A. Pierides

发表

PKD2, a Gene for Polycystic Kidney Disease That Encodes an Integral Membrane Protein

Patricia A. Gabow, William J. Kimberling, Martijn H. Breuning, 1996, Science.

Autosomal dominant polycystic kidney disease-type 2. Ultrasound, genetic and clinical correlations.

A. Pierides, C. Deltas, K. Demetriou, 2000, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Familial C3 glomerulopathy associated with CFHR5 mutations: clinical characteristics of 91 patients in 16 pedigrees.

K. Kyriacou, A. Hadjisavvas, K. Voskarides, 2011, Clinical journal of the American Society of Nephrology : CJASN.

Familial Mediterranean Fever Associated with MEFV Mutations in a Large Cohort of Cypriot Patients

A. Pierides, A. Hadjipanayis, M. Koliou, 2015, Annals of human genetics.

Familial Mediterranean fever (FMF) mutations occur frequently in the Greek-Cypriot population of Cyprus.

A. Pierides, P. Koupepidou, C. Deltas, 2002, Genetic testing.

A translation frameshift mutation induced by a cytosine insertion in the polycystic kidney disease 2 gene (PDK2).

S. Somlo, T. Mochizuki, S. Xenophontos, 1997, Human molecular genetics.

Idiopathic membranous nephropathy.

A. Pierides, D. Kerr, 1977, Nephron.

Carriers of Autosomal Recessive Alport Syndrome with Thin Basement Membrane Nephropathy Presenting as Focal Segmental Glomerulosclerosis in Later Life

K. Voskarides, A. Pierides, C. Deltas, 2015, Nephron.

Epistatic Role of the MYH9/APOL1 Region on Familial Hematuria Genes

K. Voskarides, D. Gale, A. Pierides, 2013, PloS one.

RAAS inhibition and the course of Alport syndrome.

A. Pierides, C. Deltas, I. Savva, 2016, Pharmacological research.

Serum ferritin concentration: a reliable guide to iron overload in uremic and hemodialyzed patients.

T. Feest, A. Pierides, D. Kerr, 1978, Clinical nephrology.

Effect of renal transplantation on marrow mast cell hyperplasia of chronic renal failure.

A. Pierides, H. A. Ellis, K. Peart, 1977, Journal of clinical pathology.

Recurrence of Complement Factor H-Related Protein 5 Nephropathy in a Renal Transplant

D. Gale, A. Pierides, P. Maxwell, 2011, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.

The role of molecular genetics in diagnosing familial hematuria(s)

K. Voskarides, A. Pierides, C. Deltas, 2011, Pediatric Nephrology.

Geographical clustering of low density lipoprotein receptor gene mutations (C292X; Q363X; D365E & C660X) in Cyprus

S. Xenophontos, A. Pierides, K. Demetriou, 2000, Human mutation.

Familial Homozygous Hypercholesterolemia: Effective Long-Term Treatment with Cascade Double Filtration Plasmapheresis

A. Pierides, K. Demetriou, Eleni H’Maltezou, 2001, Blood Purification.

Comparative studies of total and ionized serum calcium values in normal subjects and patients with renal disorders.

M. Burritt, K. Offord, A. Pierides, 1980, Mayo Clinic proceedings.

Pharmacology and Therapeutic Use of Vitamin D and its Analogues

A. Pierides, 1981, Drugs.

Outcome of kidney transplantation in autosomal dominant medullary cystic kidney disease type 1.

A. Pierides, C. Deltas, C. Stavrou, 2003, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Autosomal-dominant medullary cystic kidney disease type 1: clinical and molecular findings in six large Cypriot families.

K. Kyriacou, F. Hildebrandt, A. Pierides, 2002, Kidney international.

Avascular necrosis of bone following renal transplantation.

A. Pierides, F. Alvarez-ude, P. Uldall, 1975, The Quarterly journal of medicine.

Renal transplantation in Alport's syndrome: anti-glomerular basement membrane glomerulonephritis in the allograft.

A. Pierides, K. E. Holley, D. Milliner, 1982, Mayo Clinic proceedings.

Clinical aspects of cystinuria.

