Panelists at Rare Disease Day at NIH
Emily Milligan, M.P.H., executive director of the Barth Syndrome Foundation, speaks during the “There is Power in Numbers — Harnessing Patient Data through Registries” panel session at Rare Disease Day at NIH on Feb. 28, 2019. Fellow panelist Forbes Denny Porter, M.D., Ph.D., clinical director and senior investigator in NIH’s Eunice Kennedy Shriver National Institute of Child Health and Human Development, sits to her right.
Credit: Daniel Soñé Photography
Panelists at Rare Disease Day at NIH
Emily Milligan, M.P.H., executive director of the Barth Syndrome Foundation, speaks during the “There is Power in Numbers — Harnessing Patient Data through Registries” panel session at Rare Disease Day at NIH on Feb. 28, 2019. Fellow panelist Forbes Denny Porter, M.D., Ph.D., clinical director and senior investigator in NIH’s Eunice Kennedy Shriver National Institute of Child Health and Human Development, sits to her right.
Credit: Daniel Soñé Photography