[European Network for blood pressure research in children and adolescents (COST Action CA 19115)]

Autor: Lurbe E, Fernandez-Aranda F, Wuhl E, en representacion del Consorcio HyperChildNET

Publikováno v: ANALES DE PEDIATRIA
r-INCLIVA. Repositorio Institucional de Producción Científica de INCLIVA
instname

High blood pressure is a clearly established modifiable risk factor for cardiovascular and renal disease. Although most of its adverse effects develop in adulthood, it has become clear that high BP is a lifelong problem that can manifest early in lif

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::e5c1298ed79a0e3d684f4cdff90542ec
https://www.fundanet.incliva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=15636

Kidney Int

Autor: AZUKAITIS, K., JU, W., Kirchner, M., Nair, V., Smith, M., Fang, Z., THURN-VALSASSINA, D., BAYAZIT, A., NIEMIRSKA, A., CANPOLAT, N., BULUT, I. K., Yalcinkaya, F., PARIPOVIC, D., HARAMBAT, Jerome, CAKAR, N., ALPAY, H., LUGANI, F., MENCARELLI, F., CIVILIBAL, M., ERDOGAN, H., GELLERMANN, J., Vidal, E., TABEL, Y., Gimpel, C., ERTAN, P., YAVASCAN, O., MELK, A., QUERFELD, U., WUHL, E., KRETZLER, M., Schaefer, F., STUDY, C., GROUP, Escape Trial

Publikováno v: Kidney International
Kidney International, Nature Publishing Group, 2019, 96 (1), pp.214-221. ⟨10.1016/j.kint.2019.01.035⟩

Urinary epidermal growth factor (uEGF) has recently been identified as a promising biomarker of chronic kidney disease (CKD) progression in adults with glomerular disease. Low levels of uEGF predict CKD progression and appear to reflect the extent of

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::cb59abf483ffc6f0cd22f2dc5e6a4f51
https://hal.archives-ouvertes.fr/hal-03209965

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

Articles, Links Spectrum of early onset nephrotic syndrome associated with WT1 missense mutations

Autor: SCHUMACHER V, SCHARER K, WUHL E, ALTROGGE H, BONZEL KE, GUSCHMANN M, NEUHAUS TJ, POLLASTRO R.M., KUWERTZ-BROKING E, BULLA M, TONDERA AM, MUNDEL P, HELMCHEN U, WALDHERR R, WEIRICH A, ROYER-POKORA BRELATED

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3977::ca01b5bc174a9300ae661266f42e91de
http://hdl.handle.net/11591/185281

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.