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High modal number and triple trisomies are highly correlated favorable factors in childhood B-cell precursor high hyperdiploid acute lymphoblastic leukemia treated according to the NOPHO ALL 1992/2000 protocols

Haematologica (Roma), 2013-09, Vol.98 (9), p.1424-1432

2013

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Clinical and genetic features of pediatric acute lymphoblastic leukemia in Down syndrome in the Nordic countries

Journal of hematology and oncology, 2014-04, Vol.7 (1), p.32-32, Article 32

2014

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Outcome of ETV6/RUNX1‐positive childhood acute lymphoblastic leukaemia in the NOPHO‐ALL‐1992 protocol: frequent late relapses but good overall survival

British journal of haematology, 2008-03, Vol.140 (6), p.665-672

2008

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Paediatric B‐cell precursor acute lymphoblastic leukaemia with t(1;19)(q23;p13): clinical and cytogenetic characteristics of 47 cases from the Nordic countries treated according to NOPHO protocols

British journal of haematology, 2011-10, Vol.155 (2), p.235-243

2011

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Clinical and cytogenetic features of a population-based consecutive series of 285 pediatric T-cell acute lymphoblastic leukemias: Rare T-cell receptor gene rearrangements are associated with poor outcome

Genes chromosomes & cancer, 2009-09, Vol.48 (9), p.795-805

2009

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Additional aberrations of the ETV6 and RUNX1 genes have no prognostic impact in 229 t(12;21)(p13;q22)-positive B-cell precursor acute lymphoblastic leukaemias treated according to the NOPHO-ALL-2000 protocol

Leukemia research, 2012-07, Vol.36 (7), p.936-938

2012

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Cytogenetic patterns in ETV6/RUNX1-positive pediatric B-cell precursor acute lymphoblastic leukemia: A Nordic series of 245 cases and review of the literature

Genes chromosomes & cancer, 2007-05, Vol.46 (5), p.440-450

2007

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Clinical and cytogenetic features of pediatric dic(9;20)(p13.2;q11.2)-positive B-cell precursor acute lymphoblastic leukemias: A nordic series of 24 cases and review of the literature

Genes chromosomes & cancer, 2008-02, Vol.47 (2), p.149-158

2008

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Epidemiology of Primary Immunodeficiency in Iceland

Journal of clinical immunology, 2015, Vol.35 (1), p.75-79

2015

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Cytogenetic abnormalities in childhood acute myeloid leukaemia: a Nordic series comprising all children enrolled in the NOPHO‐93‐AML trial between 1993 and 2001

British journal of haematology, 2003-05, Vol.121 (4), p.566-577

2003

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Prognostic impact of karyotypic findings in childhood acute lymphoblastic leukaemia: a Nordic series comparing two treatment periods

British journal of haematology, 2000-07, Vol.110 (1), p.147-153

2000

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Familial Predisposition and Cosegregation Analysis of Adult Obstructive Sleep Apnea and the Sudden Infant Death Syndrome

American journal of respiratory and critical care medicine, 2002-09, Vol.166 (6), p.833-838

2002

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Inflammatory bowel disease in Iceland, 1990-1994: a prospective, nationwide, epidemiological study

European journal of gastroenterology & hepatology, 2000-01, Vol.12 (1), p.31-38

2000

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Cytogenetic findings in a population-based series of 787 childhood acute lymphoblastic leukemias from the Nordic countries

European journal of haematology, 2000-03, Vol.64 (3), p.194-200

2000

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Gangliogliomas: pathological and clinical correlation

Journal of neurosurgery, 1981-01, Vol.54 (1), p.58-63

1981

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A genetic contribution to inflammatory bowel disease in Iceland: A genealogic approach

Clinical gastroenterology and hepatology, 2004-09, Vol.2 (9), p.806-812

2004

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Oral lichen planus has a high rate of TP53 mutations. A study of oral mucosa in Iceland

European journal of oral sciences, 2002-06, Vol.110 (3), p.192-198

2002

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Extremely low birthweight infants in Iceland 1991-95. Risk factors for perinatal and neonatal death

Laeknabladid, 2009-02, Vol.95 (2), p.107-111

2009

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Macular Corneal Dystrophy in Iceland

