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Use of a Clinical Decision Support System (CDSS) to improve antimicrobial stewardship efforts at a single academic medical center.

Germs

Albarillo FS, Labuszewski L, Lopez J, Santarossa M, Bhatia NK.
PMID: 31341839
Germs. 2019 Jun 03;9(2):106-109. doi: 10.18683/germs.2019.1165. eCollection 2019 Jun.

No abstract available.

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Albarillo FS, Labuszewski L, Lopez J, et al. Use of a Clinical Decision Support System (CDSS) to improve antimicrobial stewardship efforts at a single academic medical center. Germs. 2019;9(2):106-109doi: 10.18683/germs.2019.1165.
Albarillo, F. S., Labuszewski, L., Lopez, J., Santarossa, M., & Bhatia, N. K. (2019). Use of a Clinical Decision Support System (CDSS) to improve antimicrobial stewardship efforts at a single academic medical center. Germs, 9(2), 106-109. https://doi.org/10.18683/germs.2019.1165
Albarillo, Fritzie S, et al. "Use of a Clinical Decision Support System (CDSS) to improve antimicrobial stewardship efforts at a single academic medical center." Germs vol. 9,2 (2019): 106-109. doi: https://doi.org/10.18683/germs.2019.1165
Albarillo FS, Labuszewski L, Lopez J, Santarossa M, Bhatia NK. Use of a Clinical Decision Support System (CDSS) to improve antimicrobial stewardship efforts at a single academic medical center. Germs. 2019 Jun 03;9(2):106-109. doi: 10.18683/germs.2019.1165. eCollection 2019 Jun. PMID: 31341839; PMCID: PMC6591524.
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Synthesis and Hydrosilylation of Vinyl-Substituted Open-Cage Silsesquioxanes with Phenylsilanes: Regioselective Synthesis of Trifunctional Silsesquioxanes.

Inorganic chemistry

Grzelak M, Januszewski R, Marciniec B.
PMID: 32436707
Inorg Chem. 2020 Jun 01;59(11):7830-7840. doi: 10.1021/acs.inorgchem.0c00947. Epub 2020 May 21.

Herein, we report an efficient synthesis and functionalization of trifunctional open-cage-type silsesquioxanes. The method proposed has been successfully applied for the synthesis of a library of incompletely condensed silsesquioxanes with vinyldiorganosilyl functional groups, which allows further modification. Detailed studies...

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Grzelak M, Januszewski R, Marciniec B. Synthesis and Hydrosilylation of Vinyl-Substituted Open-Cage Silsesquioxanes with Phenylsilanes: Regioselective Synthesis of Trifunctional Silsesquioxanes. Inorg Chem. 2020;59(11):7830-7840doi: 10.1021/acs.inorgchem.0c00947.
Grzelak, M., Januszewski, R., & Marciniec, B. (2020). Synthesis and Hydrosilylation of Vinyl-Substituted Open-Cage Silsesquioxanes with Phenylsilanes: Regioselective Synthesis of Trifunctional Silsesquioxanes. Inorganic chemistry, 59(11), 7830-7840. https://doi.org/10.1021/acs.inorgchem.0c00947
Grzelak, Magdalena, et al. "Synthesis and Hydrosilylation of Vinyl-Substituted Open-Cage Silsesquioxanes with Phenylsilanes: Regioselective Synthesis of Trifunctional Silsesquioxanes." Inorganic chemistry vol. 59,11 (2020): 7830-7840. doi: https://doi.org/10.1021/acs.inorgchem.0c00947
Grzelak M, Januszewski R, Marciniec B. Synthesis and Hydrosilylation of Vinyl-Substituted Open-Cage Silsesquioxanes with Phenylsilanes: Regioselective Synthesis of Trifunctional Silsesquioxanes. Inorg Chem. 2020 Jun 01;59(11):7830-7840. doi: 10.1021/acs.inorgchem.0c00947. Epub 2020 May 21. PMID: 32436707; PMCID: PMC7588036.
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Introduction of organogermyl functionalities to cage silsesquioxanes.

Dalton transactions (Cambridge, England : 2003)

Grzelak M, Frąckowiak D, Januszewski R, Marciniec B.
PMID: 32242191
Dalton Trans. 2020 Apr 28;49(16):5055-5063. doi: 10.1039/d0dt00557f.

