Sten A. Ivarsson

Lund, M, Sweden

Last Updated: 09/26/2026

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Found 31 publications

Month of birth and the risk of developing type 1 diabetes among children in the Swedish national Better Diabetes Diagnosis Study.

Month of birth and the risk of developing type 1 diabetes among children in the Swedish national Better Diabetes Diagnosis Study.

Journal: Acta paediatrica (Oslo, Norway : 1992)

Published: January 25, 2022

Evaluation of the RSR 3 screen ICA™ and 2 screen ICA™ as screening assays for type 1 diabetes in Sweden.

Evaluation of the RSR 3 screen ICA™ and 2 screen ICA™ as screening assays for type 1 diabetes in Sweden.

Journal: Acta diabetologica

Published: December 09, 2021

Celiac disease can be predicted by high levels of tissue transglutaminase antibodies in children and adolescents with type 1 diabetes.

Celiac disease can be predicted by high levels of tissue transglutaminase antibodies in children and adolescents with type 1 diabetes.

Journal: Pediatric diabetes

Published: July 21, 2020

Absence of Islet Autoantibodies and Modestly Raised Glucose Values at Diabetes Diagnosis Should Lead to Testing for MODY: Lessons From a 5-Year Pediatric Swedish National Cohort Study.

Absence of Islet Autoantibodies and Modestly Raised Glucose Values at Diabetes Diagnosis Should Lead to Testing for MODY: Lessons From a 5-Year Pediatric Swedish National Cohort Study.

Journal: Diabetes care

Published: April 15, 2019

Tissue transglutaminase autoantibodies in children with newly diagnosed type 1 diabetes are related to human leukocyte antigen but not to islet autoantibodies: A Swedish nationwide prospective population-based cohort study.

Tissue transglutaminase autoantibodies in children with newly diagnosed type 1 diabetes are related to human leukocyte antigen but not to islet autoantibodies: A Swedish nationwide prospective population-based cohort study.

Journal: Autoimmunity

Published: November 17, 2018

Reduced display of conformational epitopes in the N-terminal truncated GAD65 isoform: relevance for people with stiff person syndrome or DQ8/8-positive Type 1 diabetes mellitus.

Reduced display of conformational epitopes in the N-terminal truncated GAD65 isoform: relevance for people with stiff person syndrome or DQ8/8-positive Type 1 diabetes mellitus.

Journal: Diabetic medicine : a journal of the British Diabetic Association

Published: September 25, 2018

The Better Diabetes Diagnosis (BDD) study - A review of a nationwide prospective cohort study in Sweden.

The Better Diabetes Diagnosis (BDD) study - A review of a nationwide prospective cohort study in Sweden.

Journal: Diabetes research and clinical practice

Published: June 02, 2017

Building and validating a prediction model for paediatric type 1 diabetes risk using next generation targeted sequencing of class II HLA genes.

Building and validating a prediction model for paediatric type 1 diabetes risk using next generation targeted sequencing of class II HLA genes.

Journal: Diabetes/metabolism research and reviews

Published: September 28, 2016

An Increased Diagnostic Sensitivity of Truncated GAD65 Autoantibodies in Type 1 Diabetes May Be Related to HLA-DQ8.

An Increased Diagnostic Sensitivity of Truncated GAD65 Autoantibodies in Type 1 Diabetes May Be Related to HLA-DQ8.

Journal: Diabetes

Published: July 21, 2016

Thyroid and Islet Autoantibodies Predict Autoimmune Thyroid Disease at Type 1 Diabetes Diagnosis.

Thyroid and Islet Autoantibodies Predict Autoimmune Thyroid Disease at Type 1 Diabetes Diagnosis.

Journal: The Journal of clinical endocrinology and metabolism

Published: June 07, 2016

Adiposity in Children Born Small for Gestational Age Is Associated With β-Cell Function, Genetic Variants for Insulin Resistance, and Response to Growth Hormone Treatment.

Adiposity in Children Born Small for Gestational Age Is Associated With β-Cell Function, Genetic Variants for Insulin Resistance, and Response to Growth Hormone Treatment.

Journal: The Journal of clinical endocrinology and metabolism

Published: November 21, 2015

Origin of mutation in sporadic cases of severe haemophilia A in Sweden.

Origin of mutation in sporadic cases of severe haemophilia A in Sweden.

Journal: Clinical genetics

Published: September 22, 2015

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Last Updated: 09/26/2026