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Progressive increase of the mutated mitochondrial DNA fraction in Kearns-Sayre syndrome

Pediatric research, 1990-08, Vol.28 (2), p.131-136

1990

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The Risk of Celiac Disease in 107 Families With at Least Two Affected Siblings

Journal of pediatric gastroenterology and nutrition, 2004-03, Vol.38 (3), p.338-342

2004

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Longitudinal Growth in Children and Adolescents with Inflammatory Bowel Disease

Journal of pediatric gastroenterology and nutrition, 1994-02, Vol.18 (2), p.165-173

1994

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Genome-wide linkage analysis of Scandinavian affected sib-pairs supports presence of susceptibility loci for celiac disease on chromosomes 5 and 11

European journal of human genetics : EJHG, 2001-12, Vol.9 (12), p.938-944

2001

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Scandinavian CDG-Ia patients: genotype/phenotype correlation and geographic origin of founder mutations

Human genetics, 2001-05, Vol.108 (5), p.359-367

2001

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Intestinal, Pancreatic and Hepatic Involvement in Carbohydrate-Deficient Glycoprotein Syndrome Type I

Journal of pediatric gastroenterology and nutrition, 1998-07, Vol.27 (1), p.23-29

1998

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The decrease of IGF-I, IGF-binding protein-3 and bone alkaline phosphatase isoforms during gluten challenge correlates with small intestinal inflammation in children with coeliac disease

European journal of endocrinology, 2001-04, Vol.144 (4), p.417-423

2001

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The Highest Incidence of Celiac Disease in Europe: The Swedish Experience

Journal of pediatric gastroenterology and nutrition, 1997-01, Vol.24 (S1), p.3-6

1997

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Carbohydrate-deficient glycoprotein syndromes: Peculiar group of new disorders

Pediatric Neurology, 1993-07, Vol.9 (4), p.255-262

1993

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PMM2 mutation spectrum, including 10 novel mutations, in a large CDG type 1A family material with a focus on Scandinavian families

Human mutation, 2000-11, Vol.16 (5), p.395-400

2000

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The Risk of Celiac Disease in 107 Families With at Least Two Affected Siblings

Journal of pediatric gastroenterology and nutrition, 2004-03, Vol.38 (3), p.338-342

2004

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The highest incidence of celiac disease in Europe: the Swedish experience

Journal of pediatric gastroenterology and nutrition, 1997-05, Vol.24 (5), p.S3-6

1997

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Mitochondrial encephalomyopathies in childhood. I. Biochemical and morphologic investigations

The Journal of pediatrics, 1991-08, Vol.119 (2), p.242-250

1991

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Detailed mapping of the phosphomannomutase 2 (PMM2) gene and mutation detection enable improved analysis for Scandinavian CDG type I families

European journal of human genetics : EJHG, 1998-11, Vol.6 (6), p.603-611

1998

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CARNITINE DEFICIENCY INDUCED BY PIVAMPICILLIN AND PIVMECILLINAM THERAPY

The Lancet (British edition), 1989-08, Vol.334 (8661), p.469-473

1989

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Chronic Inflammatory Bowel Disease in Children and Adolescents in Sweden

Journal of pediatric gastroenterology and nutrition, 1991-10, Vol.13 (3), p.293-297

1991

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Short-term gluten challenge in children with coeliac disease does not impair spontaneous growth hormone secretion

Journal of Pediatric Endocrinology and Metabolism, 2003-06, Vol.16 (5), p.771

2003

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Linkage of a locus for carbohydrate-deficient glycoprotein syndrome type I (CDG1) to chromosome 16p, and linkage disequilibrium to microsatellite marker D16S406

Human molecular genetics, 1994-11, Vol.3 (11), p.2037-2042

1994

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Fine Mapping of the Gene for Carbohydrate-Deficient Glycoprotein Syndrome, Type I (CDG1): Linkage Disequilibrium and Founder Effect in Scandinavian Families

Genomics (San Diego, Calif.), 1997-02, Vol.39 (3), p.247-253

1997

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Childhood coeliac disease in Sweden

