LMNB1-Related Adult-Onset Autosomal Dominant Leukodystrophy Presenting as Movement Disorder: A Case Report and Review of the Literature
Author:
Publisher
Frontiers Media SA
Subject
General Neuroscience
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1. Démarche diagnostique devant une leucodystrophie métabolique de l’adulte;Pratique Neurologique - FMC;2024-03
2. LMNB1‐duplication mediated nuclear architecture alteration and demyelination of cerebral white matter in a patient with ADLD;Neuropathology and Applied Neurobiology;2024-01-24
3. Adult-Onset Genetic Leukoencephalopathies With Movement Disorders;Journal of Movement Disorders;2023-05-31
4. Nomenclature of Genetic Movement Disorders: Recommendations of the International Parkinson and Movement Disorder Society Task Force – An Update;Movement Disorders;2022-04-28
5. Adult-onset autosomal dominant leukodystrophy and neuronal intranuclear inclusion disease: lessons from two new Chinese families;Neurological Sciences;2022-04-14
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