Dab I - Search Results

1

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.

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

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

5

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.

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

7

Pathophysiology and mechanisms of gastroesophageal reflux in childhood asthma.

Malfroot A, Dab I. Malfroot A, et al. Among authors: dab i. Pediatr Pulmonol Suppl. 1995;11:55-6. doi: 10.1002/ppul.1950191129. Pediatr Pulmonol Suppl. 1995. PMID: 7547347 No abstract available.

8

Successful management of recurrent pneumothorax in cystic fibrosis by localized apical thoracoscopic talc poudrage.

Noppen M, Dhondt E, Mahler T, Malfroot A, Dab I, Vincken W. Noppen M, et al. Among authors: dab i. Chest. 1994 Jul;106(1):262-4. doi: 10.1378/chest.106.1.262. Chest. 1994. PMID: 8020281

9

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.

10

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

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

78 results

Search Page

Filters