A. Pierides, C. Deltas, 1997, Contributions to nephrology.

Novel PKD1 deletions and missense variants in a cohort of Hellenic polycystic kidney disease families

A. Pierides, C. Deltas, K. Demetriou, 2001, European Journal of Human Genetics.

Screening of the PKD1 duplicated region reveals multiple single nucleotide polymorphisms and a de novo mutation in Hellenic polycystic kidney disease families

P. Harris, A. Pierides, C. Deltas, 2000, Human mutation.

Thin glomerular basement membranes in patients with hematuria and minimal change disease.

K. Kyriacou, F. Stavrou, A. Pierides, 1999, Ultrastructural pathology.

Hemodialysis encephalopathy with osteomalacic fractures and muscle weakness.

A. Pierides, J. McCall, W. Edwards, 1980, Kidney international.

1α-Hydroxycholecalciferol in renal osteodystrophy

A. Pierides, D. Kerr, M. Ward, 1976, Calcified Tissue Research.

Barbiturate and anticonvulsant treatment in relation to osteomalacia with haemodialysis and renal transplantation.

A. Pierides, D. Kerr, F. Alvarez-ude, 1976, British medical journal.

Serum gamma glutamyl transferase and alkaline phosphatase activities in epileptics receiving anticonvulsant therapy.

A. Pierides, A. Skillen, 1976, Clinica chimica acta; international journal of clinical chemistry.

Evidence for association of endothelial cell nitric oxide synthase gene polymorphism with earlier progression to end-stage renal disease in a cohort of Hellens from Greece and Cyprus.

A. Pierides, C. Deltas, S. Trygonis, 2004, Genetic testing.

Molecular and Clinical Investigation of Cystinuria in the Greek-Cypriot Population.

K. Voskarides, A. Pierides, C. Deltas, 2015, Genetic testing and molecular biomarkers.

X‐linked Alport syndrome in Hellenic families: Phenotypic heterogeneity and mutations near interruptions of the collagen domain in COL4A5

K. Voskarides, A. Pierides, C. Deltas, 2012, Clinical genetics.

Founder Mutations in the ATP6V1B1 GeneExplain Most Cypriot Cases of Distal Renal Tubular Acidosis: First Prenatal Diagnosis

K. Voskarides, A. Pierides, C. Deltas, 2010, Nephron Clinical Practice.

Seasonal variation of serum 25-hydroxyvitamin D in patients with chronic renal failure treated by regular haemodialysis.

D. Cook, A. Pierides, G. Shannan, 1977, Clinica chimica acta; international journal of clinical chemistry.

1,25-dihydroxycholecalciferol in renal osteodystrophy. Epiphysiolysis--anticonvulsant therapy.

A. Pierides, J. Scott, H. A. Ellis, 1977, Archives of disease in childhood.

COL4A3 founder mutations in Greek-Cypriot families with thin basement membrane nephropathy and focal segmental glomerulosclerosis dating from around 18th century.

K. Voskarides, A. Pierides, C. Deltas, 2008, Genetic testing.

THE EFFECT OF lα‐HYDROXYVITAMIN D3 IN PRE‐DIALYSIS RENAL BONE DISEASE

D. Cook, A. Pierides, D. Kerr, 1977, Clinical endocrinology.

VARIABLE RESPONSE TO LONG-TERM 1α-HYDROXYCHOLECALCIFEROL IN HÆMODIALYSIS OSTEODYSTROPHY

A. Pierides, D. Kerr, M. Ward, 1976, The Lancet.

Serum alkaline phosphatase in azotemic and hemodialysis osteodystrophy: a study of isoenzyme patterns, their correlation with bone histology, and their changes in response to treatment with 1alphaOHD3 and 1,25(OH)2D3.

A. Pierides, H. A. Ellis, A. Skillen, 1979, The Journal of laboratory and clinical medicine.

Molecular genetics of familial hematuric diseases.

K. Voskarides, A. Pierides, C. Deltas, 2013, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

X-linked, COL4A5 hypomorphic Alport mutations such as G624D and P628L may only exhibit thin basement membrane nephropathy with microhematuria and late onset kidney failure.

K. Voskarides, A. Pierides, C. Deltas, 2013, Hippokratia.

On 'Incidence of renal failure and nephroprotection by RAAS inhibition in heterozygous carriers of X-chromosomal and autosomal recessive Alport mutations'.

K. Voskarides, A. Pierides, C. Deltas, 2013, Kidney international.

Full Reviews Molecular genetics of familial hematuric diseases With blog commentary

K. Voskarides, A. Pierides, C. Deltas, 2013 .

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.

