Inconsistent platelet-rich plasma product from devices cleared by the US FDA: A retrospective review of clinic data - 07/08/21
Doi : 10.1016/j.jaad.2020.12.070
Meyeneobong Inyang, MD a, Javed A. Shaik, PhD a, Noora Hussain, BS b, Maria Hordinsky, MD a, Neil Sadick, MD a, c, d, Graham Gregorich, BS e, Jessica Asiala, BS e, Rebecca Freese, MS f, Ronda S. Farah, MD a, ⁎ 
a Department of Dermatology, University of Minnesota, Minneapolis, Minnesota
b College of Continuing and Professional Studies, Minneapolis, Minnesota
c Sadick Dermatology, New York, New York
d Weill Cornell Medical College, New York, New York
e Blood Bank Quality Center, University of Minnesota Medical Center, Minneapolis, Minnesota
f Biostatistical Design and Analysis Center, Clinical and Translational Science Institute, University of Minnesota, Minneapolis, Minnesota
∗Correspondence to: Ronda S. Farah, MD, Department of Dermatology, University of Minnesota, 516 Delaware St SE, MMC 98, Minneapolis, MN 55455Department of DermatologyUniversity of Minnesota516 Delaware St SE, MMC 98MinneapolisMN55455
| Funding sources: Supported by National Institutes of Health's National Center for Advancing Translational Sciences grant UL1TR002494. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health's National Center for Advancing Translational Sciences. |
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| Disclosure: Eclipse, Emcyte and Selphyl gifted equipment to the University of Minnesota. |
|
| IRB approval status: Approved by the University of Minnesota IRB #00005562. |
© 2021
American Academy of Dermatology, Inc.. Publicado por Elsevier Masson SAS. Todos los derechos reservados.
Vol 85 - N° 3
P. 788-790 - septembre 2021 Regresar al número
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