Literature DB >> 3052191

Hereditary angioedema.

G P Moore1, W T Hurley, S A Pace.   

Abstract

Although the condition is rare, patients with hereditary angioedema often present because of abdominal pain or airway compromise. A 27-year-old woman presented to the emergency department in acute abdominal distress. Identification of the disease in this patient allowed for proper management and avoidance of invasive procedures. Pathophysiology, clinical manifestations, diagnosis, and therapy of hereditary angioedema are discussed.

Entities:  

Mesh:

Year:  1988        PMID: 3052191     DOI: 10.1016/s0196-0644(88)80450-5

Source DB:  PubMed          Journal:  Ann Emerg Med        ISSN: 0196-0644            Impact factor:   5.721


  9 in total

Review 1.  Current management of hereditary angio-oedema (C'1 esterase inhibitor deficiency).

Authors:  A Fay; M Abinun
Journal:  J Clin Pathol       Date:  2002-04       Impact factor: 3.411

Review 2.  C1 inhibitor deficiency: consensus document.

Authors:  M M Gompels; R J Lock; M Abinun; C A Bethune; G Davies; C Grattan; A C Fay; H J Longhurst; L Morrison; A Price; M Price; D Watters
Journal:  Clin Exp Immunol       Date:  2005-03       Impact factor: 4.330

3.  Hereditary angioedema: an unusual case in an African-American woman.

Authors:  M L Borum
Journal:  J Natl Med Assoc       Date:  1998-02       Impact factor: 1.798

4.  Characterizing disease manifestations and treatment outcomes among patients with orofacial granulomatosis in China.

Authors:  Minghui Wei; Cheng Xie; Yubo Liu; Yuhong Wang; Yuanyuan Wang; Xinwen Wang; Yuan Liu
Journal:  JAAD Int       Date:  2020-08-12

5.  Hereditary angioedema: New therapeutic options for a potentially deadly disorder.

Authors:  Frank J Eidelman
Journal:  BMC Blood Disord       Date:  2010-05-14

Review 6.  Brazilian guidelines for the diagnosis and treatment of hereditary angioedema.

Authors:  Pedro Giavina-Bianchi; Alfeu T França; Anete S Grumach; Abílio A Motta; Fátima R Fernandes; Regis A Campos; Solange O Valle; Nelson A Rosário; Dirceu Sole
Journal:  Clinics (Sao Paulo)       Date:  2011       Impact factor: 2.365

7.  Clinical features of hereditary angioedema and warning signs (H4AE) for its identification.

Authors:  Pedro Giavina-Bianchi; Marcelo Vivolo Aun; Juliana Fóes Bianchini Garcia; Laís Souza Gomes; Ana Júlia Ribeiro; Priscila Takejima; Rosana Câmara Agondi; Jorge Kalil; Antonio Abilio Motta
Journal:  Clinics (Sao Paulo)       Date:  2022-03-19       Impact factor: 2.365

8.  Hereditary angioedema caused by c1-esterase inhibitor deficiency: a literature-based analysis and clinical commentary on prophylaxis treatment strategies.

Authors:  Richard G Gower; Paula J Busse; Emel Aygören-Pürsün; Amin J Barakat; Teresa Caballero; Mark Davis-Lorton; Henriette Farkas; David S Hurewitz; Joshua S Jacobs; Douglas T Johnston; William Lumry; Marcus Maurer
Journal:  World Allergy Organ J       Date:  2011-02       Impact factor: 4.084

9.  Brazilian Guidelines for Hereditary Angioedema Management - 2017 Update Part 1: Definition, Classification and Diagnosis.

Authors:  Pedro Giavina-Bianchi; Luisa Karla Arruda; Marcelo V Aun; Regis A Campos; Herberto J Chong-Neto; Rosemeire N Constantino-Silva; Fátima R Fernandes; Maria F Ferraro; Mariana P L Ferriani; Alfeu T França; Gustavo Fusaro; Juliana F B Garcia; Shirley Komninakis; Luana S M Maia; Eli Mansour; Adriana S Moreno; Antonio A Motta; João B Pesquero; Nathalia Portilho; Nelson A Rosário; Faradiba S Serpa; Dirceu Solé; Priscila Takejima; Eliana Toledo; Solange O.R Valle; Camila L Veronez; Anete S Grumach
Journal:  Clinics (Sao Paulo)       Date:  2018-05-03       Impact factor: 2.365

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.