Caterina Mariotti

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 21

Top Venues

Journal of neurology, neurosurgery, and psychiatry

Movement disorders : official journal of the Movement Disorder Society

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

American journal of medical genetics. Part A

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

Publications

Thiago Junqueira Ribeiro de Rezende, Isaac Adanyaguh, Orlando G P Barsottini, Benjamin Bender, Fernando Cendes, Léo Coutinho, Andreas Deistung, Imis Dogan, Alexandra Durr, Juan Fernandez-Ruiz, Sophia L Göricke, Marina Grisoli, Carlos R Hernandez-Castillo, Christophe Lenglet, Caterina Mariotti, Alberto Rolim Muro Martinez, Breno K Massuyama, Fanny Mochel, Lorenzo Nanetti, Anna Nigri, Sergio E Ono, Gülin Öz, José Luiz Pedroso, Kathrin Reetz, Matthis Synofzik, Helio Teive, Sophia I Thomopoulos, Paul M Thompson, Dagmar Timmann, Bart P C van de Warrenburg, Judith van Gaalen, Marcondes Cavalcante de França Junior, Ian H Harding
Genotype-specific spinal cord damage in spinocerebellar ataxias: an ENIGMA-Ataxia study. Journal of neurology, neurosurgery, and psychiatry 95 (7) (2024)
Thiago Junqueira Ribeiro de Rezende, Isaac Adanyaguh, Orlando G P Barsottini, Benjamin Bender, Fernando Cendes, Léo Coutinho, Andreas Deistung, Imis Dogan, Alexandra Durr, Juan Fernandez-Ruiz, Sophia L Göricke, Marina Grisoli, Carlos R Hernandez-Castillo, Christophe Lenglet, Caterina Mariotti, Alberto Rolim Muro Martinez, Breno K Massuyama, Fanny Mochel, Lorenzo Nanetti, Anna Nigri, Sergio E Ono, Gülin Öz, José Luiz Pedroso, Kathrin Reetz, Matthis Synofzik, Helio Teive, Sophia I Thomopoulos, Paul M Thompson, Dagmar Timmann, Bart P C van de Warrenburg, Judith van Gaalen, Marcondes Cavalcante de França Junior, Ian H Harding
Genotype-specific spinal cord damage in spinocerebellar ataxias: an ENIGMA-Ataxia study. Journal of neurology, neurosurgery, and psychiatry 95 (7) (2024)
Thiago Junqueira Ribeiro de Rezende, Isaac Adanyaguh, Orlando G P Barsottini, Benjamin Bender, Fernando Cendes, Léo Coutinho, Andreas Deistung, Imis Dogan, Alexandra Durr, Juan Fernandez-Ruiz, Sophia L Göricke, Marina Grisoli, Carlos R Hernandez-Castillo, Christophe Lenglet, Caterina Mariotti, Alberto Rolim Muro Martinez, Breno K Massuyama, Fanny Mochel, Lorenzo Nanetti, Anna Nigri, Sergio E Ono, Gülin Öz, José Luiz Pedroso, Kathrin Reetz, Matthis Synofzik, Helio Teive, Sophia I Thomopoulos, Paul M Thompson, Dagmar Timmann, Bart P C van de Warrenburg, Judith van Gaalen, Marcondes Cavalcante de França Junior, Ian H Harding
Genotype-specific spinal cord damage in spinocerebellar ataxias: an ENIGMA-Ataxia study. Journal of neurology, neurosurgery, and psychiatry (2024)
Thiago Junqueira Ribeiro de Rezende, Isaac Adanyaguh, Orlando G P Barsottini, Benjamin Bender, Fernando Cendes, Léo Coutinho, Andreas Deistung, Imis Dogan, Alexandra Durr, Juan Fernandez-Ruiz, Sophia L Göricke, Marina Grisoli, Carlos R Hernandez-Castillo, Christophe Lenglet, Caterina Mariotti, Alberto Rolim Muro Martinez, Breno K Massuyama, Fanny Mochel, Lorenzo Nanetti, Anna Nigri, Sergio E Ono, Gülin Öz, José Luiz Pedroso, Kathrin Reetz, Matthis Synofzik, Helio Teive, Sophia I Thomopoulos, Paul M Thompson, Dagmar Timmann, Bart P C van de Warrenburg, Judith van Gaalen, Marcondes Cavalcante de França Junior, Ian H Harding
Genotype-specific spinal cord damage in spinocerebellar ataxias: an ENIGMA-Ataxia study. Journal of neurology, neurosurgery, and psychiatry 95 (7) (2024)
Thiago Junqueira Ribeiro de Rezende, Isaac Adanyaguh, Orlando G P Barsottini, Benjamin Bender, Fernando Cendes, Léo Coutinho, Andreas Deistung, Imis Dogan, Alexandra Durr, Juan Fernandez-Ruiz, Sophia L Göricke, Marina Grisoli, Carlos R Hernandez-Castillo, Christophe Lenglet, Caterina Mariotti, Alberto Rolim Muro Martinez, Breno K Massuyama, Fanny Mochel, Lorenzo Nanetti, Anna Nigri, Sergio E Ono, Gülin Öz, José Luiz Pedroso, Kathrin Reetz, Matthis Synofzik, Helio Teive, Sophia I Thomopoulos, Paul M Thompson, Dagmar Timmann, Bart P C van de Warrenburg, Judith van Gaalen, Marcondes Cavalcante de França Junior, Ian H Harding