Ophthalmology (Rochester, Minn.), 1996-07, Vol.103 (7), p.1111-1117

1996

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Methenamine-Silver Staining in Macular Corneal Dystrophy

American journal of ophthalmology, 1988-11, Vol.106 (5), p.630-631

1988

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Ísland í dag - Nærri tveimur áratugum síðar

Icelandic Journal of Engineering, 2020-02, Vol.26

2020

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Encephalopathy and fatty metamorphosis of the liver associated with cold-agglutinin autoimmune hemolytic anemia

The Journal of pediatrics, 1979-04, Vol.94 (4), p.569-575, Article 569

1979

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Uniparental disomy of chromosome 11 in a patient with Beckwith-Wiedemann syndrome. First reported case in Iceland

Laeknabladid, 2005-11, Vol.91 (11), p.837-840

2005

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Classification of Perinatal and Late Neonatal Deaths in Iceland: A survey from a defined population

Acta obstetricia et gynecologica Scandinavica, 1989, Vol.68 (2), p.101-108

1989

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Can we Expect to Lower Perinatal and Neonatal Mortality?

Acta obstetricia et gynecologica Scandinavica, 1989, Vol.68 (2), p.109-112

1989

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High modal number and triple trisomies are highly correlated favorable factors in childhood B-cell precursor high hyperdiploid acute lymphoblastic leukemia treated according to the NOPHO ALL 1992/2000 protocols

Clinical and genetic features of pediatric acute lymphoblastic leukemia in Down syndrome in the Nordic countries

Outcome of ETV6/RUNX1‐positive childhood acute lymphoblastic leukaemia in the NOPHO‐ALL‐1992 protocol: frequent late relapses but good overall survival

Paediatric B‐cell precursor acute lymphoblastic leukaemia with t(1;19)(q23;p13): clinical and cytogenetic characteristics of 47 cases from the Nordic countries treated according to NOPHO protocols

Clinical and cytogenetic features of a population-based consecutive series of 285 pediatric T-cell acute lymphoblastic leukemias: Rare T-cell receptor gene rearrangements are associated with poor outcome

Additional aberrations of the ETV6 and RUNX1 genes have no prognostic impact in 229 t(12;21)(p13;q22)-positive B-cell precursor acute lymphoblastic leukaemias treated according to the NOPHO-ALL-2000 protocol

Cytogenetic patterns in ETV6/RUNX1-positive pediatric B-cell precursor acute lymphoblastic leukemia: A Nordic series of 245 cases and review of the literature

Clinical and cytogenetic features of pediatric dic(9;20)(p13.2;q11.2)-positive B-cell precursor acute lymphoblastic leukemias: A nordic series of 24 cases and review of the literature

Epidemiology of Primary Immunodeficiency in Iceland

Cytogenetic abnormalities in childhood acute myeloid leukaemia: a Nordic series comprising all children enrolled in the NOPHO‐93‐AML trial between 1993 and 2001

Prognostic impact of karyotypic findings in childhood acute lymphoblastic leukaemia: a Nordic series comparing two treatment periods

Familial Predisposition and Cosegregation Analysis of Adult Obstructive Sleep Apnea and the Sudden Infant Death Syndrome

Inflammatory bowel disease in Iceland, 1990-1994: a prospective, nationwide, epidemiological study

Cytogenetic findings in a population-based series of 787 childhood acute lymphoblastic leukemias from the Nordic countries

Gangliogliomas: pathological and clinical correlation

A genetic contribution to inflammatory bowel disease in Iceland: A genealogic approach

Oral lichen planus has a high rate of TP53 mutations. A study of oral mucosa in Iceland

Extremely low birthweight infants in Iceland 1991-95. Risk factors for perinatal and neonatal death

Macular Corneal Dystrophy in Iceland

Methenamine-Silver Staining in Macular Corneal Dystrophy

Ísland í dag - Nærri tveimur áratugum síðar

Encephalopathy and fatty metamorphosis of the liver associated with cold-agglutinin autoimmune hemolytic anemia

Uniparental disomy of chromosome 11 in a patient with Beckwith-Wiedemann syndrome. First reported case in Iceland

Classification of Perinatal and Late Neonatal Deaths in Iceland: A survey from a defined population

Can we Expect to Lower Perinatal and Neonatal Mortality?

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