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Molecular Genetics and Metabolism
|
February 22, 2023
Type I Alexander disease: Update and validation of the clinical evolution-based classification
Ylenia Vaia, Eleonora Mura, Davide Tonduti
Neuropsychiatric Disease and Treatment
|
October 26, 2023
Establishing Patient-Centered Outcomes for MCT8 Deficiency: Stakeholder Engagement and Systematic Literature Review
Nina-Maria Wilpert, Davide Tonduti, Ylenia Vaia, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience
|
April 1, 2026
Early-Onset Hyperkinetic Movement Disorders Define the Most Severe Presentation of the ATP8A2-Related Phenotypic Spectrum
Fabio Bruschi, Clara E Antonello, Cecilia Parazzini, et al.
Journal of Pediatric Psychology
|
August 25, 2025
The impact of leukodystrophies on parents' lives
Laura Zampini, Laura Cordolcini, Lara Draghi, et al.
Multiple Sclerosis and Related Disorders
|
June 1, 2020
Unraveling diagnostic uncertainty in transition phase from relapsing-remitting to secondary progressive multiple sclerosis
Antonio Carotenuto, Elisabetta Signoriello, Roberta Lanzillo, et al.
Frontiers in Nutrition
|
July 29, 2024
Microbiota gut-brain axis: implications for pediatric-onset leukodystrophies
Ylenia Vaia, Fabio Bruschi, Veronica Maria Tagi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
June 8, 2026
Intracranial calcifications in DEGS1-Related Leukodystrophy: a potentially under-recognised neuroimaging feature
Ylenia Vaia, Neena Kim, Sharmila Jeyasingh, et al.
Journal of Child Neurology
|
May 22, 2025
Experiences and Hope in Caregivers of Children With Aicardi Goutières Syndrome
Francesco Gavazzi, Ashley Martin, Anjana Sevagamoorthy, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience
|
May 8, 2026
Complicated Spastic Paraparesis: Study of a Patient With a De Novo Pathogenic Variant in ELOVL1
Ylenia Vaia, Eleonora Mura, Fabio Bruschi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 27, 2025
Altered Dopamine Metabolism and Response to Treatment with Levodopa/Carbidopa in MCT8 Deficiency
Fabio Bruschi, Ylenia Vaia, Clara E Antonello, et al.
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Search research articles
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Showing results (1-10 of 21) with videos related to
Sort By:
Page
of 3
Molecular Genetics and Metabolism
|
February 22, 2023
Type I Alexander disease: Update and validation of the clinical evolution-based classification
Ylenia Vaia, Eleonora Mura, Davide Tonduti
Neuropsychiatric Disease and Treatment
|
October 26, 2023
Establishing Patient-Centered Outcomes for MCT8 Deficiency: Stakeholder Engagement and Systematic Literature Review
Nina-Maria Wilpert, Davide Tonduti, Ylenia Vaia, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience
|
April 1, 2026
Early-Onset Hyperkinetic Movement Disorders Define the Most Severe Presentation of the ATP8A2-Related Phenotypic Spectrum
Fabio Bruschi, Clara E Antonello, Cecilia Parazzini, et al.
Journal of Pediatric Psychology
|
August 25, 2025
The impact of leukodystrophies on parents' lives
Laura Zampini, Laura Cordolcini, Lara Draghi, et al.
Multiple Sclerosis and Related Disorders
|
June 1, 2020
Unraveling diagnostic uncertainty in transition phase from relapsing-remitting to secondary progressive multiple sclerosis
Antonio Carotenuto, Elisabetta Signoriello, Roberta Lanzillo, et al.
Frontiers in Nutrition
|
July 29, 2024
Microbiota gut-brain axis: implications for pediatric-onset leukodystrophies
Ylenia Vaia, Fabio Bruschi, Veronica Maria Tagi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
June 8, 2026
Intracranial calcifications in DEGS1-Related Leukodystrophy: a potentially under-recognised neuroimaging feature
Ylenia Vaia, Neena Kim, Sharmila Jeyasingh, et al.
Journal of Child Neurology
|
May 22, 2025
Experiences and Hope in Caregivers of Children With Aicardi Goutières Syndrome
Francesco Gavazzi, Ashley Martin, Anjana Sevagamoorthy, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience
|
May 8, 2026
Complicated Spastic Paraparesis: Study of a Patient With a De Novo Pathogenic Variant in ELOVL1
Ylenia Vaia, Eleonora Mura, Fabio Bruschi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 27, 2025
Altered Dopamine Metabolism and Response to Treatment with Levodopa/Carbidopa in MCT8 Deficiency
Fabio Bruschi, Ylenia Vaia, Clara E Antonello, et al.
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of 3