| For: | Nzeako UC. Diagnosis and management of angioedema with abdominal involvement: A gastroenterology perspective. World J Gastroenterol 2010; 16(39): 4913-4921 [PMID: 20954277 DOI: 10.3748/wjg.v16.i39.4913] |
|---|---|
| URL: | https://www.wjgnet.com/1007-9327/full/v16/i39/4913.htm |
| Number | Citing Articles |
| 1 |
Nilkanth L Pal, Yasmin Fernandes. Intestinal Angioedema: A Mimic of an Acute Abdomen. Cureus 2023; doi: 10.7759/cureus.34619
|
| 2 |
Laura C.G. de Graaff, Martijn van Essen, Eleonora M. Schipper, Henk Boom, Erik J.J. Duschek. Unnecessary surgery for acute abdomen secondary to angiotensin-converting enzyme inhibitor use. The American Journal of Emergency Medicine 2012; 30(8) doi: 10.1016/j.ajem.2011.10.028
|
| 3 |
Joshua Jacobs, Teresa Neeno. The importance of recognizing and managing a rare form of angioedema: hereditary angioedema due to C1-inhibitor deficiency. Postgraduate Medicine 2021; 133(6) doi: 10.1080/00325481.2021.1905364
|
| 4 |
P. Raval. A case report looking at ACE inhibitors as the cause of angioedema during dental treatment. British Dental Journal 2014; 216(2) doi: 10.1038/sj.bdj.2014.2
|
| 5 |
Eirini I Rigopoulou, Maria Ioannou, Georgia Papadamou, Georgios N Dalekos. Ascites in a patient with episodic angio-oedema and eosinophilia: thinking outside the box. BMJ Case Reports 2017; 2017 doi: 10.1136/bcr-2017-219467
|
| 6 |
Mehmet Kılınç, Fatih Çölkesen, Filiz Sadi Aykan, Recep Evcen, Eray Yıldız, Tuğba Önalan, Mehmet Emin Gerek, Şevket Arslan. An Essential Problem in Patients with Hereditary Angioedema: Irritable Bowel Syndrome. SDÜ Tıp Fakültesi Dergisi 2024; doi: 10.17343/sdutfd.1457010
|
| 7 |
B. Floccard, E. Hautin, B. Allaouchiche. Annual Update in Intensive Care and Emergency Medicine 2012. 2012; doi: 10.1007/978-3-642-25716-2_46
|
| 8 |
Andrea Zanichelli, Hilary J. Longhurst, Marcus Maurer, Laurence Bouillet, Werner Aberer, Vincent Fabien, Irmgard Andresen, Teresa Caballero, W. Aberer, A. Grumach, A. Bygum, C. Blanchard Delaunay, L. Bouillet, B. Coppere, O. Fain, B. Goichot, A. Gompel, S. Guez, P. Jeandel, G. Kanny, D. Launay, H. Maillard, L. Martin, A. Masseau, Y. Ollivier, A. Sobel, J. Arnolds, E. Aygören-Pürsün, M. Baş, A. Bauer, K. Bork, I. Martinez, M. Maurer, E. Papadopoulou-Alataki, F. Psarros, Y. Graif, S. Kivity, A. Reshef, E. Toubi, F. Arcoleo, M. Cicardi, P. Manconi, G. Marone, V. Montinaro, M.L. Baeza, T. Caballero, R. Cabañas, M. Guilarte, D. Hernandez de Rojas, C. Hernando de Larramendi, R. Lleonart, T. Lobera, B. Sáenz de San Pedro, J. Bjorkander, M. Helbert, H.J. Longhurst. Misdiagnosis trends in patients with hereditary angioedema from the real-world clinical setting. Annals of Allergy, Asthma & Immunology 2016; 117(4) doi: 10.1016/j.anai.2016.08.014
|
| 9 |
Ankur K. Jindal, Amit Rawat, Anit Kaur, Dhrubajyoti Sharma, Deepti Suri, Anju Gupta, Ravinder Garg, Sunil Dogra, Biman Saikia, Ranjana W. Minz, Surjit Singh, Marina Atanaskovic‐Markovic. Novel SERPING1 gene mutations and clinical experience of type 1 hereditary angioedema from North India. Pediatric Allergy and Immunology 2021; 32(3) doi: 10.1111/pai.13420
