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Slow progressive FSGS associated with an F392L WT1 mutation.
Kaltenis P, Schumacher V, Jankauskiene A, Laurinavicius A, Royer-Pokora B. Kaltenis P, et al. Among authors: laurinavicius a. Pediatr Nephrol. 2004 Mar;19(3):353-6. doi: 10.1007/s00467-003-1372-1. Epub 2004 Jan 27. Pediatr Nephrol. 2004. PMID: 14745636
Nationwide renal biopsy data in Lithuania 1994-2012.
Brazdziute E, Miglinas M, Gruodyte E, Priluckiene J, Tamosaitis A, Bumblyte IA, Kuzminskis V, Burbaickaja S, Sakalauskienė M, Jankauskienė A, Cerkauskiene R, Pundziene B, Laurinavicius A. Brazdziute E, et al. Among authors: laurinavicius a. Int Urol Nephrol. 2015 Apr;47(4):655-62. doi: 10.1007/s11255-015-0927-y. Epub 2015 Feb 17. Int Urol Nephrol. 2015. PMID: 25686739
Genotype⁻Phenotype Correlation in a New Fabry-Disease-Causing Mutation.
Čerkauskaitė A, Čerkauskienė R, Miglinas M, Laurinavičius A, Ding C, Rolfs A, Vencevičienė L, Barysienė J, Kazėnaitė E, Sadauskienė E. Čerkauskaitė A, et al. Among authors: laurinavicius a. Medicina (Kaunas). 2019 May 7;55(5):122. doi: 10.3390/medicina55050122. Medicina (Kaunas). 2019. PMID: 31067829 Free PMC article.
Identification of 27 Novel Variants in Genes COL4A3, COL4A4, and COL4A5 in Lithuanian Families With Alport Syndrome.
Cerkauskaite A, Savige J, Janonyte K, Jeremiciute I, Miglinas M, Kazenaite E, Laurinavicius A, Strupaite-Sileikiene R, Vainutiene V, Burnyte B, Jankauskiene A, Rolfs A, Bauer P, Schröder S, Cerkauskiene R. Cerkauskaite A, et al. Among authors: laurinavicius a. Front Med (Lausanne). 2022 Mar 28;9:859521. doi: 10.3389/fmed.2022.859521. eCollection 2022. Front Med (Lausanne). 2022. PMID: 35419377 Free PMC article.
123 results