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Quoted phrase not found in phrase index: "Hereditary angioedema with normal C1inh not related to F12 or PLG variant"
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COVID-19 and hereditary angioedema: Incidence, outcomes, and mechanistic implications.
Veronez CL, Christiansen SC, Smith TD, Riedl MA, Zuraw BL. Veronez CL, et al. Allergy Asthma Proc. 2021 Nov 1;42(6):506-514. doi: 10.2500/aap.2021.42.210083. Allergy Asthma Proc. 2021. PMID: 34871158 Free PMC article.
Background: Patients with hereditary angioedema (HAE) have been postulated to be at increased risk for coronavirus disease 2019 (COVID-19) infection due to inherent dysregulation of the plasma kallikrein-kinin system. ...The participants included subjects with HAE w …
Background: Patients with hereditary angioedema (HAE) have been postulated to be at increased risk for coronavirus disease 201 …
The role of the complement system in hereditary angioedema.
Csuka D, Veszeli N, Varga L, Prohászka Z, Farkas H. Csuka D, et al. Mol Immunol. 2017 Sep;89:59-68. doi: 10.1016/j.molimm.2017.05.020. Epub 2017 Jun 7. Mol Immunol. 2017. PMID: 28595743 Review.
Hereditary angioedema (HAE) is a rare, but potentially life-threatening disorder, characterized by acute, recurring, and self-limiting edematous episodes of the face, extremities, trunk, genitals, upper airways, or the gastrointestinal tract. HAE may be caused by th …
Hereditary angioedema (HAE) is a rare, but potentially life-threatening disorder, characterized by acute, recurring, and self- …
"Nuts and Bolts" of Laboratory Evaluation of Angioedema.
Farkas H, Veszeli N, Kajdácsi E, Cervenak L, Varga L. Farkas H, et al. Clin Rev Allergy Immunol. 2016 Oct;51(2):140-51. doi: 10.1007/s12016-016-8539-6. Clin Rev Allergy Immunol. 2016. PMID: 27142368 Review.
Hereditary angioedema with C1-inhibitor (C1-INH) deficiency type I can be diagnosed by the low C1-INH function and concentration, whereas in type II, C1-INH function is low, but its concentration is normal or even elevated. ...Diagnostic metrics are not avail …
Hereditary angioedema with C1-inhibitor (C1-INH) deficiency type I can be diagnosed by the low C1-INH function and concentrati …
Hereditary angioedema with normal C1-INH with versus without specific F12 gene mutations.
Bork K, Wulff K, Witzke G, Hardt J. Bork K, et al. Allergy. 2015 Aug;70(8):1004-12. doi: 10.1111/all.12648. Epub 2015 May 22. Allergy. 2015. PMID: 25952149
BACKGROUND: Hereditary angioedema with normal C1-INH may be linked to specific mutations in the coagulation factor 12 (FXII) gene (HAE-FXII) or mutations in genes that are still unknown (HAE-unknown). ...In families with HAE-FXII, the number of female offspri …
BACKGROUND: Hereditary angioedema with normal C1-INH may be linked to specific mutations in the coagulation factor 12 ( …
HAE update: special considerations in the female patient with hereditary angioedema.
Geng B, Riedl MA. Geng B, et al. Allergy Asthma Proc. 2013 Jan-Feb;34(1):13-8. doi: 10.2500/aap.2013.34.3635. Allergy Asthma Proc. 2013. PMID: 23406930 Review.
This review on hereditary angioedema (HAE) focuses on special topics regarding HAE in female patients. ...Finally, this review will provide an overview of the more recently characterized HAE with normal C1-INH (HAE type III) that predominantly affects women a …
This review on hereditary angioedema (HAE) focuses on special topics regarding HAE in female patients. ...Finally, this review …
Population pharmacokinetics of recombinant human C1 esterase inhibitor in children with hereditary angioedema.
