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Page 1
Severe high-molecular-weight kininogen deficiency: clinical characteristics, deficiency-causing KNG1 variants, and estimated prevalence.
Adenaeuer A, Barco S, Trinchero A, Krutmann S, Nazir HF, Ambaglio C, Rocco V, Pancione Y, Tomao L, Ruiz-Sáez A, Echenagucia M, Alesci S, Sollfrank S, Ezigbo ED, Häuser F, Lackner KJ, Lämmle B, Rossmann H. Adenaeuer A, et al. J Thromb Haemost. 2023 Feb;21(2):237-254. doi: 10.1016/j.jtha.2022.11.011. Epub 2022 Dec 22. J Thromb Haemost. 2023. PMID: 36700498 Free article.
Novel GATA1 Variant Causing a Bleeding Phenotype Associated with Combined Platelet α-/δ-Storage Pool Deficiency and Mild Dyserythropoiesis Modified by a SLC4A1 Variant.
Jurk K, Adenaeuer A, Sollfrank S, Groß K, Häuser F, Czwalinna A, Erkel J, Fritsch N, Marandiuc D, Schaller M, Lackner KJ, Rossmann H, Bergmann F. Jurk K, et al. Among authors: adenaeuer a. Cells. 2022 Sep 29;11(19):3071. doi: 10.3390/cells11193071. Cells. 2022. PMID: 36231035 Free PMC article.
Comment on "Worldwide Distribution of PK Deficiency: the Defect Seems Mainly Concentrated in West African Countries and the United States".
Barco S, Adenaeuer A, Trinchero A, Falter T, Lackner KJ, Lämmle B, Rossmann H. Barco S, et al. Among authors: adenaeuer a. Mediterr J Hematol Infect Dis. 2021 Mar 1;13(1):e2021027. doi: 10.4084/MJHID.2021.027. eCollection 2021. Mediterr J Hematol Infect Dis. 2021. PMID: 33747408 Free PMC article. No abstract available.
Severe plasma prekallikrein deficiency: Clinical characteristics, novel KLKB1 mutations, and estimated prevalence.
Barco S, Sollfrank S, Trinchero A, Adenaeuer A, Abolghasemi H, Conti L, Häuser F, Kremer Hovinga JA, Lackner KJ, Loewecke F, Miloni E, Vazifeh Shiran N, Tomao L, Wuillemin WA, Zieger B, Lämmle B, Rossmann H. Barco S, et al. Among authors: adenaeuer a. J Thromb Haemost. 2020 Jul;18(7):1598-1617. doi: 10.1111/jth.14805. Epub 2020 May 15. J Thromb Haemost. 2020. PMID: 32202057 Free article.