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ADPedKD: A Global Online Platform on the Management of Children With

Autor: De Rechter, S, Bockenhauer, D, Guay-Woodford, LM, Liu, I, Mallett, AJ, Soliman, NA, Sylvestre, LC, Schaefer, F, Liebau, MC, Mekahli, D, Adamczyk, P, Akinci, N, Alpay, H, Ardelean, C, Ayasreh, N, Aydin, Z, Bael, A, Baudouin, V, Bayrakci, US, Bensman, A, Bialkevich, H, Biebuyck, A, Boyer, O, Bjanid, O, Brylka, A, Caliskan, S, Cambier, A, Camelio, A, Carbone, V, Charbit, M, Chiodini, B, Chirita, A, Cicek, N, Cerkauskiene, R, Collard, L, Conceicao, M, Constantinescu, I, Couderc, A, Crapella, B, Cvetkovic, M, Dima, B, Diomeda, F, Docx, M, Dolan, N, Dossier, C, Drozdz, D, Drube, J, Dunand, O, Dusan, P, Eid, LA, Emma, F, Hernandez, ME, Fila, M, Furlano, M, Gafencu, M, Ghuysen, M, Giani, M, Giordano, M, Girisgen, I, Godefroid, N, Godron-Dubrasquet, A, Gojkovic, I, Gonzalez, E, Gokce, I, Groothoff, JW, Guarino, S, Guffens, A, Hansen, P, Harambat, J, Haumann, S, He, G, Heidet, L, Helmy, R, Hemery, F, Hooman, N, Ilanas, B, Jankauskiene, A, Janssens, P, Karamaria, S, Kazyra, I, Koenig, J, Krid, S, Krug, P, Kwon, V, La Manna, A, Leroy, V, Litwin, M, Lombet, J, Longo, G, Lungu, AC, Mallawaarachchi, A, Marin, A, Marzuillo, P, Massella, L, Mastrangelo, A, McCarthy, H, Miklaszewska, M, Moczulska, A, Montini, G, Morawiec-Knysak, A, Morin, D, Murer, L, Negru, I, Nobili, F, Obrycki, L, Otoukesh, H, Ozcan, S, Pape, L, Papizh, S, Parvex, P, Pawlak-Bratkowska, M, Prikhodina, L, Prytula, A, Quinlan, C, Raes, A, Ranchin, B, Ranguelov, N, Repeckiene, R, Ronit, C, Salomon, R, Santagelo, R, Saygili, SK, Schaefer, S, Schreuder, M, Schurmans, T, Seeman, T, Segers, N, Sinha, M, Snauwaert, E, Spasojevic, B, Stabouli, S, Stoica, C, Stroescu, R, Szczepanik, E, Szczepanska, M, Taranta-Janusz, K, Teixeira, A, Thumfart, J, Tkaczyk, M, Torra, R, Torres, D, Tram, N, Utsch, B, Vande Walle, J, Vieux, R, Vitkevic, R, Wilhelm-Bals, A, Wuhl, E, Yildirim, ZY, Yuksel, S, Zachwieja, K

Background: Autosomal dominant polycystic kidney disease (ADPKD) is the most common monogenic cause of renal failure. For several decades, ADPKD was regarded as an adult-onset disease. In the past decade, it has become more widely appreciated that th

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3566::5d1529778edf5ad4ec1fe6cb1827ccb4

The Clinical and Mutational Spectrum of Turkish Patients with Cystinosis

Autor: Övünç, Hacihamdioğlu, Topaloglu, R, Gulhan, B, İnözü, M, Canpolat, N, Yilmaz, A, Noyan, A, Gökçe, İ, Gürgöze, MK, Akinci, N, Baskin, E, Serdaroğlu, E, Demircioğlu, Kiliç, Yüksel, S, Korkmaz, E, Hayran, M, Ozaltin, F, contributors, of, Dursun, İSMAİL

Background and objectives Infantile nephropathic cystinosis is a severe disease that occurs due to mutations in the cystinosis gene, and it is characterized by progressive dysfunction of multiple organs; >100 cystinosis gene mutations have been ident

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::609853f9d5d65f9c5df0542c20e5b77c
https://europepmc.org/articles/PMC5628704/

Development of a medication adherence scale for familial Mediterranean fever (MASIF) in a cohort of Turkish children

Autor: Yesilkaya, S., Acikel, C., Fidanci, B. E., Polat, A., Sozeri, B., Ayaz, N. A., Makay, B. B., Simsek, D., Akinci, N., Ozcelik, G., Kavukcu, S., Emre, S., Donmez, O., Delibas, A., Yuksel, S., Berdeli, A., Poyrazoglu, H., Saldir, M., Fidanci, K., Cakar, N., Peru, H., Bakkaloglu, S., Tabel, Y., Sari, O., Aydogan, U., Ozenc, S., Basbozkurt, G., Unsal, E., Ozgur Kasapcopur, Gok, F., Ozen, S., Demirkaya, E.

Publikováno v: Scopus-Elsevier
Publons

Objective. To develop and assess the validity and reliability of an adherence scale concerning medical treatment in paediatric FMF patients. Methods. The Medication Adherence Scale in FMF Patients (MASIF) is a 18-item questionnaire that evaluates adh

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::91af8996e11dd0294ddc7f12d3b0576f