Results 101 to 110 of about 5,463 (156)

Lingual Dyskinesia as the Presenting Feature of Acquired Demyelinating Syndrome: A Case Report and Review of Differential Diagnoses

Journal of Paediatrics and Child Health, Volume 62, Issue 6, Page 1060-1065, June 2026.
Briana Davis, Ahmed Kaki, Eppie M. Yiu, Emma Macdonald‐Laurs   +3 more
wiley   +1 more source

Engineering of CD63 Enables Selective Extracellular Vesicle Cargo Loading and Enhanced Payload Delivery

Journal of Extracellular Vesicles
Extracellular vesicles (EVs) are mediators of intercellular communication through the transfer of nucleic acids, lipids and proteins between cells. This property makes bioengineered EVs promising therapeutic vectors.
Wataru Obuchi, Ayrton Zargani‐Piccardi, Kevin Leandro, David Rufino‐Ramos, Emilio Di Ianni, Dawn Madison Frederick, Katia Maalouf, Lisa Nieland, Tianhe Xiao, Pierre Repiton, Christine A. Vaine, Benjamin P. Kleinstiver, D. Cristopher Bragg, Hakho Lee, Miles A. Miller, Xandra O. Breakefield, Koen Breyne   +16 more
doaj   +1 more source

Factors influencing reduced penetrance and variable expressivity in X-linked dystonia-parkinsonism. [PDF]

Med Genet, 2022
Pozojevic J, von Holt BH, Westenberger A.   +2 more
europepmc   +1 more source

X-linked dystonia-parkinsonism: over and above a repeat disorder. [PDF]

Med Genet, 2021
Pozojevic J, Cruz JN, Westenberger A.
europepmc   +1 more source

Repeat-Associated Non-AUG Translation of AGAGGG Repeats that Cause X-Linked Dystonia-Parkinsonism. [PDF]

Mov Disord, 2022
Reyes CJ, Asano K, Todd PK, Klein C, Rakovic A.   +4 more
europepmc   +1 more source

The role of epigenetic factors in the pathogenesis of familial X-linked mental retardation (XLMR)

, 2010
Mental retardation (MR) is a handicap with severe implications not only for thosethat suffer from this disability, but also for their families, society and the welfaresystems which support them.
Carvill, Gemma
core  

Table_1_Translation, Cultural Adaptation, and Validation of the Hiligaynon Montreal Cognitive Assessment Tool (MoCA-Hil) Among Patients With X-Linked Dystonia Parkinsonism (XDP).docx

, 2019
Background: X-linked dystonia parkinsonism (XDP) is a neurodegenerative disease endemic to Filipinos with maternal lineage from Panay Island, Philippines. Patients present with dystonia concurrent with or followed by parkinsonism. Non-motor symptoms also
Nicole B. Aliling (8055059), Roland Dominic G. Jamora (8055065), Adovich S. Rivera (8055062)   +2 more
core   +1 more source

Dissection of TAF1 neuronal splicing and implications for neurodegeneration in X-linked dystonia-parkinsonism. [PDF]

Brain Commun, 2021
Capponi S, Stöffler N, Penney EB, Grütz K, Nizamuddin S, Vermunt MW, Castelijns B, Fernandez-Cerado C, Legarda GP, Velasco-Andrada MS, Muñoz EL, Ang MA, Diesta CCE, Creyghton MP, Klein C, Bragg DC, De Rijk P, Timmers HTM.   +17 more
europepmc   +1 more source

Biopsychosocial Aspect of Patients With X-Linked Dystonia-Parkinsonism: Its Implications on Quality of Life. [PDF]

Cureus, 2022
Alcachupas A, Bellosillo K, Catolico WR, Davis MC, Diaz A, Doyongan YK, Eduarte R, Gersava E, Intrepido MB, Laluma MGK, Lavalle CC, Millan JJ.   +11 more
europepmc   +1 more source

Patterns and biomarkers of X-linked dystonia parkinsonism disease progression

2024X-linked dystonia parkinsonism is a neurodegenerative movement disorder that originate from the island of Panay, Philippines. Though this is a relatively novel disease, efforts have been directed towards solving the etiology, which currently points ...
Joy, Keziah
core