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收藏DGKE Variants Cause a Glomerular Microangiopathy That Mimics Membranoproliferative GN
Ozaltin, Fatih; Li, Binghua; Rauhauser, Alysha; An, Sung-Wan; Soylemezoglu, Oguz; Gonul, Ipek Isik; Taskiran, Ekim Z.; Ibsirlioglu, Tulin; Korkmaz, Emine; Bilginer, Yelda; Duzova, Ali; Ozen, Seza; Topaloglu, Rezan; Besbas, Nesrin; Ashraf, Shazia; Du, Yong; Liang, Chaoying; Chen, Phylip; Lu, Dongmei; Vadnagara, Komal; Arbuckle, Susan; Lewis, Deborah; Wakeland, Benjamin; Quigg, Richard J.; Ransom, Richard F.; Wakeland, Edward K.; Topham, Matthew K.; Bazan, Nicolas G.; Mohan, Chandra; Hildebrandt, Friedhelm; Bakkaloglu, Aysin; Huang, Chou-Long; Attanasio, Massimo
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收藏Primary peritonitis in children with nephrotic syndrome: results of a 5-year multicenter study
Uncu, Nermin; Bulbul, Mehmet; Yildiz, Nurdan; Noyan, Aytul; Kosan, Cemlettin; Kavukcu, Salih; Caliskan, Salim; Gunduz, Zuebeyde; Besbas, Nesrin; Guven, Ayfer Guer
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收藏Peritonitis in children who receive long-term peritoneal dialysis:: A prospective evaluation of therapeutic guidelines
Warady, Bradley A.; Feneberg, Reinhard; Verrina, Enrico; Flynn, Joseph T.; Mueller-Wiefel, Dirk E.; Besbas, Nesrin; Zurowska, Aleksandra; Aksu, Nejat; Fischbach, Michel; Sojo, Ernesto; Donmez, Osman; Sever, Lale; Sirin, Aydan; Alexander, Steven R.; Schaefer, Franz
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收藏Aberrant splicing is a common mutational mechanism in MKS1, a key player in Meckel-Gruber Syndrome
Frank, Valeska; Bruechle, Nadina Ortiz; Mager, Silke; Frints, Susanna G. M.; Bohring, Axel; Du Bois, Gabriele; Debatin, Irmgard; Seidel, Heide; Senderek, Jan; Besbas, Nesrin; Todt, Unda; Kubisch, Christian; Grimm, Tiemo; Teksen, Fulya; Balci, Sevim; Zerres, Klaus; Bergman, Carsten
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收藏Novel OCRL1 mutations in patients with the phenotype of dent disease
Utsch, Boris; Boekenkamp, Arend; Benz, Marcus R.; Besbas, Nesrin; Doetsch, Joerg; Franke, Ingo; Fruend, Stefan; Gok, Faysal; Hoppe, Bernd; Karle, Stephanie; Kuwertz-Broeking, Eberhard; Laube, Guido; Neb, Margarita; Nuutinen, Matti; Ozaltin, Fatih; Rascher, Wolfgang; Ring, Troels; Tasic, Velibor; van Wijk, Joanna A. E.; Ludwig, Michael
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收藏A classification of hemolytic uremic syndrome and thrombotic thrombocytopenic purpura and related disorders
Besbas, N.; Karpman, D.; Landau, D.; Loirat, C.; Proesmans, W.; Remuzzi, G.; Rizzoni, G.; Taylor, C. M.; Van de Kar, N.; Zimmerhackl, L. B.
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收藏Juvenile polyarteritis:: Results of a multicenter survey of 110 children
Ozen, S; Anton, J; Arisoy, N; Bakkaloglu, A; Besbas, N; Brogan, P; García-Consuegra, J; Dolezalova, P; Dressler, F; Duzova, A; Ferriani, VPL; Hilário, MOE; Ibánez-Rubio, M; Kasapcopur, O; Kuis, W; Lehman, TJA; Nemcova, D; Nielsen, S; Oliveira, SK; Schikler, K; Sztajnbok, F; Terreri, MT; Zulian, F; Woo, P
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收藏MICA exon 5 microsatellite alleles in Turkish patients with FMF
Yigitbas, E; Uner, A; Dorak, MT; Ding, WZ; Tatayoglu, G; Balci, B; Duzova, A; Ozaltin, F; Ozen, S; Besbas, N; Topaloglu, R; Yilmaz, E; Bakkaloglu, A; Ozguc, M; Kansu, E; Fraser, PA
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收藏Allelic variants in genes associated with hereditary periodic fever syndromes as susceptibility factors for reactive systemic AA amyloidosis
Aganna, E; Hawkins, PN; Ozen, S; Pettersson, T; Bybee, A; McKee, S; Lachmann, H; Karenko, L; Ranki, A; Bakkaloglu, A; Besbas, N; Topaloglu, R; Hoffman, H; Hitman, G; Woo, P; McDermott, M
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