Hayes S, Farrell C, Relan A, Anderson J. Hayes S, et al. Ann Allergy Asthma Immunol. 2021 Jun;126(6):707-712. doi: 10.1016/j.anai.2021.02.010. Epub 2021 Feb 17. Ann Allergy Asthma Immunol. 2021. PMID: 33609769 Free article. Clinical Trial.
BACKGROUND: Recombinant human C1 esterase inhibitor (rhC1-INH) is indicated in the United States for the treatment of acute hereditary angioedema (HAE) attacks in adolescents and adults; it is also indicated in Europe for children aged 2 years and older. ...Simulati …
BACKGROUND: Recombinant human C1 esterase inhibitor (rhC1-INH) is indicated in the United States for the treatment of acute hereditary …
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. Zanichelli A, et al. J Allergy Clin Immunol Pract. 2017 Sep-Oct;5(5):1307-1313. doi: 10.1016/j.jaip.2016.12.032. Epub 2017 Mar 9. J Allergy Clin Immunol Pract. 2017. PMID: 28284781
OBJECTIVE: To report data on patients with C1-INH-AAE followed at Angioedema Center, Milan (from 1976 to 2015). METHODS: Diagnostic criteria included history of recurrent angioedema without wheals; decreased C1-INH antigen levels and/or functional activity of C1-INH …
OBJECTIVE: To report data on patients with C1-INH-AAE followed at Angioedema Center, Milan (from 1976 to 2015). METHODS: Diagnostic c …
How Does Pregnancy and Type of Delivery Affect the Clinical Course of Hereditary Angioedema?
Eyice Karabacak D, Can A, Demir S, Yegit OO, Colakoglu B, Buyukozturk S, Gelincik AA. Eyice Karabacak D, et al. Int Arch Allergy Immunol. 2023;184(12):1216-1224. doi: 10.1159/000531074. Epub 2023 Sep 6. Int Arch Allergy Immunol. 2023. PMID: 37673053 Free article.
INTRODUCTION: Knowledge on the clinical course of hereditary angioedema (HAE) during pregnancy, delivery, and breastfeeding is very limited. ...Lowest numbers of attacks were found in patients who did not receive anesthesia during NVD (p = 0.001). CONCLUSION: …
INTRODUCTION: Knowledge on the clinical course of hereditary angioedema (HAE) during pregnancy, delivery, and breastfee …
Applying whole-genome sequencing in relation to phenotype and outcomes in siblings with cystic fibrosis.
Wilk MA, Braun AT, Farrell PM, Laxova A, Brown DM, Holt JM, Birch CL, Sosonkina N, Wilk BM, Worthey EA. Wilk MA, et al. Cold Spring Harb Mol Case Stud. 2020 Feb 3;6(1):a004531. doi: 10.1101/mcs.a004531. Print 2020 Feb. Cold Spring Harb Mol Case Stud. 2020. PMID: 32014855 Free PMC article.
From a cohort of patients included in the Wisconsin randomized clinical trial (RCT) of newborn screening (NBS) for CF, we identified two brothers who showed discordant lung disease courses as children, with one milder and the other more severe than average, and a third, el …
From a cohort of patients included in the Wisconsin randomized clinical trial (RCT) of newborn screening (NBS) for CF, we identified two bro …
The crux of C1-INH testing in everyday lab work.
Schöffl C, Haas A, Herrmann M, Aberer W. Schöffl C, et al. J Immunol Methods. 2021 Oct;497:113109. doi: 10.1016/j.jim.2021.113109. Epub 2021 Jul 29. J Immunol Methods. 2021. PMID: 34331949 Free article.
In clinical practice, we encounter individuals with pathological values which then cannot be proved true, and HAE patients in whom the values were wrongly found to be normal under non-optimum conditions. We aimed to test realistic real-life sample processing conditions for …
In clinical practice, we encounter individuals with pathological values which then cannot be proved true, and HAE patients in whom the value …
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