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Giulia Coarelli

Showing results (41-50 of 72) with videos related to

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Cerebellum (London, England)|April 28, 2023
Quantitative Oculomotor Assessment in Hereditary Ataxia: Systematic Review and Consensus by the Ataxia Global Initiative Working Group on Digital-motor BiomarkersPilar Garces, Chrystalina A Antoniades, Anna Sobanska, et al.
Journal of Medical Genetics|January 4, 2023
Fast and reliable detection of repeat expansions in spinocerebellar ataxia using exomesJean-Loup Méreaux, Claire-Sophie Davoine, Marie Coutelier, et al.
Neurology|December 2, 2024
Patient-Relevant Digital-Motor Outcomes for Clinical Trials in Hereditary Spastic Paraplegia Type 7: A Multicenter PROSPAX StudyLukas Beichert, Jens Seemann, Christoph Kessler, et al.
American Journal of Human Genetics|April 16, 2024
CAG repeat mosaicism is gene specific in spinocerebellar ataxiasRadhia Kacher, François-Xavier Lejeune, Isabelle David, et al.
Cerebellum (London, England)|August 13, 2025
Best Oculomotor Endpoints for Clinical Trials in Hereditary Ataxias: A Systematic Review and Consensus by the Ataxia Global Initiative Working Group on Digital‑Motor BiomarkersElena Pretegiani, Pilar Garces, Chrystalina A Antoniades, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 23, 2020
Correction: Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairmentThomas Roux, Mathieu Barbier, Mélanie Papin, et al.
Neurology|February 17, 2017
Low cancer prevalence in polyglutamine expansion diseasesGiulia Coarelli, Alhassane Diallo, Morgane Sonia Thion, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 28, 2020
Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairmentThomas Roux, Mathieu Barbier, Mélanie Papin, et al.
Cardio-Oncology (London, England)|March 27, 2024
Inflammation and acute cardiotoxicity in adult hematological patients treated with CAR-T cells: results from a pilot proof-of-concept studyMassimiliano Camilli, Marcello Viscovo, Tamara Felici, et al.
Journal of Neurology|June 16, 2026
Cerebellar cognitive-affective syndrome in Friedreich AtaxiaEmilien Petit, Sabrina Sayah, Elisabetta Indelicato, et al.
Pageof 8

Showing results (41-50 of 72) with videos related to

Sort By:
Pageof 8
Cerebellum (London, England)|April 28, 2023
Quantitative Oculomotor Assessment in Hereditary Ataxia: Systematic Review and Consensus by the Ataxia Global Initiative Working Group on Digital-motor BiomarkersPilar Garces, Chrystalina A Antoniades, Anna Sobanska, et al.
Journal of Medical Genetics|January 4, 2023
Fast and reliable detection of repeat expansions in spinocerebellar ataxia using exomesJean-Loup Méreaux, Claire-Sophie Davoine, Marie Coutelier, et al.
Neurology|December 2, 2024
Patient-Relevant Digital-Motor Outcomes for Clinical Trials in Hereditary Spastic Paraplegia Type 7: A Multicenter PROSPAX StudyLukas Beichert, Jens Seemann, Christoph Kessler, et al.
American Journal of Human Genetics|April 16, 2024
CAG repeat mosaicism is gene specific in spinocerebellar ataxiasRadhia Kacher, François-Xavier Lejeune, Isabelle David, et al.
Cerebellum (London, England)|August 13, 2025
Best Oculomotor Endpoints for Clinical Trials in Hereditary Ataxias: A Systematic Review and Consensus by the Ataxia Global Initiative Working Group on Digital‑Motor BiomarkersElena Pretegiani, Pilar Garces, Chrystalina A Antoniades, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 23, 2020
Correction: Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairmentThomas Roux, Mathieu Barbier, Mélanie Papin, et al.
Neurology|February 17, 2017
Low cancer prevalence in polyglutamine expansion diseasesGiulia Coarelli, Alhassane Diallo, Morgane Sonia Thion, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 28, 2020
Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairmentThomas Roux, Mathieu Barbier, Mélanie Papin, et al.
Cardio-Oncology (London, England)|March 27, 2024
Inflammation and acute cardiotoxicity in adult hematological patients treated with CAR-T cells: results from a pilot proof-of-concept studyMassimiliano Camilli, Marcello Viscovo, Tamara Felici, et al.
Journal of Neurology|June 16, 2026
Cerebellar cognitive-affective syndrome in Friedreich AtaxiaEmilien Petit, Sabrina Sayah, Elisabetta Indelicato, et al.
Pageof 8