Caterina Garone (C Garone)

ORCID

Publication Activity (10 Years)

Years Active: 2023-2024
Publications (10 Years): 14

Top Venues

European journal of human genetics : EJHG

Journal of translational medicine

Neurology. Genetics

Brain communications

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

Publications

Ilaria Pettenuzzo, Sara Carli, Ana Sánchez-Cuesta, Federica Isidori, Francesca Montanari, Mina Grippa, Giulia Lanzoni, Irene Ambrosetti, Veronica Di Pisa, Duccio Maria Cordelli, Maria Cristina Mondardini, Tommaso Pippucci, Luca Ragni, Giovanna Cenacchi, Roberta Costa, Mario Lima, Maria Antonietta Capristo, Concetta Valentina Tropeano, Leonardo Caporali, Valerio Carelli, Elena Brunelli, Monica Maffei, Hodman Ahmed Sheikhmaye, Anna Fetta, Gloria Brea Calvo, Caterina Garone
COQ7 defect causes prenatal onset of mitochondrial CoQ 10 deficiency with cardiomyopathy and gastrointestinal obstruction. European journal of human genetics : EJHG 32 (8) (2024)
Eleonora Manzoni, Sara Carli, Pauline Gaignard, Lea Dewi Schlieben, Michio Hirano, Dario Ronchi, Emmanuel Gonzales, Masaru Shimura, Kei Murayama, Yasushi Okazaki, Ivo Barić, Danijela Petkovic Ramadza, Daniela Karall, Johannes Mayr, Diego Martinelli, Chiara La Morgia, Guido Primiano, René Santer, Serenella Servidei, Céline Bris, Aline Cano, Francesca Furlan, Serena Gasperini, Nolwenn Laborde, Costanza Lamperti, Dominic Lenz, Michelangelo Mancuso, Vincenzo Montano, Francesca Menni, Olimpia Musumeci, Victoria Nesbitt, Elena Procopio, Cécile Rouzier, Christian Staufner, Jan-Willem Taanman, Galit Tal, Chiara Ticci, Duccio Maria Cordelli, Valerio Carelli, Vincent Procaccio, Holger Prokisch, Caterina Garone
Deoxyguanosine kinase deficiency: natural history and liver transplant outcome. Brain communications 6 (3) (2024)
Ilaria Pettenuzzo, Sara Carli, Ana Sánchez-Cuesta, Federica Isidori, Francesca Montanari, Mina Grippa, Giulia Lanzoni, Irene Ambrosetti, Veronica Di Pisa, Duccio Maria Cordelli, Maria Cristina Mondardini, Tommaso Pippucci, Luca Ragni, Giovanna Cenacchi, Roberta Costa, Mario Lima, Maria Antonietta Capristo, Concetta Valentina Tropeano, Leonardo Caporali, Valerio Carelli, Elena Brunelli, Monica Maffei, Hodman Ahmed Sheikhmaye, Anna Fetta, Gloria Brea Calvo, Caterina Garone
COQ7 defect causes prenatal onset of mitochondrial CoQ 10 deficiency with cardiomyopathy and gastrointestinal obstruction. European journal of human genetics : EJHG 32 (8) (2024)
Ilaria Pettenuzzo, Sara Carli, Ana Sánchez-Cuesta, Federica Isidori, Francesca Montanari, Mina Grippa, Giulia Lanzoni, Irene Ambrosetti, Veronica Di Pisa, Duccio Maria Cordelli, Maria Cristina Mondardini, Tommaso Pippucci, Luca Ragni, Giovanna Cenacchi, Roberta Costa, Mario Lima, Maria Antonietta Capristo, Concetta Valentina Tropeano, Leonardo Caporali, Valerio Carelli, Elena Brunelli, Monica Maffei, Hodman Ahmed Sheikhmaye, Anna Fetta, Gloria Brea Calvo, Caterina Garone
COQ7 defect causes prenatal onset of mitochondrial CoQ 10 deficiency with cardiomyopathy and gastrointestinal obstruction. European journal of human genetics : EJHG (2024)
Ilaria Pettenuzzo, Sara Carli, Ana Sánchez-Cuesta, Federica Isidori, Francesca Montanari, Mina Grippa, Giulia Lanzoni, Irene Ambrosetti, Veronica Di Pisa, Duccio Maria Cordelli, Maria Cristina Mondardini, Tommaso Pippucci, Luca Ragni, Giovanna Cenacchi, Roberta Costa, Mario Lima, Maria Antonietta Capristo, Concetta Valentina Tropeano, Leonardo Caporali, Valerio Carelli, Elena Brunelli, Monica Maffei, Hodman Ahmed Sheikhmaye, Anna Fetta, Gloria Brea Calvo, Caterina Garone
