“Craniopharyngioma (CP), Rathke cleft cyst (RCC) and empty sella (ES) natural history and endocrine outcome in pediatric age: a single tertiary centre experience over the 2000-2024 period”

CP, RCC, and ES need baseline and over a prolonged period of time endocrinological and neuroradiological follow-up, in order to detect promptly endocrine defects and sellar/suprasellar region alterations, and multidisciplinary follow-up in tertiary centers is mandatory.

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Publication Details

Journal
Neuroendocrinology
Published
2025-05-19
DOI
https://doi.org/10.1159/000546493
Citations
1
Primary Topic
Pituitary Gland Disorders and Treatments
Type
article
Field-Weighted Citation Impact
1.29
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article

“Craniopharyngioma (CP), Rathke cleft cyst (RCC) and empty sella (ES) natural history and endocrine outcome in pediatric age: a single tertiary centre experience over the 2000-2024 period”

Gerdi Tuli, Jessica Munarin
1 citations
Neuroendocrinology
Pituitary Gland Disorders and Treatments
1.29
article

“Craniopharyngioma (CP), Rathke cleft cyst (RCC) and empty sella (ES) natural history and endocrine outcome in pediatric age: a single tertiary centre experience over the 2000-2024 period”

Gerdi Tuli, Jessica Munarin
article en
1 citations

Abstract

CP, RCC, and ES need baseline and over a prolonged period of time endocrinological and neuroradiological follow-up, in order to detect promptly endocrine defects and sellar/suprasellar region alterations, and multidisciplinary follow-up in tertiary centers is mandatory.

NeuroendocrinologyVol. 115(12)
Ospedale Regina Margherita (IT), University of Turin (IT)
Openalex Percentile: Top 19%
Pituitary Gland Disorders and Treatments
1.29
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