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[So many loose tasks].

Sygeplejersken

Baatrup H.
PMID: 4484013
Sygeplejersken. 1972 Jan 27;72(4):12.

No abstract available.

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Baatrup H. Sådan løses opgaven. [So many loose tasks]. Sygeplejersken. 1972;72(4):12
Baatrup, H. (1972). Sådan løses opgaven. [So many loose tasks]. Sygeplejersken, 72(4), 12.
Baatrup, H. "Sådan løses opgaven." [So many loose tasks]. Sygeplejersken vol. 72,4 (1972): 12.
Baatrup H. Sådan løses opgaven. [So many loose tasks]. Sygeplejersken. 1972 Jan 27;72(4):12. Danish. PMID: 4484013.
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Validity of data in the Danish Colorectal Cancer Screening Database.

Clinical epidemiology

Thomsen MK, Njor SH, Rasmussen M, Linnemann D, Andersen B, Baatrup G, Friis-Hansen LJ, Jørgensen JC, Mikkelsen EM.
PMID: 28255255
Clin Epidemiol. 2017 Feb 17;9:105-111. doi: 10.2147/CLEP.S124454. eCollection 2017.

BACKGROUND: In Denmark, a nationwide screening program for colorectal cancer was implemented in March 2014. Along with this, a clinical database for program monitoring and research purposes was established.OBJECTIVE: The aim of this study was to estimate the agreement...

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Thomsen MK, Njor SH, Rasmussen M, et al. Validity of data in the Danish Colorectal Cancer Screening Database. Clin Epidemiol. 2017;9:105-111doi: 10.2147/CLEP.S124454.
Thomsen, M. K., Njor, S. H., Rasmussen, M., Linnemann, D., Andersen, B., Baatrup, G., Friis-Hansen, L. J., Jørgensen, J. C., & Mikkelsen, E. M. (2017). Validity of data in the Danish Colorectal Cancer Screening Database. Clinical epidemiology, 9105-111. https://doi.org/10.2147/CLEP.S124454
Thomsen, Mette Kielsholm, et al. "Validity of data in the Danish Colorectal Cancer Screening Database." Clinical epidemiology vol. 9 (2017): 105-111. doi: https://doi.org/10.2147/CLEP.S124454
Thomsen MK, Njor SH, Rasmussen M, Linnemann D, Andersen B, Baatrup G, Friis-Hansen LJ, Jørgensen JC, Mikkelsen EM. Validity of data in the Danish Colorectal Cancer Screening Database. Clin Epidemiol. 2017 Feb 17;9:105-111. doi: 10.2147/CLEP.S124454. eCollection 2017. PMID: 28255255; PMCID: PMC5322846.
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Treatment of Clostridium difficile infection in mice with vancomycin alone is as effective as treatment with vancomycin and metronidazole in combination.

BMJ open gastroenterology

Erikstrup LT, Aarup M, Hagemann-Madsen R, Dagnaes-Hansen F, Kristensen B, Olsen KE, Fuursted K.
PMID: 26568840
BMJ Open Gastroenterol. 2015 Nov 02;2(1):e000038. doi: 10.1136/bmjgast-2015-000038. eCollection 2015.

OBJECTIVE: Clostridium difficile is a major cause of nosocomial infectious diarrhoea. Treatment of C. difficile infection (CDI) depends on disease severity. A combination of vancomycin and metronidazole is often recommended in severe cases. The aim of this study was...

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Erikstrup LT, Aarup M, Hagemann-Madsen R, et al. Treatment of Clostridium difficile infection in mice with vancomycin alone is as effective as treatment with vancomycin and metronidazole in combination. BMJ Open Gastroenterol. 2015;2(1):e000038doi: 10.1136/bmjgast-2015-000038.
Erikstrup, L. T., Aarup, M., Hagemann-Madsen, R., Dagnaes-Hansen, F., Kristensen, B., Olsen, K. E., & Fuursted, K. (2015). Treatment of Clostridium difficile infection in mice with vancomycin alone is as effective as treatment with vancomycin and metronidazole in combination. BMJ open gastroenterology, 2(1), e000038. https://doi.org/10.1136/bmjgast-2015-000038
Erikstrup, Lise Tornvig, et al. "Treatment of Clostridium difficile infection in mice with vancomycin alone is as effective as treatment with vancomycin and metronidazole in combination." BMJ open gastroenterology vol. 2,1 (2015): e000038. doi: https://doi.org/10.1136/bmjgast-2015-000038
Erikstrup LT, Aarup M, Hagemann-Madsen R, Dagnaes-Hansen F, Kristensen B, Olsen KE, Fuursted K. Treatment of Clostridium difficile infection in mice with vancomycin alone is as effective as treatment with vancomycin and metronidazole in combination. BMJ Open Gastroenterol. 2015 Nov 02;2(1):e000038. doi: 10.1136/bmjgast-2015-000038. eCollection 2015. PMID: 26568840; PMCID: PMC4641438.
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Differences in Reproductive Behavior between Spawning and Non-Spawning Zebrafish Pairs and the Effects of 17α-Ethinylestradiol (EE2).