K. Kyriacou, K. Voskarides, A. Pierides, 2009, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Co-Inheritance of Functional Podocin Variants with Heterozygous Collagen IV Mutations Predisposes to Renal Failure

K. Voskarides, A. Pierides, C. Deltas, 2015, Nephron.

Evidence that NPHS2-R229Q predisposes to proteinuria and renal failure in familial hematuria

K. Voskarides, A. Pierides, C. Deltas, 2012, Pediatric Nephrology.

Hemodialysis bone disease: correlation between clinical, histologic, and other findings.

T. Feest, A. Pierides, D. Kerr, 1978, Kidney international.

COL4A3/COL4A4 heterozygous mutations with TBMN presenting as focal segmental glomerulosclerosis.

A. Pierides, C. Deltas, 2015, Kidney international.

Incidence of Thin Basement Membrane Nephropathy in 990 Consecutive Renal Biopsies Examined with Electron Microscopy

M. Vassiliou, K. Kyriacou, A. Hadjisavvas, 2008, Ultrastructural pathology.

Ketotic hypoglycaemia of childhood

A. Pierides, J. Stansfeld, J. Anderson, 1975, Postgraduate medical journal.

Value of Ultrasonography, CT and MR Imaging in the Diagnosis of Primary Hyperparathyroidism

N. Gourtsoyiannis, A. Pierides, C. Tziakouri, 1996, Acta radiologica.

The Power of Molecular Genetics in Establishing the Diagnosis and Offering Prenatal Testing: The Case for Alport Syndrome

K. Voskarides, A. Pierides, C. Deltas, 2012 .

Novel NPR1 polymorphic variants and its exclusion as a candidate gene for medullary cystic kidney disease (ADMCKD) type 1.

F. Hildebrandt, A. Pierides, C. Deltas, 2001, Molecular and cellular probes.

Chromosome 1 localization of a gene for autosomal dominant medullary cystic kidney disease.

A. Pierides, C. Deltas, A. Eleftheriou, 1998, Human molecular genetics.

Medullary cystic kidney disease with hyperuricemia and gout in a large Cypriot family: no allelism with nephronophthisis type 1.

K. Kyriacou, C. Antignac, A. Pierides, 1998, American journal of medical genetics.

Iron and aluminum osteomalacia in hemodialysis patients.

A. Pierides, M. P. Myli, 1984, The New England journal of medicine.

HISTOPATHOLOGY OF RENAL OSTEODYSTROPHY WITH PARTICULAR REFERENCE TO THE EFFECTS OF lα‐HYDROXYVITAMIN D3 IN PATIENTS TREATED BY LONG‐TERM HAEMODIALYSIS

T. Feest, A. Pierides, D. Kerr, 1977, Clinical endocrinology.

CLOFIBRATE-INDUCED MUSCLE DAMAGE IN PATIENTS WITH CHRONIC RENAL FAILURE

A. Pierides, F. Alvarez-ude, D. Kerr, 1975, The Lancet.

Modification of the enzyme mismatch cleavage method using T7 endonuclease I and silver staining.

Richard James Mean, A. Pierides, C. Deltas, 2004, BioTechniques.

Serum alkaline phosphatase isoenzyme patterns in patients with chronic renal failure.

A. Pierides, A. Skillen, 1977, Clinica chimica acta; international journal of clinical chemistry.

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

F. Kronenberg, B. Paulweber, T. Benzing, 2017, PloS one.

COL4A3/COL4A4 Mutations Link Familial Hematuria and Focal Segmental Glomerulosclerosis. Glomerular Epithelium Destruction via Basement Membrane Thinning?

K. Voskarides, A. Pierides, C. Deltas, 2008, Connective tissue research.

COL4A3/COL4A4 mutations producing focal segmental glomerulosclerosis and renal failure in thin basement membrane nephropathy.

K. Kyriacou, K. Voskarides, A. Pierides, 2007, Journal of the American Society of Nephrology : JASN.

Genotype-renal function correlation in type 2 autosomal dominant polycystic kidney disease.

Ann M. Johnson, P. S. St George-Hyslop, E. Coto, 2003, Journal of the American Society of Nephrology : JASN.

Hemofiltration: A Viable Alternative to Conventional Hemodialysis?

