System Maintenance Notice

Please note that maintenance work is scheduled between 4 AM and 5 AM - CET. During this time, you may experience reduced performance. Thanks for your patience.

Nikoleta Printza is an expert in Pediatrics at Ippokrateio General Hospital of Thessaloniki (Greece). As of September 2026, ScienceLeadR ranks Nikoleta Printza in the top 1% of experts in Greece for Nephrosis. Nikoleta Printza has authored 183 publications, the most recent in 2026, and is an investigator in 2 clinical trials, 1 of them ongoing. SLR score: 502 (community average: 125). How the SLR is computed.

LeadR Profile

Nikoleta Printza Ippokrateio General Hospital of Thessaloniki Greece
502 ScienceLeadR Reputation 502

Unlock

Register Login
Network Map

Pediatrics

Subspecialties: Nephrology - Urology

Full career – Last 3 years

Main Topics

Publications and Clinical Studies

Publications – Clinical Studies

Profile data updated on

Expert Rankings

Top experts on the MeSH terms this expert works on

Organizations

Career arc: 2007 - 2026
Source: PubMed

Aristotle University of Thessaloniki

Publications Synthesis

Sources: PubMed, OpenAlex

Number : 183

Citations

Citations: 2 607 1st author: 18 Last author: 48 Unique author: 0

Main journals

Pediatr Nephrol 31
Hippokratia 11
Nephrol Dial Transplant 11
J Hypertens 7
Kidney Int Rep 6

Best Journals

Breakdown by type

Click a legend label to hide or show it in the chart.

Latest Publications

5 most recent indexed articles

Source: Pubmed

Title Journal Year Citations
Precision Medicine in Pediatric Nephrology: From Shared Clinical Phenotypes to Genotype-Guided Diagnosis and Management.
PMID 42792963 — thrombotic microangiopathies, research design, genomics, phenotype, kidney, kidney diseases, cystic, nephrology, genotype, precision medicine, diagnosis, therapeutics, counseling		Genes (Basel)20260
Clinical Spectrum and Early Renal Functional Variability in a Nationwide Greek Pediatric HNF1B Multicenter Cohort.
PMID 42739594 — genes, phenotype, kidney, genotype, diagnosis		J Clin Med20260
Setmelanotide Response Variability in Two Genetically Confirmed Pediatric Kidney Transplant Recipients with Bardet-Biedl Syndrome.
PMID 42737637 — hyperphagia, ciliopathies, pediatric obesity, kidney, bardet-biedl syndrome, cyclosporine, transplants, kidney transplantation, hunger, transplantation		Int J Mol Sci20260
Left Ventricular Global Longitudinal Strain as a Marker of Subclinical Myocardial Dysfunction in Youths With Type 1 Diabetes Mellitus: An Updated Systematic Review and Meta-Analysis.
PMID 42640083 — diabetes mellitus, diabetes mellitus, type 1		Diabetes Metab Res Rev20260
Heterogeneous Renal Trajectories in Pediatric IgA Nephropathy: A Single-Center Experience Highlighting the Dynamic Nature of Early Disease.
PMID 42496462 — proteinuria, disease progression, classification, recycling, biopsy, immunoglobulin a, glomerulonephritis, iga, child		Pediatr Rep20260

Clinical Studies 2

Sources: ClinicalTrials, EU CTIS

Synthesis

Principal Investigator: 1

By phase:

N/A 1
Phase 3 1

By status:

Active not recruiting 1
Unknown 1

By type:

Interventional 1
Observational 1

By Monocentric/Multicentric:

monocentric 1
multicentric2to4 0
multicentric5to9 0
multicentricup10 1

Main Topics

Cohort/Consortium Investigators 8

Ongoing Clinical Trials

Ongoing trial started since 2021, where this expert is an investigator

Source: ClinicalTrials

Study Phase Status Start
A Phase 3 Open Label Uncontrolled Study to Evaluate the Activity Safety Pharmacokinetics and Pharmacodynamics of Roxadustat for the Treatment of Anemia in Pediatric Participants with Chronic Kidney Disease
2022-501980-42-00 — kidney diseases, safety, anemia, kidney, aged, adolescent, therapeutics, child, pharmacokinetics		Phase 3Active not recruiting2023

LeadR Networks

Main global connection map

Sources: PubMed, OpenAlex, ClinicalTrials, EU CTIS