Eleni Litou is an expert in Endocrinology at AHEPA University Hospital (Greece). Eleni Litou has authored 6 publications, the most recent in 2023, and is an investigator in 1 clinical trial. SLR score: 20 (community average: 125). How the SLR is computed.

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Eleni Litou AHEPA University Hospital Greece
20 ScienceLeadR Reputation 20
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Endocrinology

Subspecialties:

Full career – Last 3 years

Main Topics

Publications and Clinical Studies

Publications – Clinical Studies

Profile data updated on

Organizations

Career arc: 2017 - 2023

Source: PubMed

Aristotle University of Thessaloniki

Publications Synthesis

Sources: PubMed, OpenAlex

Number : 6

Citations

Citations: 46 1st author: 0 Last author: 0 Unique author: 0


Best Journals

Breakdown by type

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Latest Publications

5 most recent indexed articles

Source: Pubmed

Title Journal Year Citations
Predictive Factors for Pediatric Craniopharyngioma Recurrence: An Extensive Narrative Review.
PMID 37174978 — growth, neoplasms, craniopharyngioma, adolescent, risk factors, prognosis, child
Diagnostics (Basel)202313
The Prognostic Significance of BRAF Gene Analysis in Children and Adolescents with Papillary Thyroid Carcinoma: A Systematic Review and Meta-Analysis.
PMID 36980495 — thyroid cancer, papillary, genes, neoplasms, thyroid gland, adolescent, neoplasm metastasis, mutation, prognosis, child
Diagnostics (Basel)202312
Pseudohypoparathyroidism Type 1A with Normocalcaemia, due to the Novel C.389A>G Variant of Exon 5 of the Guanine Nucleotide-Binding Protein, α-Stimulating Gene.
PMID 33730787 — genes, guanine nucleotides, maternal inheritance, phenotype, pseudohypoparathyroidism, point mutation, exons, alleles, mutation, guanine
J Bone Metab20210
Permanent damage of the sciatic nerve in an 8-year-old girl with newly diagnosed type 1 diabetes.
PMID 30739577 — insulin, child, diabetic ketoacidosis, pediatrics, diabetes mellitus, type 1, ketosis, sciatic nerve
Paediatr Int Child Health20192
46,XY Disorder of Sex Development due to 17-Beta Hydroxysteroid Dehydrogenase Type 3 Deficiency in an Infant of Greek Origin.
PMID 28739554 — genes, oxidoreductases, hydroxysteroid dehydrogenases, sex, mutation, endocrine system diseases, infant, sexual development
J Clin Res Pediatr Endocrinol201714

Clinical Studies 1

Sources: ClinicalTrials, EU CTIS

Synthesis

By phase:

N/A 1

By status:

Recruiting 1

By type:

Observational 1

By Monocentric/Multicentric:

monocentric 1
multicentric2to4 0
multicentric5to9 0
multicentricup10 0

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