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Page 1
Functional Characterization of Anti-C3bBb Autoantibodies and C3 Glomerulopathy Phenotype.
Roquigny J, Meuleman MS, El Sissy C, Cailliez M, Servais A, Roussey G, Baudouin V, Decramer S, Nobili F, Wynckel A, Sellier Leclerc AL, Lapeyraque AL, Martins PV, Meri S, Dragon-Durey MA, Chauvet S, Frémeaux-Bacchi V. Roquigny J, et al. Among authors: decramer s. J Am Soc Nephrol. 2024 Sep 26. doi: 10.1681/ASN.0000000000000499. Online ahead of print. J Am Soc Nephrol. 2024. PMID: 39325562 No abstract available.
Renal and Extrarenal Phenotypes in Patients With HNF1B Variants and Chromosome 17q12 Microdeletions.
Buffin-Meyer B, Richard J, Guigonis V, Weber S, König J, Heidet L, Moussaoui N, Vu JP, Faguer S, Casemayou A, Prakash R, Baudouin V, Hogan J, Alexandrou D, Bockenhauer D, Bacchetta J, Ranchin B, Pruhova S, Zieg J, Lahoche A, Okorn C, Antal-Kónya V, Morin D, Becherucci F, Habbig S, Liebau MC, Mauras M, Nijenhuis T, Llanas B, Mekahli D, Thumfart J, Tönshoff B, Massella L, Eckart P, Cloarec S, Cruz A, Patzer L, Roussey G, Vrillon I, Dunand O, Bessenay L, Taroni F, Zaniew M, Louillet F, Bergmann C, Schaefer F, van Eerde AM, Schanstra JP, Decramer S; HNF1B variant study group. Buffin-Meyer B, et al. Among authors: decramer s. Kidney Int Rep. 2024 May 16;9(8):2514-2526. doi: 10.1016/j.ekir.2024.05.007. eCollection 2024 Aug. Kidney Int Rep. 2024. PMID: 39156164 Free PMC article.
Rituximab treatment in children with IgA vasculitis nephritis: a case series of an international cohort.
Rohner K, Marlais M, Ali A, Decramer S, Didsbury M, Forbes TA, Koskela M, Kurt Şükür ED, La Scola C, Lopez M, Moussaoui N, Navarro AC, Nuutinen M, Oosterveld M, Pasini A, Roelofs J, Tullus K. Rohner K, et al. Among authors: decramer s. Arch Dis Child. 2024 Oct 18;109(11):958-960. doi: 10.1136/archdischild-2024-327098. Arch Dis Child. 2024. PMID: 39142824 No abstract available.
Improved prenatal assessment of kidney disease using multiple ultrasound features.
Buffin-Meyer B, Klein J, Aziza J, Fernandez M, Feuillet G, Seye M, Buléon M, Fédou C, Camus M, Burlet-Schiltz O, Martinovic J, Saulnier-Blache JS, Decramer S, Schanstra JP. Buffin-Meyer B, et al. Among authors: decramer s. Nephrol Dial Transplant. 2024 Jun 22:gfae145. doi: 10.1093/ndt/gfae145. Online ahead of print. Nephrol Dial Transplant. 2024. PMID: 38908913
Steroid-Resistant Nephrotic Syndrome due to NPHS2 Variants Is Not Associated With Posttransplant Recurrence.
Kachmar J, Boyer O, Lipska-Ziętkiewicz B, Morinière V, Gribouval O, Heidet L, Balasz-Chmielewska I, Benetti E, Cloarec S, Csaicsich D, Decramer S, Gellermann J, Guigonis V, Hogan J, Bayazit AK, Melk A, Nigmatullina N, Oh J, Ozaltin F, Ranchin B, Tsimaratos M, Trautmann A, Antignac C, Schaefer F, Dorval G; PodoNet Network. Kachmar J, et al. Among authors: decramer s. Kidney Int Rep. 2024 Jan 10;9(4):973-981. doi: 10.1016/j.ekir.2024.01.005. eCollection 2024 Apr. Kidney Int Rep. 2024. PMID: 38765578 Free PMC article.
Pediatric urogenital schistosomiasis diagnosed in France.
Percheron L, Leblanc C, Ulinski T, Fila M, Malvy D, Bacchetta J, Guigonis V, Debuisson C, Launay E, Martinez E, Morand A, Decramer S, Schanstra JP, Berry A. Percheron L, et al. Among authors: decramer s. Pediatr Nephrol. 2024 Jun;39(6):1893-1900. doi: 10.1007/s00467-023-06260-x. Epub 2024 Jan 12. Pediatr Nephrol. 2024. PMID: 38212419
Outcome of immunosuppression in children with IgA vasculitis-related nephritis.
Rohner K, Marlais M, Ahn YH, Ali A, Alsharief A, Novak AB, Brambilla M, Cakici EK, Candan C, Canpolat N, Chan EY, Decramer S, Didsbury M, Durao F, Durkan AM, Düzova A, Forbes T, Gracchi V, Güngör T, Horinouchi T, Kasap Demir B, Kobayashi Y, Koskela M, Kurt-Sukur ED, La Scola C, Langan D, Li X, Malgieri G, Mastrangelo A, Min J, Mizerska-Wasiak M, Moussaoui N, Noyan A, Nuutinen M, O'Gormon J, Okamoto T, Oni L, Oosterveld M, Pańczyk-Tomaszewska M, Parmaksiz G, Pasini A, Rianthavorn P, Roelofs J, Shen Y, Sinha R, Topaloglu R, Torres DD, Udagawa T, Wennerström M, Yap YC, Tullus K. Rohner K, et al. Among authors: decramer s. Nephrol Dial Transplant. 2024 Jul 31;39(8):1299-1309. doi: 10.1093/ndt/gfae009. Nephrol Dial Transplant. 2024. PMID: 38211969
Identification of the first homozygous intragenic deletion in the YY1AP1 gene in a consanguineous family: New insights into the phenotypic variability associated with Grange syndrome.
Viora-Dupont E, Denommé-Pichon A, Chevarin M, Patat O, Willems M, Bourgon N, Bruel A, Aubert-Mucca M, Galinier M, Itier R, Decramer S, Piton A, Gerard B, Billon C, Jeunemaitre X, Duffourd Y, Callier P, Thauvin C, Philippe C, Faivre L, Albuisson J, Vitobello A. Viora-Dupont E, et al. Among authors: decramer s. Am J Med Genet A. 2023 Nov;191(11):2728-2735. doi: 10.1002/ajmg.a.63394. Epub 2023 Sep 12. Am J Med Genet A. 2023. PMID: 37698238
141 results