Dab I - Search Results

1

A serine to proline substitution (S1255P) in the second nucleotide binding fold of the cystic fibrosis gene.

Lissens W, Bonduelle M, Malfroot A, Dab I, Liebaers I. Lissens W, et al. Among authors: dab i. Hum Mol Genet. 1992 Sep;1(6):441-2. doi: 10.1093/hmg/1.6.441. Hum Mol Genet. 1992. PMID: 1284530 No abstract available.

2

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: dab i. Hum Genet. 1990 Sep;85(4):395-6. doi: 10.1007/BF02428271. Hum Genet. 1990. PMID: 2210742

3

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: dab i. 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.

4

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: dab i. Acta Univ Carol Med (Praha). 1990;36(1-4):228-30. Acta Univ Carol Med (Praha). 1990. PMID: 2130705

5

Prenatal diagnosis of cystic fibrosis using closely linked DNA probes.

Lissens W, Vercammen M, Foulon W, De Catte L, Dab I, Malfroot A, Bonduelle M, Liebaers I. Lissens W, et al. Among authors: dab i. J Inherit Metab Dis. 1989;12 Suppl 2:308-10. doi: 10.1007/BF03335407. J Inherit Metab Dis. 1989. PMID: 2574253 No abstract available.

6

Mild pulmonary, but severe hepatic disease in a cystic fibrosis patient homozygous for a frameshift mutation in the regulatory domain of the CFTR.

Lissens W, Desmyttere S, Bonduelle M, Dab I, Liebaers I, Mercier B, Audrezet MP, Ferec C. Lissens W, et al. Among authors: dab i. J Med Genet. 1993 May;30(5):446. doi: 10.1136/jmg.30.5.446. J Med Genet. 1993. PMID: 7686577 Free PMC article. No abstract available.

7

Mild cystic fibrosis in child homozygous for G542 non-sense mutation in CF gene.

Bonduelle M, Lissens W, Liebaers I, Malfroot A, Dab I. Bonduelle M, et al. Among authors: dab i. Lancet. 1991 Jul 20;338(8760):189. doi: 10.1016/0140-6736(91)90181-n. Lancet. 1991. PMID: 1712883 No abstract available.

8

Gastroesophageal reflux: a primary defect in cystic fibrosis?

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

9

Evaluation of time interval difference digital subtraction fluoroscopy in patients with cystic fibrosis.

Desprechins B, Luypaert R, Delrée M, Freson M, Malfroot A, Dab I, Piepsz A. Desprechins B, et al. Among authors: dab i. Scand J Gastroenterol Suppl. 1988;143:86-92. doi: 10.3109/00365528809090224. Scand J Gastroenterol Suppl. 1988. PMID: 3291090

10

Therapeutic bronchoscopy in ventilated neonates.

Dab I, Malfroot A, Goossens A. Dab I, et al. Arch Dis Child. 1993 Nov;69(5 Spec No):533-7. doi: 10.1136/adc.69.5_spec_no.533. Arch Dis Child. 1993. PMID: 8285762 Free PMC article. No abstract available.

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