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Myocardial infarction in a patient with sickle cell trait. Treatment dilemmas and imaging findings at follow-up.

EuroIntervention : journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology

van Mieghem C, Ramcharitar S, Barlis P, Oosterhuis W, Kik C, de Feyter P, Serruys PW.
PMID: 19608492
EuroIntervention. 2008 Mar;3(5):627-34. doi: 10.4244/eijv3i5a112.

BACKGROUND: A 43-year-old woman with a 2-hour history of chest pain presented with an anterior infarction and was referred for primary percutaneous coronary intervention.INVESTIGATIONS: Physical examination, electrocardiography, laboratory tests, coronary angiography, abdominal angiography, cardiac CT, histology, immunohistochemistry, intravascular ultrasound.DIAGNOSIS:...

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van Mieghem C, Ramcharitar S, Barlis P, et al. Myocardial infarction in a patient with sickle cell trait. Treatment dilemmas and imaging findings at follow-up. EuroIntervention. 2008;3(5):627-34doi: 10.4244/eijv3i5a112.
van Mieghem, C., Ramcharitar, S., Barlis, P., Oosterhuis, W., Kik, C., de Feyter, P., & Serruys, P. W. (2008). Myocardial infarction in a patient with sickle cell trait. Treatment dilemmas and imaging findings at follow-up. EuroIntervention : journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology, 3(5), 627-34. https://doi.org/10.4244/eijv3i5a112
van Mieghem, Carlos, et al. "Myocardial infarction in a patient with sickle cell trait. Treatment dilemmas and imaging findings at follow-up." EuroIntervention : journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology vol. 3,5 (2008): 627-34. doi: https://doi.org/10.4244/eijv3i5a112
van Mieghem C, Ramcharitar S, Barlis P, Oosterhuis W, Kik C, de Feyter P, Serruys PW. Myocardial infarction in a patient with sickle cell trait. Treatment dilemmas and imaging findings at follow-up. EuroIntervention. 2008 Mar;3(5):627-34. doi: 10.4244/eijv3i5a112. PMID: 19608492.
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Chiral alignment of OPV chromophores: exploitation of the ureidophthalimide-based foldamer.

Journal of the American Chemical Society

Sinkeldam RW, Hoeben FJ, Pouderoijen MJ, De Cat I, Zhang J, Furukawa S, De Feyter S, Vekemans JA, Meijer EW.
PMID: 17165764
J Am Chem Soc. 2006 Dec 20;128(50):16113-21. doi: 10.1021/ja063405d.

The ability of foldamers to adopt a secondary structure in solution has been exploited to organize peripheral functionality. Our previously reported poly(ureidophthalimide) foldamer proved to be an excellent scaffold for the chiral organization of peripherally positioned oligo(p-phenylenevinylene) (OPV) chromophores....

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Sinkeldam RW, Hoeben FJ, Pouderoijen MJ, et al. Chiral alignment of OPV chromophores: exploitation of the ureidophthalimide-based foldamer. J Am Chem Soc. 2006;128(50):16113-21doi: 10.1021/ja063405d.
Sinkeldam, R. W., Hoeben, F. J., Pouderoijen, M. J., De Cat, I., Zhang, J., Furukawa, S., De Feyter, S., Vekemans, J. A., & Meijer, E. W. (2006). Chiral alignment of OPV chromophores: exploitation of the ureidophthalimide-based foldamer. Journal of the American Chemical Society, 128(50), 16113-21. https://doi.org/10.1021/ja063405d
Sinkeldam, Renatus W, et al. "Chiral alignment of OPV chromophores: exploitation of the ureidophthalimide-based foldamer." Journal of the American Chemical Society vol. 128,50 (2006): 16113-21. doi: https://doi.org/10.1021/ja063405d
Sinkeldam RW, Hoeben FJ, Pouderoijen MJ, De Cat I, Zhang J, Furukawa S, De Feyter S, Vekemans JA, Meijer EW. Chiral alignment of OPV chromophores: exploitation of the ureidophthalimide-based foldamer. J Am Chem Soc. 2006 Dec 20;128(50):16113-21. doi: 10.1021/ja063405d. PMID: 17165764.
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Temperature-induced structural phase transitions in a two-dimensional self-assembled network.

