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Br J Urol 1992;70:648-51

Studies that met the following inclusion criteria were selected: 1) A study population consisting of NAFLD or NASH patients diagnosed with biopsy or other imaging methods, 2) adult participants, 3) GLP-1RA or TZD treatment as intervention group, 4) active or placebo control group, 5) at least 3 months of treatment duration, 6) liver biopsy-based, noninvasive technique-based, biological parameters, or anthropometric parameters as outcomes

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