H. Arnqvist

HLA-DQB1 genotypes, islet antibodies and beta cell function in the classification of recent-onset diabetes among young adults in the nationwide Diabetes Incidence Study in Sweden. (2006)

Bakhtadze, E, Borg, H, Stenstrom, G, Fernlund, P, Arnqvist, H, Ekbom-Schnell, A, ...

Abstract is not available

Islet antibodies and remaining beta-cell function 8 years after diagnosis of diabetes in young adults: a prospective follow-up of the nationwide Diabetes Incidence Study in Sweden. (2004)

Schölin, A., Björklund, L., Borg, H., Arnqvist, H., Björk, E., Blohmé, G., ...

Objectives. To establish the prevalence of remaining beta-cell function 8 years after diagnosis of diabetes in young adults and relate the findings to islet antibodies at diagnosis and 8 years later....

The incidence of Type I diabetes has not increased but shifted to a younger age at diagnosis in the 0-34 years group in Sweden 1983-1998. (2002)

Pundziute-Lycka, A, Dahlquist, G, Nystrom, L, Arnqvist, H, Bjork, E, Blohme, G, ...

AIMS/HYPOTHESIS: To analyse the incidence of Type I (insulin-dependent) diabetes mellitus in the 0-34 years age group in Sweden 1983-1998. METHODS: Incidence and cumulative incidence per 100 000 and...

Nutritional assessment and muscle energy metabolism in severe chronic congestive heart failure--effects of long-term dietary supplementation (1994)

BROQVIST, M., ARNQVIST, H., DAHLSTRÖM, U., LARSSON, J., NYLANDER, E., PERMERT, J.

In order to investigate nutritional status in relation to the metabolic state of skeletal muscle in patients with severe congestive heart failure, and to explore the influence of long-term dietary...

Risk of Developing Insulin-Dependent Diabetes Mellitus (IDDM) before 35 Years of Age: Indications of Climatological Determinants for Age at Onset (1992)

NYSTRÖM, L, DAHLQUIST, G, ÖSTMAN, J, WALL, S, ARNQVIST, H, BLOHMÉ, G, ...

This study analyses data from two nationwide prospective diabetes registries now covering about 3400 cases from 19 million person-years of follow-up in the age group 0-34 years. The risk of...

Mutations in the Human Ca2+-Sensing-Receptor Gene That Cause Familial Hypocalciuric Hypercalcemia

Chou, Yah-Huei Wu, Pollak, Martin R., Brandi, Maria L., Toss, Goran, Arnqvist, H., Atkinson, A. Brew, ...

We report five novel mutations in the human Ca2+-sensing-receptor gene that cause familial hypocalciuric hypercalcemia (FHH) or neonatal severe hyperparathyroidism. Each gene defect is a missense...