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Results: 1 to 20 of 347

1.

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.

PLoS One. 2015 Apr 15;10(4):e0123525. doi: 10.1371/journal.pone.0123525. eCollection 2015.

2.

RNF216 mutations as a novel cause of autosomal recessive Huntington-like disorder.

Santens P, Van Damme T, Steyaert W, Willaert A, Sablonnière B, De Paepe A, Coucke PJ, Dermaut B.

Neurology. 2015 Apr 3. pii: 10.1212/WNL.0000000000001521. [Epub ahead of print]

PMID:
25841028
3.

Respiratory Motion, Anterior Heart Displacement and Heart Dosimetry: Comparison Between Prone (Pr) and Supine (Su) Whole Breast Irradiation.

Lakosi F, Gulyban A, Janvary L, Simoni SB, Jansen N, Seidel L, Kovacs A, Vavassis P, Coucke P.

Pathol Oncol Res. 2015 Apr 4. [Epub ahead of print]

PMID:
25840562
4.

[Working conditions, stress and burnout of Belgian professionals in radiotherapy: Comparative analysis and emotional labor exploration].

Laurent J, Bragard I, Coucke P, Hansez I.

Cancer Radiother. 2015 Mar 13. pii: S1278-3218(15)00030-X. doi: 10.1016/j.canrad.2014.12.006. [Epub ahead of print] French.

PMID:
25776195
5.

Next generation sequencing to determine the cystic fibrosis mutation spectrum in Palestinian population.

Essawi O, Farraj M, De Leeneer K, Steyaert W, De Pauw K, De Paepe A, Claes K, Essawi T, Coucke PJ.

Dis Markers. 2015;2015:458653. doi: 10.1155/2015/458653. Epub 2015 Jan 26.

6.

Defective Proteolytic Processing of Fibrillar Procollagens and Prodecorin Due to Bi-Allelic BMP1 Mutations Results in a Severe, Progressive form of Osteogenesis Imperfecta.

Syx D, Guillemyn B, Symoens S, Sousa AB, Medeira A, Whiteford M, Hermanns-Lê T, Coucke PJ, De Paepe A, Malfait F.

J Bone Miner Res. 2015 Feb 6. doi: 10.1002/jbmr.2473. [Epub ahead of print]

PMID:
25656619
7.

Gene panel sequencing in heritable thoracic aortic disorders and related entities ¿ results of comprehensive testing in a cohort of 264 patients.

Campens L, Callewaert B, Muiño Mosquera L, Renard M, Symoens S, De Paepe A, Coucke P, De Backer J.

Orphanet J Rare Dis. 2015 Feb 3;10(1):9. [Epub ahead of print]

8.

Transfer of communication skills to the workplace: impact of a 38-hour communication skills training program designed for radiotherapy teams.

Merckaert I, Delevallez F, Gibon AS, Liénard A, Libert Y, Delvaux N, Marchal S, Etienne AM, Bragard I, Reynaert C, Slachmuylder JL, Scalliet P, Van Houtte P, Coucke P, Razavi D.

J Clin Oncol. 2015 Mar 10;33(8):901-9. doi: 10.1200/JCO.2014.57.3287. Epub 2015 Jan 26.

PMID:
25624435
9.

A study of the clinical and radiological features in a cohort of 93 patients with a COL2A1 mutation causing spondyloepiphyseal dysplasia congenita or a related phenotype.

Terhal PA, Nievelstein RJ, Verver EJ, Topsakal V, van Dommelen P, Hoornaert K, Le Merrer M, Zankl A, Simon ME, Smithson SF, Marcelis C, Kerr B, Clayton-Smith J, Kinning E, Mansour S, Elmslie F, Goodwin L, van der Hout AH, Veenstra-Knol HE, Herkert JC, Lund AM, Hennekam RC, Mégarbané A, Lees MM, Wilson LC, Male A, Hurst J, Alanay Y, Annerén G, Betz RC, Bongers EM, Cormier-Daire V, Dieux A, David A, Elting MW, van den Ende J, Green A, van Hagen JM, Hertel NT, Holder-Espinasse M, den Hollander N, Homfray T, Hove HD, Price S, Raas-Rothschild A, Rohrbach M, Schroeter B, Suri M, Thompson EM, Tobias ES, Toutain A, Vreeburg M, Wakeling E, Knoers NV, Coucke P, Mortier GR.

Am J Med Genet A. 2015 Mar;167A(3):461-75. doi: 10.1002/ajmg.a.36922. Epub 2015 Jan 21.

PMID:
25604898
10.

Flexible, scalable, and efficient targeted resequencing on a benchtop sequencer for variant detection in clinical practice.

De Leeneer K, Hellemans J, Steyaert W, Lefever S, Vereecke I, Debals E, Crombez B, Baetens M, Van Heetvelde M, Coppieters F, Vandesompele J, De Jaegher A, De Baere E, Coucke P, Claes K.

Hum Mutat. 2015 Mar;36(3):379-87. doi: 10.1002/humu.22739.

