A. Mitsioni

发表

Nucleotide variations in the NPHS2 gene in Greek children with steroid-resistant nephrotic syndrome.

E. Kanavakis, J. Traeger-Synodinos, C. Stefanidis, 2009, Genetic testing and molecular biomarkers.

Plasma Urotensin II levels in children and adolescents with chronic kidney disease: a single-centre study

C. Stefanidis, A. Mitsioni, A. Garoufi, 2017, BMC Nephrology.

Routine serum biomarkers, but not Dual Energy X-ray Absorptiometry, correlate with cortical bone mineral density in children and young adults with CKD

D. Wheeler, D. Milford, J. Popoola, 2020 .

IgA nephropathy in children.

A. Mitsioni, 2001, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

A Population-Specific Formula Predicting Creatinine Excretion in Children on Chronic Peritoneal Dialysis

C. Stefanidis, A. Mitsioni, M. Bitsiori, 2003 .

Antibody‐mediated rejection with the presence of glomerular crescents in a pediatric kidney transplant recipient: A case report

V. Karava, C. Stefanidis, A. Mitsioni, 2020, Pediatric transplantation.

Results in the ESPN/ERA-EDTA Registry suggest disparities in access to kidney transplantation but little variation in graft survival of children across Europe.

B. Tönshoff, T. Seeman, A. Jankauskienė, 2020, Kidney international.

Serum osteoprotegerin, RANKL and fibroblast growth factor-23 in children with chronic kidney disease

C. Stefanidis, A. Mitsioni, N. Printza, 2011, Pediatric Nephrology.

Safety, immunogenicity and kinetics of immune response to 7-valent pneumococcal conjugate vaccine in children with idiopathic nephrotic syndrome.

C. Stefanidis, A. Mitsioni, M. Theodoridou, 2011, Vaccine.

Nephrology in Greece

P. Passadakis, A. Mitsioni, I. Boletis, 2021 .

Plasma Brain Natriuretic Peptide Levels in Children with Chronic Kidney Disease and Renal Transplant Recipients: A Single Center Study

A. Mitsioni, A. Garoufi, D. Gourgiotis, 2022, Children.

Novel and Founder Pathogenic Variants in X-Linked Alport Syndrome Families in Greece

E. Frangou, C. Deltas, A. Papagianni, 2022, Genes.

Successful treatment of steroid-resistant nephrotic syndrome associated with WT1 mutations

U. Querfeld, C. Stefanidis, A. Mitsioni, 2010, Pediatric Nephrology.

Safety and immunogenicity of booster immunization with 7-valent pneumococcal conjugate vaccine in children with idiopathic nephrotic syndrome.

C. Stefanidis, A. Mitsioni, M. Theodoridou, 2014, Vaccine.

The immunopathogenesis of idiopathic nephrotic syndrome: a narrative review of the literature

A. Mitsioni, V. Askiti, K. Kitsou, 2022, European Journal of Pediatrics.

Bone Mineral Density and Vascular Calci ﬁ cation in Children and Young Adults With CKD 4 to 5 or on Dialysis

D. Milford, N. Crabtree, K. Mortensen, 2022 .

Long-term outcome of hepatitis B after renal transplantation during childhood.

A. Mitsioni, G. Guest, M. Broyer, 1993, Transplantation proceedings.

Long‐term outcome of pediatric kidney transplantation: A single‐center experience from Greece

S. Stabouli, C. Stefanidis, A. Mitsioni, 2016, Pediatric transplantation.

Routine serum biomarkers, but not dual-energy X-ray absorptiometry, correlate with cortical bone mineral density in children and young adults with chronic kidney disease.

D. Wheeler, D. Milford, M. Leonard, 2020, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Absence of mutations in the HOXA11 and HOXD11 genes in children with congenital renal malformations

I. Georgiou, C. Stefanidis, A. Mitsioni, 2009, Pediatric Nephrology.

Novel and known nephrin gene (NPHS1) mutations in two Greek cases with congenital nephrotic syndrome including a complex genotype

S. Kitsiou‐Tzeli, E. Kanavakis, C. Stefanidis, 2013, Journal of Genetics.

Effect of the correction of anemia with recombinant human erythropoietin on growth of children treated with CAPD.

C. Stefanidis, A. Mitsioni, A. Kapogiannis, 1992, Advances in peritoneal dialysis. Conference on Peritoneal Dialysis.

Bone Mineral Density and Vascular Calcification in Children and Young Adults With CKD 4 to 5 or on Dialysis

D. Wheeler, D. Milford, J. Long, 2022, Kidney international reports.

Broad and unexpected phenotypic expression in Greek children with steroid-resistant nephrotic syndrome due to mutations in the Wilms’ tumor 1 (WT1) gene

E. Kanavakis, J. Traeger-Synodinos, C. Stefanidis, 2011, European Journal of Pediatrics.

Impact of de novo donor‐specific HLA antibodies on pediatric kidney transplant prognosis in patients with acute declined or stable allograft function

V. Karava, A. Mitsioni, M. Papachristou, 2022, Pediatric transplantation.