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Circumstances of the ambulatory prescription of quinolones in Urology and opportunities for intervention.

Journal of healthcare quality research

Tiago V, Sousa D, Luque J, Rei MJ, Borrega R, Cabedal M, Raimundo PO.
PMID: 34862151
J Healthc Qual Res. 2021 Nov 30; doi: 10.1016/j.jhqr.2021.10.011. Epub 2021 Nov 30.

INTRODUCTION AND OBJECTIVES: Antimicrobial stewardship programmes (AMSP) seldom focus on ambulatory prescribing. Our AMSP primarily supervises in-hospital prescribing, but as we aim to include the ambulatory setting, we sought opportunities for intervention on ambulatory quinolone prescription.MATERIALS AND METHODS: We...

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Tiago V, Sousa D, Luque J, et al. Circumstances of the ambulatory prescription of quinolones in Urology and opportunities for intervention. J Healthc Qual Res. 2021;doi: 10.1016/j.jhqr.2021.10.011.
Tiago, V., Sousa, D., Luque, J., Rei, M. J., Borrega, R., Cabedal, M., & Raimundo, P. O. (2021). Circumstances of the ambulatory prescription of quinolones in Urology and opportunities for intervention. Journal of healthcare quality research, . https://doi.org/10.1016/j.jhqr.2021.10.011
Tiago, V, et al. "Circumstances of the ambulatory prescription of quinolones in Urology and opportunities for intervention." Journal of healthcare quality research vol. (2021). doi: https://doi.org/10.1016/j.jhqr.2021.10.011
Tiago V, Sousa D, Luque J, Rei MJ, Borrega R, Cabedal M, Raimundo PO. Circumstances of the ambulatory prescription of quinolones in Urology and opportunities for intervention. J Healthc Qual Res. 2021 Nov 30; doi: 10.1016/j.jhqr.2021.10.011. Epub 2021 Nov 30. PMID: 34862151.
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Holotoxin disassembly by protein disulfide isomerase is less efficient for Escherichia coli heat-labile enterotoxin than cholera toxin.

Scientific reports

Serrano A, Guyette JL, Heim JB, Taylor M, Cherubin P, Krengel U, Teter K, Tatulian SA.
PMID: 34997016
Sci Rep. 2022 Jan 07;12(1):34. doi: 10.1038/s41598-021-03939-9.

Cholera toxin (CT) and Escherichia coli heat-labile enterotoxin (LT) are structurally similar AB

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Serrano A, Guyette JL, Heim JB, et al. Holotoxin disassembly by protein disulfide isomerase is less efficient for Escherichia coli heat-labile enterotoxin than cholera toxin. Sci Rep. 2022;12(1):34doi: 10.1038/s41598-021-03939-9.
Serrano, A., Guyette, J. L., Heim, J. B., Taylor, M., Cherubin, P., Krengel, U., Teter, K., & Tatulian, S. A. (2022). Holotoxin disassembly by protein disulfide isomerase is less efficient for Escherichia coli heat-labile enterotoxin than cholera toxin. Scientific reports, 12(1), 34. https://doi.org/10.1038/s41598-021-03939-9
Serrano, Albert, et al. "Holotoxin disassembly by protein disulfide isomerase is less efficient for Escherichia coli heat-labile enterotoxin than cholera toxin." Scientific reports vol. 12,1 (2022): 34. doi: https://doi.org/10.1038/s41598-021-03939-9
Serrano A, Guyette JL, Heim JB, Taylor M, Cherubin P, Krengel U, Teter K, Tatulian SA. Holotoxin disassembly by protein disulfide isomerase is less efficient for Escherichia coli heat-labile enterotoxin than cholera toxin. Sci Rep. 2022 Jan 07;12(1):34. doi: 10.1038/s41598-021-03939-9. PMID: 34997016.
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Dental education in a capitalistic society.

Journal of dental education

Hein JW.
PMID: 6575045
J Dent Educ. 1983 May;47(5):304-6.

No abstract available.

