Van Acker P - Search Results

1

Strategies for prenatal and preimplantation genetic diagnosis in Marfan syndrome (MFS).

Loeys B, Nuytinck L, Van Acker P, Walraedt S, Bonduelle M, Sermon K, Hamel B, Sanchez A, Messiaen L, De Paepe A. Loeys B, et al. Among authors: van acker p. Prenat Diagn. 2002 Jan;22(1):22-8. Prenat Diagn. 2002. PMID: 11810645

2

Mutation analysis of the FBN1 gene in patients with Marfan syndrome.

Coucke P, Van Acker P, De Paepe A. Coucke P, et al. Among authors: van acker p. Methods Mol Med. 2006;126:81-95. doi: 10.1385/1-59745-088-X:81. Methods Mol Med. 2006. PMID: 16930007

3

Comprehensive molecular screening of the FBN1 gene favors locus homogeneity of classical Marfan syndrome.

Loeys B, De Backer J, Van Acker P, Wettinck K, Pals G, Nuytinck L, Coucke P, De Paepe A. Loeys B, et al. Among authors: van acker p. Hum Mutat. 2004 Aug;24(2):140-6. doi: 10.1002/humu.20070. Hum Mutat. 2004. PMID: 15241795

4

Characterization of mutations leading to recessive dystrophic epidermolysis bullosa and Marfan syndrome in a single patient.

Gardella R, Nuytinck L, Barlati S, Van Acker P, Tadini G, De Paepe A, Colombi M. Gardella R, et al. Among authors: van acker p. Clin Exp Dermatol. 2001 Nov;26(8):710-3. doi: 10.1046/j.1365-2230.2001.00924.x. Clin Exp Dermatol. 2001. PMID: 11722462

5

Novel clinico-molecular insights in pseudoxanthoma elasticum provide an efficient molecular screening method and a comprehensive diagnostic flowchart.

Vanakker OM, Leroy BP, Coucke P, Bercovitch LG, Uitto J, Viljoen D, Terry SF, Van Acker P, Matthys D, Loeys B, De Paepe A. Vanakker OM, et al. Among authors: van acker p. Hum Mutat. 2008 Jan;29(1):205. doi: 10.1002/humu.9514. Hum Mutat. 2008. PMID: 18157818

6

Homozygosity mapping of a gene for arterial tortuosity syndrome to chromosome 20q13.

Coucke PJ, Wessels MW, Van Acker P, Gardella R, Barlati S, Willems PJ, Colombi M, De Paepe A. Coucke PJ, et al. Among authors: van acker p. J Med Genet. 2003 Oct;40(10):747-51. doi: 10.1136/jmg.40.10.747. J Med Genet. 2003. PMID: 14569121 Free PMC article.

7

Characterization of LEDGF/p75 genetic variants and association with HIV-1 disease progression.

Messiaen P, De Spiegelaere W, Alcami J, Vervisch K, Van Acker P, Verhasselt B, Meuwissen P, Calonge E, Gonzalez N, Gutierrez-Rodero F, Rodriguez-Martín C, Sermijn E, Poppe B, Vogelaers D, Verhofstede C, Vandekerckhove L. Messiaen P, et al. Among authors: van acker p. PLoS One. 2012;7(11):e50204. doi: 10.1371/journal.pone.0050204. Epub 2012 Nov 30. PLoS One. 2012. PMID: 23226247 Free PMC article.

8

High prevalence of a novel mutation in the exon 4 of the low-density lipoprotein receptor gene causing familial hypercholesterolemia in Belgium.

Descamps O, Hondekijn JC, Van Acker P, Deslypere JP, Heller FR. Descamps O, et al. Among authors: van acker p. Clin Genet. 1997 May;51(5):303-8. doi: 10.1111/j.1399-0004.1997.tb02478.x. Clin Genet. 1997. PMID: 9212177

9

Comparison of methods for in-house screening of HLA-B*57:01 to prevent abacavir hypersensitivity in HIV-1 care.

De Spiegelaere W, Philippé J, Vervisch K, Verhofstede C, Malatinkova E, Kiselinova M, Trypsteen W, Bonczkowski P, Vogelaers D, Callens S, Ruelle J, Kabeya K, De Wit S, Van Acker P, Van Sandt V, Emonds MP, Coucke P, Sermijn E, Vandekerckhove L. De Spiegelaere W, et al. Among authors: van acker p. PLoS One. 2015 Apr 15;10(4):e0123525. doi: 10.1371/journal.pone.0123525. eCollection 2015. PLoS One. 2015. PMID: 25874872 Free PMC article.

10

Low-density lipoprotein receptor gene mutations in a Southeast Asian population with familial hypercholesterolemia.

Khoo KL, van Acker P, Defesche JC, Tan H, van de Kerkhof L, Heijnen-van Eijk SJ, Kastelein JJ, Deslypere JP. Khoo KL, et al. Among authors: van acker p, van de kerkhof l. Clin Genet. 2000 Aug;58(2):98-105. doi: 10.1034/j.1399-0004.2000.580202.x. Clin Genet. 2000. PMID: 11005141

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