A. Mistry

发表

Whole genome sequencing of a sporadic primary immunodeficiency cohort

William J. Astle, Sri V. V. Deevi, Kenneth G. C. Smith, 2018, Nature.

Improving Diagnosis and Clinical Management of Acquired Systemic Autoinflammatory Diseases

S. Savic, A. Mistry, A. Al-hakim, 2022, Journal of inflammation research.

Characterization of the clinical and immunological phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations.

William J. Astle, Sri V. V. Deevi, Kenneth G. C. Smith, 2020, The Journal of allergy and clinical immunology.

Autoimmune-autoinflammatory rheumatoid arthritis overlaps: a rare but potentially important subgroup of diseases

P. Emery, D. McGonagle, R. Doffinger, 2017, RMD Open.

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

Crina Samarghitean, Vera Matser, Scott Hackett, 2018, The Journal of allergy and clinical immunology.

Interleukin-1 Blockade: An Update on Emerging Indications

S. Savic, J. V. D. van der Hilst, A. Mistry, 2017, BioDrugs.

A third generation vaccine for human visceral leishmaniasis and post kala azar dermal leishmaniasis: First-in-human trial of ChAd63-KH

R. Cortese, P. Kaye, Deborah F. Smith, 2017, PLoS neglected tropical diseases.

Whole-genome sequencing of a sporadic primary immunodeficiency cohort

William J. Astle, Sri V. V. Deevi, Kenneth G. C. Smith, 2020, Nature.

Glucose-6-Phosphatase Catalytic Subunit 3 (G6PC3) Deficiency Associated With Autoinflammatory Complications

D. Parry, R. Doffinger, S. Savic, 2017, Front. Immunol..

Bialellic Mutations in Tetratricopeptide Repeat Domain 7A (TTC7A) Cause Common Variable Immunodeficiency-Like Phenotype with Enteropathy

G. Arumugakani, S. Savic, C. Carter, 2017, Journal of Clinical Immunology.

A Case of SLC29A3 Spectrum Disorder—Unresponsive to Multiple Immunomodulatory Therapies

D. Parry, S. Savic, M. Goodfield, 2016, Journal of Clinical Immunology.

Home self‐administration of omalizumab for chronic spontaneous urticaria

S. Savic, P. Wood, K. Ford, 2016, The British journal of dermatology.

Interleukin-1 Blockade: An Update on Emerging Indications

S. Savic, J. V. D. van der Hilst, A. Mistry, 2017, BioDrugs.

Bialellic Mutations in Tetratricopeptide Repeat Domain 7A (TTC7A) Cause Common Variable Immunodeficiency-Like Phenotype with Enteropathy

D. Parry, G. Arumugakani, S. Savic, 2017, Journal of Clinical Immunology.

Inherited CD19 Deficiency Does Not Impair Plasma Cell Formation or Response to CXCL12.

Laura A. Crinnion, D. Bonthron, M. Care, 2023, Journal of clinical immunology.

Hyper‐IgM syndrome resulting from heterozygous AICDA variants: A European first?

M. Gompels, G. Arumugakani, S. Savic, 2022, Scandinavian journal of immunology.

Autosomal Dominant STAT6 Gain of Function Causes Severe Atopy Associated with Lymphoma

Sri V. V. Deevi, Eleanor F. Dewhurst, Lorena E. Lorenzo, 2023, Journal of Clinical Immunology.