Rathi V. Prasad
Charterhouse Square
London, ENG, United Kingdom
London, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 39 publications
A Case Report on Moyamoya Syndrome Associated with Noonan-Like Syndrome with Loose Anagen Hair and Growth Hormone Insufficiency.
Journal: Hormone research in paediatrics
Published: November 03, 2025
Author Correction: International consensus statement on the diagnosis and management of phaeochromocytoma and paraganglioma in children and adolescents.
Journal: Nature reviews. Endocrinology
Published: August 13, 2025
Effect of pubertal induction with combined gonadotropin therapy on testes development and spermatogenesis in males with gonadotropin deficiency: a cohort study.
Journal: Human reproduction open
Published: January 09, 2025
Author Correction: International consensus statement on the diagnosis and management of phaeochromocytoma and paraganglioma in children and adolescents.
Journal: Nature reviews. Endocrinology
Published: August 27, 2024
International consensus statement on the diagnosis and management of phaeochromocytoma and paraganglioma in children and adolescents.
Journal: Nature reviews. Endocrinology
Published: July 17, 2024
Thioredoxin Reductase 2 Variant as a Cause of Micropenis, Undescended Testis, and Selective Glucocorticoid Deficiency.
Journal: Hormone research in paediatrics
Published: May 05, 2023
Ichthyosis linked to sphingosine 1-phosphate lyase insufficiency is due to aberrant sphingolipid and calcium regulation.
Journal: Journal of lipid research
Published: October 13, 2022
A retrospective analysis of endocrine disease in sphingosine-1-phosphate lyase insufficiency: case series and literature review.
Journal: Endocrine connections
Published: June 01, 2022
Elevated sphingosine-1-phosphate lyase leads to increased metabolism and reduced survival in adrenocortical carcinoma.
Journal: European journal of endocrinology
Published: December 01, 2021
Insights From Long-term Follow-up of a Girl With Adrenal Insufficiency and Sphingosine-1-Phosphate Lyase Deficiency.
Journal: Journal of the Endocrine Society
Published: November 29, 2021
Genetic Analysis of Pediatric Primary Adrenal Insufficiency of Unknown Etiology: 25 Years' Experience in the UK.
Journal: Journal of the Endocrine Society
Published: March 19, 2021
A Sphingosine-1-Phosphate Lyase Mutation Associated With Congenital Nephrotic Syndrome and Multiple Endocrinopathy.
Journal: Frontiers in pediatrics
Published: December 10, 2019
Last Updated: 09/26/2026