Booms P - Search Results

1

Protective effect of inhaled budesonide against unlimited airway narrowing to methacholine in atopic patients with asthma.

Booms P, Cheung D, Timmers MC, Zwinderman AH, Sterk PJ. Booms P, et al. J Allergy Clin Immunol. 1997 Mar;99(3):330-7. doi: 10.1016/s0091-6749(97)70050-2. J Allergy Clin Immunol. 1997. PMID: 9058688 Clinical Trial.

2

The severity of breathlessness during challenges with inhaled methacholine and hypertonic saline in atopic asthmatic subjects. The relationship with deep breath-induced bronchodilation.

Sont JK, Booms P, Bel EH, Vandenbroucke JP, Sterk PJ. Sont JK, et al. Among authors: booms p. Am J Respir Crit Care Med. 1995 Jul;152(1):38-44. doi: 10.1164/ajrccm.152.1.7599850. Am J Respir Crit Care Med. 1995. PMID: 7599850 Clinical Trial.

3

Effect of an inhaled neutral endopeptidase inhibitor, thiorphan, on airway responsiveness to leukotriene D4 in normal and asthmatic subjects.

Diamant Z, Timmers MC, van der Veen H, Booms P, Sont JK, Sterk PJ. Diamant Z, et al. Among authors: booms p. Eur Respir J. 1994 Mar;7(3):459-66. doi: 10.1183/09031936.94.07030459. Eur Respir J. 1994. PMID: 8013602 Free article. Clinical Trial.

4

The determinants of airway hyperresponsiveness to hypertonic saline in atopic asthma in vivo. Relationship with sub-populations of peripheral blood leucocytes.

Sont JK, Booms P, Bel EH, Vandenbroucke JP, Sterk PJ. Sont JK, et al. Among authors: booms p. Clin Exp Allergy. 1993 Aug;23(8):678-88. doi: 10.1111/j.1365-2222.1993.tb01794.x. Clin Exp Allergy. 1993. PMID: 8221271 Clinical Trial.

5

A CA-repeat polymorphism near DXS418 (P122).

Van De Vosse E, Booms PF, Vossen RH, Wapenaar MC, Van Ommen GJ, Den Dunnen JT. Van De Vosse E, et al. Among authors: booms pf. Hum Mol Genet. 1993 Dec;2(12):2202. doi: 10.1093/hmg/2.12.2202-a. Hum Mol Genet. 1993. PMID: 8111402 No abstract available.

6

RGD-containing fibrillin-1 fragments upregulate matrix metalloproteinase expression in cell culture: a potential factor in the pathogenesis of the Marfan syndrome.

Booms P, Pregla R, Ney A, Barthel F, Reinhardt DP, Pletschacher A, Mundlos S, Robinson PN. Booms P, et al. Hum Genet. 2005 Jan;116(1-2):51-61. doi: 10.1007/s00439-004-1194-7. Epub 2004 Oct 23. Hum Genet. 2005. PMID: 15517394

7

TGGE screening of the entire FBN1 coding sequence in 126 individuals with marfan syndrome and related fibrillinopathies.

Katzke S, Booms P, Tiecke F, Palz M, Pletschacher A, Türkmen S, Neumann LM, Pregla R, Leitner C, Schramm C, Lorenz P, Hagemeier C, Fuchs J, Skovby F, Rosenberg T, Robinson PN. Katzke S, et al. Among authors: booms p. Hum Mutat. 2002 Sep;20(3):197-208. doi: 10.1002/humu.10112. Hum Mutat. 2002. PMID: 12203992

8

A novel de novo mutation in exon 14 of the fibrillin-1 gene associated with delayed secretion of fibrillin in a patient with a mild Marfan phenotype.

Booms P, Withers AP, Boxer M, Kaufmann UC, Hagemeier C, Vetter U, Robinson PN. Booms P, et al. Hum Genet. 1997 Aug;100(2):195-200. doi: 10.1007/s004390050489. Hum Genet. 1997. PMID: 9254848

9

Mutations of FBN1 and genotype-phenotype correlations in Marfan syndrome and related fibrillinopathies.

Robinson PN, Booms P, Katzke S, Ladewig M, Neumann L, Palz M, Pregla R, Tiecke F, Rosenberg T. Robinson PN, et al. Among authors: booms p. Hum Mutat. 2002 Sep;20(3):153-61. doi: 10.1002/humu.10113. Hum Mutat. 2002. PMID: 12203987 Review.

10

Novel exon skipping mutation in the fibrillin-1 gene: two 'hot spots' for the neonatal Marfan syndrome.

Booms P, Cisler J, Mathews KR, Godfrey M, Tiecke F, Kaufmann UC, Vetter U, Hagemeier C, Robinson PN. Booms P, et al. Clin Genet. 1999 Feb;55(2):110-7. doi: 10.1034/j.1399-0004.1999.550207.x. Clin Genet. 1999. PMID: 10189088

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