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Weight gain and the risk of knee replacement due to primary osteoarthritis: a population based, prospective cohort study of 225,908 individuals

Osteoarthritis and cartilage, 2014-05, Vol.22 (5), p.652-658

2014

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Weight gain and the risk of knee replacement due to primary osteoarthritis

Osteoarthritis and cartilage, 2014-05, Vol.22 (5), p.652-658

2014

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Weight gain and the risk of total hip replacement a population-based prospective cohort study of 265,725 individuals

Osteoarthritis and cartilage, 2011-07, Vol.19 (7), p.809-815

2011

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344 SPONTANEOUS WEIGHT CHANGE AND THE RISK FOR TOTAL HIP REPLACEMENT

Osteoarthritis and cartilage, 2008, Vol.16, p.S151-S151

2008

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P221 RISK FACTORS FOR OSTEOARTHRITIS OF THE HIP. AN INVESTIGATION OF ETHNICITY AND METABOLIC CHANGES

Osteoarthritis and cartilage, 2006, Vol.14, p.S123-S123

2006

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Screening for familial ovarian cancer: poor survival of BRCA1/2 related cancers

Journal of medical genetics, 2009-09, Vol.46 (9), p.593-597

2009

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Survival in women with MMR mutations and ovarian cancer: a multicentre study in Lynch syndrome kindreds

Journal of medical genetics, 2010-02, Vol.47 (2), p.99-102

2010

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Clinical Findings with Implications for Genetic Testing in Families with Clustering of Colorectal Cancer

The New England journal of medicine, 1998-08, Vol.339 (8), p.511-518

1998

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Survival in prospectively ascertained familial breast cancer: Analysis of a series stratified by tumour characteristics, BRCA mutations and oophorectomy

International journal of cancer, 2002-10, Vol.101 (6), p.555-559

2002

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Expression of recombinant human phenylalanine hydroxylase as fusion protein in Escherichia coli circumvents proteolytic degradation by host cell proteases. Isolation and characterization of the wild-type enzyme

Biochemical journal, 1995-03, Vol.306 ( Pt 2) (2), p.589-597

1995

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PKU mutation G46S is associated with increased aggregation and degradation of the phenylalanine hydroxylase enzyme

Human mutation, 1996, Vol.7 (3), p.228-238

1996

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Efficacy of early diagnosis and treatment in women with a family history of breast cancer

Disease markers, 1999, Vol.15 (1-3), p.179-186

1999

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PKU mutation (D143G) associated with an apparent high residual enzyme activity: Expression of a kinetic variant form of phenylalanine hydroxylase in three different systems

Human mutation, 1996, Vol.8 (3), p.236-246

1996

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Guidelines for follow-up of women at high risk for inherited breast cancer: consensus statement from the Biomed 2 Demonstration Programme on Inherited Breast Cancer

Disease markers, 1999, Vol.15 (1-3), p.207-211

1999

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Genterapi ved monogent arvelige sykdommer

Tidsskrift for den Norske Lægeforening, 2001, Vol.121 (3)

2001

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Diverse PAH transcripts in lymphocytes of PKU patients with putative nonsense (G272X, Y356X) and missense (P281L, R408Q) mutations

FEBS letters, 1999-09, Vol.457 (3), p.505-508

1999

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Complete mutation screening and haplotype characterization of the BRCA1 gene in 61 familial breast cancer patients from Norway

Disease markers, 2005, Vol.21 (1), p.29-36

2005

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Application of natural and amplification created restriction sites for the diagnosis of PKU mutations

Nucleic acids research, 1991-04, Vol.19 (7), p.1427-1430

1991

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Gene therapy for monogenic inherited diseases

Tidsskrift for den Norske Lægeforening, 2001-01, Vol.121 (3), p.349-350

2001

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Recurrence of the R408W mutation in the phenylalanine hydroxylase locus in Europeans

