Items where authors include "Longhurst, H.J."

Article

Tuijnenburg, P., Lango Allen, H., Burns, S.O. et al. (85 more authors) (2018) Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans. Journal of Allergy and Clinical Immunology, 142 (4). pp. 1285-1296. ISSN 0091-6749

Hurst, J.R., Verma, N., Lowe, D. et al. (32 more authors) (2017) British Lung Foundation/United Kingdom primary immunodeficiency network consensus statement on the definition, diagnosis, and management of granulomatous-lymphocytic interstitial lung disease in common variable immunodeficiency disorders. Journal of Allergy and Clinical Immunology: In Practice, 5 (4). pp. 938-945. ISSN 2213-2198

Coulter, T.I., Chandra, A., Bacon, C.M. et al. (55 more authors) (2017) Clinical spectrum and features of activated phosphoinositide 3-kinase δ syndrome: A large patient cohort study. Journal of Allergy and Clinical Immunology, 139 (2). 597-606.e4. ISSN 0091-6749

Proceedings Paper

Longhurst, H.J., Smith, M.D., Yea, C. et al. (1 more author) (2022) SEBETRALSTAT EFFECTIVENESS IN THE TREATMENT OF HEREDITARY ANGIOEDEMA ATTACKS RATED MILD OR MODERATE AT BASELINE IN THE PHASE 2 TRIAL. In: INTERNAL MEDICINE JOURNAL. 32nd Annual Conference of the Australasian Society of Clinical Immunology and Allergy (ASCIA), 30 Aug - 02 Sep 2022, Melbourne, Australia. , p. 29.