Clinicopathological Phenotype and Genetics of X-Linked Dystonia–Parkinsonism (XDP; DYT3; Lubag) [PDF]
Brain Sciences, 2017 X-linked dystonia–parkinsonism (XDP; OMIM314250), also referred to as DYT3 dystonia or “Lubag” disease, was first described as an endemic disease in the Philippine island of Panay.
Toshitaka Kawarai +3 more
doaj +3 more sources
Lightweight Implementation of Per-packet Service Protection in eBPF/XDP [PDF]
CoRR, 2023 Deterministic communication means reliable packet forwarding with close to zero packet loss and bounded latency. Packet loss or delay above a threshold caused by, e.g., equipment failure or malfunction could be catastrophic for applications that require deterministic communication.
Ferenc Fejes +3 more
core +4 more sources
npj Parkinson's Disease, 2017 Disease rating scale: Adressing a Philippine problem Researchers validate a tool to assess patients with X-linked dystonia parkinsonism (XDP), a movement disorder that affects men of Filipino descent.
Paul Matthew D. Pasco +8 more
doaj +2 more sources
eHDL: Turning eBPF/XDP Programs into Hardware Designs for the NIC
Proceedings of the 28th ACM International Conference on Architectural Support for Programming Languages and Operating Systems, Volume 3, 2023 Scaling network packet processing performance to meet the in- creasing speed of network ports requires software programs to carefully leverage the network devices’ hardware features. This is a complex task for network programmers, who need to learn and deal with the heterogeneity of device architectures, and re-think their software to leverage them. In
Rivitti A. +4 more
openaire +4 more sources
Striatal hyperechogenicity as an ultrasound imaging marker for prodromal X-linked dystonia-parkinsonism. [PDF]
NPJ Parkinsons DisX-linked dystonia-parkinsonism (XDP) is a neurodegenerative genetic disorder with striatal pathology. We investigated 138 participants (61 patients with XDP, 19 non-manifesting carriers (NMC), and 58 healthy controls (HC)) with transcranial sonography ...
Pauly MG +11 more
europepmc +2 more sources
Correction of the molecular phenotype of X-linked Dystonia-Parkinsonism reveals a non-canonical function of BRD4. [PDF]
Nat CommunTranscription and mRNA processing are tightly coupled regulatory layers on gene expression, and their perturbations underly human disorders. X-linked Dystonia-Parkinsonism (XDP) is a unique example of a human disease connecting aberrant mRNA processing ...
Capponi S +9 more
europepmc +2 more sources
Impact of X-linked dystonia-parkinsonism on caregiver strain, anxiety and depression. [PDF]
BMJ Neurol OpenBackground X-linked dystonia-parkinsonism (XDP) is a progressive movement disorder that predominantly affects men from the Panay Islands in the Philippines.
Cataniag P, Ong JN, Diesta CC.
europepmc +2 more sources
Alterations in energy production in a <i>Drosophila</i> model for the X-linked dystonia-parkinsonism-related Taf1 deficiency. [PDF]
Front Aging NeurosciBackgroundX-linked dystonia-parkinsonism (XDP), an adult-onset neurodegenerative disorder, is caused by an SVA insertion in the TAF1 gene, containing a hexanucleotide, the length of which is correlated to the severity of the disease.
Mandik F +4 more
europepmc +2 more sources
Neuroimaging and neuropathology studies of X-linked dystonia parkinsonism
Neurobiology of Disease, 2021 X-linked Dystonia Parkinsonism (XDP) is a recessive, genetically inherited neurodegenerative disorder endemic to Panay Island in the Philippines. Clinical symptoms include the initial appearance of dystonia, followed by parkinsonian traits after 10–15 ...
Christine J. Arasaratnam +3 more
doaj +1 more source
The Clinical, Genetic, Psychosocial, and Care Landscape of X-Linked Dystonia-Parkinsonism in Filipino Men: A Scoping Review. [PDF]
Am J Mens HealthBackground X-linked dystonia-parkinsonism (XDP) is a hereditary movement disorder predominantly affecting Filipino males from Panay Island ancestry.
Ramos MD +5 more
europepmc +2 more sources