Lise Aksglaede
0000-0001-7885-7467
Rigshospitalet
87 papers found
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Reduced serum concentrations of biomarkers reflecting Leydig and Sertoli cell function in male patients with congenital adrenal hyperplasia
Reproductive hormones, bone mineral content, body composition, and testosterone therapy in boys and adolescents with Klinefelter syndrome
Biochemical identification of prepubertal boys with Klinefelter syndrome by combined reproductive hormone profiling using machine learning
Microdissection Testicular Sperm Extraction Versus Multiple Needle-pass Percutaneous Testicular Sperm Aspiration in Men with Nonobstructive Azoospermia: A Randomized Clinical Trial
A randomized double-blind single center study of testosterone replacement therapy or placebo in testicular cancer survivors with mild Leydig cell insufficiency (Einstein-intervention)
Optimized detection of germ cell neoplasia in situ in contralateral biopsy reduces the risk of second testis cancer
Prepubertal and pubertal gonadal morphology, expression of cell lineage markers and hormonal evaluation in two 46,XY siblings with 17β-hydroxysteroid dehydrogenase 3 deficiency
Long‐term testosterone undecanoate treatment in the elderly testosterone deficient male: An observational cohort study
Serum Concentrations and Gonadal Expression of INSL3 in Eighteen Males With 45,X/46,XY Mosaicism
Testicular cancer survivors have shorter anogenital distance that is not increased by 1 year of testosterone replacement therapy
Non-Classic Congenital Adrenal Hyperplasia in Two Adolescents With Gender Dysphoria
European academy of andrology guidelines on Klinefelter Syndrome Endorsing Organization: European Society of Endocrinology
The LH/FSH ratio is not a sex-dimorphic marker after infancy: data from 6417 healthy individuals and 125 patients with Differences of Sex Development
Minipuberty of human infancy – A window of opportunity to evaluate hypogonadism and differences of sex development?
Minipuberty in Klinefelter syndrome: Current status and future directions
Voice break in boys—temporal relations with other pubertal milestones and likely causal effects of BMI
Growth disrupting mutations in epigenetic regulatory molecules are associated with abnormalities of epigenetic aging
Transcriptome analysis of the adult human Klinefelter testis and cellularity-matched controls reveals disturbed differentiation of Sertoli- and Leydig cells
The Tatton-Brown-Rahman Syndrome: A clinical study of 55 individuals with de novo constitutive DNMT3A variants.
Deletion in the uridine diphosphate glucuronyltransferase 2B17 gene is associated with delayed pubarche in healthy boys
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