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Late-Onset Cryopyrin-Associated Periodic Syndromes Caused by Somatic NLRP3 Mosaicism--UK Single Center Experience.
Published in:
Frontiers in Immunology, 2017, p. 1, doi. 10.3389/fimmu.2017.01410
By:
- Rowczenio, Dorota M.;
- Gomes, Sónia Melo;
- Aróstegui, Juan I.;
- Mensa-Vilaro, Anna;
- Omoyinmi, Ebun;
- Trojer, Hadija;
- Baginska, Anna;
- Baroja-Mazo, Alberto;
- Pelegrin, Pablo;
- Savic, Sinisa;
- Lane, Thirusha;
- Williams, Rene;
- Brogan, Paul;
- Lachmann, Helen J.;
- Hawkins, Philip N.
Publication type:
Article
Clinical characteristics in subjects with NLRP3 V198M diagnosed at a single UK center and a review of the literature.
Published in:
Arthritis Research & Therapy, 2013, v. 15, n. 1, p. 1, doi. 10.1186/ar4171
By:
- Rowczenio, Dorota M.;
- Trojer, Hadija;
- Russell, Tonia;
- Baginska, Anna;
- Lane, Thirusha;
- Stewart, Nicola M.;
- Gillmore, Julian D.;
- Hawkins, Philip N.;
- Woo, Patricia;
- Mikoluc, Bozena;
- Lachmann, Helen J.
Publication type:
Article
British kindred with dominant FMF associated with high incidence of AA amyloidosis caused by novel MEFV variant, and a review of the literature.
Published in:
Rheumatology, 2020, v. 59, n. 3, p. 554, doi. 10.1093/rheumatology/kez334
By:
- Rowczenio, Dorota M;
- Youngstein, Taryn;
- Trojer, Hadija;
- Omoyinmi, Ebun;
- Baginska, Anna;
- Brogan, Paul;
- Papadopoulou, Charalampia;
- Rezk, Tamer;
- Hawkins, Philip N;
- Lachmann, Helen J
Publication type:
Article
International multi-centre study of pregnancy outcomes with interleukin-1 inhibitors.
Published in:
Rheumatology, 2017, v. 56, n. 12, p. 2102, doi. 10.1093/rheumatology/kex305
By:
- Youngstein, Taryn;
- Hoffmann, Patrycja;
- Gül, Ahmet;
- Lane, Thirusha;
- Williams, Rene;
- Rowczenio, Dorota M.;
- Ozdogan, Huri;
- Ugurlu, Serdal;
- Ryan, John;
- Harty, Len;
- Riminton, Sean;
- Headley, Alex P.;
- Roesler, Joachim;
- Blank, Norbert;
- Kuemmerle-Deschner, Jasmin B.;
- Simon, Anna;
- Woolf, Adrian S.;
- Hawkins, Philip N.;
- Lachmann, Helen J.
Publication type:
Article
Autosomal dominant familial Mediterranean fever in Northern European Caucasians associated with deletion of p.M694 residue--a case series and genetic exploration.
Published in:
Rheumatology, 2017, v. 56, n. 2, p. 209, doi. 10.1093/rheumatology/kew058
By:
- Rowczenio, Dorota M.;
- Iancu, Daniela S.;
- Trojer, Hadija;
- Gilbertson, Janet A.;
- Gillmore, Julian D.;
- Wechalekar, Ashutosh D.;
- Tekman, Mehmet;
- Stanescu, Horia C.;
- Kleta, Robert;
- Lane, Thirusha;
- Hawkins, Philip N.;
- Lachmann, Helen J.
Publication type:
Article
Exploratory Study of MYD88 L265P, Rare NLRP3 Variants, and Clonal Hematopoiesis Prevalence in Patients With Schnitzler Syndrome.
Published in:
Arthritis & Rheumatology, 2019, v. 71, n. 12, p. 2121, doi. 10.1002/art.41030
By:
- Pathak, Shelly;
- Rowczenio, Dorota M.;
- Owen, Roger G.;
- Doody, Gina M.;
- Newton, Darren J.;
- Taylor, Claire;
- Taylor, Jan;
- Cargo, Catherine;
- Hawkins, Philip N.;
- Krause, Karoline;
- Lachmann, Helen J.;
- Savic, Sinisa
Publication type:
Article
Brief Report: Association of Tumor Necrosis Factor Receptor-Associated Periodic Syndrome With Gonosomal Mosaicism of a Novel 24-Nucleotide TNFRSF1A Deletion.
Published in:
Arthritis & Rheumatology, 2016, v. 68, n. 8, p. 2044, doi. 10.1002/art.39683
By:
- Rowczenio, Dorota M.;
- Trojer, Hadija;
- Omoyinmi, Ebun;
- Aróstegui, Juan I.;
- Arakelov, Grigor;
- Mensa‐Vilaro, Anna;
- Baginska, Anna;
- Silva Pilorz, Caroline;
- Wang, Guosu;
- Lane, Thirusha;
- Brogan, Paul;
- Hawkins, Philip N.;
- Lachmann, Helen J.
Publication type:
Article
Brief Report: Whole-Exome Sequencing Revealing Somatic NLRP3 Mosaicism in a Patient With Chronic Infantile Neurologic, Cutaneous, Articular Syndrome.
Published in:
Arthritis & Rheumatology, 2014, v. 66, n. 1, p. 197, doi. 10.1002/art.38217
By:
- Omoyinmi, Ebun;
- Melo Gomes, Sónia;
- Standing, Ariane;
- Rowczenio, Dorota M.;
- Eleftheriou, Despina;
- Klein, Nigel;
- Aróstegui, Juan I.;
- Lachmann, Helen J.;
- Hawkins, Philip N.;
- Brogan, Paul A.
Publication type:
Article
Online Registry for Mutations in Hereditary Amyloidosis Including Nomenclature Recommendations.
Published in:
Human Mutation, 2014, v. 35, n. 9, p. E2403, doi. 10.1002/humu.22619
By:
- Rowczenio, Dorota M.;
- Noor, Islam;
- Gillmore, Julian D.;
- Lachmann, Helen J.;
- Whelan, Carol;
- Hawkins, Philip N.;
- Obici, Laura;
- Westermark, Per;
- Grateau, Gilles;
- Wechalekar, Ashutosh D.
Publication type:
Article

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