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Identification of von Willebrand disease type 1 in a patient with Ehlers-Danlos syndrome classic type.

Ott HW, Perkhofer S, Coucke PJ, de Paepe A, Spannagl M.

Haemophilia. 2016 Jun 13. doi: 10.1111/hae.12931. [Epub ahead of print] No abstract available.


Glucose transporter type 10-lacking in arterial tortuosity syndrome-facilitates dehydroascorbic acid transport.

Németh CE, Marcolongo P, Gamberucci A, Fulceri R, Benedetti A, Zoppi N, Ritelli M, Chiarelli N, Colombi M, Willaert A, Callewaert BL, Coucke PJ, Gróf P, Nagy SK, Mészáros T, Bánhegyi G, Margittai É.

FEBS Lett. 2016 Jun;590(11):1630-40. doi: 10.1002/1873-3468.12204. Epub 2016 May 27.


Is it possible to improve communication around radiotherapy delivery: A randomized study to assess the efficacy of team training?

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

Radiother Oncol. 2016 May;119(2):361-7. doi: 10.1016/j.radonc.2016.03.016. Epub 2016 Apr 9.


DNA Diagnostics of Hereditary Hearing Loss: A Targeted Resequencing Approach Combined With a Mutation Classification System.

Sommen M, Schrauwen I, Vandeweyer G, Boeckx N, Corneveaux JJ, van den Ende J, Boudewyns A, De Leenheer E, Janssens S, Claes K, Verstreken M, Strenzke N, Predöhl F, Wuyts W, Mortier G, Bitner-Glindzicz M, Moser T, Coucke P, Huentelman MJ, Van Camp G.

Hum Mutat. 2016 Apr 11. doi: 10.1002/humu.22999. [Epub ahead of print]


Impacts of Ionizing Radiation on the Different Compartments of the Tumor Microenvironment.

Leroi N, Lallemand F, Coucke P, Noel A, Martinive P.

Front Pharmacol. 2016 Mar 30;7:78. doi: 10.3389/fphar.2016.00078. eCollection 2016. Review.


Mitral regurgitation as a phenotypic manifestation of nonphotosensitive trichothiodystrophy due to a splice variant in MPLKIP.

Shah K, Ali RH, Ansar M, Lee K, Chishti MS, Abbe I, Li B; University of Washington Center for Mendelian Genomics, Smith JD, Nickerson DA, Shendure J, Coucke PJ, Steyaert W, Bamshad MJ, Santos-Cortez RL, Leal SM, Ahmad W.

BMC Med Genet. 2016 Feb 16;17:13. doi: 10.1186/s12881-016-0275-5.


Zebrafish Collagen Type I: Molecular and Biochemical Characterization of the Major Structural Protein in Bone and Skin.

Gistelinck C, Gioia R, Gagliardi A, Tonelli F, Marchese L, Bianchi L, Landi C, Bini L, Huysseune A, Witten PE, Staes A, Gevaert K, De Rocker N, Menten B, Malfait F, Leikin S, Carra S, Tenni R, Rossi A, De Paepe A, Coucke P, Willaert A, Forlino A.

Sci Rep. 2016 Feb 15;6:21540. doi: 10.1038/srep21540.


FDG PET/CT texture analysis for predicting the outcome of lung cancer treated by stereotactic body radiation therapy.

Lovinfosse P, Janvary ZL, Coucke P, Jodogne S, Bernard C, Hatt M, Visvikis D, Jansen N, Duysinx B, Hustinx R.

Eur J Nucl Med Mol Imaging. 2016 Jul;43(8):1453-60. doi: 10.1007/s00259-016-3314-8. Epub 2016 Jan 30.


The Influence of Treatment Position (Prone vs. Supine) on Clip Displacement, Seroma, Tumor Bed and Partial Breast Target Volumes: Comparative Study.

Lakosi F, Gulyban A, Simoni SB, Nguyen PV, Cucchiaro S, Seidel L, Janvary L, Nicolas S, Vavassis P, Coucke P.

Pathol Oncol Res. 2016 Jul;22(3):493-500. doi: 10.1007/s12253-015-0028-3. Epub 2015 Dec 16.


Exome sequencing revealed a novel biallelic deletion in the DCAF17 gene underlying Woodhouse Sakati syndrome (WSS).

Ali RH, Shah K, Nasir A, Steyaert W, Coucke PJ, Ahmad W.