Journal of the American Chemical Society

Blunt MO, Adisoejoso J, Tahara K, Katayama K, Van der Auweraer M, Tobe Y, De Feyter S.
PMID: 23829544
J Am Chem Soc. 2013 Aug 14;135(32):12068-75. doi: 10.1021/ja405585s. Epub 2013 Aug 01.

Two-dimensional (2D) supramolecular self-assembly at liquid-solid interfaces is a thermodynamically complex process producing a variety of structures. The formation of multiple network morphologies from the same molecular building blocks is a common occurrence. We use scanning tunnelling microscopy (STM)...

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Blunt MO, Adisoejoso J, Tahara K, et al. Temperature-induced structural phase transitions in a two-dimensional self-assembled network. J Am Chem Soc. 2013;135(32):12068-75doi: 10.1021/ja405585s.
Blunt, M. O., Adisoejoso, J., Tahara, K., Katayama, K., Van der Auweraer, M., Tobe, Y., & De Feyter, S. (2013). Temperature-induced structural phase transitions in a two-dimensional self-assembled network. Journal of the American Chemical Society, 135(32), 12068-75. https://doi.org/10.1021/ja405585s
Blunt, Matthew O, et al. "Temperature-induced structural phase transitions in a two-dimensional self-assembled network." Journal of the American Chemical Society vol. 135,32 (2013): 12068-75. doi: https://doi.org/10.1021/ja405585s
Blunt MO, Adisoejoso J, Tahara K, Katayama K, Van der Auweraer M, Tobe Y, De Feyter S. Temperature-induced structural phase transitions in a two-dimensional self-assembled network. J Am Chem Soc. 2013 Aug 14;135(32):12068-75. doi: 10.1021/ja405585s. Epub 2013 Aug 01. PMID: 23829544.
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To mix or not to mix: 2D crystallization and mixing behavior of saturated and unsaturated aliphatic primary amides.

ACS nano

Mali KS, Van Averbeke B, Bhinde T, Brewer AY, Arnold T, Lazzaroni R, Clarke SM, De Feyter S.
PMID: 22011184
ACS Nano. 2011 Nov 22;5(11):9122-37. doi: 10.1021/nn203358x. Epub 2011 Oct 19.

Physisorbed monolayers based on relatively weak noncovalent interactions can serve as excellent model systems for understanding crystallization of materials in reduced dimensionality. Here we employ a powerful combination of scanning tunneling microscopy (STM), differential scanning calorimetry (DSC), and computational...

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Mali KS, Van Averbeke B, Bhinde T, et al. To mix or not to mix: 2D crystallization and mixing behavior of saturated and unsaturated aliphatic primary amides. ACS Nano. 2011;5(11):9122-37doi: 10.1021/nn203358x.
Mali, K. S., Van Averbeke, B., Bhinde, T., Brewer, A. Y., Arnold, T., Lazzaroni, R., Clarke, S. M., & De Feyter, S. (2011). To mix or not to mix: 2D crystallization and mixing behavior of saturated and unsaturated aliphatic primary amides. ACS nano, 5(11), 9122-37. https://doi.org/10.1021/nn203358x
Mali, Kunal S, et al. "To mix or not to mix: 2D crystallization and mixing behavior of saturated and unsaturated aliphatic primary amides." ACS nano vol. 5,11 (2011): 9122-37. doi: https://doi.org/10.1021/nn203358x
Mali KS, Van Averbeke B, Bhinde T, Brewer AY, Arnold T, Lazzaroni R, Clarke SM, De Feyter S. To mix or not to mix: 2D crystallization and mixing behavior of saturated and unsaturated aliphatic primary amides. ACS Nano. 2011 Nov 22;5(11):9122-37. doi: 10.1021/nn203358x. Epub 2011 Oct 19. PMID: 22011184.
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Tailoring surface-confined nanopores with photoresponsive groups.

