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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1947 1
2006 2
2009 1
2010 1
2011 1
2012 6
2013 3
2014 2
2015 4
2016 4
2017 1
2018 4
2019 7
2020 6
2021 4
2022 8
2023 2
2024 1

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49 results

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Page 1
The genetic landscape and clinical spectrum of nephronophthisis and related ciliopathies.
Petzold F, Billot K, Chen X, Henry C, Filhol E, Martin Y, Avramescu M, Douillet M, Morinière V, Krug P, Jeanpierre C, Tory K, Boyer O, Burgun A, Servais A, Salomon R, Benmerah A, Heidet L, Garcelon N, Antignac C, Zaidan M, Saunier S; INSERM–Necker Hospital NPH collaborative group. Petzold F, et al. Kidney Int. 2023 Aug;104(2):378-387. doi: 10.1016/j.kint.2023.05.007. Epub 2023 May 23. Kidney Int. 2023. PMID: 37230223 Free article.
Fatal thrombotic microangiopathy case following adeno-associated viral SMN gene therapy.
Guillou J, de Pellegars A, Porcheret F, Frémeaux-Bacchi V, Allain-Launay E, Debord C, Denis M, Péréon Y, Barnérias C, Desguerre I, Roussey G, Mercier S. Guillou J, et al. Among authors: roussey g. Blood Adv. 2022 Jul 26;6(14):4266-4270. doi: 10.1182/bloodadvances.2021006419. Blood Adv. 2022. PMID: 35584395 Free PMC article.
Treatment and outcome of congenital nephrotic syndrome.
Bérody S, Heidet L, Gribouval O, Harambat J, Niaudet P, Baudouin V, Bacchetta J, Boudaillez B, Dehennault M, de Parscau L, Dunand O, Flodrops H, Fila M, Garnier A, Louillet F, Macher MA, May A, Merieau E, Monceaux F, Pietrement C, Rousset-Rouvière C, Roussey G, Taque S, Tenenbaum J, Ulinski T, Vieux R, Zaloszyc A, Morinière V, Salomon R, Boyer O. Bérody S, et al. Among authors: roussey g. Nephrol Dial Transplant. 2019 Mar 1;34(3):458-467. doi: 10.1093/ndt/gfy015. Nephrol Dial Transplant. 2019. PMID: 29474669
Benign and malignant proliferation in idiopathic nephrotic syndrome: a French cohort study.
Cébron C, Godron-Dubrasquet A, Aladjidi N, Roussey G, Boyer O, Avramescu M, Baudouin V, Terzic J, Allain-Launay E, Rieux-Laucat F, Decramer S, Simon T, Harambat J. Cébron C, et al. Among authors: roussey g. Pediatr Nephrol. 2022 Aug;37(8):1837-1843. doi: 10.1007/s00467-021-05386-0. Epub 2022 Jan 10. Pediatr Nephrol. 2022. PMID: 35006357
Kidney Transplantation in Small Children: Association Between Body Weight and Outcome-A Report From the ESPN/ERA-EDTA Registry.
Boehm M, Bonthuis M, Aufricht C, Battelino N, Bjerre A, Edvardsson VO, Herthelius M, Hubmann H, Jahnukainen T, de Jong H, Laube GF, Mattozzi F, Molchanova EA, Muñoz M, Noyan A, Pape L, Printza N, Reusz G, Roussey G, Rubik J, Spasojevic'-Dimitrijeva B, Seeman T, Ware N, Vidal E, Harambat J, Jager KJ, Groothoff J. Boehm M, et al. Among authors: roussey g. Transplantation. 2022 Mar 1;106(3):607-614. doi: 10.1097/TP.0000000000003771. Transplantation. 2022. PMID: 33795596
[Vaccine recommendations for children with idiopathic nephrotic syndrome].
Boyer O, Baudouin V, Bérard É, Biebuyck-Gougé N, Dossier C, Guigonis V, Audard V, Klifa R, Leroy V, Ranchin B, Roussey G, Samaille C, Tellier S, Vrillon I. Boyer O, et al. Among authors: roussey g. Nephrol Ther. 2020 May;16(3):177-183. doi: 10.1016/j.nephro.2019.09.007. Epub 2020 Apr 8. Nephrol Ther. 2020. PMID: 32278737 French.
Characterization and review of MTHFD1 deficiency: four new patients, cellular delineation and response to folic and folinic acid treatment.
Burda P, Kuster A, Hjalmarson O, Suormala T, Bürer C, Lutz S, Roussey G, Christa L, Asin-Cayuela J, Kollberg G, Andersson BA, Watkins D, Rosenblatt DS, Fowler B, Holme E, Froese DS, Baumgartner MR. Burda P, et al. Among authors: roussey g. J Inherit Metab Dis. 2015 Sep;38(5):863-72. doi: 10.1007/s10545-015-9810-3. Epub 2015 Jan 30. J Inherit Metab Dis. 2015. PMID: 25633902 Free article. Review.
Ofatumumab treatment for nephrotic syndrome recurrence after pediatric renal transplantation.
Bernard J, Lalieve F, Sarlat J, Perrin J, Dehoux L, Boyer O, Godron-Dubrasquet A, Harambat J, Decramer S, Caillez M, Bruel A, Allain-Launay E, Dantal J, Roussey G. Bernard J, et al. Among authors: roussey g. Pediatr Nephrol. 2020 Aug;35(8):1499-1506. doi: 10.1007/s00467-020-04567-7. Epub 2020 Apr 18. Pediatr Nephrol. 2020. PMID: 32306087
School level of children carrying a HNF1B variant or a deletion.
Laliève F, Decramer S, Heidet L, Baudouin V, Lahoche A, Llanas B, Cochat P, Tenenbaum J, Lavocat MP, Eckart P, Broux F, Roussey G, Cloarec S, Vrillon I, Dunand O, Bessenay L, Tsimaratos M, Nobili F, Pietrement C, De Parscau L, Bonneville V, Rodier N, Saint-Martin C, Chassaing N, Michel-Calemard L, Moriniere V, Bellanné-Chantelot C, Bahans C, Guigonis V. Laliève F, et al. Among authors: roussey g. Eur J Hum Genet. 2020 Jan;28(1):56-63. doi: 10.1038/s41431-019-0490-6. Epub 2019 Sep 3. Eur J Hum Genet. 2020. PMID: 31481685 Free PMC article.
49 results