Serena Galosi

ORCID

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 12

Top Venues

Movement disorders : official journal of the Movement Disorder Society

Movement disorders clinical practice

American journal of medical genetics. Part A

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

Publications

Luca Pollini, Carlo Greco, Maria Novelli, Davide Mei, Francesco Pisani, Marina A J De Koning-Tijssen, Renzo Guerrini, Vincenzo Leuzzi, Serena Galosi
Neurophysiological Analysis of Cortical Myoclonic Tremor and Excessive Startle in ARHGEF9 Deficiency. Movement disorders clinical practice 11 (4) (2024)
Luca Pollini, Carlo Greco, Maria Novelli, Davide Mei, Francesco Pisani, Marina A J De Koning-Tijssen, Renzo Guerrini, Vincenzo Leuzzi, Serena Galosi
Neurophysiological Analysis of Cortical Myoclonic Tremor and Excessive Startle in ARHGEF9 Deficiency. Movement disorders clinical practice (2024)
Serena Galosi, Cecilia Mancini, Anna Commone, Paolo Calligari, Viviana Caputo, Francesca Nardecchia, Claudia Carducci, Lambertus P van den Heuvel, Simone Pizzi, Alessandro Bruselles, Marcello Niceta, Simone Martinelli, Richard J Rodenburg, Marco Tartaglia, Vincenzo Leuzzi
Biallelic Variants of MRPS36 Cause a New Form of Leigh Syndrome. Movement disorders : official journal of the Movement Disorder Society (2024)
Serena Galosi, Cecilia Mancini, Anna Commone, Paolo Calligari, Viviana Caputo, Francesca Nardecchia, Claudia Carducci, Lambertus P van den Heuvel, Simone Pizzi, Alessandro Bruselles, Marcello Niceta, Simone Martinelli, Richard J Rodenburg, Marco Tartaglia, Vincenzo Leuzzi
Biallelic Variants of MRPS36 Cause a New Form of Leigh Syndrome. Movement disorders : official journal of the Movement Disorder Society 39 (7) (2024)
Serena Galosi, Cecilia Mancini, Anna Commone, Paolo Calligari, Viviana Caputo, Francesca Nardecchia, Claudia Carducci, Lambertus P van den Heuvel, Simone Pizzi, Alessandro Bruselles, Marcello Niceta, Simone Martinelli, Richard J Rodenburg, Marco Tartaglia, Vincenzo Leuzzi
Biallelic Variants of MRPS36 Cause a New Form of Leigh Syndrome. Movement disorders : official journal of the Movement Disorder Society 39 (7) (2024)
Luca Pollini, Carlo Greco, Maria Novelli, Davide Mei, Francesco Pisani, Marina A J De Koning-Tijssen, Renzo Guerrini, Vincenzo Leuzzi, Serena Galosi
Neurophysiological Analysis of Cortical Myoclonic Tremor and Excessive Startle in ARHGEF9 Deficiency. Movement disorders clinical practice 11 (4) (2024)
Luca Pollini, Carlo Greco, Maria Novelli, Davide Mei, Francesco Pisani, Marina A J De Koning-Tijssen, Renzo Guerrini, Vincenzo Leuzzi, Serena Galosi
Neurophysiological Analysis of Cortical Myoclonic Tremor and Excessive Startle in ARHGEF9 Deficiency. Movement disorders clinical practice 11 (4) (2024)
Maria Novelli, Manuela Tolve, Vicente Quiroz, Claudia Carducci, Rossella Bove, Giacomina Ricciardi, Kathryn Yang, Filippo Manti, Francesco Pisani, Darius Ebrahimi-Fakhari, Serena Galosi, Vincenzo Leuzzi
Autosomal Recessive Guanosine Triphosphate Cyclohydrolase I Deficiency: Redefining the Phenotypic Spectrum and Outcomes. Movement disorders clinical practice (2024)
Serena Galosi, Cecilia Mancini, Anna Commone, Paolo Calligari, Viviana Caputo, Francesca Nardecchia, Claudia Carducci, Lambertus P van den Heuvel, Simone Pizzi, Alessandro Bruselles, Marcello Niceta, Simone Martinelli, Richard J Rodenburg, Marco Tartaglia, Vincenzo Leuzzi
Biallelic Variants of MRPS36 Cause a New Form of Leigh Syndrome. Movement disorders : official journal of the Movement Disorder Society 39 (7) (2024)
Blas Couto, Serena Galosi, Dora Steel, Manju A Kurian, Jennifer Friedman, Carolina Gorodetsky, Anthony E Lang
Severe Acute Motor Exacerbations (SAME) across Metabolic, Developmental and Genetic Disorders. Movement disorders : official journal of the Movement Disorder Society (2024)
Serena Galosi, Maria Novelli, Martina Di Rocco, Elisabetta Flex, Elena Messina, Luca Pollini, Elena Parrini, Francesco Pisani, Renzo Guerrini, Vincenzo Leuzzi, Simone Martinelli
GNAO1 Haploinsufficiency: The Milder End of the GNAO1 Phenotypic Spectrum. Movement disorders : official journal of the Movement Disorder Society (2023)
Beatrice De Maria, Simona Balestrini, Davide Mei, Federico Melani, Simona Pellacani, Tiziana Pisano, Anna Rosati, Giusi M Scaturro, Lucio Giordano, Gaetano Cantalupo, Elena Fontana, Cristina Zammarchi, Edith Said, Vincenzo Leuzzi, Mario Mastrangelo, Serena Galosi, Elena Parrini, Renzo Guerrini
Expanding the genetic and phenotypic spectrum of CHD2-related disease: From early neurodevelopmental disorders to adult-onset epilepsy. American journal of medical genetics. Part A (2021)

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Publication Activity (10 Years)

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Serena Galosi