Davide Tonduti

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 24

Top Venues

AJNR. American journal of neuroradiology

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Vittore Buzzi Children's Hospital

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

Affiliation History

Vittore Buzzi Children's Hospital Jun 16 2017

Italy

MD :: Child Neurology Unit

Fondazione IRCCS Istituto Neurologico Carlo Besta Sep 05 2013 - Jun 15 2017

Italy

MD :: Child Neurology

Publications

Federica Rey, Letizia Esposito, Erika Maghraby, Alessia Mauri, Clarissa Berardo, Eleonora Bonaventura, Davide Tonduti, Stephana Carelli, Cristina Cereda
Role of epigenetics and alterations in RNA metabolism in leukodystrophies. Wiley interdisciplinary reviews. RNA 15 (3) (2024)
Thaís Armangue, Matthew T Whitehead, Davide Tonduti, Laura Farina, Ali Reza Tavasoli, Arastoo Vossough, Mariko L Bennett, Ylenia Vaia, Geneviève Bernard, Ettore Salsano, Saadet Mercimek-Andrews, Amy Waldman, Adeline Vanderver
Brainstem Chipmunk Sign: A Diagnostic Imaging Clue across All Subtypes of Alexander Disease. AJNR. American journal of neuroradiology 45 (6) (2024)
Federica Rey, Letizia Esposito, Erika Maghraby, Alessia Mauri, Clarissa Berardo, Eleonora Bonaventura, Davide Tonduti, Stephana Carelli, Cristina Cereda
Role of epigenetics and alterations in RNA metabolism in leukodystrophies. Wiley interdisciplinary reviews. RNA 15 (3) (2024)
Federica Rey, Letizia Esposito, Erika Maghraby, Alessia Mauri, Clarissa Berardo, Eleonora Bonaventura, Davide Tonduti, Stephana Carelli, Cristina Cereda
Role of epigenetics and alterations in RNA metabolism in leukodystrophies. Wiley interdisciplinary reviews. RNA 15 (3) (2024)
Thaís Armangue, Matthew T Whitehead, Davide Tonduti, Laura Farina, Ali Reza Tavasoli, Arastoo Vossough, Mariko L Bennett, Ylenia Vaia, Geneviève Bernard, Ettore Salsano, Saadet Mercimek-Andrews, Amy Waldman, Adeline Vanderver
Brainstem Chipmunk Sign: A Diagnostic Imaging Clue across All Subtypes of Alexander Disease. AJNR. American journal of neuroradiology (2024)
Thaís Armangue, Matthew T Whitehead, Davide Tonduti, Laura Farina, Ali Reza Tavasoli, Arastoo Vossough, Mariko L Bennett, Ylenia Vaia, Geneviève Bernard, Ettore Salsano, Saadet Mercimek-Andrews, Amy Waldman, Adeline Vanderver
Brainstem Chipmunk Sign: A Diagnostic Imaging Clue across All Subtypes of Alexander Disease. AJNR. American journal of neuroradiology 45 (6) (2024)
Thaís Armangue, Matthew T Whitehead, Davide Tonduti, Laura Farina, Ali Reza Tavasoli, Arastoo Vossough, Mariko L Bennett, Ylenia Vaia, Geneviève Bernard, Ettore Salsano, Saadet Mercimek-Andrews, Amy Waldman, Adeline Vanderver
Brainstem Chipmunk Sign: A Diagnostic Imaging Clue across All Subtypes of Alexander Disease. AJNR. American journal of neuroradiology 45 (6) (2024)
Thaís Armangue, Matthew T Whitehead, Davide Tonduti, Laura Farina, Ali Reza Tavasoli, Arastoo Vossough, Mariko L Bennett, Ylenia Vaia, Geneviève Bernard, Ettore Salsano, Saadet Mercimek-Andrews, Amy Waldman, Adeline Vanderver
Brainstem Chipmunk Sign: A Diagnostic Imaging Clue across All Subtypes of Alexander Disease. AJNR. American journal of neuroradiology 45 (6) (2024)
Thaís Armangue, Matthew T Whitehead, Davide Tonduti, Laura Farina, Ali Reza Tavasoli, Arastoo Vossough, Mariko L Bennett, Ylenia Vaia, Geneviève Bernard, Ettore Salsano, Saadet Mercimek-Andrews, Amy Waldman, Adeline Vanderver
Brainstem Chipmunk Sign: A Diagnostic Imaging Clue across All Subtypes of Alexander Disease. AJNR. American journal of neuroradiology 45 (6) (2024)
