ReviewCerebellum (London, England)2025
Multifaceted Mesodiencephalic Triangles: Insights into Hypertrophic Olivary Degeneration and Oculopalatal Tremor Pathophysiology.
Review in Cerebellum (London, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
2 citing papers in PubMed.
- Hypertrophic Olivary Degeneration Following Brainstem Hemorrhage in a Patient with Tremor: A Case Report with Serial MRI Follow-Up.Journal of clinical medicine · 2026Article
- Tremor pathophysiology.Clinical parkinsonism & related disorders · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
Abstract
Oculopalatal tremor is a rare neurological disorder characterized by rhythmic oscillations of ocular and palatal muscles. This phenomenon is commonly associated with hypertrophic degeneration of the inferior olive due to loss of GABAergic cerebello-olivary fibers. Oculopalatal tremor highlights the complex interplay between cerebellar, mesodiencephalic, and olivary networks. The principal, medial accessory, and dorsal accessory subnuclei of the inferior olive exhibit rhythmic subthreshold oscillations that are hypothesized to play an important role in oculopalatal tremor. However, delayed tremor onset and variability in hypertrophic olivary degeneration challenge the hypothesis of olivary oscillation as the principal cause of tremorogenesis. A plausible alternative hypothesis is that tremorogenic oscillation emerges from maladaptive cerebellar network plasticity in response to the loss of physiologic climbing fiber activity. The anatomy and physiology of the fastigiobulbar connections are compatible with the clinical characteristics of oculopalatal tremor syndrome, and clinicopathological correlations suggest that the fastigiobulbar pathway is necessary for oculopalatal tremor. Latent brainstem oscillators, released by cerebellar dysfunction, have been proposed but do not explain the anatomical distribution of oscillation. Advanced imaging and computational models have provided insights into possible mechanisms of oscillation but underscore the need for further studies, particularly in a suitable animal model, which does not exist.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.