Items where authors include "Young, NS"

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Number of items: 4.

Article

Ferrada, MA, Savic, S orcid.org/0000-0001-7910-0554, Ospina Cardona, D et al. (29 more authors) (2022) Translation of cytoplasmic UBA1 contributes to VEXAS syndrome pathogenesis. Blood, 140 (13). pp. 1496-1506. ISSN 0006-4971

Ferrada, MA, Sikora, KA, Luo, Y et al. (32 more authors) (2021) Somatic Mutations in UBA1 Define a Distinct Subset of Relapsing Polychondritis Patients With VEXAS. Arthritis and Rheumatology, 73 (10). pp. 1886-1895. ISSN 2326-5191

Beck, DB, Ferrada, MA, Sikora, KA et al. (59 more authors) (2020) Somatic Mutations in UBA1 and Severe Adult-Onset Autoinflammatory Disease. New England Journal of Medicine. NEJMoa2026834. ISSN 0028-4793

Conference or Workshop Item

Beck, D, Ferrada, M, Sikora, K et al. (19 more authors) (2020) Somatic Mutations in a Single Residue of UBA1 Cause VEXAS, a Severe Adult-Onset Rheumatic Disease Presenting as Relapsing Polychondritis, Polyarteritis Nodosa, or Giant Cell Arteritis. In: ACR Convergence 2020, 05-09 Nov 2020, Online.

This list was generated on Mon Apr 15 02:25:41 2024 BST.