Timing and Modality of Kidney Replacement Therapy in Children and Adolescents

Autor: Cortina, G., Arbeiter, K., Dusek, J., Harambat, J., Ranchin, B., Fischbach, M., Querfeld, U., Habbig, S., Galiano, M., Büscher, R., Gimpel, C., Kemper, M., Melk, A., Thurn, D., Schaefer, F., Doyon, A., Wühl, E., Pohl, M., Wygoda, S., Jeck, N., Kranz, B., Wigger, M., Montini, G., Lugani, F., Testa, S., Vidal, E., Matteucci, C., Picca, S., Jankauskiene, A., Azukaitis, K., Zurowska, A., Drodz, D., Tkaczyk, M., Urasinski, T., Litwin, M., Szczepanska, M., Texeira, A., Peco-Antic, A., Bucher, B., Laube, G., Anarat, A., Bayazit, A.K., Yalcinkaya, F., Basin, E., Cakar, N., Soylemezoglu, O., Duzova, A., Bilginer, Y., Erdogan, H., Donmez, O., Balat, A., Kiyak, A., Caliskan, S., Canpolat, N., Candan, C., Civilibal, M., Emre, S., Ozcelik, G., Mir, S., Sözeri, B., Yavascan, O., Tabel, Y., Ertan, P., Yilmaz, E., Shroff, R., Thumfart, Julia, Wagner, Steffen, Kirchner, Marietta, Azukaitis, Karolis, Bayazit, Aysun K., Obrycki, Lukasz, Canpolat, Nur, Bulut, Ipek Kaplan, Duzova, Ali, Anarat, Ali, Bessenay, Lucie, Shroff, Rukshana, Paripovic, Dusan, Sever, Lale, Candan, Cengiz, Lugani, Francesca, Yilmaz, Alev, Yalcinkaya, Fatos, Arbeiter, Klaus, Kiyak, Aysel, Zurowska, Aleksandra, Galiano, Matthias, Querfeld, Uwe, Melk, Anette, Schaefer, Franz

Publikováno v: In Kidney International Reports September 2024 9(9):2750-2758

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Erysipelas-like erythema in children with familial Mediterranean fever

Autor: Seven, M. B., Soylemezoglu, O., GÖNEN, SEVİM, YILDIRIM, DENİZ

Objective. Erysipelas-like erythema (ELE) is a well-known pathognomonic skin lesion associated with familial Mediterranean fever (FMF). The aim of this study was to describe the clinical and demographic features and phenotypic differences between pae

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_____10046::152098e855dffec43125ddb19bc656dc
https://avesis.gazi.edu.tr/publication/details/8c2eae75-02f2-4e97-a02b-f2acbd609060/oai

children with Alport syndrome

Autor: Ozdemir, G, Gulhan, B, Atayar, E, Saygili, S, Soylemezoglu, O, Ozcakar, ZB, Eroglu, FK, Candan, C, Demir, BK, Soylu, A, Yuksel, S, Alpay, H, Agbas, A, Duzova, A, Hayran, M, Ozaltin, F, Topaloglu, R

Background Alport syndrome (AS) is an inherited glomerular disease caused by mutations in COL4A3, COL4A4, or COL4A5. Associations between clinical manifestations and genotype are not yet well defined. Our study aimed to define clinical and genetic ch

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3566::7b0cf339d48fa8b58d350d919adad602