431 related articles for article (PubMed ID: 25277223)
1. Hereditary angioedema in Greece: the first results of the greek hereditary angioedema registry.
Psarros F; Koutsostathis N; Farmaki E; Speletas MG; Germenis AE
Int Arch Allergy Immunol; 2014; 164(4):326-32. PubMed ID: 25277223
[TBL] [Abstract][Full Text] [Related]
2. Comparing acquired angioedema with hereditary angioedema (types I/II): findings from the Icatibant Outcome Survey.
Longhurst HJ; Zanichelli A; Caballero T; Bouillet L; Aberer W; Maurer M; Fain O; Fabien V; Andresen I;
Clin Exp Immunol; 2017 Apr; 188(1):148-153. PubMed ID: 27936514
[TBL] [Abstract][Full Text] [Related]
3. Diagnosis and treatment of hereditary angioedema.
Canonica GW; Rossi O
Panminerva Med; 2012 Sep; 54(3):241-53. PubMed ID: 22801442
[TBL] [Abstract][Full Text] [Related]
4. Icatibant Outcome Survey in Patients with Hereditary Angioedema: Experience in Israel Compared with Other Countries.
Toubi E; Kivity S; Graif Y; Reshef A; Botha J; Andresen I
Isr Med Assoc J; 2018 Apr; 20(4):227-232. PubMed ID: 29629730
[TBL] [Abstract][Full Text] [Related]
5. Misdiagnosis trends in patients with hereditary angioedema from the real-world clinical setting.
Zanichelli A; Longhurst HJ; Maurer M; Bouillet L; Aberer W; Fabien V; Andresen I; Caballero T;
Ann Allergy Asthma Immunol; 2016 Oct; 117(4):394-398. PubMed ID: 27742086
[TBL] [Abstract][Full Text] [Related]
6. Clinical manifestations, diagnosis, and treatment of hereditary angioedema: survey data from 94 physicians in Japan.
Ohsawa I; Honda D; Nagamachi S; Hisada A; Shimamoto M; Inoshita H; Mano S; Tomino Y
Ann Allergy Asthma Immunol; 2015 Jun; 114(6):492-8. PubMed ID: 25872948
[TBL] [Abstract][Full Text] [Related]
7. C1-inhibitor concentrate for individual replacement therapy in patients with severe hereditary angioedema refractory to danazol prophylaxis.
Kreuz W; Martinez-Saguer I; Aygören-Pürsün E; Rusicke E; Heller C; Klingebiel T
Transfusion; 2009 Sep; 49(9):1987-95. PubMed ID: 19497056
[TBL] [Abstract][Full Text] [Related]
8. Is there a need for clinical guidelines in the United States for the diagnosis of hereditary angioedema and the screening of family members of affected patients?
Lunn ML; Santos CB; Craig TJ
Ann Allergy Asthma Immunol; 2010 Mar; 104(3):211-4. PubMed ID: 20377110
[TBL] [Abstract][Full Text] [Related]
9. Parameters of the classical complement pathway predict disease severity in hereditary angioedema.
Csuka D; Füst G; Farkas H; Varga L
Clin Immunol; 2011 Apr; 139(1):85-93. PubMed ID: 21300570
[TBL] [Abstract][Full Text] [Related]
10. Characterization of patients with angioedema without wheals: the importance of F12 gene screening.
Firinu D; Bafunno V; Vecchione G; Barca MP; Manconi PE; Santacroce R; Margaglione M; Del Giacco SR
Clin Immunol; 2015 Apr; 157(2):239-48. PubMed ID: 25744496
[TBL] [Abstract][Full Text] [Related]
11. Hereditary angioedema with normal C1 inhibitor and factor XII mutation: a series of 57 patients from the French National Center of Reference for Angioedema.
Deroux A; Boccon-Gibod I; Fain O; Pralong P; Ollivier Y; Pagnier A; Djenouhat K; Du-Thanh A; Gompel A; Faisant C; Launay D; Bouillet L
Clin Exp Immunol; 2016 Sep; 185(3):332-7. PubMed ID: 27271546
[TBL] [Abstract][Full Text] [Related]
12. Diagnosis and management of hereditary angioedema.
Johnston DT
J Am Osteopath Assoc; 2011 Jan; 111(1):28-36. PubMed ID: 21258014
[TBL] [Abstract][Full Text] [Related]
13. Hereditary angioedema with normal C1-INH with versus without specific F12 gene mutations.
Bork K; Wulff K; Witzke G; Hardt J
Allergy; 2015 Aug; 70(8):1004-12. PubMed ID: 25952149
[TBL] [Abstract][Full Text] [Related]
14. Presentation, diagnosis and treatment of angioedema without wheals: a retrospective analysis of a cohort of 1058 patients.
Mansi M; Zanichelli A; Coerezza A; Suffritti C; Wu MA; Vacchini R; Stieber C; Cichon S; Cicardi M
J Intern Med; 2015 May; 277(5):585-93. PubMed ID: 25196353
[TBL] [Abstract][Full Text] [Related]
15. Health-related quality of life among children with hereditary angioedema.
Engel-Yeger B; Farkas H; Kivity S; Veszeli N; Kőhalmi KV; Kessel A
Pediatr Allergy Immunol; 2017 Jun; 28(4):370-376. PubMed ID: 28258590
[TBL] [Abstract][Full Text] [Related]
16. Comparison of chromogenic and ELISA functional C1 inhibitor tests in diagnosing hereditary angioedema.
Li HH; Busse P; Lumry WR; Frazer-Abel A; Levy H; Steele T; Dayno J; Riedl M
J Allergy Clin Immunol Pract; 2015; 3(2):200-5. PubMed ID: 25609336
[TBL] [Abstract][Full Text] [Related]
17. The diagnosis and treatment of hereditary angioedema patients in Japan: A patient reported outcome survey.
Iwamoto K; Yamamoto B; Ohsawa I; Honda D; Horiuchi T; Tanaka A; Fukunaga A; Maehara J; Yamashita K; Akita T; Hide M
Allergol Int; 2021 Apr; 70(2):235-243. PubMed ID: 33168485
[TBL] [Abstract][Full Text] [Related]
18. Diagnosis and treatment of bradykinin-mediated angioedema: outcomes from an angioedema expert consensus meeting.
Craig TJ; Bernstein JA; Farkas H; Bouillet L; Boccon-Gibod I
Int Arch Allergy Immunol; 2014; 165(2):119-27. PubMed ID: 25401373
[TBL] [Abstract][Full Text] [Related]
19. Coagulation Factor XII Gene Mutation in Brazilian Families with Hereditary Angioedema with Normal C1 Inhibitor.
Moreno AS; Valle SO; Levy S; França AT; Serpa FS; Arcuri HA; Palma MS; Campos WN; Dias MM; Ponard D; Monnier N; Lunardi J; Bork K; Silva WA; Arruda LK
Int Arch Allergy Immunol; 2015; 166(2):114-20. PubMed ID: 25790805
[TBL] [Abstract][Full Text] [Related]
20. Clinical Pattern and Acute and Long-term Management of Hereditary Angioedema Due to C1-Esterase Inhibitor Deficiency.
Gómez-Traseira C; Pérez-Fernández E; López-Serrano MC; García-Ara MC; Pedrosa M; López-Trascasa M; Caballero T
J Investig Allergol Clin Immunol; 2015; 25(5):358-64. PubMed ID: 26727765
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
