يعرض 1 - 15 نتائج من 15 نتيجة بحث عن '"Xydakis, D."', وقت الاستعلام: 0.55s تنقيح النتائج
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    Academic Journal

    المساهمون: Chatziantoniou, C

    Relation: pii: PONE-D-16-49857; Voskarides, K., Stefanou, C., Pieri, M., Demosthenous, P., Felekkis, K., Arsali, M., Athanasiou, Y., Xydakis, D., Stylianou, K., Daphnis, E., Goulielmos, G., Loizou, P., Savige, J., Hoehne, M., Voelker, L. A., Benzing, T., Maxwell, P. H., Gale, D. P., Gorski, M. ,. Deltas, C. (2017). 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. PLOS ONE, 12 (3), https://doi.org/10.1371/journal.pone.0174274.; http://hdl.handle.net/11343/258350

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    المؤلفون: Athanasiou Y, Zavros M, Arsali M, Papazachariou L, Demosthenous P, Savva I, Voskarides K, Deltas C, Pierides A, Feriozzi S, Perrin A, West M, Nicholls K, Sunder Plassmann G, Torras J, Neumann P, Cybulla M, Cofiell R, Kukreja A, Bedard K, Yan Y, Mickle A, Ogawa M, Bedrosian C, Faas S, Mészáros K, Pruess L, Gondan M, Ritz E, Schaefer F, Testa A, Spoto B, Leonardis D, Sanguedolce MC, Pisano A, Parlongo MR, Tripepi G, Mallamaci F, Zoccali C, Trujillano D, Bullich G, Ballarin J, Torra R, Estivill X, Ars E, Kleber ME, Delgado G, Grammer TB, Silbernagel G, Kraemer BK, Maerz W, Riccio E, Pisani A, Abdalla AA, Malone AF, Winn MP, Goodship T, Cronin C, Conlon PJ, Casserly LF, Nishio S, Sakuhara Y, Matsuoka N, Yamamoto J, Nakazawa D, Nakagakaki T, Abo D, Shibazaki S, Atsumi T, Mazzinghi B, Giglio S, Provenzano A, Becherucci F, Sansavini G, Ravaglia F, Roperto RM, Murer L, Lasagni L, Materassi M, Romagnani P, Schmidts M, Christou S, Cortes C, McInerney Leo A, Kayserili H, Zankl A, Peter S, Duncan E, Wicking C, Beales PL, Mitchison H, Magestro M, Vekeman F, Nichols T, Karner P, Duh MS, Srivastava B, Van Doorn Khosrovani SB, Zonnenberg BA, Ghiggeri GM, Fogazzi GB, Settanni F, BOLDORINI, Renzo Luciano, Lazzarich E, Airoldi A, Izzo C, Garrido P, Fernandes JC, Ribeiro S, Belo L, Costa EC, Reis F, Santos Silva A, Youssef DM, Alshal AS, Salah K, Rashed AE, Kingswood JC, Jozwiak S, Belousova E, Frost M, Kuperman R, Bebin EM, Korf B, Flamini JR, Kohrman MH, Sparagana S, Wu JY, Berkowitz N, Miao S, Segal S, Ridolfi A, Bissler JJ, Franz DN, Oud MM, Van Bon BW, Bongers EM, Hoischen A, Marcelis CL, De Leeuw N, Mol SJ, Mortier G, Knoers NV, Brunner HG, Roepman R, Arts HH, Van Eerde AM, Van Der Zwaag B, Lilien MR, Renkema KY, De Borst MH, Van Haaften G, Giles RH, Navis GJ, Lu KC, Su SL, Gigante M, Santangelo L, Diella S, Argentiero L, Cianciotta F, Martino M, Ranieri E, Grandaliano G, Giordano M, Gesualdo L, Fernandes J, Sereno J, Costa E, Chub O, Aires I, Polidori D, Santos AR, Brito Costa A, Simoes C, Rueff J, Nolasco F, Calado J, Van Der Tol L, Biegstraaten M, Florquin S, Vogt L, Van Den Bergh Weerman MA, Hollak CE, Hughes DA, Lachmann RH, Oliveira JP, Ortiz A, Svarstad E, Terryn W, Tøndel C, Waldek S, Wanner C, West ML, Linthorst GE, Kaesler N, Brandenburg V, Theuwissen E, Vermeer C, Floege J, Schlieper G, Krüger T, Xydakis D, Goulielmos G, Antonaki E, Stylianoy K, Sfakianaki M, Papadogiannakis A, Dafnis E, Mdimegh S, Ben Hadj Mbarek Fredj I, Moussa A, Omezzine A, Zellama D, Mabrouk S, Zouari N, Hassayoun S, Chemli J, Achour A, Bouslama A, Abroug S, Politi C, Cutrupi S, Parlongo RM, D'Arrigo G, Hohenstein Scheibenecker K, Schmidt A, Stylianou KG, Kyriazis J, Androvitsanea A, Tzanakakis M, Maragkaki E, Petrakis J, Stratakis S, Poulidaki R, Vardaki E, Petra C, Statigis S, Perakis K, Daphnis E, Metzinger Le Meuth V, Taïbi F, M'Baya Moutoula E, Louvet L, Massy Z, Metzinger L, Mani LY, Sidler D, Vogt B, Nikolskaya N, Cox JA, Smirnov A, Zarayski M, Kayukov I, Karunnaya H, Sipovski V, Kukoleva L, Dobronravov V, Fabry Outcome Survey Renal Working Group, On Behalf Of The MAURO Working Group, Uk1ok Consortium, MUSETTI, CLAUDIO, QUAGLIA, Marco, GIORDANO, Mara, STRATTA, Piero

