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48 IlicS.DrmicD.FranjicS.KolencD.CoricM.BrcicL.et al (2011a)
Food and Drug Administration (FDA) and the European Medicines Agency (EMA) will determine when these treatments can be prescribed to patients
Sotgia F, Martinez-Outschoorn UE, Lisanti MP
Diabetes (1998) 47:7649
Sejal Saheta, a customised treatment plan was initiated
The decision should involve individualized risk-benefit assessment considering the specific autoimmune diagnosis, disease activity, and concurrent medications, with coordination between the prescribing clinician and the specialist managing the autoimmune condition
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