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SAMD9 and SAMD9L in inherited predisposition to ataxia, pancytopenia, and myeloid malignancies

Leukemia, 2018-05, Vol.32 (5), p.1106-1115

2018

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Development of the Parent-to-Infant Bonding Scale: Validation in Swedish Mothers and Fathers in Community and Clinical Contexts

Child psychiatry and human development, 2024-05

2024

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Constitutional SAMD9L mutations cause familial myelodysplastic syndrome and transient monosomy 7

Haematologica (Roma), 2018-03, Vol.103 (3), p.427

2018

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A novel 33‐Gene targeted resequencing panel provides accurate, clinical‐grade diagnosis and improves patient management for rare inherited anaemias

British journal of haematology, 2016-10, Vol.175 (2), p.318-330

2016

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Twenty years' experience of immune thrombocytopenia and intracranial haemorrhage in the Nordic countries—A NOPHO study

Acta Paediatrica, 2023-05, Vol.112 (5), p.1097-1100

2023

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Parenting stress and its correlates in an infant mental health unit: a cross-sectional study

Nordic journal of psychiatry, 2020-01, Vol.74 (1), p.30-39

2020

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An Autoinflammatory Disease with Deficiency of the Interleukin-1–Receptor Antagonist

The New England journal of medicine, 2009-06, Vol.360 (23), p.2426-2437

2009

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Targeting elevated heme levels to treat a mouse model for Diamond-Blackfan Anemia

Experimental hematology, 2022-01, Vol.105, p.50-61

2022

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Recombinant versus plasma-derived factor VIII products and the development of inhibitors in previously untreated patients with severe hemophilia A: the CANAL cohort study

Blood, 2007-06, Vol.109 (11), p.4693-4697

2007

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Various regimens for prophylactic treatment of patients with haemophilia

European journal of haematology, 2015-02, Vol.94 (s77), p.11-16

2015

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Establishing a regional paediatric registry improved the overview and detection of side effects in children on anticoagulants

Acta Paediatrica, 2018-01, Vol.107 (1), p.166-167

2018

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Duration and morbidity of chronic immune thrombocytopenic purpura in children: five-year follow-up of a Nordic cohort

Acta Paediatrica, 2012-07, Vol.101 (7), p.761-766

2012

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Lupus anticoagulants in two children—bleeding due to nonphospholipid-dependent antiprothrombin antibodies

European journal of pediatrics, 2012-09, Vol.171 (9), p.1383-1387

2012

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Breath-holding spells occur disproportionately more often in children with transient erythroblastopenia

Acta Paediatrica, 2016-09, Vol.105 (9), p.1088-1093

2016

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Plastic surgical treatment of purpura fulminans: Long-term follow-up of two patients

Journal of plastic surgery and hand surgery, 2013-04, Vol.47 (2), p.147-151

2013

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Cerebral sinus venous thromboses in children with acute lymphoblastic leukaemia – a multicentre study from the Nordic Society of Paediatric Haematology and Oncology

British journal of haematology, 2015-02, Vol.168 (4), p.547-552

2015

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Prospective study of thromboembolism in 1038 children with acute lymphoblastic leukemia: a Nordic Society of Pediatric Hematology and Oncology (NOPHO) study

Journal of thrombosis and haemostasis, 2016-03, Vol.14 (3), p.485-494

2016

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Studies of chronic ITP in children and adolescents

Pediatric blood & cancer, 2006-10, Vol.47 (S5), p.660-661

2006

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A novel 33-Gene targeted resequencing panel provides accurate, clinical-grade diagnosis and improves patient management for rare inherited anaemias

British journal of haematology, 2016-10, Vol.175 (2), p.318-330

2016

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Deficiency of Interleukin-1 Receptor Antagonist (DIRA): Report of the First Indian Patient and a Novel Deletion Affecting IL1RN

Journal of clinical immunology, 2017-07, Vol.37 (5), p.445-451

2017

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Childhood idiopathic thrombocytopenic purpura in the Nordic countries : Epidemiology and predictors of chronic disease

Acta pædiatrica (Oslo), 2005-02, Vol.94 (2), p.178-184

2005

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Prenatal diagnosis of haemophilia in Sweden now more commonly used for psychological preparation than termination of pregnancy

Haemophilia : the official journal of the World Federation of Hemophilia, 2014-11, Vol.20 (6), p.854-858

2014

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SAMD9 and SAMD9L in inherited predisposition to ataxia, pancytopenia, and myeloid malignancies

Gain-of-function SAMD9L mutations cause a syndrome of cytopenia, immunodeficiency, MDS, and neurological symptoms

Development of the Parent-to-Infant Bonding Scale: Validation in Swedish Mothers and Fathers in Community and Clinical Contexts

Constitutional SAMD9L mutations cause familial myelodysplastic syndrome and transient monosomy 7

A novel 33‐Gene targeted resequencing panel provides accurate, clinical‐grade diagnosis and improves patient management for rare inherited anaemias

Twenty years' experience of immune thrombocytopenia and intracranial haemorrhage in the Nordic countries—A NOPHO study

Parenting stress and its correlates in an infant mental health unit: a cross-sectional study

An Autoinflammatory Disease with Deficiency of the Interleukin-1–Receptor Antagonist

Targeting elevated heme levels to treat a mouse model for Diamond-Blackfan Anemia

Recombinant versus plasma-derived factor VIII products and the development of inhibitors in previously untreated patients with severe hemophilia A: the CANAL cohort study

Various regimens for prophylactic treatment of patients with haemophilia

Genome-Wide Association Meta-Analysis of Single-Nucleotide Polymorphisms and Symptomatic Venous Thromboembolism during Therapy for Acute Lymphoblastic Leukemia and Lymphoma in Caucasian Children

Thromboembolism in acute lymphoblastic leukemia: results of NOPHO ALL2008 protocol treatment in patients aged 1 to 45 years

Establishing a regional paediatric registry improved the overview and detection of side effects in children on anticoagulants

Duration and morbidity of chronic immune thrombocytopenic purpura in children: five-year follow-up of a Nordic cohort

Lupus anticoagulants in two children—bleeding due to nonphospholipid-dependent antiprothrombin antibodies

Breath-holding spells occur disproportionately more often in children with transient erythroblastopenia

Plastic surgical treatment of purpura fulminans: Long-term follow-up of two patients

Cerebral sinus venous thromboses in children with acute lymphoblastic leukaemia – a multicentre study from the Nordic Society of Paediatric Haematology and Oncology

Prospective study of thromboembolism in 1038 children with acute lymphoblastic leukemia: a Nordic Society of Pediatric Hematology and Oncology (NOPHO) study

Studies of chronic ITP in children and adolescents

A novel 33-Gene targeted resequencing panel provides accurate, clinical-grade diagnosis and improves patient management for rare inherited anaemias

Deficiency of Interleukin-1 Receptor Antagonist (DIRA): Report of the First Indian Patient and a Novel Deletion Affecting IL1RN

Childhood idiopathic thrombocytopenic purpura in the Nordic countries : Epidemiology and predictors of chronic disease

Prenatal diagnosis of haemophilia in Sweden now more commonly used for psychological preparation than termination of pregnancy

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