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hereditary familial urticaria syndrome相关文献:
Cold Urticaria Syndromes: Diagnosis and Management.
Diaz VL, Gribbons KB, Yazdi-Nejad K, Kuemmerle-Deschner J, Wanderer AA, Broderick L, Hoffman HM.
J Allergy Clin Immunol Pract. 2023 Aug;11(8):2275-2285. doi: 10.1016/j.jaip.2023.05.040. Epub 2023 Jun 7.
PMID:37290539
Periodic fever syndromes.
Lachmann HJ.
Best Pract Res Clin Rheumatol. 2017 Aug;31(4):596-609. doi: 10.1016/j.berh.2017.12.001. Epub 2018 Jan 11.
PMID:29773275
Systemic autoinflammatory diseases: Clinical state of the art.
Georgin-Lavialle S, Ducharme-Benard S, Sarrabay G, Savey L, Grateau G, Hentgen V.
Best Pract Res Clin Rheumatol. 2020 Aug;34(4):101529. doi: 10.1016/j.berh.2020.101529. Epub 2020 Jun 13.
PMID:32546426
Hereditary disorders presenting with urticaria.
Kanazawa N.
Immunol Allergy Clin North Am. 2014 Feb;34(1):169-79. doi: 10.1016/j.iac.2013.08.001. Epub 2013 Sep 26.
PMID:24262697
Autoinflammatory diseases.
Grateau G.
Acta Clin Belg. 2006 Sep-Oct;61(5):264-9. doi: 10.1179/acb.2006.045.
PMID:17240743
Familial Cold Autoinflammatory Syndrome Type 1.
Mohite RS, Kotecha U, Bhattad S.
Indian J Pediatr. 2021 Aug;88(8):834. doi: 10.1007/s12098-021-03805-6. Epub 2021 May 26.
PMID:34036544
The 2021 EULAR/American College of Rheumatology Points to Consider for Diagnosis, Management and Monitoring of the Interleukin-1 Mediated Autoinflammatory Diseases: Cryopyrin-Associated Periodic Syndromes, Tumour Necrosis Factor Receptor-Associated Periodic Syndrome, Mevalonate Kinase Deficiency, and Deficiency of the Interleukin-1 Receptor Antagonist.
Romano M, Arici ZS, Piskin D, Alehashemi S, Aletaha D, Barron K, Benseler S, Berard RA, Broderick L, Dedeoglu F, Diebold M, Durrant K, Ferguson P, Foell D, Hausmann JS, Jones OY, Kastner D, Lachmann HJ, Laxer RM, Rivera D, Ruperto N, Simon A, Twilt M, Frenkel J, Hoffman HM, de Jesus AA, Kuemmerle-Deschner JB, Ozen S, Gattorno M, Goldbach-Mansky R, Demirkaya E.
Arthritis Rheumatol. 2022 Jul;74(7):1102-1121. doi: 10.1002/art.42139. Epub 2022 May 27.
PMID:35621220
The 2021 EULAR/American College of Rheumatology points to consider for diagnosis, management and monitoring of the interleukin-1 mediated autoinflammatory diseases: cryopyrin-associated periodic syndromes, tumour necrosis factor receptor-associated periodic syndrome, mevalonate kinase deficiency, and deficiency of the interleukin-1 receptor antagonist.
Romano M, Arici ZS, Piskin D, Alehashemi S, Aletaha D, Barron KS, Benseler S, Berard R, Broderick L, Dedeoglu F, Diebold M, Durrant KL, Ferguson P, Foell D, Hausmann J, Jones OY, Kastner DL, Lachmann HJ, Laxer RM, Rivera D, Ruperto N, Simon A, Twilt M, Frenkel J, Hoffman H, de Jesus AA, Kuemmerle-Deschner JB, Ozen S, Gattorno M, Goldbach-Mansky R, Demirkaya E.
Ann Rheum Dis. 2022 Jul;81(7):907-921. doi: 10.1136/annrheumdis-2021-221801. Epub 2022 May 27.
PMID:35623638
Familial atypical cold urticaria: description of a new hereditary disease.
Gandhi C, Healy C, Wanderer AA, Hoffman HM.
J Allergy Clin Immunol. 2009 Dec;124(6):1245-50. doi: 10.1016/j.jaci.2009.09.035.
PMID:19910034
Autoinflammatory syndromes.
Hashkes PJ, Toker O.
Pediatr Clin North Am. 2012 Apr;59(2):447-70. doi: 10.1016/j.pcl.2012.03.005.
PMID:22560579
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