Hypogonadotropic hypogonadism; the genetic defect. A hypothesis based on human and animal prototypes.

Central hypogonadotropic hypogonadism: genetic complexity of a complex disease.

Comment on reversal of hypogonadotropic hypogonadism in a Chinese cohort.

Familial hypogonadotropic hypogonadism with alopecia.

A network investigation on idiopathic hypogonadotropic hypogonadism in china.

Treatment of hypogonadotropic male hypogonadism: Case-based scenarios.

Hypogonadotropic hypogonadism and temporal lobe epilepsy.

A shared genetic basis for self-limited delayed puberty and idiopathic hypogonadotropic hypogonadism.

Hypogonadotropic hypogonadism in men with hereditary hemochromatosis.

The syndrome of Möbius sequence, peripheral neuropathy, and hypogonadotropic hypogonadism.

Genetics of congenital hypogonadotropic hypogonadism in Denmark.

Unexpected difficult airway with hypogonadotropic hypogonadism.

Moebius syndrome in association with hypogonadotropic hypogonadism.

Brief report: melatonin-related hypogonadotropic hypogonadism.

Congenital hypogonadotropic hypogonadism during childhood: presentation and genetic analyses in 46 boys.

A Rare Presentation of Transfusional Hemochromatosis: Hypogonadotropic Hypogonadism.

McCune-Albright syndrome. A case of primary hypogonadism obscured by hyperprolactinemic hypogonadotropic hypogonadism.

Autosomal recessive syndrome of cerebellar ataxia and hypogonadotropic hypogonadism.

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Clinical and laboratory heterogeneity in idiopathic hypogonadotropic hypogonadism.

Phenotypic spectrum and hormonal profile in hypogonadotropic hypogonadism.

Idiopathic Hypogonadotropic Hypogonadism Caused by Inactivating Mutations in SRA1.

Functional consequences of AXL sequence variants in hypogonadotropic hypogonadism.

Psychosexual development in men with congenital hypogonadotropic hypogonadism on long-term treatment: a mixed methods study.

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Central hypogonadotropic hypogonadism: genetic complexity of a complex disease.

Comment on reversal of hypogonadotropic hypogonadism in a Chinese cohort.

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A network investigation on idiopathic hypogonadotropic hypogonadism in china.

Treatment of hypogonadotropic male hypogonadism: Case-based scenarios.

Hypogonadotropic hypogonadism and temporal lobe epilepsy.

A shared genetic basis for self-limited delayed puberty and idiopathic hypogonadotropic hypogonadism.

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The syndrome of Möbius sequence, peripheral neuropathy, and hypogonadotropic hypogonadism.

Genetics of congenital hypogonadotropic hypogonadism in Denmark.

Unexpected difficult airway with hypogonadotropic hypogonadism.

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Congenital hypogonadotropic hypogonadism during childhood: presentation and genetic analyses in 46 boys.

A Rare Presentation of Transfusional Hemochromatosis: Hypogonadotropic Hypogonadism.

McCune-Albright syndrome. A case of primary hypogonadism obscured by hyperprolactinemic hypogonadotropic hypogonadism.

Autosomal recessive syndrome of cerebellar ataxia and hypogonadotropic hypogonadism.

Congenital Hypogonadotropic Hypogonadism and Kallmann Syndrome: Past, Present, and Future.

Clinical and laboratory heterogeneity in idiopathic hypogonadotropic hypogonadism.

Phenotypic spectrum and hormonal profile in hypogonadotropic hypogonadism.

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Functional consequences of AXL sequence variants in hypogonadotropic hypogonadism.

Psychosexual development in men with congenital hypogonadotropic hypogonadism on long-term treatment: a mixed methods study.

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Hypogonadotropic hypogonadism; the genetic defect. A hypothesis based on human and animal prototypes.

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