In this work, we present the first example of highly efficient platinum-catalyzed hydrosilylation of vinyl- and allylgermanes with different types of silsesquioxanes and spherosilicates. This protocol allows the straightforward introduction of organogermyl functionalities with alkyl chains linked to the...

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Grzelak M, Frąckowiak D, Januszewski R, et al. Introduction of organogermyl functionalities to cage silsesquioxanes. Dalton Trans. 2020;49(16):5055-5063doi: 10.1039/d0dt00557f.
Grzelak, M., Frąckowiak, D., Januszewski, R., & Marciniec, B. (2020). Introduction of organogermyl functionalities to cage silsesquioxanes. Dalton transactions (Cambridge, England : 2003), 49(16), 5055-5063. https://doi.org/10.1039/d0dt00557f
Grzelak, Magdalena, et al. "Introduction of organogermyl functionalities to cage silsesquioxanes." Dalton transactions (Cambridge, England : 2003) vol. 49,16 (2020): 5055-5063. doi: https://doi.org/10.1039/d0dt00557f
Grzelak M, Frąckowiak D, Januszewski R, Marciniec B. Introduction of organogermyl functionalities to cage silsesquioxanes. Dalton Trans. 2020 Apr 28;49(16):5055-5063. doi: 10.1039/d0dt00557f. PMID: 32242191.
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Double-Decker Silsesquioxanes Self-Assembled in One-Dimensional Coordination Polymeric Nanofibers with Emission Properties.

ACS applied materials & interfaces

Duszczak J, Mituła K, Santiago-Portillo A, Soumoy L, Rzonsowska M, Januszewski R, Fusaro L, Aprile C, Dudziec B.
PMID: 33961397
ACS Appl Mater Interfaces. 2021 May 19;13(19):22806-22818. doi: 10.1021/acsami.1c02510. Epub 2021 May 07.

The urgent needs for photoactive materials in industry drive fast evolution of synthetic procedures in many branches of chemistry, including the chemistry of silsesquioxanes. Here, we disclose an effective protocol for the synthesis of novel double-decker silsesquioxanes decorated with...

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Duszczak J, Mituła K, Santiago-Portillo A, et al. Double-Decker Silsesquioxanes Self-Assembled in One-Dimensional Coordination Polymeric Nanofibers with Emission Properties. ACS Appl Mater Interfaces. 2021;13(19):22806-22818doi: 10.1021/acsami.1c02510.
Duszczak, J., Mituła, K., Santiago-Portillo, A., Soumoy, L., Rzonsowska, M., Januszewski, R., Fusaro, L., Aprile, C., & Dudziec, B. (2021). Double-Decker Silsesquioxanes Self-Assembled in One-Dimensional Coordination Polymeric Nanofibers with Emission Properties. ACS applied materials & interfaces, 13(19), 22806-22818. https://doi.org/10.1021/acsami.1c02510
Duszczak, Julia, et al. "Double-Decker Silsesquioxanes Self-Assembled in One-Dimensional Coordination Polymeric Nanofibers with Emission Properties." ACS applied materials & interfaces vol. 13,19 (2021): 22806-22818. doi: https://doi.org/10.1021/acsami.1c02510
Duszczak J, Mituła K, Santiago-Portillo A, Soumoy L, Rzonsowska M, Januszewski R, Fusaro L, Aprile C, Dudziec B. Double-Decker Silsesquioxanes Self-Assembled in One-Dimensional Coordination Polymeric Nanofibers with Emission Properties. ACS Appl Mater Interfaces. 2021 May 19;13(19):22806-22818. doi: 10.1021/acsami.1c02510. Epub 2021 May 07. PMID: 33961397; PMCID: PMC8289186.
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The Role of the Mizar Mathematical Library for Interactive Proof Development in Mizar.

Journal of automated reasoning

Bancerek G, Byliński C, Grabowski A, Korniłowicz A, Matuszewski R, Naumowicz A, Pąk K.
PMID: 30069070
J Autom Reason. 2018;61(1):9-32. doi: 10.1007/s10817-017-9440-6. Epub 2017 Nov 25.

