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- 2021
-
Mark
Clinical characterization and identification of rare genetic variants in atypical hemolytic uremic syndrome : a Swedish retrospective observational study
Åkesson, Alexander LU ; Martin, Myriam LU ; Blom, Anna M LU
; Rossing, Maria
; Gabrielaite, Migle
; Zetterberg, Eva
LU
and Klintman, Jenny
LU
(2021)
In Therapeutic Apheresis and Dialysis
25(6).
p.988-1000
- Contribution to journal › Article
-
Mark
Genomic and phenotypic evolution of achromobacter xylosoxidans during chronic airway infections of patients with cystic fibrosis
Hossein Khademi, S. M. LU ; Gabrielaite, Migle ; Paulsson, Magnus LU
; Knulst, Mattis
; Touriki, Eleni
; Marvig, Rasmus L.
and Pahlman, Lisa I.
LU
(2021)
In mSystems
6(3).
- Contribution to journal › Article
-
Mark
The Copenhagen founder variant GP1BA c.58T>G is the most frequent cause of inherited thrombocytopenia in Denmark
- Contribution to journal › Article
- 2020
-
Mark
Genetic screening of children with suspected inherited bleeding disorders
Andersson, Nadine LU ; Rossing, Maria ; Fager Ferrari, Marcus LU
; Gabrielaite, Migle
; Leinøe, Eva
; Ljung, Rolf
LU
; Mårtensson, Annika
LU
; Norström, Eva
LU
and Zetterberg, Eva
LU
(2020)
In Haemophilia
26(2).
p.314-324
- Contribution to journal › Article
- 2019
-
Mark
Outcome of an enhanced diagnostic pipeline for patients suspected of inherited thrombocytopenia
- Contribution to journal › Letter