COQ7 defect causes prenatal onset of mitochondrial CoQ 10 deficiency with cardiomyopathy and gastrointestinal obstruction. European journal of human genetics : EJHG 32 (8) (2024)
Caterina Garone, F De Giorgio, S Carli
Mitochondrial metabolism in neural stem cells and implications for neurodevelopmental and neurodegenerative diseases. Journal of translational medicine 22 (1) (2024)
Ilaria Pettenuzzo, Sara Carli, Ana Sánchez-Cuesta, Federica Isidori, Francesca Montanari, Mina Grippa, Giulia Lanzoni, Irene Ambrosetti, Veronica Di Pisa, Duccio Maria Cordelli, Maria Cristina Mondardini, Tommaso Pippucci, Luca Ragni, Giovanna Cenacchi, Roberta Costa, Mario Lima, Maria Antonietta Capristo, Concetta Valentina Tropeano, Leonardo Caporali, Valerio Carelli, Elena Brunelli, Monica Maffei, Hodman Ahmed Sheikhmaye, Anna Fetta, Gloria Brea Calvo, Caterina Garone
COQ7 defect causes prenatal onset of mitochondrial CoQ 10 deficiency with cardiomyopathy and gastrointestinal obstruction. European journal of human genetics : EJHG 32 (8) (2024)
Caterina Garone, F De Giorgio, S Carli
Mitochondrial metabolism in neural stem cells and implications for neurodevelopmental and neurodegenerative diseases. Journal of translational medicine 22 (1) (2024)
Caterina Garone, F De Giorgio, S Carli
Mitochondrial metabolism in neural stem cells and implications for neurodevelopmental and neurodegenerative diseases. Journal of translational medicine 22 (1) (2024)
Caterina Garone, F De Giorgio, S Carli
Mitochondrial metabolism in neural stem cells and implications for neurodevelopmental and neurodegenerative diseases. Journal of translational medicine 22 (1) (2024)
Eleonora Manzoni, Sara Carli, Pauline Gaignard, Lea Dewi Schlieben, Michio Hirano, Dario Ronchi, Emmanuel Gonzales, Masaru Shimura, Kei Murayama, Yasushi Okazaki, Ivo Barić, Danijela Petkovic Ramadza, Daniela Karall, Johannes Mayr, Diego Martinelli, Chiara La Morgia, Guido Primiano, René Santer, Serenella Servidei, Céline Bris, Aline Cano, Francesca Furlan, Serena Gasperini, Nolwenn Laborde, Costanza Lamperti, Dominic Lenz, Michelangelo Mancuso, Vincenzo Montano, Francesca Menni, Olimpia Musumeci, Victoria Nesbitt, Elena Procopio, Cécile Rouzier, Christian Staufner, Jan-Willem Taanman, Galit Tal, Chiara Ticci, Duccio Maria Cordelli, Valerio Carelli, Vincent Procaccio, Holger Prokisch, Caterina Garone
Deoxyguanosine kinase deficiency: natural history and liver transplant outcome. Brain communications 6 (3) (2024)
Caterina Garone
Mitochondrial Cytochrome C deficiency can show the first disease signs in the prenatal stage. European journal of human genetics : EJHG (2023)
Andrea Pietra, Flavia Palombo, Melania Giannotta, Monica Maffei, Claudio Fiorini, Roberta Costa, Giovanna Cenacchi, Valerio Carelli, Duccio Maria Cordelli, Antonella Pini, Caterina Garone
Expanding the Clinical Spectrum of UBTF -Related Neurodevelopmental Disorder. Neurology. Genetics 9 (6) (2023)
Andrea Pietra, Flavia Palombo, Melania Giannotta, Monica Maffei, Claudio Fiorini, Roberta Costa, Giovanna Cenacchi, Valerio Carelli, Duccio Maria Cordelli, Antonella Pini, Caterina Garone
Expanding the Clinical Spectrum of UBTF -Related Neurodevelopmental Disorder. Neurology. Genetics 9 (6) (2023)

Caterina Garone.css-eqlu8i{font-size:small;padding-left:4px;} (C Garone)

Publication Activity (10 Years)

Top Topics

Top Venues

Caterina Garone (C Garone)