A. Pierides, 1980, The International journal of artificial organs.

A miR-1207-5p Binding Site Polymorphism Abolishes Regulation of HBEGF and Is Associated with Disease Severity in CFHR5 Nephropathy

Harsh Dweep, Norbert Gretz, Kamil Erguler, 2012, PloS one.

Central pontine myelinolysis. Two cases with associated electrolyte disturbance.

A. Pierides, W. Bradley, B. Tomlinson, 1976, The Quarterly journal of medicine.

A family with the branchio-oto-renal syndrome: clinical and genetic correlations.

A. Pierides, C. Deltas, K. Demetriou, 2002, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Genetic evidence for a trans-heterozygous model for cystogenesis in autosomal dominant polycystic kidney disease.

A. Pierides, C. Deltas, C. Deltas, 2000, Human molecular genetics.

Genetic variation of DKK3 may modify renal disease severity in ADPKD.

A. Paterson, M. Laakso, E. Coto, 2010, Journal of the American Society of Nephrology : JASN.

Identifi Cation of a Mutation in Complement Factor H-related Protein 5 in Patients of Cypriot Origin with Glomerulonephritis

Frcp, K. Kyriacou, A. Hadjisavvas, 2022 .

Chromosome 4 localization of a second gene for autosomal dominant polycystic kidney disease

R. R. Frants, R. Fossdal, L. Sandkuijl, 1993, Nature Genetics.

Loss of heterozygosity in polycystic kidney disease with a missense mutation in the repeated region of PKD1

A. Pierides, M. Koptides, P. Patsalis, 1998, Human Genetics.

Transfusion‐Induced Alloimmunization in Patients Awaiting Renal Allografts

A. Pierides, S. Sterioff, S. Moore, 1984, Vox sanguinis.

Serum gamma-glutamyl transferase activity in chronic renal failure during regular hemodialysis and after successful renal transplantation.

A. Pierides, A. Skillen, 1977, Clinica chimica acta; international journal of clinical chemistry.

Molecular investigation and long‐term clinical progress in Greek Cypriot families with recessive distal renal tubular acidosis and sensorineural deafness due to mutations in the ATP6V1B1 gene

A. Pierides, C. Deltas, M. Prikis, 2006, Clinical genetics.

Treatment of renal lithiasis associated with renal tubular acidosis.

A. Pierides, T. Bunch, C. Van den Berg, 1983, Proceedings of the European Dialysis and Transplant Association. European Dialysis and Transplant Association.

HÆMODIALYSIS ENCEPHALOPATHY: POSSIBLE ROLE OF PHOSPHATE DEPLETION

A. Pierides, D. Kerr, M. Ward, 1976, The Lancet.

Idiopathic membranous nephropathy.

A. Pierides, A. Morley, D. Kerr, 1977, The Quarterly journal of medicine.

A Simplified Method for Measuring the Thickness of Glomerular Basement Membranes

K. Kyriacou, A. Pierides, A. Karagrigoriou, 2003, Ultrastructural pathology.

Two year experience with over 500 sessions of postdilution hemofiltration.

W. J. Johnson, A. Pierides, B. Schniepp, 1981, Transactions - American Society for Artificial Internal Organs.

A. Pierides, P. Frohnert, 1981, Transactions - American Society for Artificial Internal Organs.

Dialysis dementia, osteomalacic fractures and myopathy: a syndrome due to chronic aluminum intoxication.

A. Pierides, 1978, The International journal of artificial organs.

THE NEED AND USE OF A PHOSPHATE‐ENRICHED DIALYSATE DURING REGULAR HEMODIALYSIS

A. Pierides, D. Kerr, P. Aljama, 1977, Transactions - American Society for Artificial Internal Organs.

Effect of 1alpha-hydroxycholecalciferol, 1,25-dihydroxycholecalciferol, 3 deoxy-1alpha-hydroxycholecalciferol, 24R, 25-dihydroxycholecalciferol and successful renal transplantation on calcium absorption in haemodialysis patients.

A. Pierides, D. Kerr, P. Aljama, 1978, Nephron.

THE ROLE OF PHOSPHATE IN RENAL BONE DISEASE

A. Pierides, 1977, Clinical endocrinology.

COL4A5 and LAMA5 variants co-inherited in familial hematuria: digenic inheritance or genetic modifier effect?

