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Nonsurgical healing of large periradicular lesions using a triple antibiotic paste: A case series.

Contemporary clinical dentistry

Taneja S, Kumari M, Parkash H.
PMID: 22114375
Contemp Clin Dent. 2010 Jan;1(1):31-5. doi: 10.4103/0976-237X.62519.

The infection of the root canal system is considered to be a polymicrobial infection, consisting of both aerobic and anaerobic bacteria. Because of the complexity of the root canal infection, it is unlikely that any single antibiotic could result...

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Taneja S, Kumari M, Parkash H. Nonsurgical healing of large periradicular lesions using a triple antibiotic paste: A case series. Contemp Clin Dent. 2010;1(1):31-5doi: 10.4103/0976-237X.62519.
Taneja, S., Kumari, M., & Parkash, H. (2010). Nonsurgical healing of large periradicular lesions using a triple antibiotic paste: A case series. Contemporary clinical dentistry, 1(1), 31-5. https://doi.org/10.4103/0976-237X.62519
Taneja, Sonali, et al. "Nonsurgical healing of large periradicular lesions using a triple antibiotic paste: A case series." Contemporary clinical dentistry vol. 1,1 (2010): 31-5. doi: https://doi.org/10.4103/0976-237X.62519
Taneja S, Kumari M, Parkash H. Nonsurgical healing of large periradicular lesions using a triple antibiotic paste: A case series. Contemp Clin Dent. 2010 Jan;1(1):31-5. doi: 10.4103/0976-237X.62519. PMID: 22114375; PMCID: PMC3220065.
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Disruption of the serotonergic system after neonatal hypoxia-ischemia in a rodent model.

Neurology research international

Buller KM, Wixey JA, Reinebrant HE.
PMID: 22474587
Neurol Res Int. 2012;2012:650382. doi: 10.1155/2012/650382. Epub 2012 Feb 08.

Identifying which specific neuronal phenotypes are vulnerable to neonatal hypoxia-ischemia, where in the brain they are damaged, and the mechanisms that produce neuronal losses are critical to determine the anatomical substrates responsible for neurological impairments in hypoxic-ischemic brain-injured neonates....

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Buller KM, Wixey JA, Reinebrant HE. Disruption of the serotonergic system after neonatal hypoxia-ischemia in a rodent model. Neurol Res Int. 2012;2012:650382doi: 10.1155/2012/650382.
Buller, K. M., Wixey, J. A., & Reinebrant, H. E. (2012). Disruption of the serotonergic system after neonatal hypoxia-ischemia in a rodent model. Neurology research international, 2012650382. https://doi.org/10.1155/2012/650382
Buller, Kathryn M, et al. "Disruption of the serotonergic system after neonatal hypoxia-ischemia in a rodent model." Neurology research international vol. 2012 (2012): 650382. doi: https://doi.org/10.1155/2012/650382
Buller KM, Wixey JA, Reinebrant HE. Disruption of the serotonergic system after neonatal hypoxia-ischemia in a rodent model. Neurol Res Int. 2012;2012:650382. doi: 10.1155/2012/650382. Epub 2012 Feb 08. PMID: 22474587; PMCID: PMC3306961.
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Disruption of the serotonergic system after neonatal hypoxia-ischemia in a rodent model.

Neurology research international

Buller KM, Wixey JA, Reinebrant HE.
PMID: 22474587
Neurol Res Int. 2012;2012:650382. doi: 10.1155/2012/650382. Epub 2012 Feb 08.

Identifying which specific neuronal phenotypes are vulnerable to neonatal hypoxia-ischemia, where in the brain they are damaged, and the mechanisms that produce neuronal losses are critical to determine the anatomical substrates responsible for neurological impairments in hypoxic-ischemic brain-injured neonates....

Cite
Buller KM, Wixey JA, Reinebrant HE. Disruption of the serotonergic system after neonatal hypoxia-ischemia in a rodent model. Neurol Res Int. 2012;2012:650382doi: 10.1155/2012/650382.
Buller, K. M., Wixey, J. A., & Reinebrant, H. E. (2012). Disruption of the serotonergic system after neonatal hypoxia-ischemia in a rodent model. Neurology research international, 2012650382. https://doi.org/10.1155/2012/650382
Buller, Kathryn M, et al. "Disruption of the serotonergic system after neonatal hypoxia-ischemia in a rodent model." Neurology research international vol. 2012 (2012): 650382. doi: https://doi.org/10.1155/2012/650382
Buller KM, Wixey JA, Reinebrant HE. Disruption of the serotonergic system after neonatal hypoxia-ischemia in a rodent model. Neurol Res Int. 2012;2012:650382. doi: 10.1155/2012/650382. Epub 2012 Feb 08. PMID: 22474587; PMCID: PMC3306961.
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Attenuation of diabetic retinopathy by enhanced inhibition of MMP-2 and MMP-9 using aspirin and minocycline in streptozotocin-diabetic rats.

