A founder COL4A3 pathogenic variant resulting in Alport syndrome and thin basement membrane disease: a case report series.

Autor: Tkemaladze T; Department of Molecular and Medical Genetics, Tbilisi State Medical University, Tbilisi, Georgia.; Department of Pediatrics, Givi Zhvania Pediatric Academic Clinic, Tbilisi State Medical University, Tbilisi, Georgia., Bregvadze K; Department of Molecular and Medical Genetics, Tbilisi State Medical University, Tbilisi, Georgia., Kvaratskhelia E; Department of Molecular and Medical Genetics, Tbilisi State Medical University, Tbilisi, Georgia., Abzianidze E; Department of Molecular and Medical Genetics, Tbilisi State Medical University, Tbilisi, Georgia., Davitaia T; Department of Pediatrics, Givi Zhvania Pediatric Academic Clinic, Tbilisi State Medical University, Tbilisi, Georgia.

Publikováno v: Frontiers in medicine [Front Med (Lausanne)] 2023 Dec 21; Vol. 10, pp. 1281049. Date of Electronic Publication: 2023 Dec 21 (Print Publication: 2023).

The European Society for Paediatric Nephrology study of pediatric renal care in Europe: comparative analysis 1998–2017.

Autor: Prikhodina, Larisa, Ehrich, Jochen, Shroff, Rukshana, Topaloglu, Rezan, Levtchenko, Elena, European Society for Paediatric Nephrology, Anton-Gamero, M., Arikoski, P., Aufricht, C., Awan, A., Bakkaloglu, S. A., Baylarov, R., Bjerre, A., Brandström, P., Chafai, R., Lotan, D., Davitaia, T., Dlin, V., Golubovic, E., Hadjipanayis, A.

Publikováno v: Pediatric Nephrology; Jan2020, Vol. 35 Issue 1, p103-111, 9p, 6 Charts, 1 Graph

CHARACTERISTICS OF DIARRHEAL DISEASE COMPLICATED WITH HEMOLYTIC UREMIC SYNDROME AMONG CHILDREN IN GEORGIA, 2009-2016

Autor: Chokoshvili O, Vepkhvadze N, Davitaia T, Tevzadze L, Tengiz Tsertsvadze

Publikováno v: Europe PubMed Central

Shiga toxin-producing Escherichia coli (STEC) causes illness ranging from mild diarrhea to bloody diarrhea, to the hemolytic uremic syndrome (HUS), which manifests with a triad of microangiopathic hemolytic anemia, thrombocytopenia and acute renal fa

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::47f95d9309bd7faf8272a03c8f26d640
https://pubmed.ncbi.nlm.nih.gov/30516507

Peroxisome Proliferator-Activated Receptor Alpha Stimulation Preserves Renal Tight Junction Components in a Rat Model of Early-Stage Diabetic Nephropathy.

Autor: Rosas-Martínez, Lorena^1,2 (AUTHOR) lor_ros@fisio.cinvestav.mx, Rodríguez-Muñoz, Rafael² (AUTHOR) cnamora17@hotmail.com, Namorado-Tonix, María del Carmen² (AUTHOR) fanis@fisio.cinvestav.mx, Missirlis, Fanis² (AUTHOR) jreyes@fisio.cinvestav.mx, del Valle-Mondragón, Leonardo¹ (AUTHOR) leonardodvm65@hotmail.com, Sánchez-Mendoza, Alicia¹ (AUTHOR) masanchez@gmail.com, Reyes-Sánchez, José L.² (AUTHOR), Cervantes-Pérez, Luz Graciela¹ (AUTHOR) luz.cervantes@cardiologia.org

Publikováno v: International Journal of Molecular Sciences. Dec2024, Vol. 25 Issue 23, p13152. 17p.

Characterization of two novel mutations in the claudin-16 and claudin-19 genes that cause familial hypomagnesemia with hypercalciuria and nephrocalcinosis.

Autor: Perdomo-Ramirez A; Unidad de Investigacion, Hospital Nuestra Señora de Candelaria, Santa Cruz de Tenerife, Spain., Aguirre M; Nefrologia Pediatrica, Hospital de Cruces, Baracaldo, Spain., Davitaia T; Paediatric Nephrology, M. Iashvili Childrens Hospital, Tbilisi, Georgia., Ariceta G; Nefrologia Pediatrica, Hospital Vall d' Hebron, Barcelona, Spain., Ramos-Trujillo E; Unidad de Investigacion, Hospital Nuestra Señora de Candelaria, Santa Cruz de Tenerife, Spain., Claverie-Martin F; Unidad de Investigacion, Hospital Nuestra Señora de Candelaria, Santa Cruz de Tenerife, Spain. Electronic address: fclamar@gobiernodecanarias.org.

Publikováno v: Gene [Gene] 2019 Mar 20; Vol. 689, pp. 227-234. Date of Electronic Publication: 2018 Dec 18.