The Lancet (British edition), 1994-07, Vol.344 (8918), p.340-342

1994

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Mitochondrial encephalomyopathies in childhood. II. Clinical manifestations and syndromes

The Journal of pediatrics, 1991-08, Vol.119 (2), p.251-259

1991

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Analysis of Transferrin and α 1 ‐Fetoprotein in Amniotic Fluid and Neonatal Serum: a Possible Means for Indirect Prenatal Diagnosis of the Carbohydrate‐deficient Glycoprotein Syndrome

Acta Paediatrica, 1991-05, Vol.80 (s375), p.32-38

1991

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Analysis of Transferrin and α1-Fetoprotein in Amniotic Fluid and Neonatal Serum: a Possible Means for Indirect Prenatal Diagnosis of the Carbohydrate-deficient Glycoprotein Syndrome

Acta Pædiatrica, 1991-05, Vol.80 (s375), p.32-38

1991

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Chronic Hepatitis B in Children in Gothenburg, Sweden

Scandinavian journal of infectious diseases, 1999, Vol.31 (2), p.109-114

1999

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Atypical presentation of multisystem disorders in two girls with mitochondrial DNA deletions

European journal of pediatrics, 1995, Vol.154 (1), p.35-42

1995

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Progressive increase of the mutated mitochondrial DNA fraction in Kearns-Sayre syndrome

The Risk of Celiac Disease in 107 Families With at Least Two Affected Siblings

Longitudinal Growth in Children and Adolescents with Inflammatory Bowel Disease

Genome-wide linkage analysis of Scandinavian affected sib-pairs supports presence of susceptibility loci for celiac disease on chromosomes 5 and 11

Scandinavian CDG-Ia patients: genotype/phenotype correlation and geographic origin of founder mutations

Intestinal, Pancreatic and Hepatic Involvement in Carbohydrate-Deficient Glycoprotein Syndrome Type I

The decrease of IGF-I, IGF-binding protein-3 and bone alkaline phosphatase isoforms during gluten challenge correlates with small intestinal inflammation in children with coeliac disease

The Highest Incidence of Celiac Disease in Europe: The Swedish Experience

Carbohydrate-deficient glycoprotein syndromes: Peculiar group of new disorders

PMM2 mutation spectrum, including 10 novel mutations, in a large CDG type 1A family material with a focus on Scandinavian families

The Risk of Celiac Disease in 107 Families With at Least Two Affected Siblings

The highest incidence of celiac disease in Europe: the Swedish experience

Mitochondrial encephalomyopathies in childhood. I. Biochemical and morphologic investigations

Detailed mapping of the phosphomannomutase 2 (PMM2) gene and mutation detection enable improved analysis for Scandinavian CDG type I families

CARNITINE DEFICIENCY INDUCED BY PIVAMPICILLIN AND PIVMECILLINAM THERAPY

Chronic Inflammatory Bowel Disease in Children and Adolescents in Sweden

Short-term gluten challenge in children with coeliac disease does not impair spontaneous growth hormone secretion

Linkage of a locus for carbohydrate-deficient glycoprotein syndrome type I (CDG1) to chromosome 16p, and linkage disequilibrium to microsatellite marker D16S406

Fine Mapping of the Gene for Carbohydrate-Deficient Glycoprotein Syndrome, Type I (CDG1): Linkage Disequilibrium and Founder Effect in Scandinavian Families

Childhood coeliac disease in Sweden

Mitochondrial encephalomyopathies in childhood. II. Clinical manifestations and syndromes

Analysis of Transferrin and α 1 ‐Fetoprotein in Amniotic Fluid and Neonatal Serum: a Possible Means for Indirect Prenatal Diagnosis of the Carbohydrate‐deficient Glycoprotein Syndrome

Analysis of Transferrin and α1-Fetoprotein in Amniotic Fluid and Neonatal Serum: a Possible Means for Indirect Prenatal Diagnosis of the Carbohydrate-deficient Glycoprotein Syndrome

Chronic Hepatitis B in Children in Gothenburg, Sweden

Atypical presentation of multisystem disorders in two girls with mitochondrial DNA deletions

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