American journal of translational research

Bhatt LK, Addepalli V.
PMID: 20407607
Am J Transl Res. 2010 Feb 12;2(2):181-9.

Interruptions of Matrix Metalloproteinase-2 (MMP-2) and Matrix Metalloproteinase-9 (MMP-9) have been shown to reduce the ensuing threatening risk factors of vascular complications of diabetes by alteration in Extracellular Matrix (ECM). We hypothesized that minocycline induced MMP-2 and MMP-9 inhibition...

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Bhatt LK, Addepalli V. Attenuation of diabetic retinopathy by enhanced inhibition of MMP-2 and MMP-9 using aspirin and minocycline in streptozotocin-diabetic rats. Am J Transl Res. 2010;2(2):181-9
Bhatt, L. K., & Addepalli, V. (2010). Attenuation of diabetic retinopathy by enhanced inhibition of MMP-2 and MMP-9 using aspirin and minocycline in streptozotocin-diabetic rats. American journal of translational research, 2(2), 181-9.
Bhatt, Lokesh Kumar, and Addepalli, Veeranjaneyulu. "Attenuation of diabetic retinopathy by enhanced inhibition of MMP-2 and MMP-9 using aspirin and minocycline in streptozotocin-diabetic rats." American journal of translational research vol. 2,2 (2010): 181-9.
Bhatt LK, Addepalli V. Attenuation of diabetic retinopathy by enhanced inhibition of MMP-2 and MMP-9 using aspirin and minocycline in streptozotocin-diabetic rats. Am J Transl Res. 2010 Feb 12;2(2):181-9. PMID: 20407607; PMCID: PMC2855628.
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Separation Differences Among Phenyl Hydride, UDC Cholesterol and Bidentate C8 Stationary Phases for Stability Indicating Methods of Tetracyclines: Journal of Liquid Chromatography & Related Technologies.

Journal of liquid chromatography & related technologies

Young JE, Matyska MT, Azad AK, Yoc SE, Pesek JJ.
PMID: 24748763
J Liq Chromatogr Relat Technol. 2013 Apr 01;36(7):926-942. doi: 10.1080/10826076.2012.678457.

Formulation extracts of tetracycline hydrochloride (HCl), minocycline hydrochloride (HCl), and doxycycline hyclate were degraded by strong acidic conditions and heating. Subsequently, components of the extracts were separated by Bidentate C8, Phenyl Hydride and Cholesterol (UDC) HPLC columns operating in...

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Young JE, Matyska MT, Azad AK, et al. Separation Differences Among Phenyl Hydride, UDC Cholesterol and Bidentate C8 Stationary Phases for Stability Indicating Methods of Tetracyclines: Journal of Liquid Chromatography & Related Technologies. J Liq Chromatogr Relat Technol. 2013;36(7):926-942doi: 10.1080/10826076.2012.678457.
Young, J. E., Matyska, M. T., Azad, A. K., Yoc, S. E., & Pesek, J. J. (2013). Separation Differences Among Phenyl Hydride, UDC Cholesterol and Bidentate C8 Stationary Phases for Stability Indicating Methods of Tetracyclines: Journal of Liquid Chromatography & Related Technologies. Journal of liquid chromatography & related technologies, 36(7), 926-942. https://doi.org/10.1080/10826076.2012.678457
Young, Joshua E, et al. "Separation Differences Among Phenyl Hydride, UDC Cholesterol and Bidentate C8 Stationary Phases for Stability Indicating Methods of Tetracyclines: Journal of Liquid Chromatography & Related Technologies." Journal of liquid chromatography & related technologies vol. 36,7 (2013): 926-942. doi: https://doi.org/10.1080/10826076.2012.678457
Young JE, Matyska MT, Azad AK, Yoc SE, Pesek JJ. Separation Differences Among Phenyl Hydride, UDC Cholesterol and Bidentate C8 Stationary Phases for Stability Indicating Methods of Tetracyclines: Journal of Liquid Chromatography & Related Technologies. J Liq Chromatogr Relat Technol. 2013 Apr 01;36(7):926-942. doi: 10.1080/10826076.2012.678457. PMID: 24748763; PMCID: PMC3989202.
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Integrating anti-EGFR therapies in metastatic colorectal cancer.

