1.
Reduced Frequency of Biological and Increased Frequency of Adopted Children in Males With 21-Hydroxylase Deficiency: A Swedish Population-Based National Cohort Study
by Falhammar, Henrik
The journal of clinical endocrinology and metabolism, 2017, Vol.102 (11), p.4191-4199
2.
IGF2BP2 and IGF2 genetic effects in diabetes and diabetic nephropathy
by Gu, Tianwei
Journal of diabetes and its complications, 2012, Vol.26 (5), p.393-398
3.
Increased Cardiovascular and Metabolic Morbidity in Patients With 21-Hydroxylase Deficiency: A Swedish Population-Based National Cohort Study
by Falhammar, Henrik
The journal of clinical endocrinology and metabolism, 2015, Vol.100 (9), p.3520-3528
4.
Increased Mortality in Patients With Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
by Falhammar, Henrik
The journal of clinical endocrinology and metabolism, 2014, Vol.99 (12), p.E2715-E2721
5.
Increased Psychiatric Morbidity in Men With Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
by Falhammar, Henrik
The journal of clinical endocrinology and metabolism, 2014, Vol.99 (3), p.E554-E560
6.
Genetic association analysis of the adiponectin polymorphisms in type 1 diabetes with and without diabetic nephropathy
by Ma, Jun
Journal of diabetes and its complications, 2007, Vol.21 (1), p.28-33
7.
Suboptimal Psychosocial Outcomes in Patients With Congenital Adrenal Hyperplasia: Epidemiological Studies in a Nonbiased National Cohort in Sweden
by Strandqvist, A
The journal of clinical endocrinology and metabolism, 2014, Vol.99 (4), p.1425-1432
8.
Gender Role Behavior, Sexuality, and Psychosocial Adaptation in Women with Congenital Adrenal Hyperplasia due to CYP21A2 Deficiency
by Frisén, Louise
The journal of clinical endocrinology and metabolism, 2009, Vol.94 (9), p.3432-3439
9.
Sexual Function and Surgical Outcome in Women with Congenital Adrenal Hyperplasia Due to CYP21A2 Deficiency: Clinical Perspective and the Patients’ Perception
by Nordenström, Anna
The journal of clinical endocrinology and metabolism, 2010, Vol.95 (8), p.3633-3640
10.
Type of Mutation and Surgical Procedure Affect Long-Term Quality of Life for Women with Congenital Adrenal Hyperplasia
by Nordenskjöld, Agneta
The journal of clinical endocrinology and metabolism, 2008, Vol.93 (2), p.380-386
11.
Fractures and Bone Mineral Density in Adult Women with 21-Hydroxylase Deficiency
by Falhammar, Henrik
The journal of clinical endocrinology and metabolism, 2007, Vol.92 (12), p.4643-4649
12.
Metabolic Profile and Body Composition in Adult Women with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
by Falhammar, Henrik
The journal of clinical endocrinology and metabolism, 2007, Vol.92 (1), p.110-116
13.
Sexual Function and Surgical Outcome in Women with Congenital Adrenal Hyperplasia Due toCYP21A2Deficiency: Clinical Perspective and the Patients’ Perception
by Nordenström, Anna
The journal of clinical endocrinology and metabolism, 2010, Vol.95 (8), p.3633-3640
14.
Gender Role Behavior, Sexuality, and Psychosocial Adaptation in Women with Congenital Adrenal Hyperplasia due toCYP21A2Deficiency
by Frisén, Louise
The journal of clinical endocrinology and metabolism, 2009, Vol.94 (9), p.3432-3439
