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Found 10 publications

Novel FGFR1 Variants Are Associated with Congenital Scoliosis.

Seminal Plasma Lipidomics Profiling to Identify Signatures of Kallmann Syndrome.

Mechanisms of Central Hypogonadism.

Slipped Capital Femoral Epiphysis in an Adult with Panhypopituitarism: A Case Report.

Kallmann syndrome and idiopathic hypogonadotropic hypogonadism: The role of semaphorin signaling on GnRH neurons.

Defects in GnRH Neuron Migration/Development and Hypothalamic-Pituitary Signaling Impact Clinical Variability of Kallmann Syndrome.

A Sprouty4 Mutation Identified in Kallmann Syndrome Increases the Inhibitory Potency of the Protein towards FGF and Connected Processes.

Kallmann Syndrome Due to Heterozygous Mutation in SOX10 Coexisting With Waardenburg Syndrome Type II: Case Report and Review of Literature.

Gonadotropin treatment for male partial congenital hypogonadotropic hypogonadism in Chinese patients.

Gonadotropin-releasing hormone (GnRH) deficiency under treatment: psychological and sexual functioning impacts.

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