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Page 1
A founder COL4A3 pathogenic variant resulting in Alport syndrome and thin basement membrane disease: a case report series.
Front Med (Lausanne). 2023 Dec 21;10:1281049. doi: 10.3389/fmed.2023.1281049. eCollection 2023.
Front Med (Lausanne). 2023.
PMID: 38188341
Free PMC article.
Genetic screening in adolescents with steroid-resistant nephrotic syndrome.
Lipska BS, Iatropoulos P, Maranta R, Caridi G, Ozaltin F, Anarat A, Balat A, Gellermann J, Trautmann A, Erdogan O, Saeed B, Emre S, Bogdanovic R, Azocar M, Balasz-Chmielewska I, Benetti E, Caliskan S, Mir S, Melk A, Ertan P, Baskin E, Jardim H, Davitaia T, Wasilewska A, Drozdz D, Szczepanska M, Jankauskiene A, Higuita LM, Ardissino G, Ozkaya O, Kuzma-Mroczkowska E, Soylemezoglu O, Ranchin B, Medynska A, Tkaczyk M, Peco-Antic A, Akil I, Jarmolinski T, Firszt-Adamczyk A, Dusek J, Simonetti GD, Gok F, Gheissari A, Emma F, Krmar RT, Fischbach M, Printza N, Simkova E, Mele C, Ghiggeri GM, Schaefer F; PodoNet Consortium.
Lipska BS, et al. Among authors: davitaia t.
Kidney Int. 2013 Jul;84(1):206-13. doi: 10.1038/ki.2013.93. Epub 2013 Mar 20.
Kidney Int. 2013.
PMID: 23515051
Free article.
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CHARACTERISTICS OF DIARRHEAL DISEASE COMPLICATED WITH HEMOLYTIC UREMIC SYNDROME AMONG CHILDREN IN GEORGIA, 2009-2016.
Chokoshvili O, Vepkhvadze N, Davitaia T, Tevzadze L, Tsertsvadze T.
Chokoshvili O, et al. Among authors: davitaia t.
Georgian Med News. 2018 Oct;(283):123-129.
Georgian Med News. 2018.
PMID: 30516507
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Spectrum of steroid-resistant and congenital nephrotic syndrome in children: the PodoNet registry cohort.
Trautmann A, Bodria M, Ozaltin F, Gheisari A, Melk A, Azocar M, Anarat A, Caliskan S, Emma F, Gellermann J, Oh J, Baskin E, Ksiazek J, Remuzzi G, Erdogan O, Akman S, Dusek J, Davitaia T, Özkaya O, Papachristou F, Firszt-Adamczyk A, Urasinski T, Testa S, Krmar RT, Hyla-Klekot L, Pasini A, Özcakar ZB, Sallay P, Cakar N, Galanti M, Terzic J, Aoun B, Caldas Afonso A, Szymanik-Grzelak H, Lipska BS, Schnaidt S, Schaefer F; PodoNet Consortium.
Trautmann A, et al. Among authors: davitaia t.
Clin J Am Soc Nephrol. 2015 Apr 7;10(4):592-600. doi: 10.2215/CJN.06260614. Epub 2015 Jan 29.
Clin J Am Soc Nephrol. 2015.
PMID: 25635037
Free PMC article.
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Characterization of two novel mutations in the claudin-16 and claudin-19 genes that cause familial hypomagnesemia with hypercalciuria and nephrocalcinosis.
Perdomo-Ramirez A, Aguirre M, Davitaia T, Ariceta G, Ramos-Trujillo E; RenalTube Group; Claverie-Martin F.
Perdomo-Ramirez A, et al. Among authors: davitaia t.
Gene. 2019 Mar 20;689:227-234. doi: 10.1016/j.gene.2018.12.024. Epub 2018 Dec 18.
Gene. 2019.
PMID: 30576809
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EXPANDED PHENOTYPE OF TMEM67 GENE MUTATION (CASE REPORT).
Tkemaladze T, Melikishvili G, Kherkheulidze V, Melikishvili A, Davitaia T.
Tkemaladze T, et al. Among authors: davitaia t.
Georgian Med News. 2017 Jun;(267):100-103.
Georgian Med News. 2017.
PMID: 28726664
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[Immunological parameters and ultrastructure of blood formed elements in nephrotic syndrome in children].
Davitaia T, Mandzhavidze N, Tsagareli Z, Korsantia B, Megrelishvili G.
Davitaia T, et al.
Georgian Med News. 2006 Mar;(132):81-4.
Georgian Med News. 2006.
PMID: 16636388
Russian.
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