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Hein JW. Dental education in a capitalistic society. J Dent Educ. 1983;47(5):304-6
Hein, J. W. (1983). Dental education in a capitalistic society. Journal of dental education, 47(5), 304-6.
Hein, J W. "Dental education in a capitalistic society." Journal of dental education vol. 47,5 (1983): 304-6.
Hein JW. Dental education in a capitalistic society. J Dent Educ. 1983 May;47(5):304-6. PMID: 6575045.
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Model Combining Tumor Molecular and Clinicopathologic Risk Factors Predicts Sentinel Lymph Node Metastasis in Primary Cutaneous Melanoma.

JCO precision oncology

Bellomo D, Arias-Mejias SM, Ramana C, Heim JB, Quattrocchi E, Sominidi-Damodaran S, Bridges AG, Lehman JS, Hieken TJ, Jakub JW, Pittelkow MR, DiCaudo DJ, Pockaj BA, Sluzevich JC, Cappel MA, Bagaria SP, Perniciaro C, Tjien-Fooh FJ, van Vliet MH, Dwarkasing J, Meves A.
PMID: 32405608
JCO Precis Oncol. 2020;4:319-334. doi: 10.1200/po.19.00206. Epub 2020 Apr 14.

PURPOSE: More than 80% of patients who undergo sentinel lymph node (SLN) biopsy have no nodal metastasis. Here we describe a model that combines clinicopathologic and molecular variables to identify patients with thin and intermediate thickness melanomas who may...

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Bellomo D, Arias-Mejias SM, Ramana C, et al. Model Combining Tumor Molecular and Clinicopathologic Risk Factors Predicts Sentinel Lymph Node Metastasis in Primary Cutaneous Melanoma. JCO Precis Oncol. 2020;4:319-334doi: 10.1200/po.19.00206.
Bellomo, D., Arias-Mejias, S. M., Ramana, C., Heim, J. B., Quattrocchi, E., Sominidi-Damodaran, S., Bridges, A. G., Lehman, J. S., Hieken, T. J., Jakub, J. W., Pittelkow, M. R., DiCaudo, D. J., Pockaj, B. A., Sluzevich, J. C., Cappel, M. A., Bagaria, S. P., Perniciaro, C., Tjien-Fooh, F. J., van Vliet, M. H., Dwarkasing, J., & Meves, A. (2020). Model Combining Tumor Molecular and Clinicopathologic Risk Factors Predicts Sentinel Lymph Node Metastasis in Primary Cutaneous Melanoma. JCO precision oncology, 4319-334. https://doi.org/10.1200/po.19.00206
Bellomo, Domenico, et al. "Model Combining Tumor Molecular and Clinicopathologic Risk Factors Predicts Sentinel Lymph Node Metastasis in Primary Cutaneous Melanoma." JCO precision oncology vol. 4 (2020): 319-334. doi: https://doi.org/10.1200/po.19.00206
Bellomo D, Arias-Mejias SM, Ramana C, Heim JB, Quattrocchi E, Sominidi-Damodaran S, Bridges AG, Lehman JS, Hieken TJ, Jakub JW, Pittelkow MR, DiCaudo DJ, Pockaj BA, Sluzevich JC, Cappel MA, Bagaria SP, Perniciaro C, Tjien-Fooh FJ, van Vliet MH, Dwarkasing J, Meves A. Model Combining Tumor Molecular and Clinicopathologic Risk Factors Predicts Sentinel Lymph Node Metastasis in Primary Cutaneous Melanoma. JCO Precis Oncol. 2020;4:319-334. doi: 10.1200/po.19.00206. Epub 2020 Apr 14. PMID: 32405608; PMCID: PMC7220172.
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Effect of beta-blocker therapy in patients with or without left ventricular systolic dysfunction after acute myocardial infarction.