The Mizar system is one of the pioneering systems aimed at supporting mathematical proof development on a computer that have laid the groundwork for and eventually have evolved into modern interactive proof assistants. We claim that an important milestone...

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Bancerek G, Byliński C, Grabowski A, et al. The Role of the Mizar Mathematical Library for Interactive Proof Development in Mizar. J Autom Reason. 2017;61(1):9-32doi: 10.1007/s10817-017-9440-6.
Bancerek, G., Byliński, C., Grabowski, A., Korniłowicz, A., Matuszewski, R., Naumowicz, A., & Pąk, K. (2018). The Role of the Mizar Mathematical Library for Interactive Proof Development in Mizar. Journal of automated reasoning, 61(1), 9-32. https://doi.org/10.1007/s10817-017-9440-6
Bancerek, Grzegorz, et al. "The Role of the Mizar Mathematical Library for Interactive Proof Development in Mizar." Journal of automated reasoning vol. 61,1 (2018): 9-32. doi: https://doi.org/10.1007/s10817-017-9440-6
Bancerek G, Byliński C, Grabowski A, Korniłowicz A, Matuszewski R, Naumowicz A, Pąk K. The Role of the Mizar Mathematical Library for Interactive Proof Development in Mizar. J Autom Reason. 2018;61(1):9-32. doi: 10.1007/s10817-017-9440-6. Epub 2017 Nov 25. PMID: 30069070; PMCID: PMC6044251.
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Microwave-Accelerated C,N-Cyclometalation as a Route to Chloro-Bridged Iridium(III) Binuclear Precursors of Phosphorescent Materials: Optimization, Synthesis, and Studies of the Iridium(III) Dimer Behavior in Coordinating Solvents.

Inorganic chemistry

Orwat B, Oh MJ, Zaranek M, Kubicki M, Januszewski R, Kownacki I.
PMID: 32564601
Inorg Chem. 2020 Jul 06;59(13):9163-9176. doi: 10.1021/acs.inorgchem.0c01071. Epub 2020 Jun 21.

We present the results of our research on the use of microwaves as an unconventional heat source for the acceleration of iridium(III) chloro-bridged dimer preparation. The results enabled us to revise and improve known guidelines for the very quick...

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Orwat B, Oh MJ, Zaranek M, et al. Microwave-Accelerated C,N-Cyclometalation as a Route to Chloro-Bridged Iridium(III) Binuclear Precursors of Phosphorescent Materials: Optimization, Synthesis, and Studies of the Iridium(III) Dimer Behavior in Coordinating Solvents. Inorg Chem. 2020;59(13):9163-9176doi: 10.1021/acs.inorgchem.0c01071.
Orwat, B., Oh, M. J., Zaranek, M., Kubicki, M., Januszewski, R., & Kownacki, I. (2020). Microwave-Accelerated C,N-Cyclometalation as a Route to Chloro-Bridged Iridium(III) Binuclear Precursors of Phosphorescent Materials: Optimization, Synthesis, and Studies of the Iridium(III) Dimer Behavior in Coordinating Solvents. Inorganic chemistry, 59(13), 9163-9176. https://doi.org/10.1021/acs.inorgchem.0c01071
Orwat, Bartosz, et al. "Microwave-Accelerated C,N-Cyclometalation as a Route to Chloro-Bridged Iridium(III) Binuclear Precursors of Phosphorescent Materials: Optimization, Synthesis, and Studies of the Iridium(III) Dimer Behavior in Coordinating Solvents." Inorganic chemistry vol. 59,13 (2020): 9163-9176. doi: https://doi.org/10.1021/acs.inorgchem.0c01071
Orwat B, Oh MJ, Zaranek M, Kubicki M, Januszewski R, Kownacki I. Microwave-Accelerated C,N-Cyclometalation as a Route to Chloro-Bridged Iridium(III) Binuclear Precursors of Phosphorescent Materials: Optimization, Synthesis, and Studies of the Iridium(III) Dimer Behavior in Coordinating Solvents. Inorg Chem. 2020 Jul 06;59(13):9163-9176. doi: 10.1021/acs.inorgchem.0c01071. Epub 2020 Jun 21. PMID: 32564601.
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Measurement of the longitudinal, transverse, and longitudinal-transverse structure functions in the 2H(e,e'p)n reaction.