Angewandte Chemie (International ed. in English)

Tahara K, Inukai K, Adisoejoso J, Yamaga H, Balandina T, Blunt MO, De Feyter S, Tobe Y.
PMID: 23804255
Angew Chem Int Ed Engl. 2013 Aug 05;52(32):8373-6. doi: 10.1002/anie.201303745. Epub 2013 Jun 26.

No abstract available.

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Tahara K, Inukai K, Adisoejoso J, et al. Tailoring surface-confined nanopores with photoresponsive groups. Angew Chem Int Ed Engl. 2013;52(32):8373-6doi: 10.1002/anie.201303745.
Tahara, K., Inukai, K., Adisoejoso, J., Yamaga, H., Balandina, T., Blunt, M. O., De Feyter, S., & Tobe, Y. (2013). Tailoring surface-confined nanopores with photoresponsive groups. Angewandte Chemie (International ed. in English), 52(32), 8373-6. https://doi.org/10.1002/anie.201303745
Tahara, Kazukuni, et al. "Tailoring surface-confined nanopores with photoresponsive groups." Angewandte Chemie (International ed. in English) vol. 52,32 (2013): 8373-6. doi: https://doi.org/10.1002/anie.201303745
Tahara K, Inukai K, Adisoejoso J, Yamaga H, Balandina T, Blunt MO, De Feyter S, Tobe Y. Tailoring surface-confined nanopores with photoresponsive groups. Angew Chem Int Ed Engl. 2013 Aug 05;52(32):8373-6. doi: 10.1002/anie.201303745. Epub 2013 Jun 26. PMID: 23804255.
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STM visualisation of counterions and the effect of charges on self-assembled monolayers of macrocycles.

Beilstein journal of nanotechnology

Kudernac T, Shabelina N, Mamdouh W, Höger S, De Feyter S.
PMID: 22043456
Beilstein J Nanotechnol. 2011;2:674-80. doi: 10.3762/bjnano.2.72. Epub 2011 Oct 11.

Despite their importance in self-assembly processes, the influence of charged counterions on the geometry of self-assembled organic monolayers and their direct localisation within the monolayers has been given little attention. Recently, various examples of self-assembled monolayers composed of charged...

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Kudernac T, Shabelina N, Mamdouh W, et al. STM visualisation of counterions and the effect of charges on self-assembled monolayers of macrocycles. Beilstein J Nanotechnol. 2011;2:674-80doi: 10.3762/bjnano.2.72.
Kudernac, T., Shabelina, N., Mamdouh, W., Höger, S., & De Feyter, S. (2011). STM visualisation of counterions and the effect of charges on self-assembled monolayers of macrocycles. Beilstein journal of nanotechnology, 2674-80. https://doi.org/10.3762/bjnano.2.72
Kudernac, Tibor, et al. "STM visualisation of counterions and the effect of charges on self-assembled monolayers of macrocycles." Beilstein journal of nanotechnology vol. 2 (2011): 674-80. doi: https://doi.org/10.3762/bjnano.2.72
Kudernac T, Shabelina N, Mamdouh W, Höger S, De Feyter S. STM visualisation of counterions and the effect of charges on self-assembled monolayers of macrocycles. Beilstein J Nanotechnol. 2011;2:674-80. doi: 10.3762/bjnano.2.72. Epub 2011 Oct 11. PMID: 22043456; PMCID: PMC3201620.
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The different nature of band edge absorption and emission in colloidal PbSe/CdSe core/shell quantum dots.