|
| 10 |
Abbas Shahmohammadi, Kathryn M Burtson. Acute Right Ventricular Dysfunction Secondary to Hereditary Angioedema Exacerbation . Cureus 2021; doi: 10.7759/cureus.15336
|
| 11 |
Thanita Thongtan, Anasua Deb, Genanew Bedanie, Mohamed Elmassry, Matthew Soape, Kenneth Nugent. Intestinal angioedema caused by an acquired C1 esterase inhibitor deficiency associated with underlying splenic marginal zone lymphoma. Baylor University Medical Center Proceedings 2021; 34(4) doi: 10.1080/08998280.2021.1885277
|
| 12 |
Dorde Jevtic, Adela Taylor, Igor Dumic, Erik Sviggum, Charles W. Nordstrom, Marina Antic. Recurrent Intestinal Angioedema with Normal C1-Inhibitor: A Case Report. Medicina 2025; 61(2) doi: 10.3390/medicina61020245
|
| 13 |
Sujai Jalaj, James S. Scolapio. Gastrointestinal Manifestations, Diagnosis, and Management of Hereditary Angioedema. Journal of Clinical Gastroenterology 2013; 47(10) doi: 10.1097/MCG.0b013e31829e7edf
|
| 14 |
Karim Osman, Ayse Tuba Kendi, Daniel Maselli. Isolated angioedema of the bowel caused by aspirin. Clinical Journal of Gastroenterology 2021; 14(4) doi: 10.1007/s12328-021-01430-6
|
| 15 |
Christina Mouradides, Leila Abbes, Christophe Cellier. Fleeting Gastrointestinal Thickening. Clinical Gastroenterology and Hepatology 2016; 14(4) doi: 10.1016/j.cgh.2015.12.020
|
| 16 |
Yuan-Jhen Syue, Chao-Jui Li, Wen-Liang Chen, Tsung-Han Lee, Cheng-Chieh Huang, Mei-Chueh Yang, Chih-Ming Lin, Meng-Huan Wu, Chu-Chung Chou, Chin-Fu Chang, Yan-Ren Lin. Significant predictive factors of the severity and outcomes of the first attack of acute angioedema in children. BMC Pediatrics 2019; 19(1) doi: 10.1186/s12887-019-1809-8
|
| 17 |
Eitan Rubinstein, Leslie E Stolz, Albert L Sheffer, Chris Stevens, Athos Bousvaros. Abdominal attacks and treatment in hereditary angioedema with C1-inhibitor deficiency. BMC Gastroenterology 2014; 14(1) doi: 10.1186/1471-230X-14-71
|
| 18 |
C.‐Y. Lu, M.‐S. Hsieh, K.‐C. Wei, M. Ezmerli, C.‐H. Kuo, W. Chen. Gastrointestinal involvement of primary skin diseases. Journal of the European Academy of Dermatology and Venereology 2020; 34(12) doi: 10.1111/jdv.16676
|
| 19 |
Clare E. Tange, Amrit Kaur, Nisha Verma, Alaco Hickey, Sofia Grigoriadou, Chris Scott, Sorena Kiani, Rachael Steven, Mark Ponsford, Tariq El‐Shanawany, Stephen Jolles, Stephen Harding, Antony R. Parker. Quantification of human C1 esterase inhibitor protein using an automated turbidimetric immunoassay. Journal of Clinical Laboratory Analysis 2019; 33(1) doi: 10.1002/jcla.22627
|
| 20 |
Paula J. Busse, Henriette Farkas, Aleena Banerji, William R. Lumry, Hilary J. Longhurst, Daniel J. Sexton, Marc A. Riedl. Lanadelumab for the Prophylactic Treatment of Hereditary Angioedema with C1 Inhibitor Deficiency: A Review of Preclinical and Phase I Studies. BioDrugs 2019; 33(1) doi: 10.1007/s40259-018-0325-y
|
| 21 |
