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Patients are encouraged to discuss any previous vitamin deficiencies, sensitivities, allergies, or recent health concerns prior to treatment
The first part of the study began by randomly dividing the test subjects in four groups including: wild type, APP/PS1, APP/PS1 + Dihexa administered at a dose of 1.44 mg/kg, and APP/PS1 + Dihexa administered at a dose of 2.88 mg/kg [1]
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