Quantifying the impact of symptomatic acute hepatic porphyria on well‐being via patient‐reported outcomes: Results from the Porphyria Worldwide Patient Experience Research (POWER) study

MLA

Amy Dickey, et al. “Quantifying the Impact of Symptomatic Acute Hepatic Porphyria on Well‐being via Patient‐reported Outcomes: Results from the Porphyria Worldwide Patient Experience Research (POWER) Study.” JIMD Reports, vol. 64, no. 1, Jan. 2023, pp. 104–13. EBSCOhost, https://doi.org/10.1002/jmd2.12343.

APA

Amy Dickey, Kristen Wheeden, Desiree Lyon, Sue Burrell, Sean Hegarty, Rocco Falchetto, Edrin R. Williams, Jasmin Barman‐Aksözen, Marc DeCongelio, Alison Bulkley, Joana E. Matos, Tarek Mnif, Jordanna Mora, John J. Ko, Stephen Meninger, Stephen Lombardelli, & Danielle Nance. (2023). Quantifying the impact of symptomatic acute hepatic porphyria on well‐being via patient‐reported outcomes: Results from the Porphyria Worldwide Patient Experience Research (POWER) study. JIMD Reports, 64(1), 104–113. https://doi.org/10.1002/jmd2.12343

Chicago

Amy Dickey, Kristen Wheeden, Desiree Lyon, Sue Burrell, Sean Hegarty, Rocco Falchetto, Edrin R. Williams, et al. 2023. “Quantifying the Impact of Symptomatic Acute Hepatic Porphyria on Well‐being via Patient‐reported Outcomes: Results from the Porphyria Worldwide Patient Experience Research (POWER) Study.” JIMD Reports 64 (1): 104–13. doi:10.1002/jmd2.12343.