Thaís Armangue, Matthew T Whitehead, Davide Tonduti, Laura Farina, Ali Reza Tavasoli, Arastoo Vossough, Mariko L Bennett, Ylenia Vaia, Geneviève Bernard, Ettore Salsano, Saadet Mercimek-Andrews, Amy Waldman, Adeline Vanderver
Brainstem Chipmunk Sign: A Diagnostic Imaging Clue across All Subtypes of Alexander Disease. AJNR. American journal of neuroradiology 45 (6) (2024)
Nina-Maria Wilpert, Davide Tonduti, Ylenia Vaia, Heiko Krude, Catherine Sarret, Markus Schuelke
Establishing Patient-Centered Outcomes for MCT8 Deficiency: Stakeholder Engagement and Systematic Literature Review. Neuropsychiatric disease and treatment 19 (2023)
Davide Tonduti, Alberto A Zambon, Daniele Ghezzi, Eleonora Lamantea, Rossella Izzo, Cecilia Parazzini, Cristina Baldoli, Marjo S van der Knaap, Francesca Fumagalli
Expanding the Spectrum of NUBPL-Related Leukodystrophy. Neuropediatrics (2023)
Martha Caterina Faraguna, Francesca Musto, Viola Crescitelli, Maria Iascone, Luigina Spaccini, Davide Tonduti, Tiziana Fedeli, Gaia Kullmann, Francesco Canonico, Alessandro Cattoni, Fabiola Dell'Acqua, Carmelo Rizzari, Serena Gasperini
Mucopolysaccharidosis-Plus Syndrome, a Rapidly Progressive Disease: Favorable Impact of a Very Prolonged Steroid Treatment on the Clinical Course in a Child. Genes 13 (3) (2022)
Eleonora Mura, Silvia Masnada, Clara Antonello, Cecilia Parazzini, Giana Izzo, Jessica Garau, Daisy Sproviero, Cristina Cereda, Simona Orcesi, Pierangelo Veggiotti, Gianvincenzo Zuccotti, Dario Dilillo, Francesca Penagini, Davide Tonduti
Ruxolitinib in Aicardi-Goutières syndrome. Metabolic brain disease 36 (5) (2021)
Davide Tonduti, Eleonora Mura, Silvia Masnada, Enrico Bertini, Chiara Aiello, Daniela Zini, Lucio Parmeggiani, Gaetano Cantalupo, Giacomo Talenti, Pierangelo Veggiotti, Luigina Spaccini, Maria Iascone, Cecilia Parazzini
Spinal cord involvement and paroxysmal events in "Infantile Onset Transient Hypomyelination" due to TMEM63A mutation. Journal of human genetics 66 (10) (2021)
Davide Tonduti, Anna Pichiecchio, Carla Uggetti, Stefania Maria Bova, Simona Orcesi, Cecilia Parazzini, Luisa Chiapparini
How to look for intracranial calcification in children with neurological disorders: CT, MRI, or both of them? Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology (2021)
Ferdy S van Geest, Stefan Groeneweg, Erica L T van den Akker, Iuliu Bacos, Diana Barca, Sjoerd A A van den Berg, Enrico Silvio Bertini, Doris Brunner, Nicola Brunetti-Pierri, Marco Cappa, Gerarda Cappuccio, Krishna Chatterjee, Alexander D Chesover, Peter Christian, Régis Coutant, Dana Craiu, Patricia Crock, Cheyenne Dewey, Alice Dica, Paul Dimitri, Rachana Dubey, Anina Enderli, Jan Fairchild, Jonathan Gallichan, Luigi R Garibaldi, Belinda George, Annette Hackenberg, Bianka Heinrich, Tony Huynh, Anna Kłosowska, Amy Lawson-Yuen, Michaela Linder-Lucht, Greta Lyons, Felipe Monti Lora, Carla Moran, Katalin E Müller, Laura Paone, Praveen G Paul, Michel Polak, Francesco Porta, Christina Reinauer, Yolanda B de Rijke, Rowen Seckold, Tuba Seven Menevşe, Peter Simm, Anna Simon, Marco Spada, Athanasia Stoupa, Lilla Szeifert, Davide Tonduti, Hans van Toor, Serap Turan, Joel Vanderniet, Monique de Waart, Ronald van der Wal, Adri van der Walt, Anne-Marie van Wermeskerken, Jolanta Wierzba, Federica Zibordi, Amnon Zung, Robin P Peeters, W Edward Visser
Long-term efficacy of T3 analogue Triac in children and adults with MCT8 deficiency: a real-life retrospective cohort study. The Journal of clinical endocrinology and metabolism (2021)
