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Häuser, Friederike; Rossmann, Heidi; Adenaeuer, Anke; Shrestha, Annette; Marandiuc, Dana; Paret, Claudia; Faber, Jörg; Lackner, Karl J; Lämmle, Bernhard; Beck, Olaf (2023). Hereditary Spherocytosis: Can Next-Generation Sequencing of the Five Most Frequently Affected Genes Replace Time-Consuming Functional Investigations? International journal of molecular sciences, 24(23) MDPI 10.3390/ijms242317021
Adenaeuer, Anke; Barco, Stefano; Trinchero, Alice; Krutmann, Sarah; Nazir, Hanan Fawzy; Ambaglio, Chiara; Rocco, Vincenzo; Pancione, Ylenia; Tomao, Luigi; Ruiz-Sáez, Arlette; Echenagucia, Marion; Alesci, Sonja; Sollfrank, Stefanie; Ezigbo, Eyiuche D; Häuser, Friederike; Lackner, Karl J; Lämmle, Bernhard; Rossmann, Heidi (2023). Severe high-molecular-weight kininogen deficiency: clinical characteristics, deficiency-causing KNG1 variants, and estimated prevalence. Journal of thrombosis and haemostasis, 21(2), pp. 237-254. Wiley-Blackwell 10.1016/j.jtha.2022.11.011
Adenaeuer, Anke; Barco, Stefano; Trinchero, Alice; Lackner, Karl J; Lämmle, Bernhard; Rossmann, Heidi (2022). Definite diagnosis of plasma prekallikrein deficiency should not be based exclusively on shortening of the aPTT upon prolonged pre-incubation. International journal of laboratory hematology, 44(4), e179-e180. Wiley 10.1111/ijlh.13841
Barco, Stefano; Sollfrank, Stefanie; Trinchero, Alice; Adenaeuer, Anke; Abolghasemi, Hassan; Conti, Laura; Häuser, Friederike; Kremer Hovinga, Johanna A.; Lackner, Karl J; Loewecke, Felicia; Miloni, Erwin; Vazifeh Shiran, Nader; Tomao, Luigi; Wuillemin, Walter A; Zieger, Barbara; Lämmle, Bernhard; Rossmann, Heidi (2020). Severe plasma prekallikrein deficiency: Clinical characteristics, novel KLKB1 mutations, and estimated prevalence. Journal of thrombosis and haemostasis, 18(7), pp. 1598-1617. Wiley-Blackwell 10.1111/jth.14805
