Lachaux A - Search Results

1

SERPINA1 and MAN1B1 polymorphisms are not linked to severe liver disease in a French cohort of alpha-1 antitrypsin deficiency children.

Joly P, Lachaux A, Ruiz M, Restier L, Belmalih A, Chapuis-Cellier C, Francina A, Renoux C, Bouchecareilh M. Joly P, et al. Among authors: lachaux a. Liver Int. 2017 Nov;37(11):1608-1611. doi: 10.1111/liv.13586. Epub 2017 Sep 15. Liver Int. 2017. PMID: 28887821

2

Hb Zengcheng [beta 114(G16)Leu-->Met] in a Cambodian family.

Lacan P, Aubry M, Francina A, Lachaux A. Lacan P, et al. Among authors: lachaux a. Hemoglobin. 1997 Jul;21(4):363-7. doi: 10.3109/03630269709000668. Hemoglobin. 1997. PMID: 9255614 No abstract available.

3

Association of a glucose-6-phosphate deficiency and a Gilbert syndrome as risk factors for a severe choledocholithiasis in a 2-month-old male infant.

Rivet C, Caron N, Lachaux A, Morel B, Pracros JP, Francina A, Gagnieu MC, Joly P. Rivet C, et al. Among authors: lachaux a. Pediatr Blood Cancer. 2012 Feb;58(2):316. doi: 10.1002/pbc.23261. Epub 2011 Jul 25. Pediatr Blood Cancer. 2012. PMID: 21793186 No abstract available.

4

Maternal uniparental disomy 14 revealed by alpha 1 antitrypsin deficiency.

Laverdure N, Dabadie A, Alex-Cordier MP, Odent S, Lachaux A. Laverdure N, et al. Among authors: lachaux a. Clin Res Hepatol Gastroenterol. 2014 Oct;38(5):604-6. doi: 10.1016/j.clinre.2014.01.011. Epub 2014 Mar 11. Clin Res Hepatol Gastroenterol. 2014. PMID: 24636467

5

[Hepatic involvement in hereditary alpha-1-antitrypsin deficiency].

Lachaux A, Dumortier J. Lachaux A, et al. Rev Mal Respir. 2014 Apr;31(4):357-64. doi: 10.1016/j.rmr.2013.10.651. Epub 2014 Mar 27. Rev Mal Respir. 2014. PMID: 24750955 Review. French.

6

Implementation of a computerized system in pediatric wards to improve nutritional care: a cluster randomized trial.

Duclos A, Touzet S, Restier L, Occelli P, Cour-Andlauer F, Denis A, Polazzi S, Colin C, Lachaux A, Peretti N; PREDIRE Study Group. Duclos A, et al. Among authors: lachaux a. Eur J Clin Nutr. 2015 Jul;69(7):769-75. doi: 10.1038/ejcn.2014.288. Epub 2015 Feb 4. Eur J Clin Nutr. 2015. PMID: 25649237 Clinical Trial.

7

Dramatic increase of central venous catheter-related infections associated with a high turnover of the nursing team.

Mirabel-Chambaud E, N'Guyen M, Valdeyron ML, Quessada T, Goudable J, Loras-Duclaux I, Marotte S, Heissat S, Restier L, Lachaux A, Peretti N. Mirabel-Chambaud E, et al. Among authors: lachaux a. Clin Nutr. 2016 Apr;35(2):446-452. doi: 10.1016/j.clnu.2015.03.011. Epub 2015 Mar 26. Clin Nutr. 2016. PMID: 25886708

8

Incorrect evaluation of the frequency of malnutrition and of its screening in hospitalized children by health care professionals.

Restier L, Duclos A, Jarri L, Touzet S, Denis A, Occelli P, Kassai-Koupai B, Lachaux A, Loras-Duclaux I, Colin C, Peretti N. Restier L, et al. Among authors: lachaux a. J Eval Clin Pract. 2015 Oct;21(5):958-62. doi: 10.1111/jep.12412. Epub 2015 Jul 23. J Eval Clin Pract. 2015. PMID: 26202860

9

Paediatric liver transplanted patients and prevalence of hepatitis E virus.

Laverdure N, Scholtès-Brunel C, Rivet C, Heissat S, Restier L, Bacchetta J, Boillot O, Dumortier J, Lachaux A. Laverdure N, et al. Among authors: lachaux a. J Clin Virol. 2015 Aug;69:22-6. doi: 10.1016/j.jcv.2015.04.022. Epub 2015 May 19. J Clin Virol. 2015. PMID: 26209371

10

[DEFI-ALPHA cohort and POLYGEN DEFI-ALPHA clinical research hospital programme. A study about clinical, biological and genetics factors associated with the occurrence and the evolution of hepatic complications in children with alpha-1 antitrypsin deficiency].

Joly P, Restier L, Bouchecareilh M, Lacan P, Cabet F, Chapuis-Cellier C, Francina A, Lachaux A. Joly P, et al. Among authors: lachaux a. Rev Mal Respir. 2015 Sep;32(7):759-67. doi: 10.1016/j.rmr.2015.06.010. Epub 2015 Aug 1. Rev Mal Respir. 2015. PMID: 26238925 French.

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