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Patent Foramen Ovale Closure or Antiplatelet Therapy for Cryptogenic Stroke

The New England journal of medicine, 2017-09, Vol.377 (11), p.1033-1042

2017

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One hundred years of congenital adrenal hyperplasia in Sweden: a retrospective, population-based cohort study (June, pg 22, 2013)

The lancet. Diabetes & endocrinology, 2013-08, Vol.1, p.S22

2013

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Outcome of pregnancy in patients with structural or ischaemic heart disease: results of a registry of the European Society of Cardiology

European heart journal, 2013-03, Vol.34 (9), p.657-665

2013

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Pregnancy outcomes in women with a systemic right ventricle and transposition of the great arteries results from the ESC-EORP Registry of Pregnancy and Cardiac disease (ROPAC)

Heart (British Cardiac Society), 2022-01, Vol.108 (2), p.117

2022

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Is a planned caesarean section in women with cardiac disease beneficial?

Heart (British Cardiac Society), 2015-04, Vol.101 (7), p.530-536

2015

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Mutational spectrum of the steroid 21-hydroxylase gene in Sweden : implications for genetic diagnosis and association with disease manifestation

The journal of clinical endocrinology and metabolism, 1994-05, Vol.78 (5), p.1145-1152

1994

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Genotyping is a valuable diagnostic complement to neonatal screening for congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency

The journal of clinical endocrinology and metabolism, 1999-05, Vol.84 (5), p.1505-1509

1999

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One hundred years of congenital adrenal hyperplasia in Sweden: a retrospective, population-based cohort study

The lancet. Diabetes & endocrinology, 2013-09, Vol.1 (1), p.35-42

2013

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Pregnancy Outcomes in Women After Arterial Switch Operation for Transposition of the Great Arteries: Results From ROPAC (Registry of Pregnancy and Cardiac Disease) of the European Society of Cardiology EURObservational Research Programme

Journal of the American Heart Association, 2021-01, Vol.10 (1), p.e018176

2021

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Benefits of neonatal screening for congenital adrenal hyperplasia (21-hydroxylase deficiency) in Sweden

Pediatrics (Evanston), 1998-04, Vol.101 (4), p.E11

1998

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Congenital Adrenal Hyperplasia in Sweden 1969-1986 Prevalence, Symptoms and Age at Diagnosis

Acta Paediatrica, 1990-02, Vol.79 (2), p.168-175

1990

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Incidence and prevalence of juvenile chronic arthritis: a population survey

Annals of the rheumatic diseases, 1987-04, Vol.46 (4), p.277-281

1987

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Early growth is not increased in untreated moderately severe 21-hydroxylase deficiency

Acta Paediatrica, 1995-08, Vol.84 (8), p.894-898

1995

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Fanconi's anaemia associated with haemophilia A

Clinical genetics, 1979-11, Vol.16 (5), p.364-368

1979

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Mitroflow Pericardial Bioprosthesis in the Aortic Position: Low Incidence of Structural Valve Deterioration in Elderly Patients during an 11-Year Follow-up

Scandinavian cardiovascular journal : SCJ, 2000, Vol.34 (2), p.192-196

2000

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Antihemophilic Activity in Cohn's Fraction I Prepared from Postpartum Serum

Scandinavian journal of clinical and laboratory investigation, 1955, Vol.7 (3), p.218-224

1955

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Are infants insensitive to androgen? Comments

Acta pædiatrica (Oslo), 1996-06, Vol.85 (6), p.761

1996

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A Follow-up Study of Children Treated for Acute Purulent Meningitis

Acta Paediatrica, 1957-01, Vol.46 (1), p.10-17

1957

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Are infants insensitive to androgen?

Acta Paediatrica, 1996-06, Vol.85 (6), p.760-760

1996

Volltextzugriff (PDF)

A study on the onset and prognosis of acute vascular purpura (the Schoenlein-Henoch syndrome) in children

Acta pædiatrica, 1960-05, Vol.49, p.217

1960

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Granulopoiesis in Infantile Genetic Agranulocytosis In vitro Cloning of Marrow Cells in Agar Culture

Scandinavian Journal of Haematology, 1976-01, Vol.16 (1), p.18-24

1976

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A follow-up study of children treated for acute purulent meningitis

Acta pædiatrica, 1957-01, Vol.46 (1), p.10

1957

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Catheter closure of atrial septal defect in the elderly (≥ 65 years). A worthwhile procedure

International journal of cardiology, 2016-09, Vol.218, p.25-30

2016

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Mutational spectrum of the steroid 21-hydroxylase gene in Sweden: implications for genetic diagnosis and association with disease manifestation

The journal of clinical endocrinology and metabolism, 1994-05, Vol.78 (5), p.1145-1152

1994

Volltextzugriff (PDF)

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Patent Foramen Ovale Closure or Antiplatelet Therapy for Cryptogenic Stroke

One hundred years of congenital adrenal hyperplasia in Sweden: a retrospective, population-based cohort study (June, pg 22, 2013)

Outcome of pregnancy in patients with structural or ischaemic heart disease: results of a registry of the European Society of Cardiology

Pregnancy outcomes in women with a systemic right ventricle and transposition of the great arteries results from the ESC-EORP Registry of Pregnancy and Cardiac disease (ROPAC)

Is a planned caesarean section in women with cardiac disease beneficial?

Mutational spectrum of the steroid 21-hydroxylase gene in Sweden : implications for genetic diagnosis and association with disease manifestation

Genotyping is a valuable diagnostic complement to neonatal screening for congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency

One hundred years of congenital adrenal hyperplasia in Sweden: a retrospective, population-based cohort study

Pregnancy Outcomes in Women After Arterial Switch Operation for Transposition of the Great Arteries: Results From ROPAC (Registry of Pregnancy and Cardiac Disease) of the European Society of Cardiology EURObservational Research Programme

Benefits of neonatal screening for congenital adrenal hyperplasia (21-hydroxylase deficiency) in Sweden

Congenital Adrenal Hyperplasia in Sweden 1969-1986 Prevalence, Symptoms and Age at Diagnosis

Incidence and prevalence of juvenile chronic arthritis: a population survey

2015 ESC Guidelines for the management of infective endocarditis: The Task Force for the Management of Infective Endocarditis of the European Society of Cardiology (ESC). Endorsed by: European Association for Cardio-Thoracic Surgery (EACTS), the European Association of Nuclear Medicine (EANM)

Early growth is not increased in untreated moderately severe 21-hydroxylase deficiency

Fanconi's anaemia associated with haemophilia A

Mitroflow Pericardial Bioprosthesis in the Aortic Position: Low Incidence of Structural Valve Deterioration in Elderly Patients during an 11-Year Follow-up

Antihemophilic Activity in Cohn's Fraction I Prepared from Postpartum Serum

Are infants insensitive to androgen? Comments

A Follow-up Study of Children Treated for Acute Purulent Meningitis

Are infants insensitive to androgen?

A study on the onset and prognosis of acute vascular purpura (the Schoenlein-Henoch syndrome) in children

Granulopoiesis in Infantile Genetic Agranulocytosis In vitro Cloning of Marrow Cells in Agar Culture

A follow-up study of children treated for acute purulent meningitis

Catheter closure of atrial septal defect in the elderly (≥ 65 years). A worthwhile procedure

Mutational spectrum of the steroid 21-hydroxylase gene in Sweden: implications for genetic diagnosis and association with disease manifestation

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