Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Louiza Papazachariou"'
Autor:
Louiza Papazachariou, Panayiota Demosthenous, Myrtani Pieri, Gregory Papagregoriou, Isavella Savva, Christoforos Stavrou, Michael Zavros, Yiannis Athanasiou, Kyriakos Ioannou, Charalambos Patsias, Alexia Panagides, Costas Potamitis, Kyproula Demetriou, Marios Prikis, Michael Hadjigavriel, Maria Kkolou, Panayiota Loukaidou, Androulla Pastelli, Aristos Michael, Akis Lazarou, Maria Arsali, Loukas Damianou, Ioanna Goutziamani, Andreas Soloukides, Lakis Yioukas, Avraam Elia, Ioanna Zouvani, Polycarpos Polycarpou, Alkis Pierides, Konstantinos Voskarides, Constantinos Deltas
Publikováno v:
PLoS ONE, Vol 9, Iss 12, p e115015 (2014)
Familial glomerular hematuria(s) comprise a genetically heterogeneous group of conditions which include Alport Syndrome (AS) and thin basement membrane nephropathy (TBMN). Here we investigated 57 Greek-Cypriot families presenting glomerular microscop
Externí odkaz:
https://doaj.org/article/3fce6fade7d6421f887f004d60da1484
Autor:
Konstantinos Voskarides, Panayiota Demosthenous, Louiza Papazachariou, Maria Arsali, Yiannis Athanasiou, Michalis Zavros, Kostas Stylianou, Dimitris Xydakis, Eugenios Daphnis, Daniel P Gale, Patrick H Maxwell, Avraam Elia, Cristian Pattaro, Alkis Pierides, Constantinos Deltas
Publikováno v:
PLoS ONE, Vol 8, Iss 3, p e57925 (2013)
Familial hematuria (FH) is explained by at least four different genes (see below). About 50% of patients develop late proteinuria and chronic kidney disease (CKD). We hypothesized that MYH9/APOL1, two closely linked genes associated with CKD, may be
Externí odkaz:
https://doaj.org/article/7055c818119043ffaada19dbb738d3b8
Autor:
Daniel P. Gale, Eugenios Daphnis, Dimitris Goumenos, Antonia Papadaki, Alkis Pierides, George Vergoulas, Elena Frysira, Konstantinos Voskarides, Constantina Koutsofti, Constantinos Deltas, Despina Hadjipanagi, Petros Ioannou, Dimitrios Grekas, Eleni Georgaki, Ioannis Tzanakis, Christina Melexopoulou, Garyfalia Perysinaki, Athanasios Diamantopoulos, Andreas Soloukides, Alivanis P, Louiza Papazachariou, Gregory Papagregoriou, Dimitris Xydakis, Fifi Komianou, Panagiota Demosthenous, Ioannis Boletis, Nicolaos Nikolakakis, Christos Paliouras, Nicolaos Kallivretakis, Pavlos Goudas, Kostas Stylianou
Publikováno v:
Clinical Genetics. 92:517-527
Familial microscopic hematuria (FMH) is associated with a genetically heterogeneous group of conditions including the collagen-IV nephropathies, the heritable C3/CFHR5 nephropathy and the glomerulopathy with fibronectin deposits. The clinical course
Autor:
Alkis Pierides, Panagiota Demosthenous, Louiza Papazachariou, Panos Zirogiannis, Konstantinos Voskarides, Constantinos Deltas
Publikováno v:
Diseases of Renal Parenchyma
Most Alport cases, 85%, are caused by mutations in the X-linked gene, COL4A5 that encodes the α5 chain of type IV collagen, the most abundant structural protein in the glomerular basement membrane (GBM). The remaining 15% of cases are caused by auto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::244baa2f403ab18606014ce271c93ffb
https://doi.org/10.5772/26859
https://doi.org/10.5772/26859