Anke Adenaeuer
Mainz, RP 55131, Germany
Last Updated: 09/26/2026
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Found 8 publications
Hereditary Spherocytosis: Can Next-Generation Sequencing of the Five Most Frequently Affected Genes Replace Time-Consuming Functional Investigations?
Journal: International journal of molecular sciences
Published: October 31, 2023
Novel GATA1 Variant Causing a Bleeding Phenotype Associated with Combined Platelet α-/δ-Storage Pool Deficiency and Mild Dyserythropoiesis Modified by a SLC4A1 Variant.
Journal: Cells
Published: September 03, 2022
Severe high-molecular-weight kininogen deficiency: clinical characteristics, deficiency-causing KNG1 variants, and estimated prevalence.
Journal: Journal of thrombosis and haemostasis : JTH
Published: September 01, 2022
Definite diagnosis of plasma prekallikrein deficiency should not be based exclusively on shortening of the aPTT upon prolonged pre-incubation.
Journal: International journal of laboratory hematology
Published: December 15, 2021
Comment on "Worldwide Distribution of PK Deficiency: the Defect Seems Mainly Concentrated in West African Countries and the United States".
Journal: Mediterranean journal of hematology and infectious diseases
Published: February 03, 2021
c.451dupT in KLKB1 is common in Nigerians, confirming a higher prevalence of severe prekallikrein deficiency in Africans compared to Europeans.
Journal: Journal of thrombosis and haemostasis : JTH
Published: August 20, 2020
Severe plasma prekallikrein deficiency: Clinical characteristics, novel KLKB1 mutations, and estimated prevalence.
Journal: Journal of thrombosis and haemostasis : JTH
Published: January 28, 2020
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Last Updated: 09/26/2026