American journal of human genetics, 1995, Vol.56 (1), p.278-286

1995

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Relative frequency, heterogeneity and geographic clustering of PKU mutations in Norway

European journal of human genetics : EJHG, 1996, Vol.4 (4), p.205-213

1996

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DGGE analysis as supplement to SSCP analysis of the phenylalanine hydroxylase gene: Detection of eight (one de novo, seven inherited) of nine remaining Norwegian PKU mutations

Human mutation, 1996, Vol.8 (1), p.19-22

1996

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Phenylketonuria genotypes correlated to metabolic phenotype groups in Norway

European journal of pediatrics, 1996-07, Vol.155 (7), p.554-560

1996

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Expression of wild type and mutant forms of human phenylalanine hydroxylase in E. coli

Advances in experimental medicine and biology, 1993, Vol.338, p.59

1993

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Dust from carpeted and smooth floors. I. Comparative measurements of antigenic and allergenic proteins in dust vacuumed from carpeted and non-carpeted classrooms in Norwegian schools

Clinical and experimental allergy, 1989-03, Vol.19 (2), p.217-224

1989

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Weight gain and the risk of knee replacement due to primary osteoarthritis: a population based, prospective cohort study of 225,908 individuals

Weight gain and the risk of knee replacement due to primary osteoarthritis

Weight gain and the risk of total hip replacement a population-based prospective cohort study of 265,725 individuals

344 SPONTANEOUS WEIGHT CHANGE AND THE RISK FOR TOTAL HIP REPLACEMENT

P221 RISK FACTORS FOR OSTEOARTHRITIS OF THE HIP. AN INVESTIGATION OF ETHNICITY AND METABOLIC CHANGES

Screening for familial ovarian cancer: poor survival of BRCA1/2 related cancers

Survival in women with MMR mutations and ovarian cancer: a multicentre study in Lynch syndrome kindreds

Clinical Findings with Implications for Genetic Testing in Families with Clustering of Colorectal Cancer

Survival in prospectively ascertained familial breast cancer: Analysis of a series stratified by tumour characteristics, BRCA mutations and oophorectomy

Expression of recombinant human phenylalanine hydroxylase as fusion protein in Escherichia coli circumvents proteolytic degradation by host cell proteases. Isolation and characterization of the wild-type enzyme

PKU mutation G46S is associated with increased aggregation and degradation of the phenylalanine hydroxylase enzyme

Efficacy of early diagnosis and treatment in women with a family history of breast cancer

PKU mutation (D143G) associated with an apparent high residual enzyme activity: Expression of a kinetic variant form of phenylalanine hydroxylase in three different systems

Guidelines for follow-up of women at high risk for inherited breast cancer: consensus statement from the Biomed 2 Demonstration Programme on Inherited Breast Cancer

Genterapi ved monogent arvelige sykdommer

Diverse PAH transcripts in lymphocytes of PKU patients with putative nonsense (G272X, Y356X) and missense (P281L, R408Q) mutations

Complete mutation screening and haplotype characterization of the BRCA1 gene in 61 familial breast cancer patients from Norway

Application of natural and amplification created restriction sites for the diagnosis of PKU mutations

Gene therapy for monogenic inherited diseases

Recurrence of the R408W mutation in the phenylalanine hydroxylase locus in Europeans

Relative frequency, heterogeneity and geographic clustering of PKU mutations in Norway

DGGE analysis as supplement to SSCP analysis of the phenylalanine hydroxylase gene: Detection of eight (one de novo, seven inherited) of nine remaining Norwegian PKU mutations

Phenylketonuria genotypes correlated to metabolic phenotype groups in Norway

Expression of wild type and mutant forms of human phenylalanine hydroxylase in E. coli

Dust from carpeted and smooth floors. I. Comparative measurements of antigenic and allergenic proteins in dust vacuumed from carpeted and non-carpeted classrooms in Norwegian schools

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