Toxics

Henriksen PG, Beedholm K, Baatrup E.
PMID: 29051425
Toxics. 2016 Sep 06;4(3). doi: 10.3390/toxics4030022.

Reproductive success manifested by spawning and fertilization, in most fish, depends partly on an appropriate courtship behavior by both sexes. The zebrafish reproductive behavior can be resolved in some of its constituent elements by a computerized vision system and...

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Henriksen PG, Beedholm K, Baatrup E. Differences in Reproductive Behavior between Spawning and Non-Spawning Zebrafish Pairs and the Effects of 17α-Ethinylestradiol (EE2). Toxics. 2016;4(3)doi: 10.3390/toxics4030022.
Henriksen, P. G., Beedholm, K., & Baatrup, E. (2016). Differences in Reproductive Behavior between Spawning and Non-Spawning Zebrafish Pairs and the Effects of 17α-Ethinylestradiol (EE2). Toxics, 4(3), . https://doi.org/10.3390/toxics4030022
Henriksen, Per G, et al. "Differences in Reproductive Behavior between Spawning and Non-Spawning Zebrafish Pairs and the Effects of 17α-Ethinylestradiol (EE2)." Toxics vol. 4,3 (2016). doi: https://doi.org/10.3390/toxics4030022
Henriksen PG, Beedholm K, Baatrup E. Differences in Reproductive Behavior between Spawning and Non-Spawning Zebrafish Pairs and the Effects of 17α-Ethinylestradiol (EE2). Toxics. 2016 Sep 06;4(3). doi: 10.3390/toxics4030022. PMID: 29051425; PMCID: PMC5606659.
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Selective Synthesis of 2-, 4-, and 5-Cyano Substituted Imidazoles from Imidazole N-Oxides and Trimethylsilyl Cyanide.

The Journal of organic chemistry

Alcázar J, Begtrup M, de La Hoz A.
PMID: 11667594
J Org Chem. 1996 Oct 04;61(20):6971-6973. doi: 10.1021/jo960991s.

1-Substituted 2-, 4-, and 5-cyanoimidazoles were produced by reaction of 3-cyclohexyl or 3-p-tolylimidazole 1-oxide and trimethylsilyl cyanide in the presence of triethylamine. The product composition depended on reaction temperature and solvent polarity. By proper choice of these parameters each...

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Alcázar J, Begtrup M, de La Hoz A. Selective Synthesis of 2-, 4-, and 5-Cyano Substituted Imidazoles from Imidazole N-Oxides and Trimethylsilyl Cyanide. J Org Chem. 1996;61(20):6971-6973doi: 10.1021/jo960991s.
Alcázar, J., Begtrup, M., & de La Hoz, A. (1996). Selective Synthesis of 2-, 4-, and 5-Cyano Substituted Imidazoles from Imidazole N-Oxides and Trimethylsilyl Cyanide. The Journal of organic chemistry, 61(20), 6971-6973. https://doi.org/10.1021/jo960991s
Alcázar, Jesús, et al. "Selective Synthesis of 2-, 4-, and 5-Cyano Substituted Imidazoles from Imidazole N-Oxides and Trimethylsilyl Cyanide." The Journal of organic chemistry vol. 61,20 (1996): 6971-6973. doi: https://doi.org/10.1021/jo960991s
Alcázar J, Begtrup M, de La Hoz A. Selective Synthesis of 2-, 4-, and 5-Cyano Substituted Imidazoles from Imidazole N-Oxides and Trimethylsilyl Cyanide. J Org Chem. 1996 Oct 04;61(20):6971-6973. doi: 10.1021/jo960991s. PMID: 11667594.
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Regioselective Introduction of Electrophiles in the 4-Position of 1-Hydroxypyrazole via Bromine-Lithium Exchange.

