Publications

Author

Title

Year sorteringsordning

Fulltext

Liljeholm, Maria
Vikberg, Ann-Louise
Golovleva, Irina; et al.

Congenital Dyserythropoietic Anemia Type III and Primary Hemochromatosis; Coexistence of Mutations in KIF23 and HFE.
Journal of Hematology and Blood Disorders, 1(2)

2016

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Liljeholm, Maria

Congenital Dyserythropoietic Anemia type III (CDA III): diagnostics, genetics and morbidity

2016

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Liljeholm, Maria
Vikberg, Ann-Louise
Golovleva, Irina; et al.

Congenital dyserythropoietic anemia type III and primary hemochromatosis; coexistence of mutations in KIF23 and HFE
Haematologica, 100: 594-594

2015

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Liljeholm, Maria
Grönlund, Elisabeth
Golovleva, Irina; et al.

Erythrocyte Flow Cytometric Analysis in Congenital Dyserythropoietic Anemia Type III-Evaluation of Eosin-5´-Maleimide, CD55, and CD59
Journal of Blood Disorders & Transfusion, 121(23): 4791-4799

2013

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Liljeholm, Maria
Irvine, Andrew F
Vikberg, Ann-Louise; et al.

Congenital dyserythropoietic anemia type III (CDA III) is caused by a mutation in kinesin family member, KIF23.
Blood

2013

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Abelsson, J
Merup, M
Birgegård, G; et al.

The outcome of allo-HSCT for 92 patients with myelofibrosis in the Nordic countries.
Bone Marrow Transplantation, 47(3): 380-386

2012

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Lazarevic, Vladimir Lj
Liljeholm, Maria
Forsberg, Karin; et al.

Fludarabine, cyclophosphamide and rituximab (FCR) induced pulmonary hypertension in Waldenstrom macroglobulinemia.
Leukemia & lymphoma, 49(6): 1209-1211

2008

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