Notably, for APLAs and anti‐TPO, the immune etiological group even demonstrated seemingly lower positivity rates compared with the other groups, although these differences did not reach statistical significance (0% vs. 19.3% vs. 28.1%, p = 0.21; and 0% vs. 11.0% vs. 8.8%, p = 0.88, respectively).
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Defining the role of systemic autoimmune markers in adult epilepsy: A focus on autoimmune-associated epilepsy.
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