European heart journal. Cardiovascular pharmacotherapy

Joo SJ, Kim SY, Choi JH, Park HK, Beom JW, Lee JG, Chae SC, Kim HS, Kim YJ, Cho MC, Kim CJ, Rha SW, Yoon J, Jeong MH.
PMID: 32289158
Eur Heart J Cardiovasc Pharmacother. 2021 Nov 03;7(6):475-482. doi: 10.1093/ehjcvp/pvaa029.

AIMS: This observational study aimed to investigate the association between beta-blocker therapy and clinical outcomes in patients with acute myocardial infarction (AMI), especially with mid-range or preserved left ventricular systolic function.METHODS AND RESULTS: Among 13 624 patients enrolled in...

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Joo SJ, Kim SY, Choi JH, et al. Effect of beta-blocker therapy in patients with or without left ventricular systolic dysfunction after acute myocardial infarction. Eur Heart J Cardiovasc Pharmacother. 2021;7(6):475-482doi: 10.1093/ehjcvp/pvaa029.
Joo, S. J., Kim, S. Y., Choi, J. H., Park, H. K., Beom, J. W., Lee, J. G., Chae, S. C., Kim, H. S., Kim, Y. J., Cho, M. C., Kim, C. J., Rha, S. W., Yoon, J., & Jeong, M. H. (2021). Effect of beta-blocker therapy in patients with or without left ventricular systolic dysfunction after acute myocardial infarction. European heart journal. Cardiovascular pharmacotherapy, 7(6), 475-482. https://doi.org/10.1093/ehjcvp/pvaa029
Joo, Seung-Jae, et al. "Effect of beta-blocker therapy in patients with or without left ventricular systolic dysfunction after acute myocardial infarction." European heart journal. Cardiovascular pharmacotherapy vol. 7,6 (2021): 475-482. doi: https://doi.org/10.1093/ehjcvp/pvaa029
Joo SJ, Kim SY, Choi JH, Park HK, Beom JW, Lee JG, Chae SC, Kim HS, Kim YJ, Cho MC, Kim CJ, Rha SW, Yoon J, Jeong MH. Effect of beta-blocker therapy in patients with or without left ventricular systolic dysfunction after acute myocardial infarction. Eur Heart J Cardiovasc Pharmacother. 2021 Nov 03;7(6):475-482. doi: 10.1093/ehjcvp/pvaa029. PMID: 32289158.
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Effect of Agar/AgNP Composite Film Packaging on Refrigerated Beef Loin Quality.

Membranes

Hong SI, Cho Y, Rhim JW.
PMID: 34677516
Membranes (Basel). 2021 Sep 29;11(10). doi: 10.3390/membranes11100750.

Fresh beef loin was packaged with 0-2% silver nanoparticles (AgNPs) incorporated agar films to investigate the effect of antimicrobial packaging on meat quality changes in terms of microbiological and physicochemical properties. Raw beef cuts were directly inoculated with

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Hong SI, Cho Y, Rhim JW. Effect of Agar/AgNP Composite Film Packaging on Refrigerated Beef Loin Quality. Membranes (Basel). 2021;11(10)doi: 10.3390/membranes11100750.
Hong, S. I., Cho, Y., & Rhim, J. W. (2021). Effect of Agar/AgNP Composite Film Packaging on Refrigerated Beef Loin Quality. Membranes, 11(10), . https://doi.org/10.3390/membranes11100750
Hong, Seok-In, et al. "Effect of Agar/AgNP Composite Film Packaging on Refrigerated Beef Loin Quality." Membranes vol. 11,10 (2021). doi: https://doi.org/10.3390/membranes11100750
Hong SI, Cho Y, Rhim JW. Effect of Agar/AgNP Composite Film Packaging on Refrigerated Beef Loin Quality. Membranes (Basel). 2021 Sep 29;11(10). doi: 10.3390/membranes11100750. PMID: 34677516; PMCID: PMC8538384.
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High-pressure microfluidic control in lab-on-a-chip devices using mobile polymer monoliths.

Analytical chemistry

Hasselbrink EF, Shepodd TJ, Rehm JE.
PMID: 12380812
Anal Chem. 2002 Oct 01;74(19):4913-8. doi: 10.1021/ac025761u.

