Zaccaria I - Search Results

1

Genotype-phenotype correlations in fetuses and neonates with autosomal recessive polycystic kidney disease.

Denamur E, Delezoide AL, Alberti C, Bourillon A, Gubler MC, Bouvier R, Pascaud O, Elion J, Grandchamp B, Michel-Calemard L, Missy P, Zaccaria I, Le Nagard H, Gerard B, Loirat C; Société Française de Foetopathologie; Barbet J, Beaufrère AM, Berchel C, Bessières B, Boudjemaa S, Buenerd A, Carles D, Clemenson A, Dechelotte P, Devisme L, Dijoud F, Espérandieu O, Fallet C, Gonzalès M, Hillion Y, Jacob B, Joubert M, Kermanach P, Lallemand A, Laquerrière A, Laurent N, Liprandi A, Loeuillet L, Loget P, Martinovic J, Ménez F, Narcy F, Roux JJ, Rouleau-Dubois C, Sinico M, Tantau J, Wann AR. Denamur E, et al. Among authors: zaccaria i. Kidney Int. 2010 Feb;77(4):350-8. doi: 10.1038/ki.2009.440. Epub 2009 Nov 25. Kidney Int. 2010. PMID: 19940839 Free article.

2

Long-term outcome of prenatally detected posterior urethral valves: single center study of 65 cases managed by primary valve ablation.

Sarhan O, Zaccaria I, Macher MA, Muller F, Vuillard E, Delezoide AL, Sebag G, Oury JF, Aigrain Y, El-Ghoneimi A. Sarhan O, et al. Among authors: zaccaria i. J Urol. 2008 Jan;179(1):307-12; discussion 312-3. doi: 10.1016/j.juro.2007.08.160. Epub 2007 Nov 19. J Urol. 2008. PMID: 18006017

3

Variants of the mannose-binding lectin gene in the Benin population: heterozygosity for the p.G57E allele may confer a selective advantage.

Dossou-Yovo OP, Lapoumeroulie C, Hauchecorne M, Zaccaria I, Ducrocq R, Krishnamoorthy R, Rahimy MC, Elion J. Dossou-Yovo OP, et al. Among authors: zaccaria i. Hum Biol. 2007 Dec;79(6):687-97. doi: 10.1353/hub.2008.0012. Hum Biol. 2007. PMID: 18494378

4

Time course of catch-up in adiposity influences adult anthropometry in individuals who were born small for gestational age.

Ezzahir N, Alberti C, Deghmoun S, Zaccaria I, Czernichow P, Lévy-Marchal C, Jaquet D. Ezzahir N, et al. Among authors: zaccaria i. Pediatr Res. 2005 Aug;58(2):243-7. doi: 10.1203/01.PDR.0000169980.35179.89. Epub 2005 Jul 31. Pediatr Res. 2005. PMID: 16055935

5

Inter-observer variability in chest radiograph reading for diagnosing acute lung injury in children.

Angoulvant F, Llor J, Alberti C, Kheniche A, Zaccaria I, Garel C, Dauger S. Angoulvant F, et al. Among authors: zaccaria i. Pediatr Pulmonol. 2008 Oct;43(10):987-91. doi: 10.1002/ppul.20890. Pediatr Pulmonol. 2008. PMID: 18702115

6

Alternate-site testing is reliable in children and adolescents with type 1 diabetes, except at the forearm for hypoglycemia detection.

Lucidarme N, Alberti C, Zaccaria I, Claude E, Tubiana-Rufi N. Lucidarme N, et al. Among authors: zaccaria i. Diabetes Care. 2005 Mar;28(3):710-1. doi: 10.2337/diacare.28.3.710. Diabetes Care. 2005. PMID: 15735213 No abstract available.

7

Microstructural development of human brain assessed in utero by diffusion tensor imaging.

Bui T, Daire JL, Chalard F, Zaccaria I, Alberti C, Elmaleh M, Garel C, Luton D, Blanc N, Sebag G. Bui T, et al. Among authors: zaccaria i. Pediatr Radiol. 2006 Nov;36(11):1133-40. doi: 10.1007/s00247-006-0266-3. Epub 2006 Sep 8. Pediatr Radiol. 2006. PMID: 16960686

8

Effect of transfusion therapy on cerebral vasculopathy in children with sickle-cell anemia.

Bader-Meunier B, Verlhac S, Elmaleh-Bergès M, Ithier G, Sellami F, Faid S, Missud F, Ducrocq R, Alberti C, Zaccaria I, Baruchel A, Benkerrou M. Bader-Meunier B, et al. Among authors: zaccaria i. Haematologica. 2009 Jan;94(1):123-6. doi: 10.3324/haematol.13610. Epub 2008 Dec 4. Haematologica. 2009. PMID: 19059938 Free PMC article.

9

Effects of RANTES and MBL2 gene polymorphisms in sickle cell disease clinical outcomes: association of the g.In1.1T>C RANTES variant with protection against infections.

Dossou-Yovo OP, Zaccaria I, Benkerrou M, Hauchecorne M, Alberti C, Rahimy MC, Elion J, Lapoumeroulie C. Dossou-Yovo OP, et al. Among authors: zaccaria i. Am J Hematol. 2009 Jun;84(6):378-80. doi: 10.1002/ajh.21411. Am J Hematol. 2009. PMID: 19425063 Free article. No abstract available.

10

The French Congenital Central Hypoventilation Syndrome Registry: general data, phenotype, and genotype.

Trang H, Dehan M, Beaufils F, Zaccaria I, Amiel J, Gaultier C; French CCHS Working Group. Trang H, et al. Among authors: zaccaria i. Chest. 2005 Jan;127(1):72-9. doi: 10.1378/chest.127.1.72. Chest. 2005. PMID: 15653965

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