Gedeon Loules

31 Makrigianni Street
Larisa, ESYE14 41334, Greece

Last Updated: 09/26/2026

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Found 12 publications

Liquid biopsy miRNA risk score in bladder cancer: Translational insights from patient-derived xenografts to prognostic stratification.

Liquid biopsy miRNA risk score in bladder cancer: Translational insights from patient-derived xenografts to prognostic stratification.

Journal: European journal of cancer (Oxford, England : 1990)

Published: June 24, 2026

CDKN2A copy number alteration in bladder cancer: Integrative analysis in patient-derived xenografts and cancer patients.

CDKN2A copy number alteration in bladder cancer: Integrative analysis in patient-derived xenografts and cancer patients.

Journal: Molecular therapy. Oncology

Published: October 09, 2023

Hereditary angioedema with normal C1 inhibitor associated with carboxypeptidase N deficiency.

Hereditary angioedema with normal C1 inhibitor associated with carboxypeptidase N deficiency.

Journal: The journal of allergy and clinical immunology. Global

Published: August 07, 2023

Searching for Genetic Biomarkers for Hereditary Angioedema Due to C1-Inhibitor Deficiency (C1-INH-HAE).

Searching for Genetic Biomarkers for Hereditary Angioedema Due to C1-Inhibitor Deficiency (C1-INH-HAE).

Journal: Frontiers in allergy

Published: February 02, 2022

Deciphering the Genetics of Primary Angioedema with Normal Levels of C1 Inhibitor.

Deciphering the Genetics of Primary Angioedema with Normal Levels of C1 Inhibitor.

Journal: Journal of clinical medicine

Published: September 23, 2020

A novel deep intronic SERPING1 variant as a cause of hereditary angioedema due to C1-inhibitor deficiency.

A novel deep intronic SERPING1 variant as a cause of hereditary angioedema due to C1-inhibitor deficiency.

Journal: Allergology international : official journal of the Japanese Society of Allergology

Published: October 08, 2019

A novel homozygous SACS mutation identified by whole exome sequencing-genotype phenotype correlations of all published cases.

A novel homozygous SACS mutation identified by whole exome sequencing-genotype phenotype correlations of all published cases.

Journal: Journal of molecular neuroscience : MN

Published: August 14, 2019

On the pathogenicity of the plasminogen K330E mutation for hereditary angioedema.

On the pathogenicity of the plasminogen K330E mutation for hereditary angioedema.

Journal: Allergy

Published: July 17, 2018

Targeted next-generation sequencing for the molecular diagnosis of hereditary angioedema due to C1-inhibitor deficiency.

Targeted next-generation sequencing for the molecular diagnosis of hereditary angioedema due to C1-inhibitor deficiency.

Journal: Gene

Published: December 12, 2017

Fabry disease due to D313Y and novel GLA mutations.

Fabry disease due to D313Y and novel GLA mutations.

Journal: BMJ open

Published: October 09, 2017

Genetic Determinants of C1 Inhibitor Deficiency Angioedema Age of Onset.

Genetic Determinants of C1 Inhibitor Deficiency Angioedema Age of Onset.

Journal: International archives of allergy and immunology

Published: July 05, 2017

Increased Triacylglycerol Lipase Activity in Adipose Tissue of Lean and Obese Men During Endurance Exercise.

Increased Triacylglycerol Lipase Activity in Adipose Tissue of Lean and Obese Men During Endurance Exercise.

Journal: The Journal of clinical endocrinology and metabolism

Published: January 18, 2017

Showing 1-12 of 12

Last Updated: 09/26/2026