Journal of gastrointestinal oncology

Haraldsdottir S, Bekaii-Saab T.
PMID: 23997940
J Gastrointest Oncol. 2013 Sep;4(3):285-98. doi: 10.3978/j.issn.2078-6891.2013.028.

Colorectal cancer remains one of the most common causes of cancer diagnoses and mortality in the United States. The treatment of metastatic colorectal cancer has evolved significantly over the last decade with near-tripling of patient survival rate. A significant...

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Haraldsdottir S, Bekaii-Saab T. Integrating anti-EGFR therapies in metastatic colorectal cancer. J Gastrointest Oncol. 2013;4(3):285-98doi: 10.3978/j.issn.2078-6891.2013.028.
Haraldsdottir, S., & Bekaii-Saab, T. (2013). Integrating anti-EGFR therapies in metastatic colorectal cancer. Journal of gastrointestinal oncology, 4(3), 285-98. https://doi.org/10.3978/j.issn.2078-6891.2013.028
Haraldsdottir, Sigurdis, and Bekaii-Saab, Tanios. "Integrating anti-EGFR therapies in metastatic colorectal cancer." Journal of gastrointestinal oncology vol. 4,3 (2013): 285-98. doi: https://doi.org/10.3978/j.issn.2078-6891.2013.028
Haraldsdottir S, Bekaii-Saab T. Integrating anti-EGFR therapies in metastatic colorectal cancer. J Gastrointest Oncol. 2013 Sep;4(3):285-98. doi: 10.3978/j.issn.2078-6891.2013.028. PMID: 23997940; PMCID: PMC3712294.
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Association between ward-specific antimicrobial use density and methicillin-resistant Staphylococcu aureus surveillance: a 60-month study.

Infection and drug resistance

Yoshida J, Kikuchi T, Matsubara N, Asano I, Ogami N.
PMID: 23901286
Infect Drug Resist. 2013 Jul 23;6:59-66. doi: 10.2147/IDR.S45843. Print 2013.

It is not known whether or not ward-specific antimicrobial use density (AUD) affects the ratio of methicillin-resistant Staphylococcus aureus (MRSA) in culture-positive S. aureus. A 60-month study was attempted to ascertain the association between inpatient MRSA ratio and ward-specific...

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Yoshida J, Kikuchi T, Matsubara N, et al. Association between ward-specific antimicrobial use density and methicillin-resistant Staphylococcu aureus surveillance: a 60-month study. Infect Drug Resist. 2013;6:59-66doi: 10.2147/IDR.S45843.
Yoshida, J., Kikuchi, T., Matsubara, N., Asano, I., & Ogami, N. (2013). Association between ward-specific antimicrobial use density and methicillin-resistant Staphylococcu aureus surveillance: a 60-month study. Infection and drug resistance, 659-66. https://doi.org/10.2147/IDR.S45843
Yoshida, Junichi, et al. "Association between ward-specific antimicrobial use density and methicillin-resistant Staphylococcu aureus surveillance: a 60-month study." Infection and drug resistance vol. 6 (2013): 59-66. doi: https://doi.org/10.2147/IDR.S45843
Yoshida J, Kikuchi T, Matsubara N, Asano I, Ogami N. Association between ward-specific antimicrobial use density and methicillin-resistant Staphylococcu aureus surveillance: a 60-month study. Infect Drug Resist. 2013 Jul 23;6:59-66. doi: 10.2147/IDR.S45843. Print 2013. PMID: 23901286; PMCID: PMC3726436.
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Successful treatment of cutaneous botryomycosis with a combination of minocycline and topical heat therapy.

Case reports in dermatology

Ishibashi M, Numata Y, Tagami H, Aiba S.
PMID: 22679424
Case Rep Dermatol. 2012 May;4(2):114-8. doi: 10.1159/000338798. Epub 2012 May 10.

