ReviewAnnals of medicine and surgery (2012)2025
Guillain-Barré syndrome and albuminocytological dissociation: a narrative review.
Review in Annals of medicine and surgery (2012), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
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
1 citing paper in PubMed.
- Miller Fisher Syndrome Should Only be Diagnosed if the Diagnostic Criteria are Met and All Other Differential Diagnoses Have Been Ruled Out.Journal of the American College of Emergency Physicians open · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
9 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Guillain-Barré syndrome (GBS) is an aggressively advancing rapidly autoimmune disorder often triggered by a recent infection that attacks the peripheral nerves, ultimately leading to diminished reflexes, sensory abnormalities, and muscle weakness. Albuminocytological dissociation (ACD), defined as a cerebrospinal fluid (CSF) evaluation depicting normal white blood cell counts, but high protein levels are considered as a pathognomonic feature in the diagnosis of GBS. While ACD has been well-reported in the available literature, its exact cause and etiology remain uncertain; however, some hypothesis suggests inflammation, disrupted nerve barrier function, and altered CSF flow contributes to the pathogenesis of ACD. In this narrative review, we aim to assess its diagnostic value, a viable source in predicting disease severity and evaluate the pathophysiological association between ACD and GBS. We also highlight recent advancements in CSF biomarker research and proteomics that could refine and further improve the diagnosis and treatment of GBS. By consolidating existing knowledge, this review seeks to improve clinical awareness of ACD, guide future investigations, and contribute to better patient management strategies.
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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 Socratic graph.