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- 2022
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Mark
Targeting elevated heme levels to treat a mouse model for Diamond-Blackfan Anemia
(
- Contribution to journal › Article
- 2018
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Mark
Establishing a regional paediatric registry improved the overview and detection of side effects in children on anticoagulants
(
- Contribution to journal › Article
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Mark
Constitutional SAMD9L mutations cause familial myelodysplastic syndrome and transient monosomy 7
(
- Contribution to journal › Article
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Mark
Thromboembolism in acute lymphoblastic leukemia : Results of nopho all2008 protocol treatment in patients aged 1 to 45 years
(
- Contribution to journal › Article
- 2017
-
Mark
Ataxia-pancytopenia syndrome with SAMD9L mutations
(
- Contribution to journal › Article
-
Mark
Gain-of-function SAMD9L mutations cause a syndrome of cytopenia, immunodeficiency, MDS and neurological symptoms
(
- Contribution to journal › Article
- 2016
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Mark
Prospective study of thromboembolism in 1038 children with acute lymphoblastic leukemia - a Nordic Society of Pediatric Hematology and Oncology (NOPHO) study.
(
- Contribution to journal › Article
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Mark
A novel 33-Gene targeted resequencing panel provides accurate, clinical-grade diagnosis and improves patient management for rare inherited anaemias
(
- Contribution to journal › Article
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Mark
Breath-holding spells occur disproportionately more often in children with transient erythroblastopenia
(
- Contribution to journal › Article
- 2015
-
Mark
Various regimens for prophylactic treatment of patients with haemophilia
(
- Contribution to journal › Scientific review