Translational endocrinology and rare phenotypic variation

28 days

median initial decision

100%

double-blind evaluation

450+

international reviewers

Open

immediate global access

Selected clinical findings

Recent peer-reviewed contributions documenting atypical phenotypic presentations, novel receptor pathways, and validated multi-center registry protocols.

Gonadal Dysgenesis Cohorts

Receptor Sensitivity Variants

Adrenal Hyperplasia Guidelines

Longitudinal endocrine surveillance across 312 international patients evaluating pubertal induction regimens and secondary metabolic markers.

High-throughput exome analysis identifying novel loss-of-function variants in pediatric cohorts with persistent androgen insensitivity.

Multicenter diagnostic recommendations standardizing biomarker thresholds during neonatal screening and early steroid replacement therapies.

Unifying fragmented international clinical registries through verifiable molecular pathology and open scientific dissemination.

All accepted contributions strictly adhere to Committee on Publication Ethics guidelines, ensuring transparent data provenance and open-access utility for clinical endocrinologists worldwide.

Review structural manuscript guidelines, ethical consent disclosures, and data depository policies prior to formal portal upload.