Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Jayne Gershkowitz"'
Autor:
Anna L. Bruckner, Michael Losow, Jayson Wisk, Nita Patel, Allen Reha, Hjalmar Lagast, Jamie Gault, Jayne Gershkowitz, Brett Kopelan, Michael Hund, Dedee F. Murrell
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-14 (2020)
Abstract Background Little information is available regarding the burden of living with and managing epidermolysis bullosa, including the distinct challenges faced by patients with different disease types/subtypes. Methods A 90-question/item survey w
Externí odkaz:
https://doaj.org/article/966cbe75704c431bbb56ca4693a25b76
Publikováno v:
Lysosomal Storage Disorders. :299-307
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c89dcbbdd785d51e5cd8c2e838c69a5e
https://doi.org/10.1002/9781119697312.ch28
https://doi.org/10.1002/9781119697312.ch28
Autor:
Jayson Wisk, Michael Losow, Anna L. Bruckner, Hjalmar Lagast, Nita Patel, A. Reha, Dedee F. Murrell, Jamie Gault, Jayne Gershkowitz, Michael Hund, Brett Kopelan
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-14 (2020)
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-14 (2020)
Background Little information is available regarding the burden of living with and managing epidermolysis bullosa, including the distinct challenges faced by patients with different disease types/subtypes. Methods A 90-question/item survey was develo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::820654e3cff49f6bbad1d4d68b376a67
http://europepmc.org/articles/PMC6942340
http://europepmc.org/articles/PMC6942340
Autor:
Bruckner, Anna L.1 (AUTHOR) anna.bruckner@cuanschutz.edu, Losow, Michael2 (AUTHOR), Wisk, Jayson2 (AUTHOR), Patel, Nita2 (AUTHOR), Reha, Allen2 (AUTHOR), Lagast, Hjalmar2 (AUTHOR), Gault, Jamie2 (AUTHOR), Gershkowitz, Jayne2 (AUTHOR), Kopelan, Brett3 (AUTHOR), Hund, Michael4 (AUTHOR), Murrell, Dedee F.5 (AUTHOR)
Publikováno v:
Orphanet Journal of Rare Diseases. 1/3/2020, Vol. 15 Issue 1, p1-14. 14p.
Autor:
Mulberg, Andrew E.1 amulberg@amicusrx.com, Bucci-Rechtweg, Christina2 christina.buccirechtweg@novartis.com, Giuliano, Joseph1 jgiuliano@amicusrx.com, Jacoby, David3 djacoby@bmrn.com, Johnson, Franklin K.1 fjohnson@amicusrx.com, Liu, Qing1 qliu@amicusrx.com, Marsden, Deborah4 DMarsden@ultragenyx.com, McGoohan, Scott5 Scott_McGoohan@vrtx.com, Nelson, Robert6 rnelso30@ITS.JNJ.com, Patel, Nita1 npatel@amicusrx.com, Romero, Klaus7 KRomero@c-path.org, Sinha, Vikram8 vikram.sinha@merck.com, Sitaraman, Sheela1 ssitaraman@amicusrx.com, Spaltro, John1 jspaltro@amicusrx.com, Kessler, Vivian1 vkessler@amicusrx.com
Publikováno v:
Orphanet Journal of Rare Diseases. 2/8/2019, Vol. 14 Issue 1, p1-10. 10p.
Autor:
Quilici, Elaine
Publikováno v:
Pharmaceutical Executive. Oct2020, Vol. 40 Issue 10, p22-26. 5p.
Autor:
Henderson, Lisa
Publikováno v:
Pharmaceutical Executive. Mar2019, Vol. 39 Issue 3, p12-15. 4p.