignani, Gaetano Paparella, Robbert Ramak, Ingrid Overeinder, et al.
Pagina's: 945-951 - Implementation of fetal clinical exome sequencing(2022)
Auteurs: Martina Marangoni, Guillaume Smits, Gilles Ceysens, Elena Costa, Robert Coulon, Caroline Daelemans, Caroline De Coninck, Sara Derisbourg, Kalina Gajewska, Giulia Garofalo Geymonat, et al.
Pagina's: 344-363 - The clinical relevance of intragenic NRXN1 deletions(2020)
Auteurs: Nele Cosemans, Laura Vandenhove, Annick Vogels, Koenraad Devriendt, Hilde Van Esch, Griet Van Buggenhout, Hilde Olivié, Thomy de Ravel, Els Ortibus, Eric Legius, et al.
Pagina's: 347-355