Items where authors include "Parry, D"

Article

Wei, W, Tuna, S, Keogh, MJ et al. (426 more authors) (2019) Germline selection shapes human mitochondrial DNA diversity. Science, 364 (6442). 749-+. ISSN 0036-8075

Bigley, V, Maisuria, S, Cytlak, U et al. (20 more authors) (2018) Biallelic interferon regulatory factor 8 mutation: A complex immunodeficiency syndrome with dendritic cell deficiency, monocytopenia, and immune dysregulation. Journal of Allergy and Clinical Immunology, 141 (6). pp. 2234-2248. ISSN 0091-6749

Mistry, A, Scambler, T, Parry, D et al. (5 more authors) (2017) Glucose-6-Phosphatase Catalytic Subunit 3 (G6PC3) Deficiency Associated With Autoinflammatory Complications. Frontiers in Immunology, 8. 1485. ISSN 1664-3224

Lawless, D orcid.org/0000-0001-8496-3725, Mistry, A, Wood, PM et al. (7 more authors) (2017) Bialellic Mutations in Tetratricopeptide Repeat Domain 7A (TTC7A) Cause Common Variable Immunodeficiency-Like Phenotype with Enteropathy. Journal of Clinical Immunology, 37 (7). pp. 617-622. ISSN 0271-9142

Mistry, A, Parry, D, Matthews, B et al. (3 more authors) (2016) A Case of SLC29A3 Spectrum Disorder—Unresponsive to Multiple Immunomodulatory Therapies. Journal of Clinical Immunology, 36 (5). pp. 429-433. ISSN 0271-9142

Savic, S, Parry, D, Carter, C et al. (7 more authors) (2015) A new case of Fas-associated death domain protein deficiency and update on treatment outcomes. Journal of Allergy and Clinical Immunology, 136 (2). 502 - 505. ISSN 0091-6749

Jaureguiberry, G, De la Dure-Molla, M, Parry, D et al. (68 more authors) (2013) Nephrocalcinosis (Enamel Renal Syndrome) Caused by Autosomal Recessive FAM20A Mutations. Nephron Physiology, 122 (1-2). pp. 1-6. ISSN 1660-8151