Physical review letters

Alarcon R, Beck R, Bertozzi W, Bhushan V, Boeglin W, Chen JP, Dale D, Dodson G, Dolfini S, Dow K, Dzengeleski J, Epstein MB, Farkhondeh M, Gilad S, Görgen J, Holtrop M, Joo K, Jordan D, Kelsey J, Kim W, Laszewski R, Lourie R, Mandeville J, Margaziotis D, Martinez D, McIlvain T, Miskimen R, Papanicolas CN, Penn S, Sapp W, Sarty AJ, Tieger D, Tschalaer C, Turchinetz W, Warren G, Weinstein L, Williamson S.
PMID: 10060465
Phys Rev Lett. 1996 Mar 04;76(10):1579-1582. doi: 10.1103/PhysRevLett.76.1579.

No abstract available.

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Alarcon R, Beck R, Bertozzi W, et al. Measurement of the longitudinal, transverse, and longitudinal-transverse structure functions in the 2H(e,e'p)n reaction. Phys Rev Lett. 1996;76(10):1579-1582doi: 10.1103/PhysRevLett.76.1579.
Alarcon, R., Beck, R., Bertozzi, W., Bhushan, V., Boeglin, W., Chen, J. P., Dale, D., Dodson, G., Dolfini, S., Dow, K., Dzengeleski, J., Epstein, M. B., Farkhondeh, M., Gilad, S., Görgen, J., Holtrop, M., Joo, K., Jordan, D., Kelsey, J., Kim, W., Laszewski, R., Lourie, R., Mandeville, J., Margaziotis, D., Martinez, D., McIlvain, T., Miskimen, R., Papanicolas, C. N., Penn, S., Sapp, W., Sarty, A. J., Tieger, D., Tschalaer, C., Turchinetz, W., Warren, G., Weinstein, L., & Williamson, S. (1996). Measurement of the longitudinal, transverse, and longitudinal-transverse structure functions in the 2H(e,e'p)n reaction. Physical review letters, 76(10), 1579-1582. https://doi.org/10.1103/PhysRevLett.76.1579
Alarcon, et al. "Measurement of the longitudinal, transverse, and longitudinal-transverse structure functions in the 2H(e,e'p)n reaction." Physical review letters vol. 76,10 (1996): 1579-1582. doi: https://doi.org/10.1103/PhysRevLett.76.1579
Alarcon R, Beck R, Bertozzi W, Bhushan V, Boeglin W, Chen JP, Dale D, Dodson G, Dolfini S, Dow K, Dzengeleski J, Epstein MB, Farkhondeh M, Gilad S, Görgen J, Holtrop M, Joo K, Jordan D, Kelsey J, Kim W, Laszewski R, Lourie R, Mandeville J, Margaziotis D, Martinez D, McIlvain T, Miskimen R, Papanicolas CN, Penn S, Sapp W, Sarty AJ, Tieger D, Tschalaer C, Turchinetz W, Warren G, Weinstein L, Williamson S. Measurement of the longitudinal, transverse, and longitudinal-transverse structure functions in the 2H(e,e'p)n reaction. Phys Rev Lett. 1996 Mar 04;76(10):1579-1582. doi: 10.1103/PhysRevLett.76.1579. PMID: 10060465.
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First Measurement of the Imaginary Part of the Transverse-Longitudinal Nuclear Response.

Physical review letters

Alarcon R, Beck R, Bernstein A, Bertozzi W, Boeglin W, Boffi S, Cardman L, Comfort J, Dale D, Dodson G, Dolfini S, Dow K, Epstein M, Gilad S, Görgen J, Holtrop M, Jordan D, Kim W, Kowalski S, Laszewski R, Mandeville J, Margaziotis D, Martinez D, McIlvain T, Miskimen R, Papanicolas C, Radici M, Tieger D, Turchinetz W, Weinstein L, Williamson S.
PMID: 10056169
Phys Rev Lett. 1994 May 23;72(21):3325-3328. doi: 10.1103/PhysRevLett.72.3325.

No abstract available.

