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Page 1
Molecular genetic investigation, clinical features, and response to treatment in 21 patients with Schnitzler syndrome.
Rowczenio DM, Pathak S, Arostegui JI, Mensa-Vilaro A, Omoyinmi E, Brogan P, Lipsker D, Scambler T, Owen R, Trojer H, Baginska A, Gillmore JD, Wechalekar AD, Lane T, Williams R, Youngstein T, Hawkins PN, Savic S, Lachmann HJ. Rowczenio DM, et al. Among authors: omoyinmi e. Blood. 2018 Mar 1;131(9):974-981. doi: 10.1182/blood-2017-10-810366. Epub 2017 Dec 28. Blood. 2018. PMID: 29284595 Free PMC article. Clinical Trial.
Gene hunting in autoinflammation.
Standing A, Omoyinmi E, Brogan P. Standing A, et al. Among authors: omoyinmi e. Clin Transl Allergy. 2013 Sep 26;3(1):32. doi: 10.1186/2045-7022-3-32. Clin Transl Allergy. 2013. PMID: 24070009 Free PMC article.
Stimulator of interferon genes-associated vasculitis of infancy.
Omoyinmi E, Melo Gomes S, Nanthapisal S, Woo P, Standing A, Eleftheriou D, Klein N, Brogan PA. Omoyinmi E, et al. Arthritis Rheumatol. 2015 Mar;67(3):808. doi: 10.1002/art.38998. Arthritis Rheumatol. 2015. PMID: 25510345 No abstract available.
8th International Congress of Familial Mediterranean Fever and Systemic Autoinflammatory Diseases.
Standing A, Eleftheriou D, Paisan-Ruiz C, Rowcenzio D, Hong Y, Omoyinmi E, Woo P, Hawkins P, Lachmann H, Klein N, Brogan P. Standing A, et al. Among authors: omoyinmi e. Pediatr Rheumatol Online J. 2015;13 Suppl 1(Suppl 1):O1-P211. doi: 10.1186/1546-0096-13-s1-o1. Epub 2015 Sep 28. Pediatr Rheumatol Online J. 2015. PMID: 26424586 Free PMC article. No abstract available.
Brief Report: Association of Tumor Necrosis Factor Receptor-Associated Periodic Syndrome With Gonosomal Mosaicism of a Novel 24-Nucleotide TNFRSF1A Deletion.
Rowczenio DM, Trojer H, Omoyinmi E, Aróstegui JI, Arakelov G, Mensa-Vilaro A, Baginska A, Silva Pilorz C, Wang G, Lane T, Brogan P, Hawkins PN, Lachmann HJ. Rowczenio DM, et al. Among authors: omoyinmi e. Arthritis Rheumatol. 2016 Aug;68(8):2044-9. doi: 10.1002/art.39683. Arthritis Rheumatol. 2016. PMID: 26992170
Autoinflammatory periodic fever, immunodeficiency, and thrombocytopenia (PFIT) caused by mutation in actin-regulatory gene WDR1.
Standing AS, Malinova D, Hong Y, Record J, Moulding D, Blundell MP, Nowak K, Jones H, Omoyinmi E, Gilmour KC, Medlar A, Stanescu H, Kleta R, Anderson G, Nanthapisal S, Gomes SM, Klein N, Eleftheriou D, Thrasher AJ, Brogan PA. Standing AS, et al. Among authors: omoyinmi e. J Exp Med. 2017 Jan;214(1):59-71. doi: 10.1084/jem.20161228. Epub 2016 Dec 19. J Exp Med. 2017. PMID: 27994071 Free PMC article.
46 results