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Last Updated: 10/31/2025

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Found 892 publications

Genetics of Idiopathic Hypogonadotropic Hypogonadism.

Genetics of Idiopathic Hypogonadotropic Hypogonadism.

Journal: Journal of clinical research in pediatric endocrinology
Published: September 17, 2025

Letter: Gender Dysphoria and Transition in a Patient with Kallmann Syndrome: A Case Report.

Letter: Gender Dysphoria and Transition in a Patient with Kallmann Syndrome: A Case Report.

Journal: LGBT health
Published: September 10, 2025

Modification of the Sniffin Kids Test for olfactory testing in a population of Polish children.

Modification of the Sniffin Kids Test for olfactory testing in a population of Polish children.

Journal: Rhinology
Published: September 09, 2025

Body Composition by DXA in Patients With Klinefelter and Kallmann Syndrome: The Kama Study.

Body Composition by DXA in Patients With Klinefelter and Kallmann Syndrome: The Kama Study.

Journal: The Journal of clinical endocrinology and metabolism
Published: August 01, 2025

The Lysine at Position 177 Is Essential to Limit the Inhibitory Capacities of Sprouty4 Protein in Normal and Cancer-Derived Cells.

The Lysine at Position 177 Is Essential to Limit the Inhibitory Capacities of Sprouty4 Protein in Normal and Cancer-Derived Cells.

Journal: International journal of molecular sciences
Published: June 25, 2025

Mirror Movements and Ichthyosis in a Child: A Rare Presentation of Kallmann Syndrome.

Mirror Movements and Ichthyosis in a Child: A Rare Presentation of Kallmann Syndrome.

Journal: Annals of Indian Academy of Neurology
Published: May 29, 2025

Incomplete Evidence of Bone Density Normalization Following Long-Term Reproductive Hormone Treatment in Men With Hypogonadotropic Hypogonadism.

Incomplete Evidence of Bone Density Normalization Following Long-Term Reproductive Hormone Treatment in Men With Hypogonadotropic Hypogonadism.

Journal: The Journal of clinical endocrinology and metabolism
Published: May 26, 2025

Altered glucose metabolism in default mode network and prefrontal circuit in patients with Kallmann syndrome.

Altered glucose metabolism in default mode network and prefrontal circuit in patients with Kallmann syndrome.

Journal: EJNMMI research
Published: April 24, 2025

DNA Methylation in Kallmann Syndrome: Impacts on Neuronal Development and Spermatogenesis.

DNA Methylation in Kallmann Syndrome: Impacts on Neuronal Development and Spermatogenesis.

Journal: Endocrine connections
Published: April 23, 2025

Two cases of Kallmann syndrome caused by a novel mutation in ANOS1: A case report.

Two cases of Kallmann syndrome caused by a novel mutation in ANOS1: A case report.

Journal: Medicine
Published: April 21, 2025

Identification of Novel Genetic Variants in a Cohort of Congenital Hypogonadotropic Hypogonadism: Computational Analysis of Pathogenicity Predictions.

Identification of Novel Genetic Variants in a Cohort of Congenital Hypogonadotropic Hypogonadism: Computational Analysis of Pathogenicity Predictions.

Journal: International journal of molecular sciences
Published: April 08, 2025

Spontaneous Improvement of Hypogonadotropic Hypogonadism in a Patient with PCSK1 and HS6ST1 Mutations: A Case Report.

Spontaneous Improvement of Hypogonadotropic Hypogonadism in a Patient with PCSK1 and HS6ST1 Mutations: A Case Report.

Journal: Life (Basel, Switzerland)
Published: March 21, 2025
Showing 1-12 of 892

Last Updated: 10/31/2025