PMID:
25504618
11.

Arterial Tortuosity Syndrome.

Callewaert B, De Paepe A, Coucke P.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Dolan CR, Fong CT, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2015.
2014 Nov 13.

12.

Expressed repeat elements improve RT-qPCR normalization across a wide range of zebrafish gene expression studies.

Vanhauwaert S, Van Peer G, Rihani A, Janssens E, Rondou P, Lefever S, De Paepe A, Coucke PJ, Speleman F, Vandesompele J, Willaert A.

PLoS One. 2014 Oct 13;9(10):e109091. doi: 10.1371/journal.pone.0109091. eCollection 2014.

13.

Working conditions, job strain and work engagement among Belgian radiation oncologists.

Bragard I, Hansez I, Coucke P.

Cancer Radiother. 2014 Dec;18(8):723-9. doi: 10.1016/j.canrad.2014.06.024. Epub 2014 Oct 8.

PMID:
25306448
14.

Radiotherapy staffing in the European countries: final results from the ESTRO-HERO survey.

Lievens Y, Defourny N, Coffey M, Borras JM, Dunscombe P, Slotman B, Malicki J, Bogusz M, Gasparotto C, Grau C; HERO Consortium, Kokobobo A, Sedlmayer F, Slobina E, Coucke P, Gabrovski R, Vosmik M, Eriksen JG, Jaal J, Dejean C, Polgar C, Johannsson J, Cunningham M, Atkocius V, Back C, Pirotta M, Karadjinovic V, Levernes S, Maciejewski B, Trigo ML, Šegedin B, Palacios A, Pastoors B, Beardmore C, Erridge S, Smyth G, Cleries Soler R.

Radiother Oncol. 2014 Aug;112(2):178-86. doi: 10.1016/j.radonc.2014.08.034. Epub 2014 Nov 12.

15.

Efficiency of exome sequencing for the molecular diagnosis of pseudoxanthoma elasticum.

Hosen MJ, Van Nieuwerburgh F, Steyaert W, Deforce D, Martin L, Leftheriotis G, De Paepe A, Coucke PJ, Vanakker OM.

J Invest Dermatol. 2015 Apr;135(4):992-8. doi: 10.1038/jid.2014.421. Epub 2014 Sep 29.

16.

Novel pathogenic COL11A1/COL11A2 variants in Stickler syndrome detected by targeted NGS and exome sequencing.

Acke FR, Malfait F, Vanakker OM, Steyaert W, De Leeneer K, Mortier G, Dhooge I, De Paepe A, De Leenheer EM, Coucke PJ.

Mol Genet Metab. 2014 Nov;113(3):230-5. doi: 10.1016/j.ymgme.2014.09.001. Epub 2014 Sep 8.

PMID:
25240749
17.

Anxiety at the first radiotherapy session for non-metastatic breast cancer: key communication and communication-related predictors.

Lewis F, Merckaert I, Liénard A, Libert Y, Etienne AM, Reynaert C, Slachmuylder JL, Scalliet P, Van Houtte P, Coucke P, Salamon E, Razavi D.

Radiother Oncol. 2015 Jan;114(1):35-41. doi: 10.1016/j.radonc.2014.07.017. Epub 2014 Sep 16.

PMID:
25239784
18.

Refinement of the critical 2p25.3 deletion region: the role of MYT1L in intellectual disability and obesity.

De Rocker N, Vergult S, Koolen D, Jacobs E, Hoischen A, Zeesman S, Bang B, Béna F, Bockaert N, Bongers EM, de Ravel T, Devriendt K, Giglio S, Faivre L, Joss S, Maas S, Marle N, Novara F, Nowaczyk MJ, Peeters H, Polstra A, Roelens F, Rosenberg C, Thevenon J, Tümer Z, Vanhauwaert S, Varvagiannis K, Willaert A, Willemsen M, Willems M, Zuffardi O, Coucke P, Speleman F, Eichler EE, Kleefstra T, Menten B.

Genet Med. 2014 Sep 18. doi: 10.1038/gim.2014.124. [Epub ahead of print]

PMID:
25232846
19.

FDG PET/CT for rectal carcinoma radiotherapy treatment planning: comparison of functional volume delineation algorithms and clinical challenges.

Withofs N, Bernard C, Van der Rest C, Martinive P, Hatt M, Jodogne S, Visvikis D, Lee JA, Coucke PA, Hustinx R.

J Appl Clin Med Phys. 2014 Sep 8;15(5):4696. doi: 10.1120/jacmp.v15i5.4696.

PMID:
25207560
20.

Type I procollagen C-propeptide defects: study of genotype-phenotype correlation and predictive role of crystal structure.

Symoens S, Hulmes DJ, Bourhis JM, Coucke PJ, De Paepe A, Malfait F.

Hum Mutat. 2014 Nov;35(11):1330-41. doi: 10.1002/humu.22677. Epub 2014 Oct 18.

PMID:
25146735
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