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Movement Disorders : Official Journal of the Movement Disorder Society
|
February 11, 2014
Myoclonus in mitochondrial disorders
Michelangelo Mancuso, Daniele Orsucci, Corrado Angelini, et al.
European Journal of Neurology
|
April 18, 2026
Diagnostic Criteria and Management of MELAS and Stroke-Like Episodes: Consensus-Based Statements
Michelangelo Mancuso, Marcello Bellusci, Valerio Carelli, et al.
Scientific Reports
|
February 5, 2025
Multicentre case-control study on the association between COVID-19 vaccines and neurological disorders (COVIVAX)
Elisabetta Pupillo, Elisa Bianchi, Ettore Beghi, et al.
Neurology
|
July 1, 2018
Biallelic <i>SQSTM1</i> mutations in early-onset, variably progressive neurodegeneration
Valentina Muto, Elisabetta Flex, Zachary Kupchinsky, et al.
Journal of Clinical Medicine
|
June 2, 2021
Movement Disorders in Children with a Mitochondrial Disease: A Cross-Sectional Survey from the Nationwide Italian Collaborative Network of Mitochondrial Diseases
Chiara Ticci, Daniele Orsucci, Anna Ardissone, et al.
Journal of Neurology
|
September 6, 2021
Monoallelic KIF1A-related disorders: a multicenter cross sectional study and systematic literature review
Stefania Della Vecchia, Alessandra Tessa, Claudia Dosi, et al.
Brain Communications
|
May 17, 2024
Deoxyguanosine kinase deficiency: natural history and liver transplant outcome
Eleonora Manzoni, Sara Carli, Pauline Gaignard, et al.
Frontiers in Neurology
|
June 24, 2020
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients
Carla Piano, Enrico Di Stasio, Guido Primiano, et al.
Clinical Epigenetics
|
October 23, 2024
Integrating D4Z4 methylation analysis into clinical practice: improvement of FSHD molecular diagnosis through distinct thresholds for 4qA/4qA and 4qA/4qB patients
Claudia Strafella, Domenica Megalizzi, Giulia Trastulli, et al.
Neurology
|
August 5, 2024
Clinical, Histopathologic, and Genetic Features of Patients With Myofibrillary and Distal Myopathies: Experience From the Italian Network
Sara Bortolani, Marco Savarese, Gaetano Vattemi, et al.
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of 9
Search research articles
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Showing results (71-80 of 84) with videos related to
Sort By:
Page
of 9
Movement Disorders : Official Journal of the Movement Disorder Society
|
February 11, 2014
Myoclonus in mitochondrial disorders
Michelangelo Mancuso, Daniele Orsucci, Corrado Angelini, et al.
European Journal of Neurology
|
April 18, 2026
Diagnostic Criteria and Management of MELAS and Stroke-Like Episodes: Consensus-Based Statements
Michelangelo Mancuso, Marcello Bellusci, Valerio Carelli, et al.
Scientific Reports
|
February 5, 2025
Multicentre case-control study on the association between COVID-19 vaccines and neurological disorders (COVIVAX)
Elisabetta Pupillo, Elisa Bianchi, Ettore Beghi, et al.
Neurology
|
July 1, 2018
Biallelic <i>SQSTM1</i> mutations in early-onset, variably progressive neurodegeneration
Valentina Muto, Elisabetta Flex, Zachary Kupchinsky, et al.
Journal of Clinical Medicine
|
June 2, 2021
Movement Disorders in Children with a Mitochondrial Disease: A Cross-Sectional Survey from the Nationwide Italian Collaborative Network of Mitochondrial Diseases
Chiara Ticci, Daniele Orsucci, Anna Ardissone, et al.
Journal of Neurology
|
September 6, 2021
Monoallelic KIF1A-related disorders: a multicenter cross sectional study and systematic literature review
Stefania Della Vecchia, Alessandra Tessa, Claudia Dosi, et al.
Brain Communications
|
May 17, 2024
Deoxyguanosine kinase deficiency: natural history and liver transplant outcome
Eleonora Manzoni, Sara Carli, Pauline Gaignard, et al.
Frontiers in Neurology
|
June 24, 2020
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients
Carla Piano, Enrico Di Stasio, Guido Primiano, et al.
Clinical Epigenetics
|
October 23, 2024
Integrating D4Z4 methylation analysis into clinical practice: improvement of FSHD molecular diagnosis through distinct thresholds for 4qA/4qA and 4qA/4qB patients
Claudia Strafella, Domenica Megalizzi, Giulia Trastulli, et al.
Neurology
|
August 5, 2024
Clinical, Histopathologic, and Genetic Features of Patients With Myofibrillary and Distal Myopathies: Experience From the Italian Network
Sara Bortolani, Marco Savarese, Gaetano Vattemi, et al.
Page
of 9