遗传性血管性水肿患者慢性自发性荨麻疹和血管性水肿需用奥马珠单抗治疗 - Suppr

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Chronic spontaneous urticaria and angioedema requiring treatment with omalizumab in a patient with hereditary angioedema.

作者信息

Tadros Susan, Hayman Grant R

机构信息

Immunology Department, St Helier Hospital, Surrey, United Kingdom.

出版信息

Ann Allergy Asthma Immunol. 2019 Jun;122(6):666-667. doi: 10.1016/j.anai.2019.02.019. Epub 2019 Mar 1.

DOI:10.1016/j.anai.2019.02.019

PMID:30831259

Abstract

摘要

相似文献

Chronic spontaneous urticaria and angioedema requiring treatment with omalizumab in a patient with hereditary angioedema.

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引用本文的文献

Prediction of hereditary angioedema during attacks in patients with recurrent angioedema: Awareness at a glance with the hereditary angioedema prediction score.

Clin Transl Allergy. 2025 Apr;15(4):e70040. doi: 10.1002/clt2.70040.

The international WAO/EAACI guideline for the management of hereditary angioedema - The 2021 revision and update.

World Allergy Organ J. 2022 Apr 7;15(3):100627. doi: 10.1016/j.waojou.2022.100627. eCollection 2022 Mar.

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Chronic spontaneous urticaria and angioedema requiring treatment with omalizumab in a patient with hereditary angioedema.

作者信息

Tadros Susan, Hayman Grant R

机构信息

Immunology Department, St Helier Hospital, Surrey, United Kingdom.

出版信息

Ann Allergy Asthma Immunol. 2019 Jun;122(6):666-667. doi: 10.1016/j.anai.2019.02.019. Epub 2019 Mar 1.

DOI:10.1016/j.anai.2019.02.019

PMID:30831259

Abstract

摘要

相似文献

Chronic spontaneous urticaria and angioedema requiring treatment with omalizumab in a patient with hereditary angioedema.

Ann Allergy Asthma Immunol. 2019 Jun;122(6):666-667. doi: 10.1016/j.anai.2019.02.019. Epub 2019 Mar 1.

A case of hereditary angioedema involving recurrent abdominal attacks.

Intern Med. 2011;50(23):2911-4. doi: 10.2169/internalmedicine.50.6224. Epub 2011 Dec 1.

[Hereditary angioedema: strange cause of abdominal pain].

Cir Cir. 2014 Sep-Oct;82(5):563-6.

Acute Pancreatitis in the Context of Abdominal Attack of Hereditary Angioedema.

J Investig Allergol Clin Immunol. 2020 Aug;30(4):281-283. doi: 10.18176/jiaci.0490.

Hereditary angioedema as the cause of death from asphyxia: postmortem computed tomography study.

Allergol Int. 2014 Sep;63(3):493-4. doi: 10.2332/allergolint.13-LE-0655.

Genotype-phenotype correlations in Brazilian patients with hereditary angioedema due to C1 inhibitor deficiency.

Allergy. 2019 May;74(5):1013-1016. doi: 10.1111/all.13699. Epub 2019 Jan 22.

Daily subcutaneous administration of human C1 inhibitor in a child with hereditary angioedema type 1.

Pediatr Allergy Immunol. 2016 Mar;27(2):223-4. doi: 10.1111/pai.12495. Epub 2015 Nov 27.

Acquired complement C1 esterase inhibitor deficiency in a patient with a rare variant with unknown significance.

BMJ Case Rep. 2019 Sep 4;12(9):e231122. doi: 10.1136/bcr-2019-231122.

J Allergy Clin Immunol Pract. 2019 Apr;7(4):1352-1354.e3. doi: 10.1016/j.jaip.2018.10.005. Epub 2018 Oct 16.

Angioedema is an unfavorable factor for the response to omalizumab in chronic spontaneous urticaria: A retrospective study.

Dermatol Ther. 2019 Jan;32(1):e12752. doi: 10.1111/dth.12752. Epub 2018 Oct 30.

引用本文的文献

Prediction of hereditary angioedema during attacks in patients with recurrent angioedema: Awareness at a glance with the hereditary angioedema prediction score.

Clin Transl Allergy. 2025 Apr;15(4):e70040. doi: 10.1002/clt2.70040.

The international WAO/EAACI guideline for the management of hereditary angioedema - The 2021 revision and update.

World Allergy Organ J. 2022 Apr 7;15(3):100627. doi: 10.1016/j.waojou.2022.100627. eCollection 2022 Mar.