The Journal of organic chemistry

Balle T, Vedsø P, Begtrup M.
PMID: 11674594
J Org Chem. 1999 Jul 23;64(15):5366-5370. doi: 10.1021/jo981970w.

Two protocols for introduction of electrophiles at the 4-position of 1-hydroxypyrazoles have been developed. The first is deprotonation of 4-bromo-1-[(tert-butyldiphenylsilyl)oxy]pyrazole (6) with LDA to produce the 5-lithio derivative in which the silyl group migrates spontaneously from oxygen to C-5...

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Balle T, Vedsø P, Begtrup M. Regioselective Introduction of Electrophiles in the 4-Position of 1-Hydroxypyrazole via Bromine-Lithium Exchange. J Org Chem. 1999;64(15):5366-5370doi: 10.1021/jo981970w.
Balle, T., Vedsø, P., & Begtrup, M. (1999). Regioselective Introduction of Electrophiles in the 4-Position of 1-Hydroxypyrazole via Bromine-Lithium Exchange. The Journal of organic chemistry, 64(15), 5366-5370. https://doi.org/10.1021/jo981970w
Balle, Thomas, et al. "Regioselective Introduction of Electrophiles in the 4-Position of 1-Hydroxypyrazole via Bromine-Lithium Exchange." The Journal of organic chemistry vol. 64,15 (1999): 5366-5370. doi: https://doi.org/10.1021/jo981970w
Balle T, Vedsø P, Begtrup M. Regioselective Introduction of Electrophiles in the 4-Position of 1-Hydroxypyrazole via Bromine-Lithium Exchange. J Org Chem. 1999 Jul 23;64(15):5366-5370. doi: 10.1021/jo981970w. PMID: 11674594.
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Convergent synthesis of 6-substituted phenanthridines via anionic ring closure.

Organic letters

Lysén M, Kristensen JL, Vedsø P, Begtrup M.
PMID: 11796064
Org Lett. 2002 Jan 24;4(2):257-9. doi: 10.1021/ol0170051.

[reaction: see text] The addition of organometallic derivatives to the cyano group of 2-(2-fluorophenyl)benzonitrile followed by intramolecular nucleophilic substitution produces 6-substituted phenanthridines. Alkyllithiums, aryllithiums, and sterically nondemanding lithium amides reacted at -78 degrees C to produce the 6-substituted phenanthridines...

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Lysén M, Kristensen JL, Vedsø P, et al. Convergent synthesis of 6-substituted phenanthridines via anionic ring closure. Org Lett. 2002;4(2):257-9doi: 10.1021/ol0170051.
Lysén, M., Kristensen, J. L., Vedsø, P., & Begtrup, M. (2002). Convergent synthesis of 6-substituted phenanthridines via anionic ring closure. Organic letters, 4(2), 257-9. https://doi.org/10.1021/ol0170051
Lysén, Morten, et al. "Convergent synthesis of 6-substituted phenanthridines via anionic ring closure." Organic letters vol. 4,2 (2002): 257-9. doi: https://doi.org/10.1021/ol0170051
Lysén M, Kristensen JL, Vedsø P, Begtrup M. Convergent synthesis of 6-substituted phenanthridines via anionic ring closure. Org Lett. 2002 Jan 24;4(2):257-9. doi: 10.1021/ol0170051. PMID: 11796064.
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Synthesis of ortho substituted arylboronic esters by in situ trapping of unstable lithio intermediates.

Organic letters

Kristensen J, Lysén M, Vedsø P, Begtrup M.
PMID: 11388835
Org Lett. 2001 May 17;3(10):1435-7. doi: 10.1021/ol015598+.

[reaction: see text] Ortho lithiation-in situ boration using lithium 2,2,6,6-tetramethylpiperidide (LTMP) in combination with triisopropylborate (B(OiPr)(3)) is a highly efficient and experimentally straightforward process for the preparation of ortho substituted arylboronic esters. The mild reaction conditions allow the presence...