RaeAnn Hirschy, Tanvi Shah, Tamara Davis, Megan A. Rech. Treatment of Life-Threatening ACE-Inhibitor–Induced Angioedema. Advanced Emergency Nursing Journal 2018; 40(4) doi: 10.1097/TME.0000000000000211
|
| 22 |
Ammar Hassan, Simcha Weissman, Michael A. Sciarra, John Sotiriadis. Isolated Intestinal Angioedema Secondary to a Food Allergen. ACG Case Reports Journal 2019; 6(9) doi: 10.14309/crj.0000000000000222
|
| 23 |
Tanja Oostergo, Gerrie Prins, Yvonne C. Schrama, Ivonne Leeuwenburgh. Small bowel angioedema due to acquired C1 inhibitor deficiency. European Journal of Gastroenterology & Hepatology 2013; 25(4) doi: 10.1097/MEG.0b013e32835c94ff
|
| 24 |
Bernard Floccard, Jullien Crozon, Brigitte Coppere, Laurence Bouillet, Bernard Allaouchiche. Uncommon Diseases in the ICU. 2014; doi: 10.1007/978-3-319-04576-4_16
|
| 25 |
S. Alagheband, P. Malet, D. Katz, M. Davis-Lorton. Angioedema of the small intestine: A great imitator. Clinics and Research in Hepatology and Gastroenterology 2017; 41(2) doi: 10.1016/j.clinre.2016.09.007
|
| 26 |
Benoit Coffin, Henri Duboc. Review article: diagnostic and therapeutic approach to persistent abdominal pain beyond irritable bowel syndrome. Alimentary Pharmacology & Therapeutics 2022; 56(3) doi: 10.1111/apt.17064
|
| 27 |
Poovizhi Bharathi Rajaduraivelpandian, Rashmi R. Rao, Ashwin Kamath. Drug-Induced Intestinal Angioedema: A Disproportionality Analysis Using the United States Food and Drug Administration Adverse Event Reporting System Database and Literature Review. Medical Sciences 2025; 13(4) doi: 10.3390/medsci13040327
|
| 28 |
Bernard Floccard, Nicolas Javaud, Jullien Crozon, Thomas Rimmelé. Prise en charge en urgence des angiœdèmes bradykiniques. La Presse Médicale 2015; 44(1) doi: 10.1016/j.lpm.2014.09.012
|
| 29 |
Janina Hahn, Alisa Hoess, Daniel Thomas Friedrich, Benjamin Mayer, Lucia Schauf, Thomas K. Hoffmann, Jens Greve. Unnecessary abdominal interventions in patients with hereditary angioedema. JDDG: Journal der Deutschen Dermatologischen Gesellschaft 2018; 16(12) doi: 10.1111/ddg.13698
|
| 30 |
Zahra Kamal, Hannah Wakefield, Kathleen Head, Jonathan Mathis, Patricia McBurney. Expanding Your Differential for Abdominal Distention in the Pediatric Patient. Clinical Pediatrics 2017; 56(4) doi: 10.1177/0009922816650397
|
| 31 |
Parwinder Gill, Stephen D. Betschel. The Clinical Evaluation of Angioedema. Immunology and Allergy Clinics of North America 2017; 37(3) doi: 10.1016/j.iac.2017.04.007
|
| 32 |
Fumiaki Kawara, Takanori Matsuura, Kodai Yamanaka, Chiharu Nishioka. A Case of Duodenal Edema-related Undiagnosed Hereditary Angioedema. Internal Medicine 2023; 62(15) doi: 10.2169/internalmedicine.0869-22
|
| 33 |
Intestinal Angioedema: Case Report and Literature Review. Journal of Gastroenterology & Digestive Systems 2018; 2(2) doi: 10.33140/JGDS/02/02/00003
|
| 34 |
Kyle Staller, Anthony Lembo, Aleena Banerji, Jonathan A. Bernstein, Eric D. Shah, Marc A. Riedl. Consider Hereditary Angioedema in the Differential Diagnosis for Unexplained Recurring Abdominal Pain. Journal of Clinical Gastroenterology 2022; 56(9) doi: 10.1097/MCG.0000000000001744