We have developed a nonstick polymer formulation for creating moving parts inside of microfluidic channels and have applied the technique to create piston-based devices that overcome several microfluidic flow control challenges. The parts were created bycompletely filling the channels...

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Hasselbrink EF, Shepodd TJ, Rehm JE. High-pressure microfluidic control in lab-on-a-chip devices using mobile polymer monoliths. Anal Chem. 2002;74(19):4913-8doi: 10.1021/ac025761u.
Hasselbrink, E. F., Shepodd, T. J., & Rehm, J. E. (2002). High-pressure microfluidic control in lab-on-a-chip devices using mobile polymer monoliths. Analytical chemistry, 74(19), 4913-8. https://doi.org/10.1021/ac025761u
Hasselbrink, Ernest F, et al. "High-pressure microfluidic control in lab-on-a-chip devices using mobile polymer monoliths." Analytical chemistry vol. 74,19 (2002): 4913-8. doi: https://doi.org/10.1021/ac025761u
Hasselbrink EF, Shepodd TJ, Rehm JE. High-pressure microfluidic control in lab-on-a-chip devices using mobile polymer monoliths. Anal Chem. 2002 Oct 01;74(19):4913-8. doi: 10.1021/ac025761u. PMID: 12380812.
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Impact of Antibiotic Prescribing Patterns on Susceptibilities of Uropathogens in Children below 24 Months Old.

Antibiotics (Basel, Switzerland)

Park JY, Kang HM, Kwak EM, Rhim JW, Ahn YH, Lee H, Jeong DC, Kang JH.
PMID: 33339282
Antibiotics (Basel). 2020 Dec 16;9(12). doi: 10.3390/antibiotics9120915.

Monitoring regional antibiotic resistance patterns of uropathogens are important for deciding suitable empirical antibiotics for urinary tract infections (UTIs) in children. This study aimed to investigate regional differences in antimicrobial susceptibility patterns of

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Park JY, Kang HM, Kwak EM, et al. Impact of Antibiotic Prescribing Patterns on Susceptibilities of Uropathogens in Children below 24 Months Old. Antibiotics (Basel). 2020;9(12)doi: 10.3390/antibiotics9120915.
Park, J. Y., Kang, H. M., Kwak, E. M., Rhim, J. W., Ahn, Y. H., Lee, H., Jeong, D. C., & Kang, J. H. (2020). Impact of Antibiotic Prescribing Patterns on Susceptibilities of Uropathogens in Children below 24 Months Old. Antibiotics (Basel, Switzerland), 9(12), . https://doi.org/10.3390/antibiotics9120915
Park, Ji Young, et al. "Impact of Antibiotic Prescribing Patterns on Susceptibilities of Uropathogens in Children below 24 Months Old." Antibiotics (Basel, Switzerland) vol. 9,12 (2020). doi: https://doi.org/10.3390/antibiotics9120915
Park JY, Kang HM, Kwak EM, Rhim JW, Ahn YH, Lee H, Jeong DC, Kang JH. Impact of Antibiotic Prescribing Patterns on Susceptibilities of Uropathogens in Children below 24 Months Old. Antibiotics (Basel). 2020 Dec 16;9(12). doi: 10.3390/antibiotics9120915. PMID: 33339282; PMCID: PMC7767190.
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Musculoskeletal Ultrasound: Basic Principles.

Seminars in musculoskeletal radiology

Read JW.
PMID: 11387102
Semin Musculoskelet Radiol. 1998;2(3):203-210. doi: 10.1055/s-2008-1080102.

Equipment selection and examination technique are critical issues in the practice of musculoskeletal ultrasound.

