Sorena Kiani‐Alikhan

The international WAO/EAACI guideline for the management of hereditary angioedema—The 2021 revision and update

Marcus Maurer, Markus Magerl, Stephen Betschel et al. · Allergy · 2022 · 441 citations · Full text

Thrombosis, Type 1, Cardiovascular Disease +14

KLRG1 signaling induces defective Akt (ser473) phosphorylation and proliferative dysfunction of highly differentiated CD8+ T cells

Siân M. Henson, Ornella Franzese, R. Macaulay et al. · Blood · 2009 · 266 citations · Full text

Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans

Paul Tuijnenburg, Hana Lango Allen, Siobhan O. Burns et al. · Journal of Allergy and Clinical Immunology · 2018 · 227 citations · Full text

Primary Immunodeficiency, Disease Susceptibility, Immune Cell Development +15

The international WAO/EAACI guideline for the management of hereditary angioedema – The 2021 revision and update

Marcus Maurer, Markus Magerl, Stephen Betschel et al. · World Allergy Organization Journal · 2022 · 139 citations · Full text

Cardiovascular Disease, Hereditary Angioedema, Vascular Malformation +6

Hypogammaglobulinaemia after rituximab treatment--incidence and outcomes

Melina Makatsori, Sorena Kiani‐Alikhan, A L Manson et al. · QJM · 2014 · 134 citations · Full text