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Dive into the research topics where Ernest E. Lee is active.

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Featured researches published by Ernest E. Lee.


International Journal of Dermatology | 2005

UVB phototherapy and skin cancer risk: a review of the literature

Ernest E. Lee; John Koo; Tim Berger

Background  UVB phototherapy is a common treatment modality for psoriasis and other skin diseases. Although UVB has been in use for many decades, many clinicians are hesitant to use this type of phototherapy because of concern over increasing the skin cancer risk. Over the past 20 years, numerous studies have been published examining this issue, but a consensus or analysis of the skin cancer risk is required for the dermatologist to make an educated risk–benefit analysis.


International Journal of Dermatology | 2005

Effect of ethnicity on the risk of developing nonmelanoma skin cancer following long-term PUVA therapy.

Jenny E. Murase; Ernest E. Lee; John Koo

Background  Research demonstrating an increased incidence of skin cancer with psoralen plus ultraviolet A (PUVA) therapy has reflected the Caucasian experience. Our objective was to review the literature on skin cancer risk associated with long‐term PUVA therapy in non‐Caucasians.


American Journal of Clinical Dermatology | 2001

Treatment of urticaria. An evidence-based evaluation of antihistamines.

Ernest E. Lee; Howard I. Maibach

Urticaria is a cutaneous syndrome characterized by dermal edema (wheal) and erythema (flare) that blanches with pressure. The lesions typically last less than 24 hours and are usually pruritic. In 1983, Christensen and Maibach summarized the theory behind the use of histamine H1 receptor antagonists (antihistamines) in clinical dermatology. These agents remain the mainstay of treatment for urticaria.This article reviews the medical literature on the effectiveness of antihistamines in urticarial syndromes, including acute, chronic idiopathic and the physical urticarias.Older antihistamines, such as chlorpheniramine and hydroxyzine, are effective in the treatment of urticarias, but they also have marked sedative and anticholinergic effects. Newer nonsedating antihistamines (second-generation antihistamines) have been developed that have reduced adverse effects because they do not cross the blood-brain barrier; these agents (acrivastine, cetirizine, loratadine, mizolastine, fexofenadine, ebastine, azelastine and epinastine) cause significantly less sedation and psychomotor impairment than their older counterparts.A review of the literature reveals that there are few studies which document the efficacy of second-generation antihistamines in the treatment of acute urticaria, a biologic entity that usually resolves within 3 weeks. We did not identify controlled studies that suggested superiority of any antihistamine in the treatment of acute urticaria. Loratadine or cetirizine, and possibly mizolastine, appear to be treatments of choice for chronic idiopathic urticaria. For symptomatic dermatographism, the combination of an antihistamine and an H2 antagonist, e.g. chlorpheniramine and cimetidine, appears to be effective. Very few studies have been conducted on the use of antihistamines in the treatment of cold, cholinergic, and pressure urticaria.Antihistamines are the mainstay of urticarial therapy. This evidence-based review suggests that there are efficacy differences between newer, nonsedating antihistamines and older agents in some forms of the disorder. Clearly, further well-controlled clinical trials in larger numbers of patients are needed to clarify the role of these agents in the treatment of urticaria.


Contact Dermatitis | 2001

Is contact allergy in man lifelong? An overview of patch test follow-ups

Ernest E. Lee; Howard I. Maibach

In contradistinction from certain strains of mice, contact allergy in man is hypothesized to be either lifelong or at least to last for years. We examined follow‐up studies on contact allergy, as evaluated by patch testing, attempting to quantify its natural history. The allergens include colophonium, gold sodium thiosulfate, nickel, and cobalt. At present, due to technical limitations, we cannot state in quantitative terms whether contact allergy in man is lifelong and whether its clinical manifestations change. Thus, we list some criteria for future studies which may help resolve the above question.


Exogenous Dermatology | 2002

Role of Vehicles in Diagnosing Contact Allergy: An Update

Ernest E. Lee; Howard I. Maibach

In suspected allergic contact dermatitis, the proper choice of vehicles for patch testing may be critical. The role of vehicles in diagnostic patch testing has been summarized, suggesting that improved delivery systems might significantly increase the reproducibility and reliability of patch tests. We review the literature subsequent to 1992 for advances in our knowledge of the optimization of vehicles for patch testing. A universal vehicle more efficient than petrolatum or water remains elusive; in vitro percutaneous penetration data provide insight that questions standard dogma.


Archive | 2012

Pharmacogenetics and Dermatology

Tsippora Shainhouse; Ernest E. Lee; Howard I. Maibach


Archive | 2007

Is Contact Allergy Lifelong in Humans? An Overview of Patch-Test Follow-Ups

Ernest E. Lee; Howard I. Maibach


Exogenous Dermatology | 2002

Symposium III: First International Symposium on Diagnosis, Treatment, and Prevention of Dermatological Conditions in Health Care Workers

S. Moshe; A. Ingber; D. Slodovnik; Y. Lerman; Ernest E. Lee; Howard I. Maibach


Exogenous Dermatology | 2002

Symposium V: Evidence-Based Contact Dermatitis

S. Moshe; A. Ingber; D. Slodovnik; Y. Lerman; Ernest E. Lee; Howard I. Maibach


Exogenous Dermatology | 2002

Symposium II: Contact, Occupational and Environmental Dermatitis in Latin America

S. Moshe; A. Ingber; D. Slodovnik; Y. Lerman; Ernest E. Lee; Howard I. Maibach

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John Koo

University of California

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Tim Berger

University of California

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