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

Autor: Stéphanie De Rechter, Detlef Bockenhauer, Lisa M. Guay-Woodford, Isaac Liu, Andrew J. Mallett, Neveen A. Soliman, Lucimary C. Sylvestre, Franz Schaefer, Max C. Liebau, Djalila Mekahli, P. Adamczyk, N. Akinci, H. Alpay, C. Ardelean, N. Ayasreh, Z. Aydin, A. Bael, V. Baudouin, U.S. Bayrakci, A. Bensman, H. Bialkevich, A. Biebuyck, O. Boyer, O. Bjanid, A. Bryłka, S. Çalışkan, A. Cambier, A. Camelio, V. Carbone, M. Charbit, B. Chiodini, A. Chirita, N. Çiçek, R. Cerkauskiene, L. Collard, M. Conceiçao, I. Constantinescu, A. Couderc, B. Crapella, M. Cvetkovic, B. Dima, F. Diomeda, M. Docx, N. Dolan, C. Dossier, D. Drozdz, J. Drube, O. Dunand, P. Dusan, L.A. Eid, F. Emma, M. Espino Hernandez, M. Fila, M. Furlano, M. Gafencu, M.S. Ghuysen, M. Giani, M. Giordano, I. Girisgen, N. Godefroid, A. Godron-Dubrasquet, I. Gojkovic, E. Gonzalez, I. Gökçe, J.W. Groothoff, S. Guarino, A. Guffens, P. Hansen, J. Harambat, S. Haumann, G. He, L. Heidet, R. Helmy, F. Hemery, N. Hooman, B. llanas, A. Jankauskiene, P. Janssens, S. Karamaria, I. Kazyra, J. Koenig, S. Krid, P. Krug, V. Kwon, A. La Manna, V. Leroy, M. Litwin, J. Lombet, G. Longo, A.C. Lungu, A. Mallawaarachchi, A. Marin, P. Marzuillo, L. Massella, A. Mastrangelo, H. McCarthy, M. Miklaszewska, A. Moczulska, G. Montini, A. Morawiec-Knysak, D. Morin, L. Murer, I. Negru, F. Nobili, L. Obrycki, H. Otoukesh, S. Özcan, L. Pape, S. Papizh, P. Parvex, M. Pawlak-Bratkowska, L. Prikhodina, A. Prytula, C. Quinlan, A. Raes, B. Ranchin, N. Ranguelov, R. Repeckiene, C. Ronit, R. Salomon, R. Santagelo, S.K. Saygılı, S. Schaefer, M. Schreuder, T. Schurmans, T. Seeman, N. Segers, M. Sinha, E. Snauwaert, B. Spasojevic, S. Stabouli, C. Stoica, R. Stroescu, E. Szczepanik, M. Szczepańska, K. Taranta-Janusz, A. Teixeira, J. Thumfart, M. Tkaczyk, R. Torra, D. Torres, N. Tram, B. Utsch, J. Vande Walle, R. Vieux, R. Vitkevic, A. Wilhelm-Bals, E. Wühl, Z.Y. Yildirim, S. Yüksel, K. Zachwieja

Publikováno v: Kidney International Reports, Vol 4, Iss 9, Pp 1271-1284 (2019)

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://doaj.org/article/a1f3859f23d4489db4d7640a8d721983

Polykystose rénale autosomique dominante associée aux variants monoalléliques de IFT140 : une nouvelle entité clinique

Autor: A. Calamel, V.G.V. Pillay, L. Olivier Faivre, C. Freguin, B. Llanas, Y. Le Meur, M.P. Audrezet, E. Cornec Le Gall

Publikováno v: Néphrologie & Thérapeutique. 18:300

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::c2264ce9936fb0716599813afa533256
https://doi.org/10.1016/j.nephro.2022.07.221

Intérêt de l’examen des urines à la bandelette en cas de retard de croissance

Autor: N. Bendelac, R. Novo, Aurélia Bertholet-Thomas, Gabriel Choukroun, Stéphane Decramer, C. Goizet, Aude Servais, B. Llanas

Publikováno v: Archives de Pédiatrie. 22:756-762

Resume Tout retard de croissance staturo-ponderale conduit generalement le medecin referent a adresser l’enfant a une equipe hospitaliere. Souvent, a l’issue d’un bilan complementaire, un diagnostic est pose et un traitement instaure. Mais cert

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b82e7dcc1a5348f0ac2fbb28399a0ec3
https://doi.org/10.1016/j.arcped.2015.04.016

Caractéristiques cliniques et biochimiques des lithiases urinaires de l’enfant

Autor: Emmanuel Richard, A. Giraudon, B. Llanas, E. Dobremez, Pascal Barat, A. Godron, A Bouty, Jean-Marc Blouin, Jérôme Harambat

Publikováno v: Archives de Pédiatrie. 21:1322-1329

Resume Objectifs Les lithiases urinaires sont rares chez l’enfant mais leur incidence a augmente au cours des dernieres decennies. Cette etude avait pour objectif de decrire la presentation clinique, les caracteristiques biochimiques, l’etiologie

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::0f42f9e73a2fc832ede438833dc1b828
https://doi.org/10.1016/j.arcped.2014.08.027

[Solitary kidney: Management and outcome]

Autor: A, Godron-Dubrasquet, C, Didailler, J, Harambat, B, Llanas

Publikováno v: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 24(11)

Solitary functioning kidneys form an important subgroup of congenital anomalies of the kidney and urinary tract (CAKUT). A solitary kidney can be congenital or acquired after unilateral nephrectomy and is often associated with ipsilateral urogenital

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::45ec388ccb0e060f220e6f5ea5307f82
https://pubmed.ncbi.nlm.nih.gov/28939448