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Adenaeuer, Anke
21
results:
Search for persons
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Format
Online (21)
Mediatypes
Articles (Online) (7)
OpenAccess-fulltext (14)
Sorted by: Relevance
Sorted by: Year
?
1
Severe high-molecular-weight kininogen deficiency: clinical..:
Adenaeuer, Anke
;
Barco, Stefano
;
Trinchero, Alice
...
Journal of Thrombosis and Haemostasis. 21 (2023) 2 - p. 237-254 , 2023
Link:
https://doi.org/10.1016/..
?
2
Hereditary Spherocytosis: Can Next-Generation Sequencing of..:
Häuser, Friederike
;
Rossmann, Heidi
;
Adenaeuer, Anke
...
International Journal of Molecular Sciences. 24 (2023) 23 - p. 17021 , 2023
Link:
https://doi.org/10.3390/..
?
3
Novel GATA1 Variant Causing a Bleeding Phenotype Associated..:
Jurk, Kerstin
;
Adenaeuer, Anke
;
Sollfrank, Stefanie
...
Cells. 11 (2022) 19 - p. 3071 , 2022
Link:
https://doi.org/10.3390/..
?
4
Definite diagnosis of plasma prekallikrein deficiency shoul..:
Adenaeuer, Anke
;
Barco, Stefano
;
Trinchero, Alice
...
International Journal of Laboratory Hematology. 44 (2022) 4 - p. , 2022
Link:
https://doi.org/10.1111/..
?
5
Second MAFA Variant Causing a Phosphorylation Defect in the..:
Fottner, Christian
;
Sollfrank, Stefanie
;
Ghiasi, Mursal
...
Cancers. 14 (2022) 7 - p. 1798 , 2022
Link:
https://doi.org/10.3390/..
?
6
c.451dupT in KLKB1 is common in Nigerians, confirming a hig..:
Adenaeuer, Anke
;
Ezigbo, Eyiuche D.
;
Fawzy Nazir, Hanan
...
Journal of Thrombosis and Haemostasis. 19 (2021) 1 - p. 147-152 , 2021
Link:
https://doi.org/10.1111/..
?
7
Severe plasma prekallikrein deficiency: Clinical characteri..:
Barco, Stefano
;
Sollfrank, Stefanie
;
Trinchero, Alice
...
Journal of Thrombosis and Haemostasis. 18 (2020) 7 - p. 1598-1617 , 2020
Link:
https://doi.org/10.1111/..
?
8
Severe high-molecular-weight kininogen deficiency: clinical..:
Adenaeuer, Anke
;
Barco, Stefano
;
Trinchero, Alice
...
https://boris.unibe.ch/177969/. , 2023
Link:
https://boris.unibe.ch/1..
?
9
Hereditary spherocytosis : can next-generation sequencing o..:
Häuser, Friederike
;
Rossmann, Heidi
;
Adenaeuer, Anke
...
http://doi.org/10.25358/openscience-9760. , 2023
Link:
https://openscience.ub.u..
?
10
Hereditary Spherocytosis: Can Next-Generation Sequencing of..:
Häuser, Friederike
;
Rossmann, Heidi
;
Adenaeuer, Anke
...
https://boris.unibe.ch/190092/. , 2023
Link:
https://boris.unibe.ch/1..
?
11
Second MAFA Variant Causing a Phosphorylation Defect in the..:
Fottner, Christian
;
Sollfrank, Stefanie
;
Ghiasi, Mursal
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8997416/. , 2022
Link:
http://www.ncbi.nlm.nih...
?
12
Second MAFA variant causing a phosphorylation defect in the..:
Fottner, Christian
;
Sollfrank, Stefanie
;
Ghiasi, Mursal
...
http://doi.org/10.25358/openscience-7026. , 2022
Link:
https://openscience.ub.u..
?
13
c.451dupT in KLKB1 is common in Nigerians, confirming a hig..:
Adenaeuer, Anke
;
Ezigbo, D. Eyiuche
;
Nazir, Hanan Fawzy
...
http://doi.org/10.25358/openscience-6169. , 2021
Link:
https://openscience.ub.u..
?
14
Severe plasma prekallikrein deficiency: Clinical characteri..:
Barco, Stefano
;
Sollfrank, Stefanie
;
Trinchero, Alice
...
https://boris.unibe.ch/149801/. , 2020
Link:
https://boris.unibe.ch/1..
?
15
Severe plasma prekallikrein deficiency : clinical character..:
Barco, Stefano
;
Sollfrank, Stefanie
;
Trinchero, Alice
...
http://doi.org/10.25358/openscience-6292. , 2020
Link:
https://openscience.ub.u..
1-15
