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Items: 1 to 20 of 99

1.

Hereditary angioedema-presenting as recurrent abdominal pain.

Killedar MM, Malani AS.

Indian J Surg. 2011 Dec;73(6):444-6. doi: 10.1007/s12262-011-0255-0. Epub 2011 Apr 12.

2.

Initial presentation of hereditary angioedema as abdominal pain and ascites in puerperium: case report.

Salamon L, Morović-Vergles J.

Acta Dermatovenerol Croat. 2010;18(4):261-3.

PMID:
21251443
3.

[Ascites and suspected acute abdomen in hereditary angioedema due to C1 inhibitor deficiency].

Bork K, Bindewald H, Böckers M, Eckardt V.

Dtsch Med Wochenschr. 1997 Oct 31;122(44):1347-50. German.

PMID:
9410707
4.

[Hereditary angioedema. A rare cause of acute abdominal pain with ascites].

Goti F, Melcher GA, Späth P, Wüthrich B.

Dtsch Med Wochenschr. 1998 Oct 2;123(40):1166-71. German.

PMID:
9793531
5.

Hereditary angioedema: A rare cause of recurrent abdominal pain.

Chen X, Yang YX, Liu YL, Gan HT, Wen ZH.

Pak J Med Sci. 2014 Sep;30(5):1147-9. doi: 10.12669/pjms.305.5524.

6.

Hereditary angioedema: an infrequent cause of abdominal pain with ascites.

Talavera A, Larraona JL, Ramos JL, López T, Maraver A, Arias J, Barrios A.

Am J Gastroenterol. 1995 Mar;90(3):471-4.

PMID:
7872288
7.

[Abdominal pain and ascites as manifestations of hereditary angioneurotic edema].

Mundi Sánchez-Ramade JL, Carmona Soria I, Lavín Castejón I, Trapero Martínez A, Fernández Pérez R, Palacios Pérez A, Salmerón Escobar J.

Gastroenterol Hepatol. 1998 May;21(5):230-2. Spanish.

PMID:
9644877
8.

Acquired C1-esterase inhibitor deficiency: a rare cause of episodic acute abdominal pain and ascites.

Vantroyen B, Knockaert DC.

Eur J Emerg Med. 2003 Sep;10(3):246-9.

PMID:
12972907
9.

Gastrointestinal manifestations, diagnosis, and management of hereditary angioedema.

Jalaj S, Scolapio JS.

J Clin Gastroenterol. 2013 Nov-Dec;47(10):817-23. doi: 10.1097/MCG.0b013e31829e7edf. Review.

PMID:
24141983
10.

[Hereditary deficiency of C1-esterase inhibitor presenting with recurrent abdominal pain].

Steiss JO, Mayser P, Gortner L, Alzen G.

Klin Padiatr. 2002 Jan-Feb;214(1):20-1. German.

PMID:
11823949
11.

[Hereditary angioedema, a rare cause of recurrent abdominal pains. A report of 2 clinical cases and comments of a general nature].

Parisi G, Chiarelli A, Squadrone NP, Galante E.

Minerva Pediatr. 1991 May;43(5):413-7. Italian.

PMID:
1842037
12.

Many faces of angioedema: focus on the diagnosis and management of abdominal manifestations of hereditary angioedema.

Nzeako UC, Longhurst HJ.

Eur J Gastroenterol Hepatol. 2012 Apr;24(4):353-61. doi: 10.1097/MEG.0b013e3283517998. Review.

PMID:
22410711
13.

Ultrasonography in the diagnosis and monitoring of ascites in acute abdominal attacks of hereditary angioneurotic oedema.

Farkas H, Harmat G, Kaposi PN, Karádi I, Fekete B, Füst G, Fáy K, Vass A, Varga L.

Eur J Gastroenterol Hepatol. 2001 Oct;13(10):1225-30.

PMID:
11711780
14.

Hereditary angioedema: a case with ascites yet no symptoms in the family.

Shinzato T, Nakamura H, Kuniyoshi T, Higashionna A, Uehara T, Oshiro J, Uechi H, Shikiya K, Sakugawa H, Kinjo F, et al.

Intern Med. 1992 May;31(5):633-5.

15.

[Hereditary angioedema type II with predominantly abdominal symptoms].

von Schönfeld J, Olbricht T, Breuer N.

Dtsch Med Wochenschr. 1991 Jun 21;116(25):973-6. German.

PMID:
2049985
16.

A case of angioedema due to acquired C1 esterase inhibitor deficiency masquerading as suspected peritonitis: a case report.

Hong SB, Kim CW, Kim JH, Kim JS, Han SB.

J Emerg Med. 2011 Nov;41(5):e99-e101. doi: 10.1016/j.jemermed.2008.04.004. Epub 2008 May 16.

PMID:
18486406
17.

Hereditary angioedema: diagnosis and management.

Chng HH, Boey ML.

Singapore Med J. 1990 Apr;31(2):177-9.

PMID:
2371584
18.

[A case of acquired angioedema].

Garcia-Hejl C, Harnois F, El Jahiri Y, Bigaillon C, Mennecier D, Ceppa F, Thiolet C, Fabre R.

Ann Biol Clin (Paris). 2006 Mar-Apr;64(2):166-9. French.

PMID:
16556528
19.
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