Search Results - "Spruance, Spotswood L"
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Novel Composite Efficacy Measure To Demonstrate the Rationale and Efficacy of Combination Antiviral–Anti-Inflammatory Treatment for Recurrent Herpes Simplex Labialis
Published in Antimicrobial Agents and Chemotherapy (01-03-2014)“…Classifications Services AAC Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit…”
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2
Single-dose, patient-initiated famciclovir: A randomized, double-blind, placebo-controlled trial for episodic treatment of herpes labialis
Published in Journal of the American Academy of Dermatology (01-07-2006)“…The brief period of viral replication in recurrent herpes labialis lesions suggests shorter therapeutic regimens are a logical episodic treatment strategy. We…”
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Acyclovir Cream for Treatment of Herpes Simplex Labialis: Results of Two Randomized, Double-Blind, Vehicle-Controlled, Multicenter Clinical Trials
Published in Antimicrobial Agents and Chemotherapy (01-07-2002)“…Classifications Services AAC Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit…”
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4
Early treatment of cold sores with topical ME-609 decreases the frequency of ulcerative lesions: A randomized, double-blind, placebo-controlled, patient-initiated clinical trial
Published in Journal of the American Academy of Dermatology (2011)“…Background Prior pilot studies support the use of antiviral medications with topical corticosteroids for herpes simplex labialis (HSL). ME-609 (Xerese,…”
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High-Dose, Short-Duration, Early Valacyclovir Therapy for Episodic Treatment of Cold Sores: Results of Two Randomized, Placebo-Controlled, Multicenter Studies
Published in Antimicrobial Agents and Chemotherapy (01-03-2003)“…Classifications Services AAC Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit…”
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6
Topical Iontophoretic Administration of Acyclovir for the Episodic Treatment of Herpes Labialis: A Randomized, Double-Blind, Placebo-Controlled, Clinic-Initiated Trial
Published in Clinical infectious diseases (15-08-2006)“…Background. Multiple studies of the use of acyclovir for the treatment of herpes labialis have suggested that the nominal efficacy of the topical formulation…”
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Application of a Topical Immune Response Modifier, Resiquimod Gel, to Modify the Recurrence Rate of Recurrent Genital Herpes: A Pilot Study
Published in The Journal of infectious diseases (15-07-2001)“…Resiquimod (R-848), a topically active immune response modifier, induced production of interferon-α and interleukin-12 in cultured blood mononuclear cells and…”
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Evaluation of Imiquimod 5% Cream to Modify the Natural History of Herpes Labialis: A Pilot Study
Published in Clinical infectious diseases (15-09-2005)“…Background. Imiquimod is currently approved for the treatment of genital warts and has been shown to decrease recurrences of genital herpes in the guinea pig…”
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9
Hazard ratio in clinical trials
Published in Antimicrobial agents and chemotherapy (01-08-2004)Get full text
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Recurrent Antiviral-Resistant Genital Herpes in an Immunocompetent Patient
Published in The Journal of infectious diseases (01-07-2005)“…Herpes simplex virus type 2 (HSV-2) resistance to antiviral drugs has been described primarily in immunocompromised patients. We report an apparently…”
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Glycoprotein-D–Adjuvant Vaccine to Prevent Genital Herpes
Published in The New England journal of medicine (21-11-2002)“…Two double-blind, controlled trials assessed the efficacy of a glycoprotein-D–subunit vaccine to prevent genital herpes disease. The vaccine elicited humoral…”
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Peroral Famciclovir in the Treatment of Experimental Ultraviolet Radiation-Induced Herpes Simplex Labialis: A Double-Blind, Dose-Ranging, Placebo-Controlled, Multicenter Trial
Published in The Journal of infectious diseases (01-02-1999)“…Three doses of famciclovir were tested for treatment of experimental ultraviolet radiation (UVR)-induced herpes labialis. Patients received 125, 250, or 500 mg…”
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Transcranial Doppler quantification of residual shunt after percutaneous patent foramen ovale closure: correlation of device efficacy with intracardiac anatomic measures
Published in Journal of interventional cardiology (01-06-2012)“…Percutaneous, mechanical closure of defects of the atrial septum fails to completely resolve shunting in up to 20% of cases. Little is known about the factors…”
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Transcranial doppler quantification of residual shunt after percutaneous patent foramen ovale closure: efficacy of the GORE(®) HELEX septal occluder
Published in Journal of interventional cardiology (01-08-2011)“…Ideally, percutaneous, mechanical closure of defects of the atrial septum should completely resolve shunt. To achieve this goal, more information is needed…”
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Low-Intensity Laser Therapy for Recurrent Herpes Labialis
Published in Journal of investigative dermatology (01-07-2000)Get full text
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Prospects for Control of Herpes Simplex Virus Disease through Immunization
Published in Clinical infectious diseases (01-03-2000)“…Herpes simplex viruses (HSVs) can cause a variety of infections, including genital herpes. Despite effective antiviral therapy, HSV infections remain a…”
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Herpes simplex virus as a cause of Bell's palsy
Published in Reviews in medical virology (01-09-2000)Get full text
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N-docosanol (Abreva) for herpes labialis: Problems and questions
Published in Journal of the American Academy of Dermatology (01-09-2002)Get full text
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Clinical significance of antiviral therapy for episodic treatment of herpes labialis: exploratory analyses of the combined data from two valaciclovir trials
Published in Journal of antimicrobial chemotherapy (01-05-2004)“…Valaciclovir (Valtrex) 2 g twice daily for 1 day was recently approved in the United States for treatment of cold sores. In order to apply more clinically…”
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Effective treatment of herpes simplex labialis with penciclovir cream: combined results of two trials
Published in The Journal of the American Dental Association (1939) (01-03-2002)“…Two randomized, double-blind, parallel-group clinical trials were conducted in Europe and North America to compare the efficacy and safety of topical 1 percent…”
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