Bacchetta J - Search Results

1

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: bacchetta j. 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.

2

The case: familial renal failure with ocular abnormality.

Bacchetta J, Habault C, Liutkus A, Cochat P. Bacchetta J, et al. Kidney Int. 2008 Apr;73(8):977-8. doi: 10.1038/ki.2008.12. Kidney Int. 2008. PMID: 18379529 Free article. No abstract available.

3

Precocious puberty and unlicensed paediatric drugs for severe hyperparathyroidism.

Bacchetta J, Plotton I, Ranchin B, Vial T, Nicolino M, Morel Y, Cochat P. Bacchetta J, et al. Nephrol Dial Transplant. 2009 Aug;24(8):2595-8. doi: 10.1093/ndt/gfp211. Epub 2009 May 6. Nephrol Dial Transplant. 2009. PMID: 19420106

4

Autoimmune hypoparathyroidism in a 12-year-old girl with McKusick cartilage hair hypoplasia.

Bacchetta J, Ranchin B, Brunet AS, Bouvier R, Duquesne A, Edery P, Fabien N, Peretti N. Bacchetta J, et al. Pediatr Nephrol. 2009 Dec;24(12):2449-53. doi: 10.1007/s00467-009-1256-0. Epub 2009 Jul 22. Pediatr Nephrol. 2009. PMID: 19626344

5

The influence of glomerular filtration rate and age on fibroblast growth factor 23 serum levels in pediatric chronic kidney disease.

Bacchetta J, Dubourg L, Harambat J, Ranchin B, Abou-Jaoude P, Arnaud S, Carlier MC, Richard M, Cochat P. Bacchetta J, et al. J Clin Endocrinol Metab. 2010 Apr;95(4):1741-8. doi: 10.1210/jc.2009-1576. Epub 2010 Feb 15. J Clin Endocrinol Metab. 2010. PMID: 20157196

6

Congenital versus acquired solitary kidney: is the difference relevant?

Abou Jaoudé P, Dubourg L, Bacchetta J, Berthiller J, Ranchin B, Cochat P. Abou Jaoudé P, et al. Among authors: bacchetta j. Nephrol Dial Transplant. 2011 Jul;26(7):2188-94. doi: 10.1093/ndt/gfq659. Epub 2010 Nov 2. Nephrol Dial Transplant. 2011. PMID: 21045075

7

Which creatinine and cystatin C equations can be reliably used in children?

Bacchetta J, Cochat P, Rognant N, Ranchin B, Hadj-Aissa A, Dubourg L. Bacchetta J, et al. Clin J Am Soc Nephrol. 2011 Mar;6(3):552-60. doi: 10.2215/CJN.04180510. Epub 2010 Nov 29. Clin J Am Soc Nephrol. 2011. PMID: 21115623 Free PMC article.

8

Bone assessment in children with chronic kidney disease: data from two new bone imaging techniques in a single-center pilot study.

Bacchetta J, Boutroy S, Vilayphiou N, Ranchin B, Fouque-Aubert A, Basmaison O, Cochat P. Bacchetta J, et al. Pediatr Nephrol. 2011 Apr;26(4):587-95. doi: 10.1007/s00467-010-1745-1. Epub 2011 Jan 20. Pediatr Nephrol. 2011. PMID: 21246220

9

What about the renal function during childhood of children born from dialysed mothers?

Abou-Jaoude P, Dubourg L, Bessenay L, Pinçon A, Jolivot A, Guebre-Egziabher F, Cochat P, Bacchetta J. Abou-Jaoude P, et al. Among authors: bacchetta j. Nephrol Dial Transplant. 2012 Jun;27(6):2365-9. doi: 10.1093/ndt/gfr617. Epub 2011 Nov 9. Nephrol Dial Transplant. 2012. PMID: 22076429 Clinical Trial.

10

From bone abnormalities to mineral metabolism dysregulation in autosomal dominant polycystic kidney disease.

Mekahli D, Bacchetta J. Mekahli D, et al. Among authors: bacchetta j. Pediatr Nephrol. 2013 Nov;28(11):2089-96. doi: 10.1007/s00467-012-2384-5. Epub 2013 Jan 24. Pediatr Nephrol. 2013. PMID: 23340856 Review.

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