ACS nano

De Geyter B, Justo Y, Moreels I, Lambert K, Smet PF, Van Thourhout D, Houtepen AJ, Grodzinska D, de Mello Donega C, Meijerink A, Vanmaekelbergh D, Hens Z.
PMID: 21189031
ACS Nano. 2011 Jan 25;5(1):58-66. doi: 10.1021/nn102980e. Epub 2010 Dec 28.

We present a quantitative analysis of the absorption and luminescence of colloidal PbSe/CdSe core/shell quantum dots (QDs). In absorption, both the energy and the oscillator strength of the first exciton transition coincide with that of plain PbSe QDs. In...

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De Geyter B, Justo Y, Moreels I, et al. The different nature of band edge absorption and emission in colloidal PbSe/CdSe core/shell quantum dots. ACS Nano. 2010;5(1):58-66doi: 10.1021/nn102980e.
De Geyter, B., Justo, Y., Moreels, I., Lambert, K., Smet, P. F., Van Thourhout, D., Houtepen, A. J., Grodzinska, D., de Mello Donega, C., Meijerink, A., Vanmaekelbergh, D., & Hens, Z. (2011). The different nature of band edge absorption and emission in colloidal PbSe/CdSe core/shell quantum dots. ACS nano, 5(1), 58-66. https://doi.org/10.1021/nn102980e
De Geyter, Bram, et al. "The different nature of band edge absorption and emission in colloidal PbSe/CdSe core/shell quantum dots." ACS nano vol. 5,1 (2011): 58-66. doi: https://doi.org/10.1021/nn102980e
De Geyter B, Justo Y, Moreels I, Lambert K, Smet PF, Van Thourhout D, Houtepen AJ, Grodzinska D, de Mello Donega C, Meijerink A, Vanmaekelbergh D, Hens Z. The different nature of band edge absorption and emission in colloidal PbSe/CdSe core/shell quantum dots. ACS Nano. 2011 Jan 25;5(1):58-66. doi: 10.1021/nn102980e. Epub 2010 Dec 28. PMID: 21189031.
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Forced to align: flow-induced long-range alignment of hierarchical molecular assemblies from 2D to 3D.

Journal of the American Chemical Society

Lee SL, Yuan Z, Chen L, Mali KS, Müllen K, De Feyter S.
PMID: 24588617
J Am Chem Soc. 2014 Mar 19;136(11):4117-20. doi: 10.1021/ja5005202. Epub 2014 Mar 10.

Nanostructured molecular thin films adsorbed on solid surfaces form the basis of numerous applications. Long-range order within adsorbed molecules is very often a desirable property for such systems. In this contribution, we report a simple and efficient method to...

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Lee SL, Yuan Z, Chen L, et al. Forced to align: flow-induced long-range alignment of hierarchical molecular assemblies from 2D to 3D. J Am Chem Soc. 2014;136(11):4117-20doi: 10.1021/ja5005202.
Lee, S. L., Yuan, Z., Chen, L., Mali, K. S., Müllen, K., & De Feyter, S. (2014). Forced to align: flow-induced long-range alignment of hierarchical molecular assemblies from 2D to 3D. Journal of the American Chemical Society, 136(11), 4117-20. https://doi.org/10.1021/ja5005202
Lee, Shern-Long, et al. "Forced to align: flow-induced long-range alignment of hierarchical molecular assemblies from 2D to 3D." Journal of the American Chemical Society vol. 136,11 (2014): 4117-20. doi: https://doi.org/10.1021/ja5005202
Lee SL, Yuan Z, Chen L, Mali KS, Müllen K, De Feyter S. Forced to align: flow-induced long-range alignment of hierarchical molecular assemblies from 2D to 3D. J Am Chem Soc. 2014 Mar 19;136(11):4117-20. doi: 10.1021/ja5005202. Epub 2014 Mar 10. PMID: 24588617.
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Efficient molecular recognition based on nonspecific van der Waals interaction at the solid/liquid interface.

Chemical communications (Cambridge, England)

Cao L, Xu L, Zhao D, Tahara K, Tobe Y, De Feyter S, Lei S.
PMID: 25162067
Chem Commun (Camb). 2014 Oct 14;50(80):11946-9. doi: 10.1039/c4cc03658a.