    المساهمون: Athanasiou, Y, Zavros, M, Arsali, M, Papazachariou, L, Demosthenous, P, Savva, I, Voskarides, K, Deltas, C, Pierides, A, Feriozzi, S, Perrin, A, West, M, Nicholls, K, Sunder Plassmann, G, Torras, J, Neumann, P, Cybulla, M, Cofiell, R, Kukreja, A, Bedard, K, Yan, Y, Mickle, A, Ogawa, M, Bedrosian, C, Faas, S, Mészáros, K, Pruess, L, Gondan, M, Ritz, E, Schaefer, F, Testa, A, Spoto, B, Leonardis, D, Sanguedolce, Mc, Pisano, A, Parlongo, Mr, Tripepi, G, Mallamaci, F, Zoccali, C, Trujillano, D, Bullich, G, Ballarin, J, Torra, R, Estivill, X, Ars, E, Kleber, Me, Delgado, G, Grammer, Tb, Silbernagel, G, Kraemer, Bk, Maerz, W, Riccio, E, Pisani, A, Abdalla, Aa, Malone, Af, Winn, Mp, Goodship, T, Cronin, C, Conlon, Pj, Casserly, Lf, Nishio, S, Sakuhara, Y, Matsuoka, N, Yamamoto, J, Nakazawa, D, Nakagakaki, T, Abo, D, Shibazaki, S, Atsumi, T, Mazzinghi, B, Giglio, S, Provenzano, A, Becherucci, F, Sansavini, G, Ravaglia, F, Roperto, Rm, Murer, L, Lasagni, L, Materassi, M, Romagnani, P, Schmidts, M, Christou, S, Cortes, C, McInerney Leo, A, Kayserili, H, Zankl, A, Peter, S, Duncan, E, Wicking, C, Beales, Pl, Mitchison, H, Magestro, M, Vekeman, F, Nichols, T, Karner, P, Duh, M, Srivastava, B, Van Doorn Khosrovani, Sb, Zonnenberg, Ba, Musetti, Claudio

    Relation: info:eu-repo/semantics/altIdentifier/pmid/24849976; info:eu-repo/semantics/altIdentifier/wos/WOS:000342935600026; volume:29; issue:Suppl. 3; firstpage:339; lastpage:350; numberofpages:12; journal:NEPHROLOGY DIALYSIS TRANSPLANTATION; http://hdl.handle.net/11579/41786

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    المساهمون: Constantinou-Deltas, Constantinos D. [0000-0001-5549-9169]

    المصدر: PLoS ONE
    PLoS ONE, Vol 8, Iss 3, p e57925 (2013)

    مصطلحات موضوعية: Male, Pathology, genetic association, kidney disease, genetic risk, urologic and male genital diseases, Gastroenterology, Linkage Disequilibrium, lcsh:Science, quantitative analysis, adult, thin basement membrane nephropathy, Molecular Motor Proteins, allele, Apolipoprotein L1, Proteinuria, real time polymerase chain reaction, Nephrology, Cohort, Disease Progression, Medicine, disease severity, Lipoproteins, HDL, marker gene, medicine.medical_specialty, phenotype, Single-nucleotide polymorphism, glomerulopathy, Nephropathy, complement component C3, Molecular Genetics, Genetic Mutation, Genetics, Humans, human, Renal Insufficiency, Chronic, genetic epistasis, Biology, COL4A3 gene, Alleles, Aged, Hematuria, Myosin Heavy Chains, lcsh:R, medicine.disease, major clinical study, gene linkage disequilibrium, gene function, Apolipoproteins, lcsh:Q, Dialysis, haplotype, lcsh:Medicine, Epigenesis, Genetic, hereditary hematuria, APOL1 gene, single nucleotide polymorphism, genetic variability, Molecular Cell Biology, Chronic Kidney Disease, gene mutation, Multidisciplinary, messenger RNA, article, COL4A4 gene, Exons, Middle Aged, biological marker, female, CFHR5 gene, Female, Research Article, Clinical Pathology, sex difference, Polymorphism, Single Nucleotide, male, Glomerulopathy, Diagnostic Medicine, Internal medicine, medicine, controlled study, complement component C3 gene, Alport syndrome, Genetic Association Studies, Clinical Genetics, business.industry, Mutation Types, Human Genetics, gene structure, myosin heavy chain 9 gene, hematuria, Haplotypes, Genetics of Disease, CFHR5 nephropathy, business, CFHR5, Kidney disease

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