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Kristensen J, Lysén M, Vedsø P, et al. Synthesis of ortho substituted arylboronic esters by in situ trapping of unstable lithio intermediates. Org Lett. 2001;3(10):1435-7doi: 10.1021/ol015598+.
Kristensen, J., Lysén, M., Vedsø, P., & Begtrup, M. (2001). Synthesis of ortho substituted arylboronic esters by in situ trapping of unstable lithio intermediates. Organic letters, 3(10), 1435-7. https://doi.org/10.1021/ol015598+
Kristensen, J, et al. "Synthesis of ortho substituted arylboronic esters by in situ trapping of unstable lithio intermediates." Organic letters vol. 3,10 (2001): 1435-7. doi: https://doi.org/10.1021/ol015598+
Kristensen J, Lysén M, Vedsø P, Begtrup M. Synthesis of ortho substituted arylboronic esters by in situ trapping of unstable lithio intermediates. Org Lett. 2001 May 17;3(10):1435-7. doi: 10.1021/ol015598+. PMID: 11388835.
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Current issues in Danish psychiatry.

Nordic journal of psychiatry

Fink-Jensen A, Kastrup M, Lolk A.
PMID: 19958259
Nord J Psychiatry. 2009 Nov;63(6):517-8. doi: 10.3109/08039480903444393.

No abstract available.

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Fink-Jensen A, Kastrup M, Lolk A. Current issues in Danish psychiatry. Nord J Psychiatry. 2009;63(6):517-8doi: 10.3109/08039480903444393.
Fink-Jensen, A., Kastrup, M., & Lolk, A. (2009). Current issues in Danish psychiatry. Nordic journal of psychiatry, 63(6), 517-8. https://doi.org/10.3109/08039480903444393
Fink-Jensen, Anders, et al. "Current issues in Danish psychiatry." Nordic journal of psychiatry vol. 63,6 (2009): 517-8. doi: https://doi.org/10.3109/08039480903444393
Fink-Jensen A, Kastrup M, Lolk A. Current issues in Danish psychiatry. Nord J Psychiatry. 2009 Nov;63(6):517-8. doi: 10.3109/08039480903444393. PMID: 19958259.
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WPA guidance on how to combat stigmatization of psychiatry and psychiatrists.

World psychiatry : official journal of the World Psychiatric Association (WPA)

Sartorius N, Gaebel W, Cleveland HR, Stuart H, Akiyama T, Arboleda-Flórez J, Baumann AE, Gureje O, Jorge MR, Kastrup M, Suzuki Y, Tasman A.
PMID: 20975855
World Psychiatry. 2010 Oct;9(3):131-44. doi: 10.1002/j.2051-5545.2010.tb00296.x.

In 2009 the WPA President established a Task Force that was to examine available evidence about the stigmatization of psychiatry and psychiatrists and to make recommendations about action that national psychiatric societies and psychiatrists as professionals could do to...

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Sartorius N, Gaebel W, Cleveland HR, et al. WPA guidance on how to combat stigmatization of psychiatry and psychiatrists. World Psychiatry. 2010;9(3):131-44doi: 10.1002/j.2051-5545.2010.tb00296.x.
Sartorius, N., Gaebel, W., Cleveland, H. R., Stuart, H., Akiyama, T., Arboleda-Flórez, J., Baumann, A. E., Gureje, O., Jorge, M. R., Kastrup, M., Suzuki, Y., & Tasman, A. (2010). WPA guidance on how to combat stigmatization of psychiatry and psychiatrists. World psychiatry : official journal of the World Psychiatric Association (WPA), 9(3), 131-44. https://doi.org/10.1002/j.2051-5545.2010.tb00296.x
Sartorius, Norman, et al. "WPA guidance on how to combat stigmatization of psychiatry and psychiatrists." World psychiatry : official journal of the World Psychiatric Association (WPA) vol. 9,3 (2010): 131-44. doi: https://doi.org/10.1002/j.2051-5545.2010.tb00296.x
Sartorius N, Gaebel W, Cleveland HR, Stuart H, Akiyama T, Arboleda-Flórez J, Baumann AE, Gureje O, Jorge MR, Kastrup M, Suzuki Y, Tasman A. WPA guidance on how to combat stigmatization of psychiatry and psychiatrists. World Psychiatry. 2010 Oct;9(3):131-44. doi: 10.1002/j.2051-5545.2010.tb00296.x. PMID: 20975855; PMCID: PMC2948719.
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Polaron stability in semiconducting polymer neat films.

