Publications by authors named "Alkis Pierides"

Claim this Profile
C
COL4A5 and LAMA5 variants co-inherited in familial hematuria: digenic inheritance or genetic modifier effect?
Konstantinos Voskarides, Gregory Papagregoriou, Despina Hadjipanagi, Ioanelli Petrou, Isavella Savva, Alkis Pierides

BMC Nephrol· May 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A functional variant in NEPH3 gene confers high risk of renal failure in primary hematuric glomerulopathies. Evidence for predisposition to microalbuminuria in the general population.
Konstantinos Voskarides, Charalambos Stefanou, Myrtani Pieri, Panayiota Demosthenous, Kyriakos Felekkis, Alkis Pierides

PLoS One· August 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Co-Inheritance of Functional Podocin Variants with Heterozygous Collagen IV Mutations Predisposes to Renal Failure.
Charalambos Stefanou, Myrtani Pieri, Isavella Savva, Georgia Georgiou, Alkis Pierides

Nephron· May 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Carriers of Autosomal Recessive Alport Syndrome with Thin Basement Membrane Nephropathy Presenting as Focal Segmental Glomerulosclerosis in Later Life.
Constantinos Deltas, Isavella Savva, Konstantinos Voskarides, Louiza Papazachariou, Alkis Pierides

Nephron· May 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
RAAS inhibition and the course of Alport syndrome.
Isavella Savva, Alkis Pierides, Constantinos Deltas

Pharmacol Res· May 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Frequency of COL4A3/COL4A4 mutations amongst families segregating glomerular microscopic hematuria and evidence for activation of the unfolded protein response. Focal and segmental glomerulosclerosis is a frequent development during ageing.
Louiza Papazachariou, Panayiota Demosthenous, Myrtani Pieri, Gregory Papagregoriou, Isavella Savva, Alkis Pierides

PLoS One· February 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Molecular and Clinical Investigation of Cystinuria in the Greek-Cypriot Population.
Yiannis Athanasiou, Konstantinos Voskarides, Anthi Chatzikyriakidou, Anastasia Ignatiou, Panayiota Demosthenous, Alkis Pierides

Genet Test Mol Biomarkers· November 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
COL4A3/COL4A4 heterozygous mutations with TBMN presenting as focal segmental glomerulosclerosis.
Constantinos Deltas, Alkis Pierides

Kidney Int· April 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Familial Mediterranean fever associated with MEFV mutations in a large cohort of Cypriot patients.
Vassos Neocleous, Constantina Costi, Christina Kyriakou, Tassos C Kyriakides, Christos Shammas, Alkis Pierides

Ann Hum Genet· January 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Molecular genetics of familial hematuric diseases.
Constantinos Deltas, Alkis Pierides, Konstantinos Voskarides

Nephrol Dial Transplant· December 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Epistatic role of the MYH9/APOL1 region on familial hematuria genes.
Konstantinos Voskarides, Panayiota Demosthenous, Louiza Papazachariou, Maria Arsali, Yiannis Athanasiou, Alkis Pierides

PLoS One· September 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
C3 glomerulonephritis/CFHR5 nephropathy is an endemic disease in Cyprus: clinical and molecular findings in 21 families.
Constantinos Deltas, Daniel Gale, Terence Cook, Konstantinos Voskarides, Yiannis Athanasiou, Alkis Pierides

Adv Exp Med Biol· March 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
O
On 'Incidence of renal failure and nephroprotection by RAAS inhibition in heterozygous carriers of X-chromosomal and autosomal recessive Alport mutations'.
Konstantinos Voskarides, Alkis Pierides, Constantinos Deltas

Kidney Int· February 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A miR-1207-5p binding site polymorphism abolishes regulation of HBEGF and is associated with disease severity in CFHR5 nephropathy.
Gregory Papagregoriou, Kamil Erguler, Harsh Dweep, Konstantinos Voskarides, Panayiota Koupepidou, Alkis Pierides

PLoS One· September 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The role of molecular genetics in diagnosing familial hematuria(s).
Constantinos Deltas, Alkis Pierides, Konstantinos Voskarides

Pediatr Nephrol· August 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Evidence that NPHS2-R229Q predisposes to proteinuria and renal failure in familial hematuria.
Konstantinos Voskarides, Maria Arsali, Yiannis Athanasiou, Avraam Elia, Alkis Pierides

Pediatr Nephrol· April 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Founder mutations in the ATP6V1B1 gene explain most Cypriot cases of distal renal tubular acidosis: first prenatal diagnosis.
Avraam Elia, Konstantinos Voskarides, Panayiota Demosthenous, Aikaterini Michalopoulou, Maria-Adamantia Malliarou, Alkis Pierides

Nephron Clin Pract· January 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Familial C3 glomerulopathy associated with CFHR5 mutations: clinical characteristics of 91 patients in 16 pedigrees.
Yiannis Athanasiou, Konstantinos Voskarides, Daniel P Gale, Loukas Damianou, Charalambos Patsias, Alkis Pierides

Clin J Am Soc Nephrol· June 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genetic variation of DKK3 may modify renal disease severity in ADPKD.
Michelle Liu, Sally Shi, Sean Senthilnathan, Julie Yu, Elliot Wu, Alkis Pierides

J Am Soc Nephrol· September 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Identification of a mutation in complement factor H-related protein 5 in patients of Cypriot origin with glomerulonephritis.
Daniel P Gale, Elena Goicoechea de Jorge, H Terence Cook, Rubén Martinez-Barricarte, Andreas Hadjisavvas, Alkis Pierides

Lancet· September 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Clinico-pathological correlations in 127 patients in 11 large pedigrees, segregating one of three heterozygous mutations in the COL4A3/ COL4A4 genes associated with familial haematuria and significant late progression to proteinuria and chronic kidney disease from focal segmental glomerulosclerosis.
Alkis Pierides, Konstantinos Voskarides, Yiannis Athanasiou, Kyriacos Ioannou, Loukas Damianou, Michael Pierides

Nephrol Dial Transplant· September 2009

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Incidence of thin basement membrane nephropathy in 990 consecutive renal biopsies examined with electron microscopy.
Ioanna Zouvani, Sophia Aristodemou, Andreas Hadjisavvas, Thalia Michael, Mary Vassiliou, Alkis Pierides

Ultrastruct Pathol· March 2009

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
COL4A3/COL4A4 mutations link familial hematuria and focal segmental glomerulosclerosis. glomerular epithelium destruction via basement membrane thinning?
Konstantinos Voskarides, Alkis Pierides, Constantinos Deltas

Connect Tissue Res· September 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
NPHS2 screening with SURVEYOR in Hellenic children with steroid-resistant nephrotic syndrome.
Konstantinos Voskarides, Christiana Makariou, Gregory Papagregoriou, Nicolaos Stergiou, Nicoletta Printza, Alkis Pierides

Pediatr Nephrol· August 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
COL4A3 founder mutations in Greek-Cypriot families with thin basement membrane nephropathy and focal segmental glomerulosclerosis dating from around 18th century.
Konstantinos Voskarides, Charalampos Patsias, Alkis Pierides, Constantinos Deltas

Genet Test· June 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis