Maternal pregestational or gestational diabetes and childhood wheezing: A population‐based cohort study
Abstract
1. Maurer M, Magerl M, Ansotegui I, et al. The international WAO/ EAACI guideline for the management of hereditary angioedema‐The 2017 revision and update. Allergy. 2018;73:1575‐1596. 2. Dewald G, Bork K. Missense mutations in the coagulation factor XII (Hageman factor) gene in hereditary angioedema with normal C1 inhibitor. Biochem Biophys Res Commun. 2006;343:1286‐1289. 3. Bork K, Wulff K, Meinke P, Wagner N, Hardt J, Witzke G. A novel mutation in the coagulation factor 12 gene in subjects with hereditary angioedema and normal C1‐inhibitor. Clin Immunol. 2011;141:31‐35. 4. Kiss N, Barabás E, Várnai K, et al. Novel duplication in the F12 gene in a patient with recurrent angioedema. Clin Immunol. 2013;149:142‐145. 5. Veronez CL, Moreno AS, Constantino-Silva RN, et al. Hereditary angioedema with normal C1 inhibitor and F12 mutations in 42 Brazilian families. J Allergy Clin Immunol Pract. 2017 Nov 8. pii: S2213-2198 (17)30755-9. https://doi.org/10.1016/j.jaip.2017.09.025. [Epub ahead of print] 6. Bork K, Wulff K, Witzke G, Hardt J. Hereditary angioedema with normal C1‐INH with versus without specific F12 gene mutations. Allergy. 2015;70:1004‐1012. 7. Bork K, Wulff K, Steinmüller-Magin L, et al. Hereditary angioedema with a mutation in the plasminogen gene. Allergy. 2018;73:442‐450. 8. Dewald G. A missense mutation in the plasminogen gene, within the plasminogen kringle 3 domain, in hereditary angioedema with normal C1 inhibitor. Biochem Biophys Res Commun. 2018;498:193‐198. 9.…
How strong is the evidence?
Evidence Hub reads this as a cohort study, done in people. Its evidence level is 3 of 5 (Moderate · trial / cohort / secondary analysis). Trials without a large randomized design, cohorts and secondary analyses give moderate evidence. Reported size: 12 participants or records.
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