Cite
Alarcon R, Beck R, Bernstein A, et al. First Measurement of the Imaginary Part of the Transverse-Longitudinal Nuclear Response. Phys Rev Lett. 1994;72(21):3325-3328doi: 10.1103/PhysRevLett.72.3325.
Alarcon, R., Beck, R., Bernstein, A., Bertozzi, W., Boeglin, W., Boffi, S., Cardman, L., Comfort, J., Dale, D., Dodson, G., Dolfini, S., Dow, K., Epstein, M., Gilad, S., Görgen, J., Holtrop, M., Jordan, D., Kim, W., Kowalski, S., Laszewski, R., Mandeville, J., Margaziotis, D., Martinez, D., McIlvain, T., Miskimen, R., Papanicolas, C., Radici, M., Tieger, D., Turchinetz, W., Weinstein, L., & Williamson, S. (1994). First Measurement of the Imaginary Part of the Transverse-Longitudinal Nuclear Response. Physical review letters, 72(21), 3325-3328. https://doi.org/10.1103/PhysRevLett.72.3325
Alarcon, et al. "First Measurement of the Imaginary Part of the Transverse-Longitudinal Nuclear Response." Physical review letters vol. 72,21 (1994): 3325-3328. doi: https://doi.org/10.1103/PhysRevLett.72.3325
Alarcon R, Beck R, Bernstein A, Bertozzi W, Boeglin W, Boffi S, Cardman L, Comfort J, Dale D, Dodson G, Dolfini S, Dow K, Epstein M, Gilad S, Görgen J, Holtrop M, Jordan D, Kim W, Kowalski S, Laszewski R, Mandeville J, Margaziotis D, Martinez D, McIlvain T, Miskimen R, Papanicolas C, Radici M, Tieger D, Turchinetz W, Weinstein L, Williamson S. First Measurement of the Imaginary Part of the Transverse-Longitudinal Nuclear Response. Phys Rev Lett. 1994 May 23;72(21):3325-3328. doi: 10.1103/PhysRevLett.72.3325. PMID: 10056169.
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Synthesis of bifunctional disiloxanes via subsequent hydrosilylation of alkenes and alkynes.

Chemical communications (Cambridge, England)

Szyling J, Januszewski R, Jankowska K, Walkowiak J, Kownacki I, Franczyk A.
PMID: 33954327
Chem Commun (Camb). 2021 May 07;57(37):4504-4507. doi: 10.1039/d1cc01253c. Epub 2021 Apr 08.

The first protocol for the synthesis of unsymmetrical bifunctional 1,1,3,3-tetramethyldisiloxane derivatives via subsequent hydrosilylation of alkenes and alkynes is presented. The methodology described has vast functional group tolerance and is extremely efficient towards the formation of novel disiloxane-based building...

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Szyling J, Januszewski R, Jankowska K, et al. Synthesis of bifunctional disiloxanes via subsequent hydrosilylation of alkenes and alkynes. Chem Commun (Camb). 2021;57(37):4504-4507doi: 10.1039/d1cc01253c.
Szyling, J., Januszewski, R., Jankowska, K., Walkowiak, J., Kownacki, I., & Franczyk, A. (2021). Synthesis of bifunctional disiloxanes via subsequent hydrosilylation of alkenes and alkynes. Chemical communications (Cambridge, England), 57(37), 4504-4507. https://doi.org/10.1039/d1cc01253c
Szyling, Jakub, et al. "Synthesis of bifunctional disiloxanes via subsequent hydrosilylation of alkenes and alkynes." Chemical communications (Cambridge, England) vol. 57,37 (2021): 4504-4507. doi: https://doi.org/10.1039/d1cc01253c
Szyling J, Januszewski R, Jankowska K, Walkowiak J, Kownacki I, Franczyk A. Synthesis of bifunctional disiloxanes via subsequent hydrosilylation of alkenes and alkynes. Chem Commun (Camb). 2021 May 07;57(37):4504-4507. doi: 10.1039/d1cc01253c. Epub 2021 Apr 08. PMID: 33954327.
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Pt(0)-Catalysed synthesis of new bifunctional silanes.

Dalton transactions (Cambridge, England : 2003)

Januszewski R, Dutkiewicz M, Franczyk A, Kownacki I.
PMID: 32510084
Dalton Trans. 2020 Jun 21;49(23):7697-7700. doi: 10.1039/d0dt01668c. Epub 2020 Jun 08.

