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Margin status did not change the natural course of disease.
The administration of an anti-mouse IL-17A mAb did not alter the course of disease.
No significant correlation between the course of disease and electrophysiologic parameters was seen.
The possible modifications in pain characteristics during the course of disease, including paroxysms duration and intensity, were also examined.
During the course of disease, paroxysms worsened in intensity in 3% of patients, and paroxysms duration increased in 2%.
We also analyzed the possible change in pain characteristics during the course of disease, including paroxysms duration and intensity.
To explore which brain regions might relate to the course of disease, a correlation analysis was performed.
Results have improved, especially for patients transplanted earlier in the course of disease.
Autoreactive T cells may contribute to lung injury late in the course of disease.
The course of disease ranged from relatively slow progression to aggressive disease.
Extent of organ tropism and severity of lesions corroborate with the course of disease.
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CEO of Professional Science Editing for Scientists @ prosciediting.com