Novel mutations in the duplicated region of PKD1 gene.

Autor: Perrichot, R, Mercier, B, Quere, I, Carre, A, Simon, P, Whebe, B, Cledes, J, Ferec, C

Publikováno v: European Journal of Human Genetics. May2000, Vol. 8 Issue 5, p353. 7p.

Kidney transplantation in patients with Fabry disease

Autor: Cybulla M, Walter KN, Schwarting A, Divito R, Feriozzi S, Sunder Plassmann G, Binder C, Kotanko P, Kroepfl T, Plecko B, Bodamer O, Hauser AC, Kleinert J, Kristoferitsch W, Schreiber W, Georges B, Nassogne MC, Pirson Y, Dehout F, Henry F, Roland D, Vauthier L, Goyens P, Mazoin N, Van Maldergem L, Eyskens F, Bultas J, Karetová D, Linhart A, Dostalova G, Choukroun G, Berthelot J, Hardy P, Carey Reomonnay S, Lacombe D, Bataille P, Benziane S, Mittelberger JM, Thevenot C, Dobbelaere D, Hachulla E, Dussol B, Reade R, Khau van Kien A, Kaminsky P, Guyot C, Lino M, Ghafari T, Germain DP, Knebelmann B, Lidove O, Ouali N, Touati G, Monlun E, Jaussaud R, Richalet B, Klotz V, Andres E, Caraman D, Bazex J, Perrichot R, Hennermann J, von Arnim Baas A, Stolz S, Hoffmann B, Chrobot E, Grabbe S, Jansen T, Neumann HP, Schluh G, Gal A, Muschol N, Shäfer E, Ullrich K, Das A, Illsinger S, Lücke T, Bähner F, Baron K, Beck M, Bruns K, Delgado Sanchez S, Hartung R, Kalkum G, Kampmann C, Keilmann A, Lackner K, Pitz S, Whybra C, Wiethoff C, Koletzko B, Pontz B, Böttcher T, Miethe S, Rolfs A, Davydenko I, Wanner C, Maródi L, Gabrielli O, Gobbi S, Concolino D, Zampetti A, Borsini W, Buchner S, Menni F, Parini R, Ravaglia R, Santus F, Di Vito R, Burlina A, Burlina AP, Manara R, Antuzzi D, Castorina M, Ricci R, Kaarbøe Ø, Skarbøvik A, Houge G, Svarstad E, Tøndel C, Barba MA, Botella R, Franco A, Torras J, Gómez Huertas E, Torregrosa V, Fernández V, Paniagua J, Rodriguez F, Herrera J, Febrer I, Perez Garcia A, Martin I, Barbado FJ, Garcia de Lorenzo A, López M, González J, Ballarin J, Torra R, Hernández S, Ara J, Bonal J, Pintos G, Andreu J, Rivera A, Oqvist B, Huyen Do U, Barbey F, Hayoz D, Theytaz J, Schärer M, Schulthess G, Steinmann B, Walter K, Widmer U, Hollak C, Ormel E, van Duinen A, Vetter A, Corcoran M, Cox TM, Deegan P, Ramaswami U, Wright N, Baker R, Blincoe M, Bruce R, Burns A, Close L, Davey C, Elliott J, Elliott P, Evans S, Ginsberg L, Hajioff D, Hughes D, Ioannidis A, Keshav S, Mehta A, Milligan A, Orteu C, Richfield L., STRISCIUGLIO, PIETRO

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3730::20ede5c4651daeb1c39580f8b9c0d12f
http://hdl.handle.net/11588/490290

Aberrant glycosylation of IgA from patients with IgA nephropathy

Autor: Le Corre R, Pierre Youinou, D. Baharaki, Maryvonne Dueymes, J. Clèdes, Basset C, Perrichot R

Publikováno v: Glycoconjugate journal. 13(4)

Despite the prominent role of IgA, particularly IgA1, in the pathogenesis of IgA nephropathy (IgAN), the precise role of this molecule in the process remains unclear. Four biotin-conjugated lectins in sandwich-type enzyme-linked immunosorbent assays

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bcdad23e1d91a007dd29bcf0aadd9b90
https://pubmed.ncbi.nlm.nih.gov/8872105

Peut-on prédire l’âge de survenue de l’insuffisance rénale terminale dans la polykystose rénale autosomique dominante ? Construction d’un nouveau modèle pronostique

Autor: Cornec-Le Gall, E., Hourmant, M., Morin, M.P., Charasse, C., Perrichot, R., Renaudineau, E., Treguer, L., Whebe, B., Jousset, P., Audrezet, M.P., Ferec, C., Le Meur, Y.

Publikováno v: In Néphrologie & Thérapeutique September 2013 9(5):276-276

Idiopathic and secondary membranous nephropathy and polymorphism at TAP1 and HLA-DMA loci.

Autor: Chevrier, D., Giral, M., Perrichot, R., Latinne, D., Coville, P., Muller, J. Y., Soulillou, J. P., Bignon, J. D.

Publikováno v: Tissue Antigens; Aug1997, Vol. 50 Issue 2, p164-169, 6p