Multiple sclerosis in patients with hereditary spastic paraplegia: a case report and systematic review
Author:
Publisher
Springer Science and Business Media LLC
Subject
Psychiatry and Mental health,Neurology (clinical),Dermatology,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s10072-022-06145-1.pdf
Reference30 articles.
1. Mackay-Sim A (2021) Hereditary spastic paraplegia: from genes, cells and networks to novel pathways for drug discovery. Brain Sci 11:403
2. McGinley MP, Goldschmidt CH, Rae-Grant AD (2021) Diagnosis and treatment of multiple sclerosis: a review. JAMA 325:765
3. DeLuca GC, Ramagopalan SV, Cader MZ et al (2007) The role of hereditary spastic paraplegia related genes in multiple sclerosis: a study of disease susceptibility and clinical outcome. J Neurol 254:1221–1226
4. Criscuolo C, Carbone R, Lieto M, Peluso S, Guacci A, Filla A, Quarantelli M, Lanzillo R, Brescia Morra V, De Michele G (2016) SPG5 and multiple sclerosis: clinical and genetic overlap? Acta Neurol Scand 133:410–414
5. Jia X, Madireddy L, Caillier S et al (2018) Genome sequencing uncovers phenocopies in primary progressive multiple sclerosis. Ann Neurol 84:51–63
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