194 related articles for article (PubMed ID: 26812872)
1. New mutations in SERPING1 gene of Brazilian patients with hereditary angioedema.
Cagini N; Veronez CL; Constantino-Silva RN; Buzolin M; Martin RP; Grumach AS; Velloso LA; Mansour E; Pesquero JB
Biol Chem; 2016 Apr; 397(4):337-44. PubMed ID: 26812872
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. Identification of a novel and recurrent mutation in the SERPING1 gene in patients with hereditary angioedema.
Firinu D; Colomba P; Manconi PE; Barca MP; Fenu L; Piseddu G; Zizzo C; Del Giacco SR; Duro G
Clin Immunol; 2013 May; 147(2):129-32. PubMed ID: 23583915
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Analysis of SERPING1 expression on hereditary angioedema patients: quantitative analysis of full-length and exon 3 splicing variants.
de la Cruz RM; López-Lera A; López-Trascasa M
Immunol Lett; 2012 Jan; 141(2):158-64. PubMed ID: 22001489
[TBL] [Abstract][Full Text] [Related]
8. Mutational spectrum of the SERPING1 gene in Swiss patients with hereditary angioedema.
Steiner UC; Keller M; Schmid P; Cichon S; Wuillemin WA
Clin Exp Immunol; 2017 Jun; 188(3):430-436. PubMed ID: 28194776
[TBL] [Abstract][Full Text] [Related]
9. A novel deep intronic SERPING1 variant as a cause of hereditary angioedema due to C1-inhibitor deficiency.
Vatsiou S; Zamanakou M; Loules G; Psarros F; Parsopoulou F; Csuka D; Valerieva A; Staevska M; Porebski G; Obtulowicz K; Magerl M; Maurer M; Speletas M; Farkas H; Germenis AE
Allergol Int; 2020 Jul; 69(3):443-449. PubMed ID: 31959500
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Hereditary angioedema in a Jordanian family with a novel missense mutation in the C1-inhibitor N-terminal domain.
Jaradat SA; Caccia S; Rawashdeh R; Melhem M; Al-Hawamdeh A; Carzaniga T; Haddad H
Mol Immunol; 2016 Mar; 71():123-130. PubMed ID: 26895475
[TBL] [Abstract][Full Text] [Related]
12. Mutational spectrum of the c1 inhibitor gene in a cohort of Italian patients with hereditary angioedema: description of nine novel mutations.
Bafunno V; Bova M; Loffredo S; Divella C; Petraroli A; Marone G; Montinaro V; Margaglione M; Triggiani M
Ann Hum Genet; 2014 Mar; 78(2):73-82. PubMed ID: 24456027
[TBL] [Abstract][Full Text] [Related]
13. A single nucleotide deletion at the C1 inhibitor gene as the cause of hereditary angioedema: insights from a Brazilian family.
Ferraro MF; Moreno AS; Castelli EC; Donadi EA; Palma MS; Arcuri HA; Lange AP; Bork K; Sarti W; Arruda LK
Allergy; 2011 Oct; 66(10):1384-90. PubMed ID: 21623829
[TBL] [Abstract][Full Text] [Related]
14. Hereditary angioedema in Greek families caused by novel and recurrent mutations.
Speletas M; Boukas K; Papadopoulou-Alataki E; Tsitsami E; Germenis AE
Hum Immunol; 2009 Nov; 70(11):925-9. PubMed ID: 19706314
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Gene mapping strategy for Alu elements rearrangements: Detection of new large deletions in the SERPING1 gene causing hereditary angioedema in Brazilian families.
Nicolicht P; Faria DOS; Martins-Silva L; Maia LSM; Moreno AS; Arruda LK; Motta AA; Grumach AS; Pesquero JB
Gene; 2019 Feb; 685():179-185. PubMed ID: 30389558
[TBL] [Abstract][Full Text] [Related]
17. Hereditary Angioedema with Normal C1 Inhibitor and F12 Mutations in 42 Brazilian Families.
Veronez CL; Moreno AS; Constantino-Silva RN; Maia LSM; Ferriani MPL; Castro FFM; Valle SR; Nakamura VK; Cagini N; Gonçalves RF; Mansour E; Serpa FS; Coelho Dias GA; Piccirillo MA; Toledo E; de Souza Bernardes M; Cichon S; Stieber C; Arruda LK; Pesquero JB; Grumach AS
J Allergy Clin Immunol Pract; 2018; 6(4):1209-1216.e8. PubMed ID: 29128335
[TBL] [Abstract][Full Text] [Related]
18. Identification and characterization of a novel splice site mutation in the SERPING1 gene in a family with hereditary angioedema.
Colobran R; Lois S; de la Cruz X; Pujol-Borrell R; Hernández-González M; Guilarte M
Clin Immunol; 2014 Feb; 150(2):143-8. PubMed ID: 24412907
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]
