223 related articles for article (PubMed ID: 29661499)
1. The relationship between complement levels and disease activity in Japanese family cases of hereditary angioedema with C1-INH deficiency.
Fukunaga A; Tsuchiyama S; Lee K; Washio K; Hashimura C; Horiuchi T; Nishigori C
Allergol Int; 2018 Oct; 67(4):518-520. PubMed ID: 29661499
[No Abstract] [Full Text] [Related]
2. The role of the complement system in hereditary angioedema.
Csuka D; Veszeli N; Varga L; Prohászka Z; Farkas H
Mol Immunol; 2017 Sep; 89():59-68. PubMed ID: 28595743
[TBL] [Abstract][Full Text] [Related]
3. Deletions in SERPING1 Lead to Lower C1 Inhibitor Function: Lower C1 Inhibitor Function Can Predict Disease Severity.
Mete Gökmen N; Gülbahar O; Onay H; Peker Koc Z; Özgül S; Köse T; Gelincik A; Büyüköztürk S; Sin AZ
Int Arch Allergy Immunol; 2019; 178(1):50-59. PubMed ID: 30278448
[TBL] [Abstract][Full Text] [Related]
4. The Role of Complement in Hereditary Angioedema.
Levi M; Cohn DM
Transfus Med Rev; 2019 Oct; 33(4):243-247. PubMed ID: 31676220
[TBL] [Abstract][Full Text] [Related]
5. Clinical and genetic features of hereditary angioedema with and without C1-inhibitor (C1-INH) deficiency in Japan.
Hashimura C; Kiyohara C; Fukushi JI; Hirose T; Ohsawa I; Tahira T; Horiuchi T
Allergy; 2021 Nov; 76(11):3529-3534. PubMed ID: 34343365
[No Abstract] [Full Text] [Related]
6. Baseline level of functional C1-inhibitor correlates with disease severity scores in hereditary angioedema.
Kelemen Z; Moldovan D; Mihály E; Visy B; Széplaki G; Csuka D; Füst G; Farkas H; Varga L
Clin Immunol; 2010 Mar; 134(3):354-8. PubMed ID: 19945350
[TBL] [Abstract][Full Text] [Related]
7. Genetics of Hereditary Angioedema Revisited.
Germenis AE; Speletas M
Clin Rev Allergy Immunol; 2016 Oct; 51(2):170-82. PubMed ID: 27116602
[TBL] [Abstract][Full Text] [Related]
8. A novel C1 inhibitor gene mutation in a family with hereditary angioedema: Use of genetic analysis to facilitate early diagnosis.
Yokoyama K; Horiuchi T; Hashimura C; Yoshida A
Allergol Int; 2020 Jan; 69(1):148-149. PubMed ID: 31409531
[No Abstract] [Full Text] [Related]
9. [Hereditary angioedema biological diagnosis].
Ponard D
Presse Med; 2015 Jan; 44(1):57-64. PubMed ID: 25511654
[TBL] [Abstract][Full Text] [Related]
10. Successful Use of Recombinant Human C1-INH in a Patient with Acquired Angioedema due to C1 Inhibitor Deficiency and an Unusually High Titer of Anti-C1-Inhibitor Autoantibodies.
Jesenak M; Brndiarova M; Banovcin P; Varga L; Farkas H
J Investig Allergol Clin Immunol; 2021 Jun; 31(3):255-256. PubMed ID: 32732186
[No Abstract] [Full Text] [Related]
11. Diagnosis, Course, and Management of Angioedema in Patients With Acquired C1-Inhibitor Deficiency.
Zanichelli A; Azin GM; Wu MA; Suffritti C; Maggioni L; Caccia S; Perego F; Vacchini R; Cicardi M
J Allergy Clin Immunol Pract; 2017; 5(5):1307-1313. PubMed ID: 28284781
[TBL] [Abstract][Full Text] [Related]
12. Targeted next-generation sequencing for the molecular diagnosis of hereditary angioedema due to C1-inhibitor deficiency.
Loules G; Zamanakou M; Parsopoulou F; Vatsiou S; Psarros F; Csuka D; Porebski G; Obtulowicz K; Valerieva A; Staevska M; López-Lera A; López-Trascasa M; Moldovan D; Magerl M; Maurer M; Speletas M; Farkas H; Germenis AE
Gene; 2018 Aug; 667():76-82. PubMed ID: 29753808
[TBL] [Abstract][Full Text] [Related]
13. Hereditary angioedema and chronic urticaria: is there a possible association?
Jorge AS; Dortas SD; Valle SO; França AT
J Investig Allergol Clin Immunol; 2009; 19(4):327-8. PubMed ID: 19639735
[No Abstract] [Full Text] [Related]
14. 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]
15. Hereditary angioedema caused by a novel intronic variant of SERPING1.
López-Martínez R; Martínez-Borra J; Fernández-González P; Coto E; Toyos-González P
Pediatr Allergy Immunol; 2022 Jan; 33(1):e13681. PubMed ID: 34971012
[No Abstract] [Full Text] [Related]
16. The Janus faces of acquired angioedema: C1-inhibitor deficiency, lymphoproliferation and autoimmunity.
Wu MA; Castelli R
Clin Chem Lab Med; 2016 Feb; 54(2):207-14. PubMed ID: 26068904
[TBL] [Abstract][Full Text] [Related]
17. Hereditary and acquired C1-inhibitor-dependent angioedema: from pathophysiology to treatment.
Zeerleder S; Levi M
Ann Med; 2016; 48(4):256-67. PubMed ID: 27018196
[TBL] [Abstract][Full Text] [Related]
18. [Hereditary angioedema].
Kreuz W
Kinderkrankenschwester; 2009 Dec; 28(12):520-1. PubMed ID: 20063658
[No Abstract] [Full Text] [Related]
19. Shortened Activated Partial Thromboplastin Time May Help in Diagnosing Hereditary and Acquired Angioedema.
Bork K; Witzke G
Int Arch Allergy Immunol; 2016; 170(2):101-7. PubMed ID: 27463190
[TBL] [Abstract][Full Text] [Related]
20. A recombinant C1 esterase inhibitor (Ruconest) for hereditary angioedema.
Med Lett Drugs Ther; 2016 Mar; 58(1491):e44-5. PubMed ID: 27027690
[No Abstract] [Full Text] [Related]
[Next] [New Search]