K. Voskarides, A. Pierides, C. Deltas, 2018, BMC Nephrology.

Detection of a novel nonsense mutation and an intragenic polymorphism in the PKD1 gene of a Cypriot family with autosomal dominant polycystic kidney disease

A. Pierides, C. Deltas, R. Constantinides, 1996, Human Genetics.

The pregnant patient with partial lipodystrophy developing acute renal failure--onset of de novo membranoproliferative glomerulonephritis.

K. Kyriacou, A. Pierides, K. Demetriou, 1998, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Variable response to long-term 1alpha-hydroxycholecalciferol in haemodialysis osteodystrophy.

A. Pierides, D. Kerr, M. Ward, 1976, Lancet.

1 alpha-hydroxycholecalciferol in hemodialysis renal osteodystrophy. Adverse effects of anticonvulsant therapy.

H. DeLuca, A. Pierides, D. Kerr, 1976, Clinical nephrology.

Frequent COL4 mutations in familial microhematuria accompanied by later‐onset Alport nephropathy due to focal segmental glomerulosclerosis

K. Voskarides, D. Gale, A. Pierides, 2017, Clinical genetics.

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

K. Voskarides, A. Pierides, C. Deltas, 2014, PloS one.

Study on a family with anderson--Fabry's disease and associated familial spastic paraplegia.

D. F. Roberts, S. Gardiner, A. Pierides, 1976, Journal of medical genetics.

Ultrafiltration followed by haemodialysis. A longterm trial and acute studies.

W. J. Johnson, A. Pierides, S. Kurtz, 1978, Journal of Dialysis.

Elimination kinetics of captopril in patients with renal failure.

S. Singhvi, A. Pierides, K. Duchin, 1984, Kidney international.

Germinal and somatic mutations in the PKD2 gene of renal cysts in autosomal dominant polycystic kidney disease.

A. Pierides, P. Koupepidou, C. Deltas, 1999, Human molecular genetics.

Genetic heterogeneity in adult dominant polycystic kidney disease in Cypriot families

A. Pierides, M. Breuning, D. Peters, 1995, Human Genetics.

The MTHFR 677TT and 677CT/1298AC genotypes in Cypriot patients may be predisposing to hypertensive nephrosclerosis and chronic renal failure.

A. Pierides, C. Deltas, P. Koupepidou, 2005, International Angiology.

Dialysis encephalopathy syndrome

A. Pierides, D. Kerr, R. Perry, 1976 .

Long term therapy with 1,25(OH)2D3 in dialysis bone disease.

A. Pierides, D. Kerr, F. Alvarez-ude, 1976, Proceedings of the European Dialysis and Transplant Association. European Dialysis and Transplant Association.

C3 glomerulonephritis/CFHR5 nephropathy is an endemic disease in Cyprus: clinical and molecular findings in 21 families.

K. Voskarides, A. Pierides, C. Deltas, 2013, Advances in experimental medicine and biology.

Supplementary webappendix

Jonathan E. Dickerson, K. Kyriacou, R. Hennekam, 2013 .

Supplementary webappendix

Jonathan E. Dickerson, K. Kyriacou, R. Hennekam, 2010 .

Autosomal dominant medullary cystic kidney disease: evidence of gene locus heterogeneity.

F. Hildebrandt, T. Feest, A. Pierides, 1998, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Idiopathic membranous nephropathy.

A. Pierides, D. Kerr, 1978, Nephron.

Reversible nonoliguric acute renal failure associated with zomepirac therapy.

A. Pierides, G. Schwartz, T. J. Blair, 1982, Mayo Clinic proceedings.

Photon absorptiometry of bone after successful renal transplantation.

A. Pierides, E. Aird, 1977, The British journal of radiology.

COL4A3/COL4A4 Mutations Link Familial Hematuria and Focal Segmental Glomerulosclerosis. Glomerular Epithelium Destruction via Basement Membrane Thinning?

K. Voskarides, A. Pierides, C. Deltas, 2008, Connective tissue research.

COL4A3 founder mutations in Greek-Cypriot families with thin basement membrane nephropathy and focal segmental glomerulosclerosis dating from around 18th century.

K. Voskarides, A. Pierides, C. Deltas, 2008, Genetic testing.

Hemofiltration and vascular stability.

L. Henderson, A. Pierides, E. Ritz, 1982, Contributions to nephrology.

Calcium, phosphorus and parathyroid hormone metabolism in chronic hemofiltration.

M. Burritt, A. Pierides, D. Giacherio, 1982, Contributions to nephrology.