I agree that this site is using cookies. You can find further informations
here
.
X
Login
My folder (
0
)
Home
About us
Home About us
Our history
Profile
Press & public relations
Friends
The library in figures
Exhibitions
Projects
Training, internships, careers
Films
Services & Information
Home Services & Information
Lending and interlibrary loans
Returns and renewals
Training and library tours
My Account
Library cards
New to the library?
Download Information
Opening hours
Learning spaces
PC, WLAN, copy, scan and print
Catalogs and collections
Home Catalogs and Collections
Rare books and manuscripts
Digital collections
Subject Areas
Our sites
Home Our sites
Central Library
Law Library (Juridicum)
BB Business and Economics (BB11)
BB Physics and Electrical Engineering
TB Engineering and Social Sciences
TB Economics and Nautical Sciences
TB Music
TB Art & Design
TB Bremerhaven
Contact the library
Home Contact the library
Staff Directory
Open access & publishing
Home Open access & publishing
Reference management: Citavi & RefWorks
Publishing documents
Open Access in Bremen
Show Desktop-Version
Toggle navigation
Adenaeuer, Anke
21
results:
Search for persons
X
Format
Online (21)
Mediatypes
Articles (Online) (7)
OpenAccess-fulltext (14)
Sorted by: Year
Sorted by: Relevance
?
1
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/..
?
2
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/..
?
3
Hereditary Spherocytosis: Can Next-Generation Sequencing of..:
Friederike Häuser
;
Heidi Rossmann
;
Anke Adenaeuer
...
https://www.mdpi.com/1422-0067/24/23/17021. , 2023
Link:
https://doi.org/10.3390/..
?
4
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..
?
5
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..
?
6
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..
?
7
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/..
?
8
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/..
?
9
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/..
?
10
Novel GATA1 Variant Causing a Bleeding Phenotype Associated..:
Kerstin Jurk
;
Anke Adenaeuer
;
Stefanie Sollfrank
...
Cellular Pathology. , 2022
Link:
https://doi.org/10.3390/..
?
11
Second MAFA Variant Causing a Phosphorylation Defect in the..:
Christian Fottner
;
Stefanie Sollfrank
;
Mursal Ghiasi
...
Cancer Therapy. , 2022
Link:
https://doi.org/10.3390/..
?
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
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/..
?
14
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...
?
15
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/..
1-15
