214 related articles for article (PubMed ID: 32351099)
1. Characteristics of patients with C1 esterase inhibitor deficiency: a single center study.
Soyak Aytekin E; Çağdaş D; Tan C; Tezcan İ
Eur Ann Allergy Clin Immunol; 2021 Mar; 53(2):75-79. PubMed ID: 32351099
[TBL] [Abstract][Full Text] [Related]
2. Hereditary angioedema due to C1-inhibitor deficiency in Macedonia: clinical characteristics, novel SERPING1 mutations and genetic factors modifying the clinical phenotype.
Grivčeva-Panovska V; Košnik M; Korošec P; Andrejević S; Karadža-Lapić L; Rijavec M
Ann Med; 2018 May; 50(3):269-276. PubMed ID: 29513108
[TBL] [Abstract][Full Text] [Related]
3. Clinical Evaluation of Pediatric Patients with Hereditary Angioedema.
Kırmızıtaş Aydoğdu A; Ürel Demir G
Tohoku J Exp Med; 2024 Jan; 262(1):23-27. PubMed ID: 37793880
[TBL] [Abstract][Full Text] [Related]
4. A Nationwide Study of Norwegian Patients with Hereditary Angioedema with C1 Inhibitor Deficiency Identified Six Novel Mutations in SERPING1.
Johnsrud I; Kulseth MA; Rødningen OK; Landrø L; Helsing P; Waage Nielsen E; Heimdal K
PLoS One; 2015; 10(7):e0131637. PubMed ID: 26154504
[TBL] [Abstract][Full Text] [Related]
5. Frequent life-threatening laryngeal attacks in two Croatian families with hereditary angioedema due to C1 inhibitor deficiency harbouring a novel frameshift mutation in SERPING1.
Karadža-Lapić L; Korošec P; Šilar M; Košnik M; Cikojević D; Lozić B; Rijavec M
Ann Med; 2016 Nov; 48(7):485-491. PubMed ID: 27187751
[TBL] [Abstract][Full Text] [Related]
6. Unnecessary Abdominal Surgeries in Attacks of Hereditary Angioedema with Normal C1 Inhibitor.
Gutierrez M; Veronez CL; Rodrigues Valle SO; Gonçalves RF; Ferriani MPL; Moreno AS; Arruda LK; Aun MV; Giavina-Bianchi P; Alonso MLO; Pesquero JB; Grumach AS
Clin Rev Allergy Immunol; 2021 Aug; 61(1):60-65. PubMed ID: 33755867
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Repeated attacks of hereditary angioedema in pediatric female.
Abass MK; Dabosy A; Walid Khawaja K; Fischer PR
Paediatr Int Child Health; 2024 May; 44(1):39-41. PubMed ID: 38404177
[TBL] [Abstract][Full Text] [Related]
9. Molecular diagnosis and management of hereditary angioedema in a Greek family.
Papadopoulou-Alataki E; Foerster T; Antari V; Pavlitou-Tsiontsi A; Varlamis G
Int Arch Allergy Immunol; 2008; 147(2):166-70. PubMed ID: 18535392
[TBL] [Abstract][Full Text] [Related]
10. A novel prophylaxis with C1-inhibitor concentrate in hereditary angioedema during erythema marginatum.
Kőhalmi KV; Veszeli N; Cervenak L; Varga L; Farkas H
Immunol Lett; 2017 Sep; 189():90-93. PubMed ID: 28577900
[TBL] [Abstract][Full Text] [Related]
11. A missense mutation in the plasminogen gene, within the plasminogen kringle 3 domain, in hereditary angioedema with normal C1 inhibitor.
Dewald G
Biochem Biophys Res Commun; 2018 Mar; 498(1):193-198. PubMed ID: 29548426
[TBL] [Abstract][Full Text] [Related]
12. Evidence for a dominant-negative effect of a missense mutation in the SERPING1 gene responsible for hereditary angioedema type I.
Yasuno S; Ansai O; Hayashi R; Nakamura S; Shimomura Y
J Dermatol; 2021 Aug; 48(8):1243-1249. PubMed ID: 33914953
[TBL] [Abstract][Full Text] [Related]
13. A Missense Mutation of the Plasminogen Gene in a Japanese Family with Hereditary Angioedema with Normal C1 Inhibitor: Third Family Survey in Asia.
Yakushiji H; Yamagami K; Hashimura C; Iwasaki H; Horiuchi T
Intern Med; 2023 Jul; 62(13):2005-2008. PubMed ID: 36418094
[TBL] [Abstract][Full Text] [Related]
14. Definition and classification of hereditary angioedema.
Proper SP; Lavery WJ; Bernstein JA
Allergy Asthma Proc; 2020 Nov; 41(Suppl 1):S03-S07. PubMed ID: 33109317
[TBL] [Abstract][Full Text] [Related]
15. The importance of recognizing and managing a rare form of angioedema: hereditary angioedema due to C1-inhibitor deficiency.
Jacobs J; Neeno T
Postgrad Med; 2021 Aug; 133(6):639-650. PubMed ID: 33993830
[TBL] [Abstract][Full Text] [Related]
16. Long-Term Efficacy of Subcutaneous C1 Inhibitor in Pediatric Patients with Hereditary Angioedema.
Levy D; Caballero T; Hussain I; Reshef A; Anderson J; Baker J; Schwartz LB; Cicardi M; Prusty S; Feuersenger H; Pragst I; Manning ME
Pediatr Allergy Immunol Pulmonol; 2020 Sep; 33(3):136-141. PubMed ID: 32953229
[No Abstract] [Full Text] [Related]
17. Novel SERPING1 gene mutations and clinical experience of type 1 hereditary angioedema from North India.
Jindal AK; Rawat A; Kaur A; Sharma D; Suri D; Gupta A; Garg R; Dogra S; Saikia B; Minz RW; Singh S
Pediatr Allergy Immunol; 2021 Apr; 32(3):599-611. PubMed ID: 33220126
[TBL] [Abstract][Full Text] [Related]
18. Hereditary angioedema nationwide study in Slovenia reveals four novel mutations in SERPING1 gene.
Rijavec M; Korošec P; Šilar M; Zidarn M; Miljković J; Košnik M
PLoS One; 2013; 8(2):e56712. PubMed ID: 23437219
[TBL] [Abstract][Full Text] [Related]
19. Outcomes of long term treatments of type I hereditary angioedema in a Turkish family.
Akoglu G; Kesim B; Yildiz G; Metin A
An Bras Dermatol; 2017; 92(5):655-660. PubMed ID: 29166502
[TBL] [Abstract][Full Text] [Related]
20. Hereditary Angioedema Due to C1 Inhibitor Deficiency in Serbia: Two Novel Mutations and Evidence of Genotype-Phenotype Association.
Andrejević S; Korošec P; Šilar M; Košnik M; Mijanović R; Bonači-Nikolić B; Rijavec M
PLoS One; 2015; 10(11):e0142174. PubMed ID: 26535898
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