A highly efficient recognition phenomenon was observed between alkoxylated arylene-ethynylene macrocycles bearing identical side chains but different core size, which is based on van der Waals interactions between alkoxy chains. The ratio of both molecules and the environment of...

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Cao L, Xu L, Zhao D, et al. Efficient molecular recognition based on nonspecific van der Waals interaction at the solid/liquid interface. Chem Commun (Camb). 2014;50(80):11946-9doi: 10.1039/c4cc03658a.
Cao, L., Xu, L., Zhao, D., Tahara, K., Tobe, Y., De Feyter, S., & Lei, S. (2014). Efficient molecular recognition based on nonspecific van der Waals interaction at the solid/liquid interface. Chemical communications (Cambridge, England), 50(80), 11946-9. https://doi.org/10.1039/c4cc03658a
Cao, Lili, et al. "Efficient molecular recognition based on nonspecific van der Waals interaction at the solid/liquid interface." Chemical communications (Cambridge, England) vol. 50,80 (2014): 11946-9. doi: https://doi.org/10.1039/c4cc03658a
Cao L, Xu L, Zhao D, Tahara K, Tobe Y, De Feyter S, Lei S. Efficient molecular recognition based on nonspecific van der Waals interaction at the solid/liquid interface. Chem Commun (Camb). 2014 Oct 14;50(80):11946-9. doi: 10.1039/c4cc03658a. PMID: 25162067.
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Pasteurian segregation on a surface imaged in situ at the molecular level.

Angewandte Chemie (International ed. in English)

Xu H, Saletra WJ, Iavicoli P, Van Averbeke B, Ghijsens E, Mali KS, Schenning AP, Beljonne D, Lazzaroni R, Amabilino DB, De Feyter S.
PMID: 23097143
Angew Chem Int Ed Engl. 2012 Nov 26;51(48):11981-5. doi: 10.1002/anie.201202081. Epub 2012 Oct 24.

No abstract available.

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Xu H, Saletra WJ, Iavicoli P, et al. Pasteurian segregation on a surface imaged in situ at the molecular level. Angew Chem Int Ed Engl. 2012;51(48):11981-5doi: 10.1002/anie.201202081.
Xu, H., Saletra, W. J., Iavicoli, P., Van Averbeke, B., Ghijsens, E., Mali, K. S., Schenning, A. P., Beljonne, D., Lazzaroni, R., Amabilino, D. B., & De Feyter, S. (2012). Pasteurian segregation on a surface imaged in situ at the molecular level. Angewandte Chemie (International ed. in English), 51(48), 11981-5. https://doi.org/10.1002/anie.201202081
Xu, Hong, et al. "Pasteurian segregation on a surface imaged in situ at the molecular level." Angewandte Chemie (International ed. in English) vol. 51,48 (2012): 11981-5. doi: https://doi.org/10.1002/anie.201202081
Xu H, Saletra WJ, Iavicoli P, Van Averbeke B, Ghijsens E, Mali KS, Schenning AP, Beljonne D, Lazzaroni R, Amabilino DB, De Feyter S. Pasteurian segregation on a surface imaged in situ at the molecular level. Angew Chem Int Ed Engl. 2012 Nov 26;51(48):11981-5. doi: 10.1002/anie.201202081. Epub 2012 Oct 24. PMID: 23097143.
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Tailoring atomic layer growth at the liquid-metal interface.

Nature communications

Cao H, Waghray D, Knoppe S, Dehaen W, Verbiest T, De Feyter S.
PMID: 30459306
Nat Commun. 2018 Nov 20;9(1):4889. doi: 10.1038/s41467-018-07381-w.

Engineering atomic structures at metal surfaces represents an important step in the development of novel nanomaterials and nanodevices, but relies predominantly on atomic/molecular beam epitaxy under ultrahigh vacuum conditions, where controlling the deposition processes remains challenging. By using solution-borne...

