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/vufind/Search/Results?lookfor=%22Pierides%2C+Alkis%22&type=Person&sort=year
/vufind/Search/Results?lookfor=%22Pierides%2C+Alkis%22&type=Person&sort=year
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PubPharm (80)
1
COL4A5 and LAMA5 variants co-inherited in familial hematuria : digenic inheritance or genetic modifier effect?
enthalten in:
BMC nephrology
| 2018
von
Voskarides, K.
|
Papagregoriou, G.
|
Hadjipanagi, D.
| +10
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2
COL4A5 and LAMA5 variants co-inherited in familial hematuria: digenic inheritance or genetic modifier effect?
enthalten in:
BMC nephrology
| 2018
von
Voskarides, K.
|
Papagregoriou, G.
|
Hadjipanagi, D.
| +10
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3
COL4A5 and LAMA5 variants co-inherited in familial hematuria: digenic inheritance or genetic modifier effect?
enthalten in:
BMC nephrology
| 2018
von
Voskarides, K.
|
Papagregoriou, G.
|
Hadjipanagi, D.
| +10
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4
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
enthalten in:
PloS one
| 2017
von
Voskarides, K.
|
Stefanou, C.
|
Pieri, M.
| +23
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5
RAAS inhibition and the course of Alport syndrome
enthalten in:
Pharmacological research
| 2016
von
Savva, I.
|
Pierides, A.
|
Deltas, C.
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6
RAAS inhibition and the course of Alport syndrome
enthalten in:
Pharmacological research
| 2016
von
Savva, I.
|
Pierides, A.
|
Deltas, C.
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7
Molecular and Clinical Investigation of Cystinuria in the Greek-Cypriot Population
enthalten in:
Genetic testing and molecular biomarkers
| 2015
von
Athanasiou, Y.
|
Voskarides, K.
|
Chatzikyriakidou, A.
| +7
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8
COL4A3/COL4A4 heterozygous mutations with TBMN presenting as focal segmental glomerulosclerosis
enthalten in:
Kidney international
| 2015
von
Deltas, C.
|
Pierides, A.
CommentOn: Kidney Int. 2014 Dec;86(6):1253-9. - PMID 25229338
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9
Carriers of Autosomal Recessive Alport Syndrome with Thin Basement Membrane Nephropathy Presenting as Focal Segmental Glomerulosclerosis in Later Life
enthalten in:
Nephron
| 2015
von
Deltas, C.
|
Savva, I.
|
Voskarides, K.
| +2
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10
Co-Inheritance of Functional Podocin Variants with Heterozygous Collagen IV Mutations Predisposes to Renal Failure
enthalten in:
Nephron
| 2015
von
Stefanou, C.
|
Pieri, M.
|
Savva, I.
| +4
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Pediatric nephrology
8
Nephrology, dialysis, transplantation
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Genetic testing
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Kidney international
4
Human genetics
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Human genetics <Berlin>
4
Nephrology, dialysis, transplantation : officia...
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PloS one
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Pediatric nephrology (Berlin, Germany)
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1
American journal of medical genetics
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Thema
30
Journal Article
26
Research Support, Non-U.S. Gov't
12
Collagen Type IV
9
Collagen IV
8
Autoantigens
7
Alport syndrome
7
type IV collagen alpha3 chain
6
9007-36-7
6
CFHR5 protein, human
6
COL4A4 protein, human
6
Complement System Proteins
6
FSGS
6
Familial hematuria
5
Membrane Proteins
5
Review
3
C3 glomerulonephritis
3
CFHR5
3
CFHR5 nephropathy
3
COL4A3/COL4A4
3
Complement
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Erscheinungszeitraum
69
2000-
10
1900-1999
Erscheinungsjahr(e)
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Sprache
57
Englisch
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