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

Year Number of Results
1991 1
1992 2
1995 1
1996 1
1997 2
1998 2
1999 1
2000 1
2001 3
2002 3
2004 1
2005 2
2006 2
2011 1
2012 2
2013 3
2014 1
2015 1
2017 1
2018 3
2019 2
2020 3
2021 1
2023 0

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37 results

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Page 1
[The new drunks].
Mortamet G, Eckart P. Mortamet G, et al. Among authors: eckart p. Arch Pediatr. 2012 Dec;19(12):1279-81. doi: 10.1016/j.arcped.2012.09.007. Epub 2012 Nov 17. Arch Pediatr. 2012. PMID: 23164473 French. No abstract available.
[Reflux nephropathy].
Eckart P, Broyer M. Eckart P, et al. Rev Prat. 1992 Feb 15;42(4):447-51. Rev Prat. 1992. PMID: 1604164 Review. French.
NPHS2 mutations in steroid-resistant nephrotic syndrome: a mutation update and the associated phenotypic spectrum.
Bouchireb K, Boyer O, Gribouval O, Nevo F, Huynh-Cong E, Morinière V, Campait R, Ars E, Brackman D, Dantal J, Eckart P, Gigante M, Lipska BS, Liutkus A, Megarbane A, Mohsin N, Ozaltin F, Saleem MA, Schaefer F, Soulami K, Torra R, Garcelon N, Mollet G, Dahan K, Antignac C. Bouchireb K, et al. Among authors: eckart p. Hum Mutat. 2014 Feb;35(2):178-86. doi: 10.1002/humu.22485. Epub 2013 Dec 9. Hum Mutat. 2014. PMID: 24227627 Review.
A very uncommon cause of acute kidney injury in infancy.
Dorval G, Balducci E, Kaltenbach S, Chomton M, Krid S, Rabant M, Porcheret F, Duong Van Huyen JP, Eckart P, Mortamet G, Delacourt C, de Saint-Blanquat L, Dehoux L, Picard C, Salomon R, Neven B, Boyer O. Dorval G, et al. Among authors: eckart p. Kidney Int. 2021 Oct;100(4):948-950. doi: 10.1016/j.kint.2021.06.024. Kidney Int. 2021. PMID: 34556303 No abstract available.
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: eckart p. 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.
Radiation-induced cataract in astronauts and cosmonauts.
Rastegar N, Eckart P, Mertz M. Rastegar N, et al. Among authors: eckart p. Graefes Arch Clin Exp Ophthalmol. 2002 Jul;240(7):543-7. doi: 10.1007/s00417-002-0489-4. Epub 2002 Jun 7. Graefes Arch Clin Exp Ophthalmol. 2002. PMID: 12136284
Eculizumab treatment in severe pediatric STEC-HUS: a multicenter retrospective study.
Percheron L, Gramada R, Tellier S, Salomon R, Harambat J, Llanas B, Fila M, Allain-Launay E, Lapeyraque AL, Leroy V, Adra AL, Bérard E, Bourdat-Michel G, Chehade H, Eckart P, Merieau E, Piètrement C, Sellier-Leclerc AL, Frémeaux-Bacchi V, Dimeglio C, Garnier A. Percheron L, et al. Among authors: eckart p. Pediatr Nephrol. 2018 Aug;33(8):1385-1394. doi: 10.1007/s00467-018-3903-9. Epub 2018 Mar 23. Pediatr Nephrol. 2018. PMID: 29572749
[Legionella pneumonia in an immunocompetent child].
Akou'ou MH, Oger M, Gras G, Eckart P, Penniello MJ, Vergnaud M, Guillois B. Akou'ou MH, et al. Among authors: eckart p. Arch Pediatr. 2005 Apr;12 Suppl 1:S49-53. doi: 10.1016/s0929-693x(05)80012-0. Arch Pediatr. 2005. PMID: 15893239 Free PMC article. French.
CYP24A1 Mutations in a Cohort of Hypercalcemic Patients: Evidence for a Recessive Trait.
Molin A, Baudoin R, Kaufmann M, Souberbielle JC, Ryckewaert A, Vantyghem MC, Eckart P, Bacchetta J, Deschenes G, Kesler-Roussey G, Coudray N, Richard N, Wraich M, Bonafiglia Q, Tiulpakov A, Jones G, Kottler ML. Molin A, et al. Among authors: eckart p. J Clin Endocrinol Metab. 2015 Oct;100(10):E1343-52. doi: 10.1210/jc.2014-4387. Epub 2015 Jul 27. J Clin Endocrinol Metab. 2015. PMID: 26214117
37 results