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Stefanie Sollfrank
16
results:
Search for persons
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Online (16)
Mediatypes
Articles (Online) (6)
OpenAccess-fulltext (10)
Sorted by: Relevance
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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
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/..
?
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
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/..
?
5
A non-invasive diagnostic assay for rapid detection and cha..:
Häuser, Friederike
;
Gökce, Seyfullah
;
Werner, Gesa
...
Molecular Genetics and Metabolism. 130 (2020) 1 - p. 27-35 , 2020
Link:
https://doi.org/10.1016/..
?
6
Phenotypic Variability and Risk of Malignancy inSDHC-Linked..:
Bickmann, Julia K.
;
Sollfrank, Stefanie
;
Schad, Arno
...
The Journal of Clinical Endocrinology & Metabolism. 99 (2014) 3 - p. E489-E496 , 2014
Link:
https://doi.org/10.1210/..
?
7
Novel GATA1 Variant Causing a Bleeding Phenotype Associated..:
Kerstin Jurk
;
Anke Adenaeuer
;
Stefanie Sollfrank
...
Cellular Pathology. , 2022
Link:
https://doi.org/10.3390/..
?
8
Second MAFA Variant Causing a Phosphorylation Defect in the..:
Christian Fottner
;
Stefanie Sollfrank
;
Mursal Ghiasi
...
Cancer Therapy. , 2022
Link:
https://doi.org/10.3390/..
?
9
Novel GATA1 Variant Causing a Bleeding Phenotype Associated..:
Kerstin Jurk
;
Anke Adenaeuer
;
Stefanie Sollfrank
...
https://www.mdpi.com/2073-4409/11/19/3071. , 2022
Link:
https://doi.org/10.3390/..
?
10
Second MAFA Variant Causing a Phosphorylation Defect in the..:
Christian Fottner
;
Stefanie Sollfrank
;
Mursal Ghiasi
...
https://www.mdpi.com/2072-6694/14/7/1798. , 2022
Link:
https://doi.org/10.3390/..
?
11
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..
?
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
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...
?
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