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Read JW. Musculoskeletal Ultrasound: Basic Principles. Semin Musculoskelet Radiol. 1998;2(3):203-210doi: 10.1055/s-2008-1080102.
Read, J. W. (1998). Musculoskeletal Ultrasound: Basic Principles. Seminars in musculoskeletal radiology, 2(3), 203-210. https://doi.org/10.1055/s-2008-1080102
Read, J.W.. "Musculoskeletal Ultrasound: Basic Principles." Seminars in musculoskeletal radiology vol. 2,3 (1998): 203-210. doi: https://doi.org/10.1055/s-2008-1080102
Read JW. Musculoskeletal Ultrasound: Basic Principles. Semin Musculoskelet Radiol. 1998;2(3):203-210. doi: 10.1055/s-2008-1080102. PMID: 11387102.
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Development of an intelligent polymerized crystalline colloidal array colorimetric reagent.

Analytical chemistry

Reese E, Baltusavich ME, Keim JP, Asher SA.
PMID: 11721897
Anal Chem. 2001 Nov 01;73(21):5038-42. doi: 10.1021/ac010667j.

We have developed a novel colorimetric reagent for the determination of Pb2+, pH, and temperature. This colorimetric reagent consists of a dispersion of approximately 100-microm particles composed of an intelligent polymerized crystalline colloidal array (IPCCA). The IPCCA particles are...

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Reese E, Baltusavich ME, Keim JP, et al. Development of an intelligent polymerized crystalline colloidal array colorimetric reagent. Anal Chem. 2001;73(21):5038-42doi: 10.1021/ac010667j.
Reese, E., Baltusavich, M. E., Keim, J. P., & Asher, S. A. (2001). Development of an intelligent polymerized crystalline colloidal array colorimetric reagent. Analytical chemistry, 73(21), 5038-42. https://doi.org/10.1021/ac010667j
Reese, E, et al. "Development of an intelligent polymerized crystalline colloidal array colorimetric reagent." Analytical chemistry vol. 73,21 (2001): 5038-42. doi: https://doi.org/10.1021/ac010667j
Reese E, Baltusavich ME, Keim JP, Asher SA. Development of an intelligent polymerized crystalline colloidal array colorimetric reagent. Anal Chem. 2001 Nov 01;73(21):5038-42. doi: 10.1021/ac010667j. PMID: 11721897.
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Guest editorial.

Missouri medicine

KEIM JH.
PMID: 13565877
Mo Med. 1958 Aug;55(8):889-90.

No abstract available.

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KEIM JH. Guest editorial. Mo Med. 1958;55(8):889-90
KEIM, J. H. (1958). Guest editorial. Missouri medicine, 55(8), 889-90.
KEIM, J H. "Guest editorial." Missouri medicine vol. 55,8 (1958): 889-90.
KEIM JH. Guest editorial. Mo Med. 1958 Aug;55(8):889-90. PMID: 13565877.
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The attractiveness of choice alternatives when freedom to choose is eliminated by a social agent.

Journal of personality

Hammock T, Brehm JW.
PMID: 5971672
J Pers. 1966 Dec;34(4):546-54. doi: 10.1111/j.1467-6494.1966.tb02370.x.

No abstract available.

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Hammock T, Brehm JW. The attractiveness of choice alternatives when freedom to choose is eliminated by a social agent. J Pers. 1966;34(4):546-54doi: 10.1111/j.1467-6494.1966.tb02370.x.
Hammock, T., & Brehm, J. W. (1966). The attractiveness of choice alternatives when freedom to choose is eliminated by a social agent. Journal of personality, 34(4), 546-54. https://doi.org/10.1111/j.1467-6494.1966.tb02370.x
Hammock, T, and Brehm, J W. "The attractiveness of choice alternatives when freedom to choose is eliminated by a social agent." Journal of personality vol. 34,4 (1966): 546-54. doi: https://doi.org/10.1111/j.1467-6494.1966.tb02370.x
Hammock T, Brehm JW. The attractiveness of choice alternatives when freedom to choose is eliminated by a social agent. J Pers. 1966 Dec;34(4):546-54. doi: 10.1111/j.1467-6494.1966.tb02370.x. PMID: 5971672.
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Showing 25 to 36 of 184 entries