Journal of Movement Disorders

Tongue Myorhythmia as a Manifestation of IgLON 5 Disease: Abeer Goel, Sahil Mehta, Shreshtha Gupta, Dhanush Mallesh, Sidharth Chand, Vivek Lal; J Mov Disord. 2025;18(4):396-396. Published online July 18, 2025; DOI: https://doi.org/10.14802/jmd.25161

Early-Onset Cataracts as a Clinical Indicator of DJ-1-Related Parkinsonism: Sahil Mehta, Jagdeep Singh, Saurabh Mishra, Vivek Lal; J Mov Disord. 2025;18(2):193-195. Published online March 24, 2025; DOI: https://doi.org/10.14802/jmd.25016

DHDDS Mutation: A Rare Cause of Refractory Epilepsy and Hyperkinetic Movement Disorder: Sahil Mehta, Vivek Lal; J Mov Disord. 2023;16(1):107-109. Published online January 12, 2023; DOI: https://doi.org/10.14802/jmd.22154

Citations

Citations to this article as recorded by

Niemann-Pick C-like Endolysosomal Dysfunction in DHDDS Patient Cells, a Congenital Disorder of Glycosylation, Can Be Treated with Miglustat
Hannah L. Best, Sophie R. Cook, Helen Waller-Evans, Emyr Lloyd-Evans
International Journal of Molecular Sciences.2025; 26(4): 1471. CrossRef
Evaluation, Diagnosis, and Treatment of Concomitant Movement Disorders in Genetic Epilepsies
Jordan Garris, Megan Abbott, Erika Axeen, Laura Tochen, John M. Schreiber
Epilepsy Currents.2025; 25(6): 378. CrossRef
Genetic disorders of dolichol synthesis and utilization
Eline Pieters, Jaak Jaeken, Matthew P. Wilson
Molecular Genetics and Metabolism.2025; 146(1-2): 109226. CrossRef
DHDDS and NUS1: A Converging Pathway and Common Phenotype
Laura J. Williams, Sophie Waller, Jessica Qiu, Emily Innes, Noha Elserafy, Peter Procopis, Hugo Sampaio, Neil Mahant, Michel C. Tchan, Shekeeb S. Mohammad, Hugo Morales‐Briceño, Victor S.C. Fung
Movement Disorders Clinical Practice.2024; 11(1): 76. CrossRef

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