Cutaneous botryomycosis is a chronic focal infection characterized by a granulomatous inflammatory response to bacterial pathogens such as Staphylococcus aureus. Treatment requires antibiotic therapy and may also require surgical debridement. We employed topical heat therapy and oral minocycline. The...

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Ishibashi M, Numata Y, Tagami H, et al. Successful treatment of cutaneous botryomycosis with a combination of minocycline and topical heat therapy. Case Rep Dermatol. 2012;4(2):114-8doi: 10.1159/000338798.
Ishibashi, M., Numata, Y., Tagami, H., & Aiba, S. (2012). Successful treatment of cutaneous botryomycosis with a combination of minocycline and topical heat therapy. Case reports in dermatology, 4(2), 114-8. https://doi.org/10.1159/000338798
Ishibashi, Masaya, et al. "Successful treatment of cutaneous botryomycosis with a combination of minocycline and topical heat therapy." Case reports in dermatology vol. 4,2 (2012): 114-8. doi: https://doi.org/10.1159/000338798
Ishibashi M, Numata Y, Tagami H, Aiba S. Successful treatment of cutaneous botryomycosis with a combination of minocycline and topical heat therapy. Case Rep Dermatol. 2012 May;4(2):114-8. doi: 10.1159/000338798. Epub 2012 May 10. PMID: 22679424; PMCID: PMC3369419.
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Dialysis: Minocycline-EDTA lock reduces bacteremia in dialysis catheters.

Nature reviews. Nephrology

Ireland R.
PMID: 21894184
Nat Rev Nephrol. 2011 Sep 06;7(10):547. doi: 10.1038/nrneph.2011.120.

No abstract available.

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Ireland R. Dialysis: Minocycline-EDTA lock reduces bacteremia in dialysis catheters. Nat Rev Nephrol. 2011;7(10):547doi: 10.1038/nrneph.2011.120.
Ireland, R. (2011). Dialysis: Minocycline-EDTA lock reduces bacteremia in dialysis catheters. Nature reviews. Nephrology, 7(10), 547. https://doi.org/10.1038/nrneph.2011.120
Ireland, Rebecca. "Dialysis: Minocycline-EDTA lock reduces bacteremia in dialysis catheters." Nature reviews. Nephrology vol. 7,10 (2011): 547. doi: https://doi.org/10.1038/nrneph.2011.120
Ireland R. Dialysis: Minocycline-EDTA lock reduces bacteremia in dialysis catheters. Nat Rev Nephrol. 2011 Sep 06;7(10):547. doi: 10.1038/nrneph.2011.120. PMID: 21894184.
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Lymphocutaneous nocardiosis caused by Nocardia otitidiscaviarum: A case report and review of literature.

Journal of natural science, biology, and medicine

Shahapur PR, Peerapur BV, Shahapur RP, Honnutagi RM, Biradar MS.
PMID: 24678228
J Nat Sci Biol Med. 2014 Jan;5(1):197-201. doi: 10.4103/0976-9668.127328.

Nocardia otitidiscaviarum is a rare clinical isolate of primary cutaneous infections. This report describes a case of lymphocutaneous nocardiosis caused by N. otitidiscaviarum. Analysis of 16S ribosomal RNA gene of the isolate and the type strain of N. otitidiscaviarum...

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Shahapur PR, Peerapur BV, Shahapur RP, et al. Lymphocutaneous nocardiosis caused by Nocardia otitidiscaviarum: A case report and review of literature. J Nat Sci Biol Med. 2014;5(1):197-201doi: 10.4103/0976-9668.127328.
Shahapur, P. R., Peerapur, B. V., Shahapur, R. P., Honnutagi, R. M., & Biradar, M. S. (2014). Lymphocutaneous nocardiosis caused by Nocardia otitidiscaviarum: A case report and review of literature. Journal of natural science, biology, and medicine, 5(1), 197-201. https://doi.org/10.4103/0976-9668.127328
Shahapur, Praveen R, et al. "Lymphocutaneous nocardiosis caused by Nocardia otitidiscaviarum: A case report and review of literature." Journal of natural science, biology, and medicine vol. 5,1 (2014): 197-201. doi: https://doi.org/10.4103/0976-9668.127328
Shahapur PR, Peerapur BV, Shahapur RP, Honnutagi RM, Biradar MS. Lymphocutaneous nocardiosis caused by Nocardia otitidiscaviarum: A case report and review of literature. J Nat Sci Biol Med. 2014 Jan;5(1):197-201. doi: 10.4103/0976-9668.127328. PMID: 24678228; PMCID: PMC3961935.
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Antibiotic coated catheter to decrease infection: pilot study.

