
Adalimumab (Humira, AbbVie) is demonstrating effectiveness in early trials for the treatment of hidradenitis suppurativa, a condition that as of yet has no approved treatment.

Adalimumab (Humira, AbbVie) is demonstrating effectiveness in early trials for the treatment of hidradenitis suppurativa, a condition that as of yet has no approved treatment.

The Food and Drug Administration has granted 510(k) clearance to Nucletron for Esteya, an electronic brachytherapy system for high-precision skin cancer treatment.

Cimzia (certolizumab pegol, UCB) has been approved by the Food and Drug Administration for the treatment of psoriatic arthritis in adult patients.

Long-term analysis of patients with advanced melanoma taking ipilimumab demonstrated survival rates of up to 10 years, according to recent research.

Strathspey Crown Holdings has acquired Evolus, which will allow Strathspey Crown’s wholly-owned subsidiary, Alphaeon Corporation, the exclusive license to market the botulinum toxin type A product Evosyal.

Among the most troublesome stage 2 requirements of the Medicare and Medicaid EHR Incentive Programs is the requirement that 5 percent of patients use the Internet to communicate with practices, an expert says.

New genetic testing methods may not only help identify the potential risk for individuals to develop certain diseases but may also open the door for more targeted therapies and management strategies, which could be of particular benefit in higher risk patient populations.

Vitamin D has been in and out of favor with physicians and their patients over the years. Even today, the controversies over the embattled vitamin still continue regarding its safe and beneficial daily allowance. According to the recent research, however, and guidelines from the Institute of Medicine (IOM), the majority of Americans are taking enough vitamin D.

In the European Union (EU), a simple approval process for hyaluronic acid (HA) products has yielded a broader array of offerings than what’s available in the United States, an expert says. Easier EU approvals also have given HA a virtual lock on the European filler market, he adds.

Dermatologists are using an evolving collection of combination therapies designed to address different aspects of disease, monotherapy limitations and failures, as well as enhance treatment.

Factors including UV exposure and psychological stress can accelerate the aging process, partly through their influence on telomeres, an expert says. Research is beginning to uncover strategies to counter these forces, however.

Not all botulinum toxins are equally safe for neurons, according to a new study by Harvard researchers.

Nobody likes overly busy presentation slides - especially the audience members who must decipher them on the fly, an expert says.

Dermatologists generally know that the sensitivity of many pathogens to the antibiotics used to treat them is decreasing, experts say. But many dermatologists may not appreciate their specialty’s role in potentially fueling the problem.

Dr. Derm owns 15 dermatology practices. Dr. Skin owns 12 similar practices. Recently a venture capitalist bought all of these practices and merged them as one practice. All of the dermatologists were given a 20-mile, two-year restrictive covenant.

The Food and Drug Administration has approved Stelara (ustekinumab, Janssen Biotech) alone or in combination with methotrexate for the treatment of psoriatic arthritis in patients ages 18 and older.

Researchers have identified a specific type of T cell that summons other immune cells to the site of skin injuries, shedding light on how these “first responders” contribute to wound healing.

There appears to be a rebirth of measles among unvaccinated children and adults, despite high immunization rates among children in the United States, according to the Centers for Disease Control and Prevention (CDC).

Sleep deprivation can increase the signs of aging in the skin and decrease the skin’s ability to recover after sun exposure, a recent clinical trial indicates.

Women who suffer from migraines may have a slightly higher risk of rosacea, a study suggests.

Technology in devices being used for airport security could lead to the development of more advanced skin cancer screening, recent research suggests.

The Food and Drug Administration has approved Botox (onabotulinumtoxinA, Allergan) for the temporary improvement of moderate-to-severe lateral canthal lines.

As many of half of the warts in children ages 4 to 12 will resolve without treatment, a recent study indicates.

For many physicians, no matter their specialty, the one thing that keeps them up at night is fear of medical malpractice lawsuits. Here are the top ways to avoid medical malpractice lawsuits.

A fractional nonablative laser module, the ResurFX for the Lumenis M22 platform, has been given 510(k) clearance from the Food and Drug Administration.

Take a look at these new products available for dermatologists.

Giving a great lecture requires ongoing refinement and the ability to be honest with one’s audience and oneself, according to an expert.

Alma Lasers begins offering Practice for Success seminars this month.

The Food and Drug Administration has approved Galderma’s topical gel Mirvaso (brimonidine 0.33 percent) for the treatment of facial erythema from rosacea.

Physicians discussed sunscreen use with patients at less than 1 percent of visits, according to recent study results.