Genetic forms of male hypogonadism

Prader-Willi syndrome: a review of clinical, genetic, and endocrine findings.

Journal of endocrinological investigation·2015

Limb lengthening in children.

Orthopedics·2014

Characterization of two novel homozygous missense mutations involving codon 6 and 259 of type II 3beta-hydroxysteroid dehydrogenase (3betaHSD) gene causing, respectively, nonsalt-wasting and salt-wasting 3betaHSD deficiency disorder.

The Journal of clinical endocrinology and metabolism·2000

Effects of growth hormone and testosterone on cortical bone formation and bone density in aged orchiectomized rats.

Bone·1999

Photoanthropometric study of craniofacial traits in individuals with Prader-Willi syndrome on short-term growth hormone therapy.

Clinical genetics·1998

Macrotestes associated with hyperprolactinemia.

Journal of pediatric endocrinology & metabolism : JPEM·1996

Post-operative Urinary Tract Infection After Pediatric Pyeloplasty: A Multicenter Analysis of Drain Type, Surgical Approach, and Prophylactic Antibiotics.

Urology·2026

Evaluation of AI Chatbot Responses to Pediatric Urology Frequently Asked Questions.

Urology·2026

Convergent Validity of Stamey's Incontinence Scoring System in Assessing Post-Prostatectomy Urinary Incontinence.

Urology·2026

Urinary Biomarkers in Childhood Cancer Survivors with Lower Urinary Tract Dysfunction.

Urology·2026

Item Level Analysis of Patient-Reported Outcomes After Ureteroscopy for Kidney Stones- Plan Your Chores, Cancel Your Plans.

Urology·2026

Trends in Urodynamic Study Claims Billed by Physicians and Advanced Practice Providers in the United States between 2010 and 2024.

Urology·2026

Preimplantation genetic testing and prenatal diagnosis of TANGO2 deficiency disorder with biallelic pathogenic variants using single-nucleotide polymorphism-based haplotyping and gap-polymerase chain reaction.

Frontiers in genetics·2026

Clinical and genetic features of syndromic craniosynostosis in 18 Chinese probands: novel candidate genes and phenotypes of known pathogenic genes.

Frontiers in genetics·2026

Notch-Regulated Hematopoiesis in Drosophila: Parallels and Contrasts with Vertebrate Blood Development.

Developmental biology·2026

Serotonin deficiency caused by inactivation of Tph2 in mice leads to widespread sex-dependent changes in cerebral oxidative metabolic activity.

Journal of neural transmission (Vienna, Austria : 1996)·2026

Haplotype-resolved genome assembly of a male Dioscorea alata cultivar reveals the structure and evolution of young sex chromosomes.

The Plant journal : for cell and molecular biology·2026

Low-Level Viremia and Spatial Heterogeneity Among Individuals on Dolutegravir-Based Antiretroviral Therapy in Botswana: A Nationwide Study (2016-2022).

The Journal of infectious diseases·2026

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Genetic forms of male hypogonadism

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Prader-Willi syndrome: a review of clinical, genetic, and endocrine findings.

Limb lengthening in children.

Characterization of two novel homozygous missense mutations involving codon 6 and 259 of type II 3beta-hydroxysteroid dehydrogenase (3betaHSD) gene causing, respectively, nonsalt-wasting and salt-wasting 3betaHSD deficiency disorder.

Effects of growth hormone and testosterone on cortical bone formation and bone density in aged orchiectomized rats.

Photoanthropometric study of craniofacial traits in individuals with Prader-Willi syndrome on short-term growth hormone therapy.

Macrotestes associated with hyperprolactinemia.

Post-operative Urinary Tract Infection After Pediatric Pyeloplasty: A Multicenter Analysis of Drain Type, Surgical Approach, and Prophylactic Antibiotics.

Evaluation of AI Chatbot Responses to Pediatric Urology Frequently Asked Questions.

Convergent Validity of Stamey's Incontinence Scoring System in Assessing Post-Prostatectomy Urinary Incontinence.

Urinary Biomarkers in Childhood Cancer Survivors with Lower Urinary Tract Dysfunction.

Item Level Analysis of Patient-Reported Outcomes After Ureteroscopy for Kidney Stones- Plan Your Chores, Cancel Your Plans.

Trends in Urodynamic Study Claims Billed by Physicians and Advanced Practice Providers in the United States between 2010 and 2024.

Preimplantation genetic testing and prenatal diagnosis of TANGO2 deficiency disorder with biallelic pathogenic variants using single-nucleotide polymorphism-based haplotyping and gap-polymerase chain reaction.

Clinical and genetic features of syndromic craniosynostosis in 18 Chinese probands: novel candidate genes and phenotypes of known pathogenic genes.

Notch-Regulated Hematopoiesis in Drosophila: Parallels and Contrasts with Vertebrate Blood Development.

Serotonin deficiency caused by inactivation of Tph2 in mice leads to widespread sex-dependent changes in cerebral oxidative metabolic activity.

Haplotype-resolved genome assembly of a male Dioscorea alata cultivar reveals the structure and evolution of young sex chromosomes.

Low-Level Viremia and Spatial Heterogeneity Among Individuals on Dolutegravir-Based Antiretroviral Therapy in Botswana: A Nationwide Study (2016-2022).

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Genetic forms of male hypogonadism

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