Increased Risk of Autoimmune Disorders in 21-Hydroxylase Deficiency: A Swedish Population-Based National Cohort Study-Reference-Cited by-同舟云学术

Increased Risk of Autoimmune Disorders in 21-Hydroxylase Deficiency: A Swedish Population-Based National Cohort Study

Author:

Falhammar Henrik¹²^ORCID,Frisén Louise³⁴,Hirschberg Angelica Linden⁵⁶,Nordenskjöld Agneta⁵⁷⁸,Almqvist Catarina⁹¹⁰,Nordenström Anna⁵¹¹

Affiliation:

1. Department of Endocrinology, Metabolism and Diabetes, Karolinska University Hospital, Stockholm, Sweden

2. Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden

3. Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden

4. Child and Adolescent Psychiatry Research Center, Stockholm, Sweden

5. Department of Women’s and Children’s Health, Karolinska Institutet, Stockholm, Sweden

6. Department of Gynecology and Reproductive Medicine, Karolinska University Hospital, Stockholm, Sweden

7. Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden

8. Pediatric Surgery, Astrid Lindgren Children’s Hospital, Karolinska University Hospital, Stockholm, Sweden

9. Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden

10. Lung and Allergy Unit, Astrid Lindgren Children’s Hospital, Karolinska University Hospital

11. Department of Pediatric Endocrinology, Astrid Lindgren Children’s Hospital, Karolinska University Hospital, Stockholm, Sweden

Funder

Medicinska Forskningsrådet

Magnus Bergvalls Stiftelse

Publisher

The Endocrine Society

Subject

Endocrinology, Diabetes and Metabolism

Link

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