Chemical communications (Cambridge, England)

Beatrup D, Wade J, Biniek L, Bronstein H, Hurhangee M, Kim JS, McCulloch I, Durrant JR.
PMID: 25302346
Chem Commun (Camb). 2014 Nov 28;50(92):14425-8. doi: 10.1039/c4cc06193d.

We describe a spectroelectrochemical approach to accelerated electrochemical stability studies of conjugated polymers under oxidative stress. The polaron stabilities of alternating copolymers based on (i) thiophene and thiazole, namely PTTz, and (ii) bithiophene and thiazole, namely PTTTz, are compared...

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Beatrup D, Wade J, Biniek L, et al. Polaron stability in semiconducting polymer neat films. Chem Commun (Camb). 2014;50(92):14425-8doi: 10.1039/c4cc06193d.
Beatrup, D., Wade, J., Biniek, L., Bronstein, H., Hurhangee, M., Kim, J. S., McCulloch, I., & Durrant, J. R. (2014). Polaron stability in semiconducting polymer neat films. Chemical communications (Cambridge, England), 50(92), 14425-8. https://doi.org/10.1039/c4cc06193d
Beatrup, Daniel, et al. "Polaron stability in semiconducting polymer neat films." Chemical communications (Cambridge, England) vol. 50,92 (2014): 14425-8. doi: https://doi.org/10.1039/c4cc06193d
Beatrup D, Wade J, Biniek L, Bronstein H, Hurhangee M, Kim JS, McCulloch I, Durrant JR. Polaron stability in semiconducting polymer neat films. Chem Commun (Camb). 2014 Nov 28;50(92):14425-8. doi: 10.1039/c4cc06193d. PMID: 25302346.
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Photocurrent enhancement from diketopyrrolopyrrole polymer solar cells through alkyl-chain branching point manipulation.

Journal of the American Chemical Society

Meager I, Ashraf RS, Mollinger S, Schroeder BC, Bronstein H, Beatrup D, Vezie MS, Kirchartz T, Salleo A, Nelson J, McCulloch I.
PMID: 23876163
J Am Chem Soc. 2013 Aug 07;135(31):11537-40. doi: 10.1021/ja406934j. Epub 2013 Jul 29.

Systematically moving the alkyl-chain branching position away from the polymer backbone afforded two new thieno[3,2-b]thiophene-diketopyrrolopyrrole (DPPTT-T) polymers. When used as donor materials in polymer:fullerene solar cells, efficiencies exceeding 7% were achieved without the use of processing additives. The effect...

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Meager I, Ashraf RS, Mollinger S, et al. Photocurrent enhancement from diketopyrrolopyrrole polymer solar cells through alkyl-chain branching point manipulation. J Am Chem Soc. 2013;135(31):11537-40doi: 10.1021/ja406934j.
Meager, I., Ashraf, R. S., Mollinger, S., Schroeder, B. C., Bronstein, H., Beatrup, D., Vezie, M. S., Kirchartz, T., Salleo, A., Nelson, J., & McCulloch, I. (2013). Photocurrent enhancement from diketopyrrolopyrrole polymer solar cells through alkyl-chain branching point manipulation. Journal of the American Chemical Society, 135(31), 11537-40. https://doi.org/10.1021/ja406934j
Meager, Iain, et al. "Photocurrent enhancement from diketopyrrolopyrrole polymer solar cells through alkyl-chain branching point manipulation." Journal of the American Chemical Society vol. 135,31 (2013): 11537-40. doi: https://doi.org/10.1021/ja406934j
Meager I, Ashraf RS, Mollinger S, Schroeder BC, Bronstein H, Beatrup D, Vezie MS, Kirchartz T, Salleo A, Nelson J, McCulloch I. Photocurrent enhancement from diketopyrrolopyrrole polymer solar cells through alkyl-chain branching point manipulation. J Am Chem Soc. 2013 Aug 07;135(31):11537-40. doi: 10.1021/ja406934j. Epub 2013 Jul 29. PMID: 23876163.
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