Revista Brasileira de terapia intensiva

Kurtz P, Rosa P, Penna G, Braga F, Kezen J, Drumond LE, Freitas M, Almeida G, Vegni R, Kalichsztein M, Nobre G.
PMID: 25307004
Rev Bras Ter Intensiva. 2008 Jun;20(2):160-4.

BACKGROUND AND OBJECTIVES: Nosocomial catheter related bloodstream infections (CR-BSI) increase morbidity and mortality in critically ill patients. Central venous catheters (CVC) coated with rifampin and minocycline (RM) decrease rates of colonization and CR-BSI. However, recent trials challenged the clinical...

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Kurtz P, Rosa P, Penna G, et al. Cateter venoso profundo recoberto com antibiótico para reduzir infecção: estudo piloto. Antibiotic coated catheter to decrease infection: pilot study. Rev Bras Ter Intensiva. 2008;20(2):160-4
Kurtz, P., Rosa, P., Penna, G., Braga, F., Kezen, J., Drumond, L. E., Freitas, M., Almeida, G., Vegni, R., Kalichsztein, M., & Nobre, G. (2008). Cateter venoso profundo recoberto com antibiótico para reduzir infecção: estudo piloto. Antibiotic coated catheter to decrease infection: pilot study. Revista Brasileira de terapia intensiva, 20(2), 160-4.
Kurtz, Pedro, et al. "Cateter venoso profundo recoberto com antibiótico para reduzir infecção: estudo piloto." Antibiotic coated catheter to decrease infection: pilot study. Revista Brasileira de terapia intensiva vol. 20,2 (2008): 160-4.
Kurtz P, Rosa P, Penna G, Braga F, Kezen J, Drumond LE, Freitas M, Almeida G, Vegni R, Kalichsztein M, Nobre G. Cateter venoso profundo recoberto com antibiótico para reduzir infecção: estudo piloto. Antibiotic coated catheter to decrease infection: pilot study. Rev Bras Ter Intensiva. 2008 Jun;20(2):160-4. Portuguese. PMID: 25307004.
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Risk factors and antibiotic resistance of pneumonia caused by multidrug resistant Acinetobacter baumannii in pediatric intensive care unit.

World journal of emergency medicine

Cai XF, Sun JM, Bao LS, Li WB.
PMID: 25215064
World J Emerg Med. 2012;3(3):202-7. doi: 10.5847/wjem.j.issn.1920-8642.2012.03.008.

BACKGROUND: With beta-lactam drugs and immunosuppressants widely used, the infection caused by Acinetobacter baumannii (Ab) has become more and more serious with multidrug resistant Acinetobacter baumannii (MDRAb) emerging and worsening rapidly. Compared with other patients, the incidence and multidrug...

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Cai XF, Sun JM, Bao LS, et al. Risk factors and antibiotic resistance of pneumonia caused by multidrug resistant Acinetobacter baumannii in pediatric intensive care unit. World J Emerg Med. 2012;3(3):202-7doi: 10.5847/wjem.j.issn.1920-8642.2012.03.008.
Cai, X. F., Sun, J. M., Bao, L. S., & Li, W. B. (2012). Risk factors and antibiotic resistance of pneumonia caused by multidrug resistant Acinetobacter baumannii in pediatric intensive care unit. World journal of emergency medicine, 3(3), 202-7. https://doi.org/10.5847/wjem.j.issn.1920-8642.2012.03.008
Cai, Xiao-Fang, et al. "Risk factors and antibiotic resistance of pneumonia caused by multidrug resistant Acinetobacter baumannii in pediatric intensive care unit." World journal of emergency medicine vol. 3,3 (2012): 202-7. doi: https://doi.org/10.5847/wjem.j.issn.1920-8642.2012.03.008
Cai XF, Sun JM, Bao LS, Li WB. Risk factors and antibiotic resistance of pneumonia caused by multidrug resistant Acinetobacter baumannii in pediatric intensive care unit. World J Emerg Med. 2012;3(3):202-7. doi: 10.5847/wjem.j.issn.1920-8642.2012.03.008. PMID: 25215064; PMCID: PMC4129778.
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Showing 25 to 36 of 799 entries