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2018 | 4 |
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Page 1
MAPK inhibition and growth hormone: a promising therapy in XLH.
FASEB J. 2019 Jul;33(7):8349-8362. doi: 10.1096/fj.201802007R. Epub 2019 Apr 11.
FASEB J. 2019.
PMID: 30974062
Bone Disease in Nephropathic Cystinosis: Beyond Renal Osteodystrophy.
Machuca-Gayet I, Quinaux T, Bertholet-Thomas A, Gaillard S, Claramunt-Taberner D, Acquaviva-Bourdain C, Bacchetta J.
Machuca-Gayet I, et al. Among authors: claramunt taberner d.
Int J Mol Sci. 2020 Apr 28;21(9):3109. doi: 10.3390/ijms21093109.
Int J Mol Sci. 2020.
PMID: 32354056
Free PMC article.
Review.
Item in Clipboard
Clinical and laboratory approaches in the diagnosis of renal tubular acidosis.
Santos F, Ordóñez FA, Claramunt-Taberner D, Gil-Peña H.
Santos F, et al. Among authors: claramunt taberner d.
Pediatr Nephrol. 2015 Dec;30(12):2099-107. doi: 10.1007/s00467-015-3083-9. Epub 2015 Apr 1.
Pediatr Nephrol. 2015.
PMID: 25823989
Review.
Item in Clipboard
Bone disease in nephropathic cystinosis is related to cystinosin-induced osteoclastic dysfunction.
Claramunt-Taberner D, Flammier S, Gaillard S, Cochat P, Peyruchaud O, Machuca-Gayet I, Bacchetta J.
Claramunt-Taberner D, et al.
Nephrol Dial Transplant. 2018 Sep 1;33(9):1525-1532. doi: 10.1093/ndt/gfx362.
Nephrol Dial Transplant. 2018.
PMID: 29365190
Item in Clipboard
Teenagers and young adults with nephropathic cystinosis display significant bone disease and cortical impairment.
Bertholet-Thomas A, Claramunt-Taberner D, Gaillard S, Deschênes G, Sornay-Rendu E, Szulc P, Cohen-Solal M, Pelletier S, Carlier MC, Cochat P, Bacchetta J.
Bertholet-Thomas A, et al. Among authors: claramunt taberner d.
Pediatr Nephrol. 2018 Jul;33(7):1165-1172. doi: 10.1007/s00467-018-3902-x. Epub 2018 Feb 12.
Pediatr Nephrol. 2018.
PMID: 29435659
Clinical Trial.
Item in Clipboard
Marked alterations in the structure, dynamics and maturation of growth plate likely explain growth retardation and bone deformities of young Hyp mice.
Fuente R, Gil-Peña H, Claramunt-Taberner D, Hernández-Frías O, Fernández-Iglesias Á, Hermida-Prado F, Anes-González G, Rubio-Aliaga I, Lopez JM, Santos F.
Fuente R, et al. Among authors: claramunt taberner d.
Bone. 2018 Nov;116:187-195. doi: 10.1016/j.bone.2018.08.004. Epub 2018 Aug 8.
Bone. 2018.
PMID: 30096468
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Hyperphosphatemic tumoral calcinosis caused by FGF23 compound heterozygous mutations: what are the therapeutic options for a better control of phosphatemia?
Claramunt-Taberner D, Bertholet-Thomas A, Carlier MC, Dijoud F, Chotel F, Silve C, Bacchetta J.
Claramunt-Taberner D, et al.
Pediatr Nephrol. 2018 Jul;33(7):1263-1267. doi: 10.1007/s00467-018-3945-z. Epub 2018 Mar 28.
Pediatr Nephrol. 2018.
PMID: 29594503
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