Clin Genet. 2015 Nov 26. doi: 10.1111/cge.12700. [Epub ahead of print]


Ehlers-Danlos Syndrome, Hypermobility Type, Is Linked to Chromosome 8p22-8p21.1 in an Extended Belgian Family.

Syx D, Symoens S, Steyaert W, De Paepe A, Coucke PJ, Malfait F.

Dis Markers. 2015;2015:828970. doi: 10.1155/2015/828970. Epub 2015 Oct 4.


[(18)F]FPRGD2 PET/CT imaging of integrin αvβ3 levels in patients with locally advanced rectal carcinoma.

Withofs N, Martinive P, Vanderick J, Bletard N, Scagnol I, Mievis F, Giacomelli F, Coucke P, Delvenne P, Cataldo D, Gambhir SS, Hustinx R.

Eur J Nucl Med Mol Imaging. 2016 Apr;43(4):654-62. doi: 10.1007/s00259-015-3219-y. Epub 2015 Oct 22.


The timing of surgery after neoadjuvant radiotherapy influences tumor dissemination in a preclinical model.

Leroi N, Sounni NE, Van Overmeire E, Blacher S, Marée R, Van Ginderachter J, Lallemand F, Lenaerts E, Coucke P, Noel A, Martinive P.

Oncotarget. 2015 Nov 3;6(34):36825-37. doi: 10.18632/oncotarget.5931.


Clinical efficacy and toxicity of radio-chemotherapy and magnetic resonance imaging-guided brachytherapy for locally advanced cervical cancer patients: A mono-institutional experience.

Lakosi F, de Cuypere M, Viet Nguyen P, Jansen N, Warlimont B, Gulyban A, Gennigens C, Seidel L, Delbecque K, Coucke P, Hermesse J, Kridelka F.

Acta Oncol. 2015;54(9):1558-66. doi: 10.3109/0284186X.2015.1062542. Epub 2015 Sep 25.


Genetic Defects in TAPT1 Disrupt Ciliogenesis and Cause a Complex Lethal Osteochondrodysplasia.

Symoens S, Barnes AM, Gistelinck C, Malfait F, Guillemyn B, Steyaert W, Syx D, D'hondt S, Biervliet M, De Backer J, Witten EP, Leikin S, Makareeva E, Gillessen-Kaesbach G, Huysseune A, Vleminckx K, Willaert A, De Paepe A, Marini JC, Coucke PJ.

Am J Hum Genet. 2015 Oct 1;97(4):521-34. doi: 10.1016/j.ajhg.2015.08.009. Epub 2015 Sep 10.


Association between Kniest dysplasia and chondrosarcoma in a child.

Hochart A, Dieux A, Coucke P, Fron D, Fayoux P, Labalette P, Boutry N, Escande F, Aubert S, Renaud F, Rocourt N, Vinchon M, Leblond P.

Am J Med Genet A. 2015 Dec;167A(12):3204-8. doi: 10.1002/ajmg.a.37361. Epub 2015 Sep 8.


Marfan Syndrome and Related Heritable Thoracic Aortic Aneurysms and Dissections.

De Backer J, Renard M, Campens L, Mosquera LM, De Paepe A, Coucke P, Callewaert B, Kodolitsch Yv.

Curr Pharm Des. 2015;21(28):4061-75.


Altered cytoskeletal organization characterized lethal but not surviving Brtl+/- mice: insight on phenotypic variability in osteogenesis imperfecta.

Bianchi L, Gagliardi A, Maruelli S, Besio R, Landi C, Gioia R, Kozloff KM, Khoury BM, Coucke PJ, Symoens S, Marini JC, Rossi A, Bini L, Forlino A.

Hum Mol Genet. 2015 Nov 1;24(21):6118-33. doi: 10.1093/hmg/ddv328. Epub 2015 Aug 11.


Hearing loss in Waardenburg syndrome: a systematic review.

Song J, Feng Y, Acke FR, Coucke P, Vleminckx K, Dhooge IJ.

Clin Genet. 2015 Jun 22. doi: 10.1111/cge.12631. [Epub ahead of print]


The Genetics of Soft Connective Tissue Disorders.

Vanakker O, Callewaert B, Malfait F, Coucke P.

Annu Rev Genomics Hum Genet. 2015;16:229-55. doi: 10.1146/annurev-genom-090314-050039. Epub 2015 May 18. Review.

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