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Risk of Non‐Hodgkin's Lymphoma in Primary Sjögren's Syndrome: A Population‐Based Study

Arthritis care & research (2010), 2013-05, Vol.65 (5), p.816-821

2013

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Association of Genes in the NF‐κB Pathway with Antibody‐Positive Primary Sjögren's Syndrome

Scandinavian journal of immunology, 2013-11, Vol.78 (5), p.447-454

2013

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Symptom-based stratification of patients with primary Sjögren's syndrome: multi-dimensional characterisation of international observational cohorts and reanalyses of randomised clinical trials

The Lancet. Rheumatology, 2019-10, Vol.1 (2), p.e85-e94

2019

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Association of Genes in the NF-[kappa]B Pathway with Antibody-Positive Primary Sjögren's Syndrome

Scandinavian journal of immunology, 2013-11, Vol.78 (5), p.447

2013

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DNA Methylation-Based Interferon Scores Associate With Sub-Phenotypes in Primary Sjögren's Syndrome

Frontiers in immunology, 2021-07, Vol.12, p.702037-702037

2021

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Association between genetic variants in the tumour necrosis factor/lymphotoxin α/lymphotoxin β locus and primary Sjögren's syndrome in Scandinavian samples

Annals of the rheumatic diseases, 2012-06, Vol.71 (6), p.981-988

2012

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Genetic associations to germinal centre formation in primary Sjögren's syndrome

Annals of the rheumatic diseases, 2014-06, Vol.73 (6), p.1253-1258

2014

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Complement C4 Copy Number Variation is Linked to SSA/Ro and SSB/La Autoantibodies in Systemic Inflammatory Autoimmune Diseases

Arthritis & rheumatology (Hoboken, N.J.), 2022-08, Vol.74 (8), p.1440-1450

2022

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Genetic variants at the RTP4/MASP1 locus are associated with fatigue in Scandinavian patients with primary Sjögren’s syndrome

Rheumatic & musculoskeletal diseases open, 2021-12, Vol.7 (3), p.e001832

2021

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Strong Association of Combined Genetic Deficiencies in the Classical Complement Pathway With Risk of Systemic Lupus Erythematosus and Primary Sjögren's Syndrome

Arthritis & rheumatology (Hoboken, N.J.), 2022-11, Vol.74 (11), p.1842-1850

2022

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The Conceptual Roles of Negative and Positive Affectivity in the Stressor-Strain Relationship

Europe's journal of psychology, 2013-02, Vol.9 (1), p.93-103

2013

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Preoperative Octreotide Treatment in Newly Diagnosed Acromegalic Patients with Macroadenomas Increases Cure Short-Term Postoperative Rates: A Prospective, Randomized Trial

The journal of clinical endocrinology and metabolism, 2008-08, Vol.93 (8), p.2984-2990

2008

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Relational interventions in psychotherapy: development of a therapy process rating scale

BMC psychiatry, 2016-09, Vol.16 (1), p.310-310, Article 310

2016

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Difference in Clinical Presentation between Female and Male Patients with Primary Sjogren's Syndrome at Diagnosis and in Long-Term Follow-up

ARTHRITIS & RHEUMATOLOGY, 2017, Vol.69 (S10)

2017

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Social support in a wired world: Use of online mental health forums in Norway

Nordic journal of psychiatry, 2002, Vol.56 (1), p.59-65

2002

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Long-term follow-up in primary Sjögren's syndrome reveals differences in clinical presentation between female and male patients

Biology of sex differences, 2017-08, Vol.8 (1), p.25-25, Article 25

2017

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The EXTERNAL Experience on System and Enterprise Integration

Lecture notes in computer science, 2004, p.158-174

2004

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NMR spectroscopy study of the effect of 3-nitropropionic acid on glutamate metabolism in cultured astrocytes

Journal of neuroscience research, 1997-03, Vol.47 (6), p.642-649

1997

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α‐Ketoisocaproate Alters the Production of Both Lactate and Aspartate from [U‐13C]Glutamate in Astrocytes: A 13C NMR Study

Journal of neurochemistry, 1998-03, Vol.70 (3), p.1001-1008

1998

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Prader-Willi syndrome in a brother and sister without cytogenetic or detectable molecular genetic abnormality at chromosome 15q11q13

American journal of medical genetics, 1992-11, Vol.44 (4), p.534-538

1992

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Risk of Non‐Hodgkin's Lymphoma in Primary Sjögren's Syndrome: A Population‐Based Study

Association of Genes in the NF‐κB Pathway with Antibody‐Positive Primary Sjögren's Syndrome

Symptom-based stratification of patients with primary Sjögren's syndrome: multi-dimensional characterisation of international observational cohorts and reanalyses of randomised clinical trials

Association of Genes in the NF-[kappa]B Pathway with Antibody-Positive Primary Sjögren's Syndrome

DNA Methylation-Based Interferon Scores Associate With Sub-Phenotypes in Primary Sjögren's Syndrome

Association between genetic variants in the tumour necrosis factor/lymphotoxin α/lymphotoxin β locus and primary Sjögren's syndrome in Scandinavian samples

Genetic associations to germinal centre formation in primary Sjögren's syndrome

Complement C4 Copy Number Variation is Linked to SSA/Ro and SSB/La Autoantibodies in Systemic Inflammatory Autoimmune Diseases

Genetic variants at the RTP4/MASP1 locus are associated with fatigue in Scandinavian patients with primary Sjögren’s syndrome

Strong Association of Combined Genetic Deficiencies in the Classical Complement Pathway With Risk of Systemic Lupus Erythematosus and Primary Sjögren's Syndrome

The Conceptual Roles of Negative and Positive Affectivity in the Stressor-Strain Relationship

Genetic and clinical basis for two distinct subtypes of primary Sjögren’s syndrome

Preoperative Octreotide Treatment in Newly Diagnosed Acromegalic Patients with Macroadenomas Increases Cure Short-Term Postoperative Rates: A Prospective, Randomized Trial

Relational interventions in psychotherapy: development of a therapy process rating scale

Difference in Clinical Presentation between Female and Male Patients with Primary Sjogren's Syndrome at Diagnosis and in Long-Term Follow-up

Social support in a wired world: Use of online mental health forums in Norway

Long-term follow-up in primary Sjögren's syndrome reveals differences in clinical presentation between female and male patients

The EXTERNAL Experience on System and Enterprise Integration

NMR spectroscopy study of the effect of 3-nitropropionic acid on glutamate metabolism in cultured astrocytes

α‐Ketoisocaproate Alters the Production of Both Lactate and Aspartate from [U‐13C]Glutamate in Astrocytes: A 13C NMR Study

Prader-Willi syndrome in a brother and sister without cytogenetic or detectable molecular genetic abnormality at chromosome 15q11q13

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