|
| 35 |
Jameel Uddeen. Atlas of Dermatological Manifestations of Gastrointestinal Disease. 2013; doi: 10.1007/978-1-4614-6191-3_53
|
| 36 |
Hilary J Longhurst, Ugo C Nzeako. Diagnosis and treatment of hereditary angio-oedema attacks. British Journal of Hospital Medicine 2012; 73(3) doi: 10.12968/hmed.2012.73.3.148
|
| 37 |
Bernard Floccard, Nicolas Javaud, Jullien Crozon, Thomas Rimmelé. Prise en charge en urgence des angiœdèmes bradykiniques. Journal Européen des Urgences et de Réanimation 2015; 27(1) doi: 10.1016/j.jeurea.2015.02.003
|
| 38 |
Philippa Adams, Stephanie Kilinç. The lived experience of women who have Hereditary Angioedema: An exploratory study. Health Psychology Update 2019; 28(1) doi: 10.53841/bpshpu.2019.28.1.23
|
| 39 |
Janina Hahn, Alisa Hoess, Daniel Thomas Friedrich, Benjamin Mayer, Lucia Schauf, Thomas K. Hoffmann, Jens Greve. Unnötige abdominelle Eingriffe bei Patienten mit hereditärem Angioödem. JDDG: Journal der Deutschen Dermatologischen Gesellschaft 2018; 16(12) doi: 10.1111/ddg.13698_g
|
| 40 |
Nayla Mumneh, Matthew Tick, Marie Borum. Angioedema with severe acute abdominal pain: Think of hereditary angioedema. Clinics and Research in Hepatology and Gastroenterology 2021; 45(4) doi: 10.1016/j.clinre.2021.101702
|
| 41 |
Maria Pedrosa, Alicia Prieto-García, Anna Sala-Cunill, T. Caballero, M. L. Baeza, R. Cabañas, A. Campos, S. Cimbollek, C. Gómez-Traseira, T. González Quevedo, M. Guilarte, J. Jurado-Palomo, T. Lobera, M. C. López-Serrano, C. Marcos, M. Piñero-Saavedra, N. Prior, B. Sáenz de San Pedro, M. Ferrer, J. M. Barceló, A. Daschner, M. Echechipía, M. Garcés, P. Iriarte, I. Jáuregui, M. Lázaro, M. Quiñones, B. Veleiro, O. Villareal. Management of angioedema without urticaria in the emergency department. Annals of Medicine 2014; 46(8) doi: 10.3109/07853890.2014.949300
|
| 42 |
P. Ilkova, Z. Stoyneva, N. Dimitrova. Current aspects in the differential diagnosis of angioneurotic edema. Trakia Journal of Sciences 2021; 19(1) doi: 10.15547/tjs.2021.01.015
|
| 43 |
Batya Engel‐Yeger, Henriette Farkas, Shmuel Kivity, Nóra Veszeli, Kinga Viktória Kőhalmi, Aharon Kessel. Health‐related quality of life among children with hereditary angioedema. Pediatric Allergy and Immunology 2017; 28(4) doi: 10.1111/pai.12712
|
| 44 |
N.T.M.L. Fragnan, A.L.N. Tolentino, G.B. Borba, A.C. Oliveira, J.A. Simões, S.M.U. Palma, R.N. Constantino-Silva, A.S. Grumach. Hereditary angioedema with C1 inhibitor (C1-INH) deficit: the strength of recognition (51 cases). Brazilian Journal of Medical and Biological Research 2018; 51(12) doi: 10.1590/1414-431x20187813
|
| 45 |
A.S. Grumach, S.O.R. Valle, E. Toledo, D. de Moraes Vasconcelos, M.M.S. Villela, E. Mansour, J.A. Pinto, R.A. Campos, A.T. França. Hereditary angioedema: first report of the Brazilian registry and challenges. Journal of the European Academy of Dermatology and Venereology 2013; 27(3) doi: 10.1111/j.1468-3083.2012.04670.x
|