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Page 1
[Is detection of vesicoureteral reflux mandatory?].
Bouissou F, Brochard K, Garnier A, Bandin F, Decramer S. Bouissou F, et al. Among authors: brochard k. Arch Pediatr. 2009 Jun;16(6):906-8. doi: 10.1016/S0929-693X(09)74199-5. Arch Pediatr. 2009. PMID: 19541217 French. No abstract available.
Phenotype-genotype correlation in antenatal and neonatal variants of Bartter syndrome.
Brochard K, Boyer O, Blanchard A, Loirat C, Niaudet P, Macher MA, Deschenes G, Bensman A, Decramer S, Cochat P, Morin D, Broux F, Caillez M, Guyot C, Novo R, Jeunemaître X, Vargas-Poussou R. Brochard K, et al. Nephrol Dial Transplant. 2009 May;24(5):1455-64. doi: 10.1093/ndt/gfn689. Epub 2008 Dec 18. Nephrol Dial Transplant. 2009. PMID: 19096086
[Cystic and hyperechogenic kidneys in children].
Brochard K, Decramer S. Brochard K, et al. Nephrol Ther. 2010 Jul;6(4):272-9. doi: 10.1016/j.nephro.2010.03.006. Epub 2010 Apr 28. Nephrol Ther. 2010. PMID: 20430711 French.
[Atypical onset of Churg and Strauss syndrome in a child].
Tellier S, Dallocchio A, Brochard K, Pajot C, Garnier A, Bandin F, Mazereeuw J, Vial J, Decramer S. Tellier S, et al. Among authors: brochard k. Arch Pediatr. 2012 Jun;19(6):620-3. doi: 10.1016/j.arcped.2012.03.006. Epub 2012 Apr 27. Arch Pediatr. 2012. PMID: 22541509 French.
Long-term outcome of children treated with rituximab for idiopathic nephrotic syndrome.
Tellier S, Brochard K, Garnier A, Bandin F, Llanas B, Guigonis V, Cailliez M, Pietrement C, Dunand O, Nathanson S, Bertholet-Thomas A, Ichay L, Decramer S. Tellier S, et al. Among authors: brochard k. Pediatr Nephrol. 2013 Jun;28(6):911-8. doi: 10.1007/s00467-012-2406-3. Epub 2013 Jan 23. Pediatr Nephrol. 2013. PMID: 23340857
[Bartter and Gitelman syndromes].
Brochard K. Brochard K. Arch Pediatr. 2015 May;22(5 Suppl 1):46-7. doi: 10.1016/S0929-693X(15)30024-5. Arch Pediatr. 2015. PMID: 26112515 French. No abstract available.
Mycophenolic Acid Pharmacokinetics and Relapse in Children with Steroid-Dependent Idiopathic Nephrotic Syndrome.
Tellier S, Dallocchio A, Guigonis V, Saint-Marcoux F, Llanas B, Ichay L, Bandin F, Godron A, Morin D, Brochard K, Gandia P, Bouchet S, Marquet P, Decramer S, Harambat J. Tellier S, et al. Among authors: brochard k. Clin J Am Soc Nephrol. 2016 Oct 7;11(10):1777-1782. doi: 10.2215/CJN.00320116. Epub 2016 Jul 21. Clin J Am Soc Nephrol. 2016. PMID: 27445161 Free PMC article.
French expert opinion for the management of juvenile dermatomyositis.
Bader-Meunier B, Gitiaux C, Belot A, Brochard K, Mouy R, Ponce D, Bughin V, Jouen F, Musset L, Allenbach Y, Hachulla E, Maillard H, Meyer A, Bourrat E, Benveniste O; French Network of rare autoimmune, autoinflammatory diseases FAI2R. Bader-Meunier B, et al. Among authors: brochard k. Arch Pediatr. 2019 Feb;26(2):120-125. doi: 10.1016/j.arcped.2018.12.002. Epub 2019 Jan 10. Arch Pediatr. 2019. PMID: 30638764
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.
31 results