Genotype-specific spinal cord damage in spinocerebellar ataxias: an ENIGMA-Ataxia study. Journal of neurology, neurosurgery, and psychiatry 95 (7) (2024)
Luca Porcu, Mario Fichera, Lorenzo Nanetti, Eliana Rulli, Paola Giunti, Michael H Parkinson, Alexandra Durr, Claire Ewenczyk, Sylvia Boesch, Wolfgang Nachbauer, Elisabetta Indelicato, Thomas Klopstock, Claudia Stendel, Francisco Javier Rodríguez de Rivera, Ludger Schöls, Zofia Fleszar, Ilaria Giordano, Claire Didszun, Anna Castaldo, Myriam Rai, Thomas Klockgether, Massimo Pandolfo, Jörg Bernhard Schulz, Kathrin Reetz, Caterina Mariotti, null null
Longitudinal changes of SARA scale in Friedreich ataxia: Strong influence of baseline score and age at onset. Annals of clinical and translational neurology (2023)
Elisabetta Indelicato, Kathrin Reetz, Sarah Maier, Wolfgang Nachbauer, Matthias Amprosi, Paola Giunti, Caterina Mariotti, Alexandra Durr, Francisco J R de Rivera Garrido, Thomas Klopstock, Ludger Schöls, Thomas Klockgether, Katrin Bürk, Massimo Pandolfo, Claire Didszun, Marcus Grobe-Einsler, Lorenzo Nanetti, Lukas Nenning, Stefan Kiechl, Wolfgang Dichtl, Hanno Ulmer, Jörg B Schulz, Sylvia Boesch, null null
Predictors of Survival in Friedreich's Ataxia: A Prospective Cohort Study. Movement disorders : official journal of the Movement Disorder Society 39 (3) (2023)
Anna Castaldo, Mariangela Farinotti, Mario Fichera, Lorenzo Nanetti, Filippo Fortuna, Caterina Mariotti, Alessandra Solari
Italian cross-cultural adaptation of the patient-reported outcome measure of ataxia. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology (2023)
Lorenzo Nanetti, Mary Kearney, Sylvia Boesch, Lucie Stovickova, Juan Darío Ortigoza-Escobar, Alfons Macaya, David Gomez-Andres, Emmanuel Roze, Maria-Judit Molnar, Nicole I Wolf, Alejandra Darling, Gessica Vasco, Enrico Bertini, Elisabetta Indelicato, David Neubauer, Tobias B Haack, Judit C Sagi, Federica R Danti, Deborah Sival, Ginevra Zanni, Anneli Kolk, Odile Boespflug-Tanguy, Ludger Schols, Bart van de Warrenburg, Marie Vidailhet, Michèl A Willemsen, Annemieke I Buizer, Enrico Orzes, Sophie Ripp, Carola Reinhard, Isabella Moroni, Caterina Mariotti, null null
Child-to-adult transition: a survey of current practices within the European Reference Network for Rare Neurological Diseases (ERN-RND). Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology (2023)
Lorenzo Nanetti, Stefania Magri, Mario Fichera, Anna Castaldo, Anna Nigri, Chiara Pinardi, Alessia Mongelli, Lidia Sarro, Davide Pareyson, Marina Grisoli, Cinzia Gellera, Daniela Di Bella, Caterina Mariotti, Franco Taroni
Complex Ataxia-Dementia Phenotype in Patients with Digenic TBP/STUB1 Spinocerebellar Ataxia. Movement disorders : official journal of the Movement Disorder Society (2023)
Elisabetta Indelicato, Kathrin Reetz, Sarah Maier, Wolfgang Nachbauer, Matthias Amprosi, Paola Giunti, Caterina Mariotti, Alexandra Durr, Francisco J R de Rivera Garrido, Thomas Klopstock, Ludger Schöls, Thomas Klockgether, Katrin Bürk, Massimo Pandolfo, Claire Didszun, Marcus Grobe-Einsler, Lorenzo Nanetti, Lukas Nenning, Stefan Kiechl, Wolfgang Dichtl, Hanno Ulmer, Jörg B Schulz, Sylvia Boesch, null null
Predictors of Survival in Friedreich's Ataxia: A Prospective Cohort Study. Movement disorders : official journal of the Movement Disorder Society (2023)
David R Lynch, Angie Goldsberry, Christian Rummey, Jennifer Farmer, Sylvia Boesch, Martin B Delatycki, Paola Giunti, J Chad Hoyle, Caterina Mariotti, Katherine D Mathews, Wolfgang Nachbauer, Susan Perlman, Sub H Subramony, George Wilmot, Theresa Zesiewicz, Lisa Weissfeld, Colin Meyer
