G. Loules

发表

Foxp3 expression in human cancer cells

K. Gourgoulianis, V. Karanikas, M. Speletas, 2008, Journal of Translational Medicine.

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

Á. Szilágyi, H. Farkas, M. Maurer, 2022, Frontiers in Allergy.

Analysis of SLC40A1 gene at the mRNA level reveals rapidly the causative mutations in patients with hereditary hemochromatosis type IV.

P. Hytiroglou, M. Speletas, A. Germenis, 2008, Blood cells, molecules & diseases.

Aspects of hereditary angioedema genotyping in the era of NGS: The case of F12 gene

H. Farkas, M. Bova, M. Magerl, 2018 .

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

A. Jamurtas, I. Papassotiriou, I. Fatouros, 2017, The Journal of clinical endocrinology and metabolism.

FIP1L1-PDGFRA molecular analysis in the differential diagnosis of eosinophilia

N. Giannakoulas, M. Speletas, P. Matsouka, 2009, BMC blood disorders.

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

M. López-Trascasa, H. Farkas, M. Maurer, 2018, Gene.

Abstracts from the 10th C1-inhibitor deficiency workshop

William H. Yang, A. Szilágyi, M. Margaglione, 2017, Allergy, Asthma & Clinical Immunology.

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

H. Farkas, M. Maurer, M. Magerl, 2020, Allergology international : official journal of the Japanese Society of Allergology.

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

H. Farkas, M. Bova, S. D. Del Giacco, 2020, Journal of clinical medicine.

On the pathogenicity of the plasminogen K330E mutation for hereditary angioedema

I. Braenne, K. Bork, K. Wulff, 2018, Allergy.

Genetic Determinants of C1 Inhibitor Deficiency Angioedema Age of Onset

H. Farkas, M. Maurer, M. Magerl, 2017, International Archives of Allergy and Immunology.

Fabry disease due to D313Y and novel GLA mutations

J. Kyriazis, M. Speletas, A. Germenis, 2017, BMJ Open.

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

G. Hadjigeorgiou, G. Xiromerisiou, P. Stathis, 2019, Journal of Molecular Neuroscience.

CorrigendumCorrigendum to: Analysis of SLC40A1 gene at the mRNA level reveals rapidly the causative mutations in patients with hereditary hemochromatosis type IV [Blood Cells Mol. Dis. 40:3 (2008) 353–359]

P. Hytiroglou, M. Speletas, A. Germenis, 2013 .