We report herein very efficient syntheses of new functional silanes obtained via olefin hydrosilylation. New bifunctional compounds contain attractive functional groups such as epoxy, fluoroalkyl, trisilylamine, chloropropyl, and methacroiloxy which can play different roles in molecular systems. Moreover, the...

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Januszewski R, Dutkiewicz M, Franczyk A, et al. Pt(0)-Catalysed synthesis of new bifunctional silanes. Dalton Trans. 2020;49(23):7697-7700doi: 10.1039/d0dt01668c.
Januszewski, R., Dutkiewicz, M., Franczyk, A., & Kownacki, I. (2020). Pt(0)-Catalysed synthesis of new bifunctional silanes. Dalton transactions (Cambridge, England : 2003), 49(23), 7697-7700. https://doi.org/10.1039/d0dt01668c
Januszewski, Rafał, et al. "Pt(0)-Catalysed synthesis of new bifunctional silanes." Dalton transactions (Cambridge, England : 2003) vol. 49,23 (2020): 7697-7700. doi: https://doi.org/10.1039/d0dt01668c
Januszewski R, Dutkiewicz M, Franczyk A, Kownacki I. Pt(0)-Catalysed synthesis of new bifunctional silanes. Dalton Trans. 2020 Jun 21;49(23):7697-7700. doi: 10.1039/d0dt01668c. Epub 2020 Jun 08. PMID: 32510084.
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Out-of-plane quasielastic scattering from deuterium using polarized electrons.

Physical review. C, Nuclear physics

Alarcon R, Arenhövel H, Beck R, Bernstein A, Bertozzi W, Boeglin W, Cardman L, Comfort J, Dale D, Dodson G, Dolfini S, Dow K, Epstein M, Farkhondeh M, Gilad S, Görgen J, Holtrop M, Jordan D, Kim W, Kowalski S, Laszewski R, Mandeville J, Margaziotis D, Martinez D, McIlvain T, Miskimen R, Papanicolas C, Tieger D, Turchinetz W, Weinstein L, Williamson S.
PMID: 9970453
Phys Rev C Nucl Phys. 1995 Jun;51(6):3479-3482. doi: 10.1103/physrevc.51.3479.

No abstract available.

Cite
Alarcon R, Arenhövel H, Beck R, et al. Out-of-plane quasielastic scattering from deuterium using polarized electrons. Phys Rev C Nucl Phys. 1995;51(6):3479-3482doi: 10.1103/physrevc.51.3479.
Alarcon, R., Arenhövel, H., Beck, R., Bernstein, A., Bertozzi, W., Boeglin, W., Cardman, L., Comfort, J., Dale, D., Dodson, G., Dolfini, S., Dow, K., Epstein, M., Farkhondeh, M., Gilad, S., Görgen, J., Holtrop, M., Jordan, D., Kim, W., Kowalski, S., Laszewski, R., Mandeville, J., Margaziotis, D., Martinez, D., McIlvain, T., Miskimen, R., Papanicolas, C., Tieger, D., Turchinetz, W., Weinstein, L., & Williamson, S. (1995). Out-of-plane quasielastic scattering from deuterium using polarized electrons. Physical review. C, Nuclear physics, 51(6), 3479-3482. https://doi.org/10.1103/physrevc.51.3479
Alarcon, et al. "Out-of-plane quasielastic scattering from deuterium using polarized electrons." Physical review. C, Nuclear physics vol. 51,6 (1995): 3479-3482. doi: https://doi.org/10.1103/physrevc.51.3479
Alarcon R, Arenhövel H, Beck R, Bernstein A, Bertozzi W, Boeglin W, Cardman L, Comfort J, Dale D, Dodson G, Dolfini S, Dow K, Epstein M, Farkhondeh M, Gilad S, Görgen J, Holtrop M, Jordan D, Kim W, Kowalski S, Laszewski R, Mandeville J, Margaziotis D, Martinez D, McIlvain T, Miskimen R, Papanicolas C, Tieger D, Turchinetz W, Weinstein L, Williamson S. Out-of-plane quasielastic scattering from deuterium using polarized electrons. Phys Rev C Nucl Phys. 1995 Jun;51(6):3479-3482. doi: 10.1103/physrevc.51.3479. PMID: 9970453.
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