Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Stavrou, Christoforos V."'
Autor:
Stavrou, Christoforos V., Constantinou-Deltas, Constantinos D., Christofides, Tasos C., Pierides, Alkis M.
Publikováno v:
Nephrology Dialysis Transplantation
Nephrol.Dial.Transplant.
Nephrol.Dial.Transplant.
Background. Autosomal dominant medullary cystic kidney disease (ADMCKD) is an inherited, distinct, chronic, tubulointerstitial, cystic-type nephropathy, often described together with juvenile nephronophthisis as a single disease complex (NPH-MCD). Ho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5ddee2297e43b4bed88a57c50290ea4
https://doi.org/10.1093/ndt/gfg196
https://doi.org/10.1093/ndt/gfg196
Autor:
Papazachariou, Louiza, Demosthenous, Panayiota, Pieri, Myrtani, Papagregoriou, Gregory N., Savva, Isavella, Stavrou, Christoforos V., Zavros, Michalis, Athanasiou, Yiannis, Ioannou, Kyriakos, Patsias, Charalambos, Panagides, Alexia, Potamitis, Costas, Demetriou, Kyproula, Prikis, Marios, Hadjigavriel, Michalis, Kkolou, Maria, Loukaidou, Panayiota, Pastelli, Androulla, Michael, Aristos, Lazarou, Akis, Arsali, Maria, Damianou, Loukas, Goutziamani, Ioanna, Soloukides, Andreas P., Yioukas, Lakis, Elia, Avraam, Zouvani, Ioanna, Polycarpou, Polycarpos, Pierides, Alkis M., Voskarides, Konstantinos, Constantinou-Deltas, Constantinos D., Demosthenous, Panayiota M., Voskarides, Konstantinos A.
Publikováno v:
PLoS ONE
PLoS ONE, Vol 9, Iss 12, p e115015 (2014)
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::32984464412a53ae87b82ad46ecd525e
http://gnosis.library.ucy.ac.cy/handle/7/54780
http://gnosis.library.ucy.ac.cy/handle/7/54780
Autor:
Christodoulou, Kyproula, Tsingis, Marios, Stavrou, Christoforos V., Eleftheriou, Andri, Papapavlou, Petros, Patsalis, Philippos C., Ioannou, Panayiotis A., Pierides, Alkis M., Constantinou-Deltas, Constantinos D.
Publikováno v:
Human molecular genetics
Hum.Mol.Genet.
Hum.Mol.Genet.
There is a group of inherited cystic nephropathies that are characterized by juvenile onset recessive inheritance (familial juvenile nephronophthisis, FJN) or by adult onset dominant inheritance (medullary cystic disease, MCD) and share similar clini
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9a012aeccdb616773a36799a1389ade
https://doi.org/10.1093/hmg/7.5.905
https://doi.org/10.1093/hmg/7.5.905
Autor:
Soloukides, Andreas P., Moutzouris, Dimitrios Anestis D., Papagregoriou, Gregory N., Stavrou, Christoforos V., Constantinou-Deltas, Constantinos D., Tzanatos, Helen A.
Publikováno v:
Journal of nephrology
J.Nephrol.
J.Nephrol.
Background: Medullary cystic kidney disease (MCKD) is an inherited interstitial nephritis, leading to endstage renal disease (ESRD) between the fourth and seventh decade of life. MCKD shares clinical and morphological features with nephronophthisis,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::deb29142b7fe8d0236d25d6628738669
http://gnosis.library.ucy.ac.cy/handle/7/53398
http://gnosis.library.ucy.ac.cy/handle/7/53398
Autor:
Demosthenous, Panayiota, Voskarides, Konstantinos, Stylianou, Konstantinos G., Hadjigavriel, Michalis, Arsali, Maria, Patsias, Charalambos, Georgaki, Eleni, Zirogiannis, P., Stavrou, Christoforos V., Daphnis, Eugenios K., Pierides, Alkis M., Constantinou-Deltas, Constantinos D.
Publikováno v:
Clinical genetics
Clin.Genet.
Clin.Genet.
