Malfroot A - Search Results

1

Burkholderia (Pseudomonas) cepacia and cystic fibrosis: the epidemiology in Belgium.

Revets H, Vandamme P, Van Zeebroeck A, De Boeck K, Struelens MJ, Verhaegen J, Ursi JP, Verschraegen G, Franckx H, Malfroot A, Dab I, Lauwers S. Revets H, et al. Among authors: malfroot a. Acta Clin Belg. 1996;51(4):222-30. doi: 10.1080/22953337.1996.11718514. Acta Clin Belg. 1996. PMID: 8858887

2

Molecular typing of Bordetella pertussis isolates recovered from Belgian children and their household members.

De Schutter I, Malfroot A, Dab I, Hoebrekx N, Muyldermans G, Piérard D, Lauwers S. De Schutter I, et al. Among authors: malfroot a. Clin Infect Dis. 2003 Jun 1;36(11):1391-6. doi: 10.1086/375071. Epub 2003 May 21. Clin Infect Dis. 2003. PMID: 12766833

3

Immunisation in the current management of cystic fibrosis patients.

Malfroot A, Adam G, Ciofu O, Döring G, Knoop C, Lang AB, Van Damme P, Dab I, Bush A; European Cystic Fibrosis Society (ECFS) Vaccination Group. Malfroot A, et al. J Cyst Fibros. 2005 May;4(2):77-87. doi: 10.1016/j.jcf.2004.10.003. J Cyst Fibros. 2005. PMID: 15978534 Free article.

4

New insights on gastro-oesophageal reflux in cystic fibrosis by longitudinal follow up.

Malfroot A, Dab I. Malfroot A, et al. Arch Dis Child. 1991 Nov;66(11):1339-45. doi: 10.1136/adc.66.11.1339. Arch Dis Child. 1991. PMID: 1755649 Free PMC article.

5

The prevalence of the deletion F508 in a Belgian cystic fibrosis population.

Lissens W, Bonduelle M, Malfroot A, Dab I, Liebaers I. Lissens W, et al. Among authors: malfroot a. Adv Exp Med Biol. 1991;290:369-70. doi: 10.1007/978-1-4684-5934-0_40. Adv Exp Med Biol. 1991. PMID: 1950750 No abstract available.

6

Adolescent and adult cystic fibrosis patients: how to leave home when you are depending on it?

Lampo A, Dab I, Malfroot A. Lampo A, et al. Among authors: malfroot a. Acta Univ Carol Med (Praha). 1990;36(1-4):228-30. Acta Univ Carol Med (Praha). 1990. PMID: 2130705

7

The deletion F508 is the major gene mutation in a representative Belgian cystic fibrosis population.

Bonduelle M, Lissens W, Malfroot A, Dab I, Liebaers I. Bonduelle M, et al. Among authors: malfroot a. Hum Genet. 1990 Sep;85(4):395-6. doi: 10.1007/BF02428271. Hum Genet. 1990. PMID: 2210742

8

Gastroesophageal reflux: a primary defect in cystic fibrosis?

Dab I, Malfroot A. Dab I, et al. Among authors: malfroot a. Scand J Gastroenterol Suppl. 1988;143:125-31. doi: 10.3109/00365528809090232. Scand J Gastroenterol Suppl. 1988. PMID: 3164497

9

Epidemiology of Burkholderia cepacia complex colonisation in cystic fibrosis patients.

De Boeck K, Malfroot A, Van Schil L, Lebecque P, Knoop C, Govan JR, Doherty C, Laevens S, Vandamme P; Belgian Burkholderia cepacia Study Group. De Boeck K, et al. Among authors: malfroot a. Eur Respir J. 2004 Jun;23(6):851-6. doi: 10.1183/09031936.04.00118804. Eur Respir J. 2004. PMID: 15218997 Free article.

10

National survey of molecular epidemiology of Staphylococcus aureus colonization in Belgian cystic fibrosis patients.

Vergison A, Denis O, Deplano A, Casimir G, Claeys G, DeBaets F, DeBoeck K, Douat N, Franckx H, Gigi J, Ieven M, Knoop C, Lebeque P, Lebrun F, Malfroot A, Paucquay F, Pierard D, Van Eldere J, Struelens MJ. Vergison A, et al. Among authors: malfroot a. J Antimicrob Chemother. 2007 May;59(5):893-9. doi: 10.1093/jac/dkm037. Epub 2007 Mar 6. J Antimicrob Chemother. 2007. PMID: 17341469

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