Ceballos-Picot I - Search Results

1

Adenine phosphoribosyltransferase deficiency in children.

Harambat J, Bollée G, Daudon M, Ceballos-Picot I, Bensman A; APRT Study Group. Harambat J, et al. Pediatr Nephrol. 2012 Apr;27(4):571-9. doi: 10.1007/s00467-011-2037-0. Epub 2012 Jan 3. Pediatr Nephrol. 2012. PMID: 22212387

2

Phenotype and genotype characterization of adenine phosphoribosyltransferase deficiency.

Bollée G, Dollinger C, Boutaud L, Guillemot D, Bensman A, Harambat J, Deteix P, Daudon M, Knebelmann B, Ceballos-Picot I. Bollée G, et al. J Am Soc Nephrol. 2010 Apr;21(4):679-88. doi: 10.1681/ASN.2009080808. Epub 2010 Feb 11. J Am Soc Nephrol. 2010. PMID: 20150536 Free PMC article.

3

Decreased kidney function and crystal deposition in the tubules after kidney transplant.

Stratta P, Fogazzi GB, Canavese C, Airoldi A, Fenoglio R, Bozzola C, Ceballos-Picot I, Bollée G, Daudon M. Stratta P, et al. Am J Kidney Dis. 2010 Sep;56(3):585-90. doi: 10.1053/j.ajkd.2009.12.028. Epub 2010 Mar 19. Am J Kidney Dis. 2010. PMID: 20303634

4

Maternal uniparental disomy of chromosome 16 in a patient with adenine phosphoribosyltransferase deficiency.

Ceballos-Picot I, Guest G, Moriniere V, Mockel L, Daudon M, Malan V, Antignac C, Heidet L. Ceballos-Picot I, et al. Clin Genet. 2011 Aug;80(2):199-201. doi: 10.1111/j.1399-0004.2011.01626.x. Clin Genet. 2011. PMID: 21749366 No abstract available.

5

Adenine phosphoribosyltransferase deficiency.

Bollée G, Harambat J, Bensman A, Knebelmann B, Daudon M, Ceballos-Picot I. Bollée G, et al. Clin J Am Soc Nephrol. 2012 Sep;7(9):1521-7. doi: 10.2215/CJN.02320312. Epub 2012 Jun 14. Clin J Am Soc Nephrol. 2012. PMID: 22700886 Review.

6

2,8-Dihydroxyadenine urolithiasis: a not so rare inborn error of purine metabolism.

Ceballos-Picot I, Daudon M, Harambat J, Bensman A, Knebelmann B, Bollée G. Ceballos-Picot I, et al. Nucleosides Nucleotides Nucleic Acids. 2014;33(4-6):241-52. doi: 10.1080/15257770.2013.853780. Nucleosides Nucleotides Nucleic Acids. 2014. PMID: 24940675 Review.

7

Recurrent 2,8-dihydroxyadenine nephropathy: a rare but preventable cause of renal allograft failure.

Zaidan M, Palsson R, Merieau E, Cornec-Le Gall E, Garstka A, Maggiore U, Deteix P, Battista M, Gagné ER, Ceballos-Picot I, Duong Van Huyen JP, Legendre C, Daudon M, Edvardsson VO, Knebelmann B. Zaidan M, et al. Am J Transplant. 2014 Nov;14(11):2623-32. doi: 10.1111/ajt.12926. Epub 2014 Oct 10. Am J Transplant. 2014. PMID: 25307253 Free PMC article.

8

Chronic tubulointerstitial kidney disease in untreated adenine phosphoribosyl transferase (APRT) deficiency: A case report .

Cochran B, Kovačíková T, Hodaňová K, Živná M, Hnízda A, Niehaus AG, Bonnecaze A, Balasubraminiam G, Ceballos-Picot I, Hawfield A, Kidd K, Kmoch S, Bleyer AJ. Cochran B, et al. Among authors: ceballos picot i. Clin Nephrol. 2018 Oct;90(4):296-301. doi: 10.5414/CN109460. Clin Nephrol. 2018. PMID: 30106368 Review.

9

2,8-Dihydroxyadenine urolithiasis, an underdiagnosed disease.

Ceballos-Picot I, Perignon JL, Hamet M, Daudon M, Kamoun P. Ceballos-Picot I, et al. Lancet. 1992 Apr 25;339(8800):1050-1. Lancet. 1992. PMID: 1349069 No abstract available.

10

Structural Insights into the Forward and Reverse Enzymatic Reactions in Human Adenine Phosphoribosyltransferase.

Huyet J, Ozeir M, Burgevin MC, Pinson B, Chesney F, Remy JM, Siddiqi AR, Lupoli R, Pinon G, Saint-Marc C, Gibert JF, Morales R, Ceballos-Picot I, Barouki R, Daignan-Fornier B, Olivier-Bandini A, Augé F, Nioche P. Huyet J, et al. Among authors: ceballos picot i. Cell Chem Biol. 2018 Jun 21;25(6):666-676.e4. doi: 10.1016/j.chembiol.2018.02.011. Epub 2018 Mar 22. Cell Chem Biol. 2018. PMID: 29576532 Free article.

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