The X-linked Alport syndrome (ATS) is caused by mutations in COL4A5 and exhibits a widely variable expression. Usually ATS is heralded with continuous microhematuria which rapidly progresses to proteinuria, hypertension and chronic or end-stage renal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::625ea8b36141ff1a3dc2a226b929d54f
http://gnosis.library.ucy.ac.cy/handle/7/53052
http://gnosis.library.ucy.ac.cy/handle/7/53052
Autor:
Koptides, Michael, Mean, R., Stavrou, Christoforos V., Pierides, Alkis M., Demetriou, Kyproula, Nakayama, T., Hildebrandt, F., Fuchshuber, A., Constantinou-Deltas, Constantinos D.
Publikováno v:
Molecular and cellular probes
Mol.Cell.Probes
Mol.Cell.Probes
Autosomal dominant medullary cystic kidney disease (ADMCKD) is an adult-onset heterogeneous genetic nephropathy characterized by salt wasting and end-stage renal failure. The gene responsible for ADMCKD-1 was mapped on chromosome 1 q21 and it is flan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ddf5d249a7a59a0b278f08918b110c14
https://pubmed.ncbi.nlm.nih.gov/11851379
https://pubmed.ncbi.nlm.nih.gov/11851379
Autor:
Stavrou, Christoforos V., Koptides, Michael, Tombazos, C., Psara, E., Patsias, Charalambos, Zouvani, Ioanna, Kyriacou, Kyriacos C., Hildebrandt, F., Christofides, Tasos C., Pierides, Alkis M., Constantinou-Deltas, Constantinos D.
Publikováno v:
Kidney international
Kidney Int.
Kidney Int.
Background. Autosomal-dominant medullary cystic kidney disease (ADMCKD), a hereditary chronic interstitial nephropathy, recently attracted attention because of the cloning or mapping of certain gene loci, namely NPHP1, NPHP2 and NPHP3 for familial ju
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4485::ec2d38cc84544fb9bf343ad229351398
http://gnosis.library.ucy.ac.cy/handle/7/57657
http://gnosis.library.ucy.ac.cy/handle/7/57657
Autor:
Fuchshuber, A., Constantinou-Deltas, Constantinos D., Berthold, S., Stavrou, Christoforos V., Vollmer, M., Burton, C., Feest, T., Krieter, D., Gal, A., Brandis, M., Pierides, Alkis M., Hildebrandt, F.
Publikováno v:
Nephrology Dialysis Transplantation
Nephrol.Dial.Transplant.
Nephrol.Dial.Transplant.
Autosomal dominant medullary cystic kidney disease (ADMCKD synonym: medullary cystic disease, MCD) is an autosomal dominant kidney disorder, sharing morphological and clinical features with recessive juvenile nephronophthisis (NPH), such as reduced u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23294b631df6ca857ded4276224ae893
http://gnosis.library.ucy.ac.cy/handle/7/53076
http://gnosis.library.ucy.ac.cy/handle/7/53076
Autor:
Stavrou, Christoforos V., Pierides, Alkis M., Zouvani, Ioanna, Kyriacou, Kyriacos C., Antignac, C., Neophytou, Pavlos, Christodoulou, Kyproula, Constantinou-Deltas, Constantinos D.
Publikováno v:
American Journal of Medical Genetics
Am.J.Med.Genet.
Am.J.Med.Genet.
We describe a large Cypriot family with an interstitial type of nephropathy, inherited as an autosomal dominant trait that led to end stage renal failure between 51 to 78 years of age (mean 62.2 years). Twenty-three people are known to be affected, b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4485::3cf444ccfa054a414d29197a54578a69
http://gnosis.library.ucy.ac.cy/handle/7/53404
http://gnosis.library.ucy.ac.cy/handle/7/53404
Autor:
Soloukides AP; Nefrologiko Athinon Dialysis Center, Athens, Greece. soloukides@yahoo.gr, Moutzouris DA, Papagregoriou GN, Stavrou CV, Deltas CC, Tzanatos HA
Publikováno v:
Journal of nephrology [J Nephrol] 2013 Jul-Aug; Vol. 26 (4), pp. 793-8. Date of Electronic Publication: 2013 Feb 25.