Leal T - Search Results

1

Mutations of the cystic fibrosis gene and intermediate sweat chloride levels in children.

Lebecque P, Leal T, De Boeck C, Jaspers M, Cuppens H, Cassiman JJ. Lebecque P, et al. Among authors: leal t. Am J Respir Crit Care Med. 2002 Mar 15;165(6):757-61. doi: 10.1164/ajrccm.165.6.2104073. Am J Respir Crit Care Med. 2002. PMID: 11897640

2

A specific database for providing local and national level of integration of clinical data in cystic fibrosis.

Leal T, Reychler G, Mailleux P, Gigi J, Godding V, Lebecque P. Leal T, et al. J Cyst Fibros. 2007 May;6(3):187-93. doi: 10.1016/j.jcf.2006.07.002. Epub 2006 Oct 5. J Cyst Fibros. 2007. PMID: 17027346 Free article.

3

Inhaled phosphodiesterase type 5 inhibitors restore chloride transport in cystic fibrosis mice.

Lubamba B, Lebacq J, Reychler G, Marbaix E, Wallemacq P, Lebecque P, Leal T. Lubamba B, et al. Among authors: leal t. Eur Respir J. 2011 Jan;37(1):72-8. doi: 10.1183/09031936.00013510. Epub 2010 Jun 18. Eur Respir J. 2011. PMID: 20562123 Free article.

4

Biological variability of the sweat chloride in diagnostic sweat tests: A retrospective analysis.

Vermeulen F, Lebecque P, De Boeck K, Leal T. Vermeulen F, et al. Among authors: leal t. J Cyst Fibros. 2017 Jan;16(1):30-35. doi: 10.1016/j.jcf.2016.11.008. Epub 2016 Dec 22. J Cyst Fibros. 2017. PMID: 28017620 Free article.

5

Early referral to cystic fibrosis specialist centre impacts on respiratory outcome.

Lebecque P, Leonard A, De Boeck K, De Baets F, Malfroot A, Casimir G, Desager K, Godding V, Leal T. Lebecque P, et al. Among authors: leal t. J Cyst Fibros. 2009 Jan;8(1):26-30. doi: 10.1016/j.jcf.2008.07.005. Epub 2008 Oct 5. J Cyst Fibros. 2009. PMID: 18838309 Free article.

6

Sweat potassium concentration may help to identify falsification of sweat test: a case report.

Leonard A, Leal T, Godding V, Villanueva P, Wallemacq P, Lebecque P. Leonard A, et al. Among authors: leal t. Clin Biochem. 2008 Sep;41(13):1110-2. doi: 10.1016/j.clinbiochem.2008.05.006. Epub 2008 May 27. Clin Biochem. 2008. PMID: 18554505

7

[Cystic fibrosis and pseudomonas aeruginosa current and future strategies].

Leonard A, Leal T, Lebecque P. Leonard A, et al. Among authors: leal t. J Pharm Belg. 2007;62(1):25-8. J Pharm Belg. 2007. PMID: 17508664 Review. French.

8

[Cystic fibrosis and normal sweat chloride values: a case-report].

Lebecque P, Leal T, Godding V. Lebecque P, et al. Among authors: leal t. Rev Mal Respir. 2001 Sep;18(4 Pt 1):443-5. Rev Mal Respir. 2001. PMID: 11547256 French.

9

CFTR biomarkers: time for promotion to surrogate end-point.

De Boeck K, Kent L, Davies J, Derichs N, Amaral M, Rowe SM, Middleton P, de Jonge H, Bronsveld I, Wilschanski M, Melotti P, Danner-Boucher I, Boerner S, Fajac I, Southern K, de Nooijer RA, Bot A, de Rijke Y, de Wachter E, Leal T, Vermeulen F, Hug MJ, Rault G, Nguyen-Khoa T, Barreto C, Proesmans M, Sermet-Gaudelus I; European Cystic Fibrosis Society Clinical Trial Network Standardisation Committee. De Boeck K, et al. Among authors: leal t. Eur Respir J. 2013 Jan;41(1):203-16. doi: 10.1183/09031936.00057512. Epub 2012 Aug 9. Eur Respir J. 2013. PMID: 22878883 Free article. Review.

10

Effect of continuous positive airway pressure combined to nebulization on lung deposition measured by urinary excretion of amikacin.

Reychler G, Leal T, Roeseler J, Thys F, Delvau N, Liistro G. Reychler G, et al. Among authors: leal t. Respir Med. 2007 Oct;101(10):2051-5. doi: 10.1016/j.rmed.2007.06.003. Epub 2007 Jul 12. Respir Med. 2007. PMID: 17628465 Free article.

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