Fiona Moghaddas
Fiona Moghaddas
The Walter and Eliza Hall Institute of Medical Research, The Royal Melbourne Hospital
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Familial autoinflammation with neutrophilic dermatosis reveals a regulatory mechanism of pyrin activation
SL Masters, V Lagou, I Jéru, PJ Baker, L Van Eyck, DA Parry, D Lawless, ...
Science translational medicine 8 (332), 332ra45-332ra45, 2016
A novel Pyrin-Associated Autoinflammation with Neutrophilic Dermatosis mutation further defines 14-3-3 binding of pyrin and distinction to Familial Mediterranean Fever
F Moghaddas, R Llamas, D De Nardo, H Martinez-Banaclocha, ...
Annals of the rheumatic diseases 76 (12), 2085-2094, 2017
A mutation outside the dimerization domain causing atypical STING-associated vasculopathy with onset in infancy
RG Saldanha, KR Balka, S Davidson, BK Wainstein, M Wong, ...
Frontiers in immunology 9, 1535, 2018
Monogenic autoinflammatory diseases: cytokinopathies
F Moghaddas, SL Masters
Cytokine 74 (2), 237-246, 2015
Autoinflammatory mutation in NLRC4 reveals a leucine-rich repeat (LRR)–LRR oligomerization interface
F Moghaddas, P Zeng, Y Zhang, H Schützle, S Brenner, SR Hofmann, ...
Journal of Allergy and Clinical Immunology 142 (6), 1956-1967. e6, 2018
Posttranslational modification as a critical determinant of cytoplasmic innate immune recognition
PJ Baker, D De Nardo, F Moghaddas, LS Tran, A Bachem, T Nguyen, ...
Physiological reviews 97 (3), 1165-1209, 2017
The classification, genetic diagnosis and modelling of monogenic autoinflammatory disorders
F Moghaddas, SL Masters
Clinical Science 132 (17), 1901-1924, 2018
Need for intensive care in patients admitted for asthma: red flags from the social history
F Moghaddas, C Smith, D Pilcher, R O'Hehir, M Hew, E Dabscheck
Respirology 21 (7), 1251-1254, 2016
Novel genes and mechanisms in monogenic autoinflammatory disorders
FE Moghaddas
Autoantibodies directed to centromere protein F in a patient with BRCA1 gene mutation
F Moghaddas, F Joshua, R Taylor, MJ Fritzler, BH Toh
BMC research notes 9 (1), 1-4, 2016
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