Propensity matched comparison of omaveloxolone treatment to Friedreich ataxia natural history data. Annals of clinical and translational neurology (2023)
Elisabetta Indelicato, Kathrin Reetz, Sarah Maier, Wolfgang Nachbauer, Matthias Amprosi, Paola Giunti, Caterina Mariotti, Alexandra Durr, Francisco J R de Rivera Garrido, Thomas Klopstock, Ludger Schöls, Thomas Klockgether, Katrin Bürk, Massimo Pandolfo, Claire Didszun, Marcus Grobe-Einsler, Lorenzo Nanetti, Lukas Nenning, Stefan Kiechl, Wolfgang Dichtl, Hanno Ulmer, Jörg B Schulz, Sylvia Boesch, null null
Predictors of Survival in Friedreich's Ataxia: A Prospective Cohort Study. Movement disorders : official journal of the Movement Disorder Society 39 (3) (2023)
David R Lynch, Melanie P Chin, Sylvia Boesch, Martin B Delatycki, Paola Giunti, Angie Goldsberry, J Chad Hoyle, Caterina Mariotti, Katherine D Mathews, Wolfgang Nachbauer, Megan O'Grady, Susan Perlman, S H Subramony, George Wilmot, Theresa Zesiewicz, Colin J Meyer
Efficacy of Omaveloxolone in Friedreich's Ataxia: Delayed-Start Analysis of the MOXIe Extension. Movement disorders : official journal of the Movement Disorder Society (2022)
Simone Migliore, Giulia D'Aurizio, Sabrina Maffi, Consuelo Ceccarelli, Giovanni Ristori, Massimiliano Mirabella, Anna Castaldo, Caterina Mariotti, Giuseppe Curcio, Ferdinando Squitieri
Cognitive and behavioral associated changes in manifest Huntington disease: A retrospective cross-sectional study. Brain and behavior 11 (7) (2021)
Marta Gatti, Stefania Magri, Daniela Di Bella, Elisa Sarto, Franco Taroni, Caterina Mariotti, Lorenzo Nanetti
Spastic paraplegia type 46: novel and recurrent GBA2 gene variants in a compound heterozygous Italian patient with spastic ataxia phenotype. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 42 (11) (2021)
Anna Nigri, Lidia Sarro, Alessia Mongelli, Anna Castaldo, Luca Porcu, Chiara Pinardi, Marina Grisoli, Stefania Ferraro, Laura Canafoglia, Elisa Visani, Maria Grazia Bruzzone, Lorenzo Nanetti, Franco Taroni, Caterina Mariotti
Spinocerebellar Ataxia Type 1: One-Year Longitudinal Study to Identify Clinical and MRI Measures of Disease Progression in Patients and Presymptomatic Carriers. Cerebellum (London, England) (2021)
Alessia Mongelli, Stefania Magri, Elena Salvatore, Elena Rizzo, Anna De Rosa, Tommasina Fico, Marta Gatti, Cinzia Gellera, Franco Taroni, Caterina Mariotti, Lorenzo Nanetti
Frequency and distribution of polyQ disease intermediate-length repeat alleles in healthy Italian population. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 41 (6) (2020)
Stefania Magri, Lorenzo Nanetti, Alessia Mongelli, Elena Rizzo, Franco Taroni, Caterina Mariotti, Cinzia Gellera
Missing the pathological expansion in Huntington disease: de novo c.51C>G variant on the expanded allele causing intrafamilial allele dropout. American journal of medical genetics. Part A 185 (2) (2020)
Marta Gatti, Stefania Magri, Lorenzo Nanetti, Elisa Sarto, Daniela Di Bella, Ettore Salsano, Chiara Pantaleoni, Caterina Mariotti, Franco Taroni
From congenital microcephaly to adult onset cerebellar ataxia: Distinct and overlapping phenotypes in patients with PNKP gene mutations. American journal of medical genetics. Part A 179 (11) (2019)
Lorenzo Nanetti, Elisa Sarto, Anna Castaldo, Stefania Magri, Alessia Mongelli, Davide Rossi Sebastiano, Laura Canafoglia, Marina Grisoli, Chiara Malaguti, Francesca Rivieri, Maria Chiara D'Amico, Daniela Di Bella, Silvana Franceschetti, Caterina Mariotti, Franco Taroni
ANO10 mutational screening in recessive ataxia: genetic findings and refinement of the clinical phenotype. Journal of neurology 266 (2) (2018)

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Publication Activity (10 Years)

Top Topics

Top Venues

Caterina Mariotti