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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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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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Gain-of-Function SAMD9L Mutations Cause a Syndrome of Cytopenia, Immunodeficiency, Myelodysplastic Syndrome and Neurological Symptoms

LEUKEMIA RESEARCH, 2017, Vol.55, p.S11-S12

2017

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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.427-437

2018

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Reproductive choices of haemophilia carriers

British journal of haematology, 1999-08, Vol.106 (2), p.421-426

1999

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Risk stratification for inhibitor development at first treatment for severe hemophilia A: a tool for clinical practice

Journal of thrombosis and haemostasis, 2008-12, Vol.6 (12), p.2048-2054

2008

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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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21 - Gain-of-Function SAMD9L Mutations Cause a Syndrome of Cytopenia, Immunodeficiency, Myelodysplastic Syndrome and Neurological Symptoms

Leukemia research, 2017-04, Vol.55, p.S11-S12

2017

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Carrier testing and prenatal diagnosis of haemophilia - utilisation and psychological consequences

Haemophilia : the official journal of the World Federation of Hemophilia, 1998-07, Vol.4 (4), p.365-369

1998

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Long-term psychological effects of carrier testing and prenatal diagnosis of haemophilia: comparison with a control group

Prenatal diagnosis, 1999-05, Vol.19 (5), p.411-417

1999

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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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How do carriers of hemophilia and their spouses experience prenatal diagnosis by chorionic villus sampling?

Clinical genetics, 1999-01, Vol.55 (1), p.26-33

1999

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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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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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Identifying carriers at high risk for negative reactions when performing prenatal diagnosis of haemophilia

Haemophilia : the official journal of the World Federation of Hemophilia, 1997-04, Vol.3 (2), p.123-130

1997

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Emergence of novel transient clonal chromosomal bone marrow changes in remission of acute lymphoblastic leukemia

Leukemia, 1996-02, Vol.10 (2), p.378-383

1996

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Haemophilia Care in Europe: the ESCHQoL study

Haemophilia : the official journal of the World Federation of Hemophilia, 2012-09, Vol.18 (5), p.729-737

2012

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Genetic Counseling of Hemophilia Carriers

Seminars in thrombosis and hemostasis, 2003, Vol.29 (1), p.031-036

2003

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Small Molecule Screens Identify CDK8-Inhibitors As Candidate Diamond-Blackfan Anemia Drugs

BLOOD, 2018-11, Vol.132 (Supplement 1), p.753-753

2018

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How do carriers of hemophilia experience prenatal diagnosis by fetal blood sampling?

Clinical genetics, 1987-05, Vol.31 (5), p.297-302

1987

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Gain-of-function SAMD9L mutations cause a syndrome with cytopenia, myelodysplastic syndrome, immunodeficiency and neurological disease

EUROPEAN JOURNAL OF HUMAN GENETICS, 2018, Vol.26, p.315

2018

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Venous Thromboembolism in Children with Acute Lymphoblastic Leukemia in Northern Europe

BLOOD, 2014-12, Vol.124 (21), p.3652-3652

2014

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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

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

Gain-of-Function SAMD9L Mutations Cause a Syndrome of Cytopenia, Immunodeficiency, Myelodysplastic Syndrome and Neurological Symptoms

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

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

Constitutional SAMD9L mutations cause familial myelodysplastic syndrome and transient monosomy 7

Reproductive choices of haemophilia carriers

Risk stratification for inhibitor development at first treatment for severe hemophilia A: a tool for clinical practice

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

21 - Gain-of-Function SAMD9L Mutations Cause a Syndrome of Cytopenia, Immunodeficiency, Myelodysplastic Syndrome and Neurological Symptoms

Carrier testing and prenatal diagnosis of haemophilia - utilisation and psychological consequences

Long-term psychological effects of carrier testing and prenatal diagnosis of haemophilia: comparison with a control group

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

How do carriers of hemophilia and their spouses experience prenatal diagnosis by chorionic villus sampling?

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

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

Cytopenia, Predisposition to Myelodysplastic Syndrome, Immunodeficiency, and Neurological Disease Caused By Gain-of-Function SAMD9L Mutations Is Frequently Ameliorated By Hematopoietic Revertant Mosaicism

Identifying carriers at high risk for negative reactions when performing prenatal diagnosis of haemophilia

Emergence of novel transient clonal chromosomal bone marrow changes in remission of acute lymphoblastic leukemia

Haemophilia Care in Europe: the ESCHQoL study

Genetic Counseling of Hemophilia Carriers

Small Molecule Screens Identify CDK8-Inhibitors As Candidate Diamond-Blackfan Anemia Drugs

How do carriers of hemophilia experience prenatal diagnosis by fetal blood sampling?

Gain-of-function SAMD9L mutations cause a syndrome with cytopenia, myelodysplastic syndrome, immunodeficiency and neurological disease

Venous Thromboembolism in Children with Acute Lymphoblastic Leukemia in Northern Europe

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