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Cao H, Waghray D, Knoppe S, et al. Tailoring atomic layer growth at the liquid-metal interface. Nat Commun. 2018;9(1):4889doi: 10.1038/s41467-018-07381-w.
Cao, H., Waghray, D., Knoppe, S., Dehaen, W., Verbiest, T., & De Feyter, S. (2018). Tailoring atomic layer growth at the liquid-metal interface. Nature communications, 9(1), 4889. https://doi.org/10.1038/s41467-018-07381-w
Cao, Hai, et al. "Tailoring atomic layer growth at the liquid-metal interface." Nature communications vol. 9,1 (2018): 4889. doi: https://doi.org/10.1038/s41467-018-07381-w
Cao H, Waghray D, Knoppe S, Dehaen W, Verbiest T, De Feyter S. Tailoring atomic layer growth at the liquid-metal interface. Nat Commun. 2018 Nov 20;9(1):4889. doi: 10.1038/s41467-018-07381-w. PMID: 30459306; PMCID: PMC6244000.
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Chemical Vapor Deposition Synthesis and Terahertz Photoconductivity of Low-Band-Gap N = 9 Armchair Graphene Nanoribbons.

Journal of the American Chemical Society

Chen Z, Wang HI, Teyssandier J, Mali KS, Dumslaff T, Ivanov I, Zhang W, Ruffieux P, Fasel R, Räder HJ, Turchinovich D, De Feyter S, Feng X, Kläui M, Narita A, Bonn M, Müllen K.
PMID: 28248492
J Am Chem Soc. 2017 Mar 15;139(10):3635-3638. doi: 10.1021/jacs.7b00776. Epub 2017 Mar 06.

Recent advances in bottom-up synthesis of atomically defined graphene nanoribbons (GNRs) with various microstructures and properties have demonstrated their promise in electronic and optoelectronic devices. Here we synthesized N = 9 armchair graphene nanoribbons (9-AGNRs) with a low optical...

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Chen Z, Wang HI, Teyssandier J, et al. Chemical Vapor Deposition Synthesis and Terahertz Photoconductivity of Low-Band-Gap N = 9 Armchair Graphene Nanoribbons. J Am Chem Soc. 2017;139(10):3635-3638doi: 10.1021/jacs.7b00776.
Chen, Z., Wang, H. I., Teyssandier, J., Mali, K. S., Dumslaff, T., Ivanov, I., Zhang, W., Ruffieux, P., Fasel, R., Räder, H. J., Turchinovich, D., De Feyter, S., Feng, X., Kläui, M., Narita, A., Bonn, M., & Müllen, K. (2017). Chemical Vapor Deposition Synthesis and Terahertz Photoconductivity of Low-Band-Gap N = 9 Armchair Graphene Nanoribbons. Journal of the American Chemical Society, 139(10), 3635-3638. https://doi.org/10.1021/jacs.7b00776
Chen, Zongping, et al. "Chemical Vapor Deposition Synthesis and Terahertz Photoconductivity of Low-Band-Gap N = 9 Armchair Graphene Nanoribbons." Journal of the American Chemical Society vol. 139,10 (2017): 3635-3638. doi: https://doi.org/10.1021/jacs.7b00776
Chen Z, Wang HI, Teyssandier J, Mali KS, Dumslaff T, Ivanov I, Zhang W, Ruffieux P, Fasel R, Räder HJ, Turchinovich D, De Feyter S, Feng X, Kläui M, Narita A, Bonn M, Müllen K. Chemical Vapor Deposition Synthesis and Terahertz Photoconductivity of Low-Band-Gap N = 9 Armchair Graphene Nanoribbons. J Am Chem Soc. 2017 Mar 15;139(10):3635-3638. doi: 10.1021/jacs.7b00776. Epub 2017 Mar 06. PMID: 28248492.
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Showing 25 to 36 of 301 entries