Silvia Masnada, Diego Martinelli, Marta Correa-Vela, Emanuele Agolini, Heidy Baide-Mairena, Anna Marcé-Grau, Cecilia Parazzini, Pierangelo Veggiotti, Belen Perez-Duenas, Davide Tonduti
PRKRA-Related Disorders: Bilateral Striatal Degeneration in Addition to DYT16 Spectrum. Movement disorders : official journal of the Movement Disorder Society 36 (4) (2021)
Carolina Uggenti, Alice Lepelley, Marine Depp, Andrew P Badrock, Mathieu P Rodero, Marie-Thérèse El-Daher, Gillian I Rice, Somdutta Dhir, Ann P Wheeler, Ashish Dhir, Waad Albawardi, Marie-Louise Frémond, Luis Seabra, Jennifer Doig, Natalie Blair, Maria José Martin-Niclos, Erika Della Mina, Alejandro Rubio-Roldán, Jose Luis García-Pérez, Duncan Sproul, Jan Rehwinkel, Jonny Hertzog, Anne Boland-Auge, Robert Olaso, Jean François Deleuze, Julien Baruteau, Karine Brochard, Jonathan Buckley, Vanessa Cavallera, Cristina Cereda, Liesbeth M H De Waele, Angus Dobbie, Diane Doummar, Frances Elmslie, Margarete Koch-Hogrebe, Ram Kumar, Kate Lamb, John H Livingston, Anirban Majumdar, Charles Marques Lorenço, Simona Orcesi, Sylviane Peudenier, Kevin Rostasy, Caroline A Salmon, Christiaan Scott, Davide Tonduti, Guy Touati, Marialuisa Valente, Hélio van der Linden, Hilde Van Esch, Marie Vermelle, Kate Webb, Andrew P Jackson, Martin A M Reijns, Nick Gilbert, Yanick J Crow
cGAS-mediated induction of type I interferon due to inborn errors of histone pre-mRNA processing. Nature genetics 52 (12) (2020)
Davide Tonduti, Elisa Fazzi, Raffaele Badolato, Simona Orcesi
Novel and emerging treatments for Aicardi-Goutières syndrome. Expert review of clinical immunology 16 (2) (2020)
Silvia Masnada, Stefan Groenweg, Veronica Saletti, Luisa Chiapparini, Barbara Castellotti, Ettore Salsano, W Edward Visser, Davide Tonduti
Novel mutations in SLC16A2 associated with a less severe phenotype of MCT8 deficiency. Metabolic brain disease 34 (6) (2019)
Jessica Garau, Vanessa Cavallera, Marialuisa Valente, Davide Tonduti, Daisy Sproviero, Susanna Zucca, Domenica Battaglia, Roberta Battini, Enrico Bertini, Silvia Cappanera, Luisa Chiapparini, Camilla Crasà, Giovanni Crichiutti, Elvio Dalla Giustina, Stefano D'Arrigo, Valentina De Giorgis, Micaela De Simone, Jessica Galli, Roberta La Piana, Tullio Messana, Isabella Moroni, Nardo Nardocci, Celeste Panteghini, Cecilia Parazzini, Anna Pichiecchio, Antonella Pini, Federica Ricci, Veronica Saletti, Elisabetta Salvatici, Filippo M Santorelli, Stefano Sartori, Francesca Tinelli, Carla Uggetti, Edvige Veneselli, Giovanna Zorzi, Barbara Garavaglia, Elisa Fazzi, Simona Orcesi, Cristina Cereda
Molecular Genetics and Interferon Signature in the Italian Aicardi Goutières Syndrome Cohort: Report of 12 New Cases and Literature Review. Journal of clinical medicine 8 (5) (2019)
Davide Tonduti, Celeste Panteghini, Anna Pichiecchio, Alice Decio, Miryam Carecchio, Chiara Reale, Isabella Moroni, Nardo Nardocci, Jaume Campistol, Angela Garcia-Cazorla, Belen Perez Duenas, null null, Luisa Chiapparini, Barbara Garavaglia, Simona Orcesi
Encephalopathies with intracranial calcification in children: clinical and genetic characterization. Orphanet journal of rare diseases 13 (1) (2018)
Davide Tonduti, Anna Ardissone, Isabella Ceccherini, Giorgio Giaccone, Laura Farina, Isabella Moroni
Unusual presentations and intrafamilial phenotypic variability in infantile onset Alexander disease. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 37 (6) (2016)

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Publication Activity (10 Years)

Top Topics

Top Venues

Davide Tonduti