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Website Value | $1091 |
Alexa Rank | 623008 |
Monthly Visits | 12112 |
Daily Visits | 404 |
Monthly Earnings | $60.56 |
Daily Earnings | $2.02 |
Country: United States
Metropolitan Area: Ashburn
Postal Reference Code: 20149
Latitude: 39.0481
Longitude: -77.4728
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Title: | JDD: Scientific, Peer-Reviewed Dermatology Journal Indexed with | |
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JDD: Scientific, Peer-Reviewed Dermatology Journal Indexed with MEDLINE/PubMed |
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/articles/dermatology/S1545961604P0081X: | |
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Cutaneous Vasculitis Secondary to Ramipril: Scientific, Peer-Reviewed Dermatology Article Indexed with MEDLINE/PubMed |
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Scientific, peer-reviewed Dermatology article, indexed with MEDLINE/PubMed: Cutaneous Vasculitis Secondary to Ramipril : A 61-year-old patient who had been treated with lisinopril in the past without any problems was commenced on ramipril for left ventricular dysfunction. He developed a painful symmetrical purpuric eruption over both feet after three days. A full vasculitis screen was negative. Ramipril was stopped and he required a course of steroids after which the rash improved slowly. The ACE inhibitors can cause various skin side effects; however, it rarely causes cutaneous vasculitis. Ramipril-induced cutaneous vasculitis is particularly rare and our case was atypical because the patient had tolerated lisinopril before. Previous successful treatment with one ACE inhibitor does not rule out the vasculitis caused by the drug from the same group. Here we report ramipril-induced cutaneous vasculitis in a patient who required steroid therapy to control it. |
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/articles/dermatology/S1545961616S0021X: | |
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A New Approach in Topical Hyaluronic Acid: Going Beyond Instant Benefits to Restore Epidermal HA Homeostasis: Scientific, Peer-Reviewed Dermatology Article Indexed with MEDLINE/PubMed |
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Scientific, peer-reviewed Dermatology article, indexed with MEDLINE/PubMed: A New Approach in Topical Hyaluronic Acid: Going Beyond Instant Benefits to Restore Epidermal HA Homeostasis : Skin aging is a combination of multifactorial mechanisms that are not fully understood. Intrinsic and extrinsic factors modulate skin aging, activating distinctive processes that share similar molecular pathways. One of the main characteristics of youthful skin is its large capacity to retain water, and this decreases significantly as we age. A key molecule involved in maintaining skin hydration is hyaluronic acid (HA). Concentration of HA in the skin is determined by the complex balance between its synthesis, deposition, ociation with cellular structures, and degradation. HA bio-equivalency and bio-compatibility have been fundamental in keeping this macromolecule as the favorite of the skincare industry for decades. Scientific evidence now shows that topically applied HA is unable to penetrate the skin and is rapidly degraded on the skin surface. [censored]
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/articles/dermatology/S1545961606P0370X: | |
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Non-Sarcoidal, Non- r id Granuloma in Common Variable Immunodeficiency: Scientific, Peer-Reviewed Dermatology Article Indexed with MEDLINE/PubMed [censored]
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Scientific, peer-reviewed Dermatology article, indexed with MEDLINE/PubMed: Non-Sarcoidal, Non- r id Granuloma in Common Variable Immunodeficiency : Sarcoidal (non-caseating) or r id granulomas are cutaneous manifestations of common variable immunodeficiency (CVID). In this case report, we describe a patient with CVID but with non-sarcoidal, non- r id granuloma. The 29- year-old Egyptian male patient presented with a vitiliginous patch on the chin of 1 year duration and multiple recurrent warts on the hands and feet of 8 years duration. He is a known case of CVID with chronic diarrhea, recurrent otitis media, pneumonia, purulent conjunctivitis, septic arthritis, hepato-splenomegaly, and generalized lymphadenopathy. In addition, he had evidence of multiple non-tender subcutaneous nodules predominantly juxta-articular and recurrent rheumatoid-like arthritis. The skin overlying the nodules was either normal or slightly erythematous. Laboratory findings revealed markedly reduced serum immunoglobulins (IgG 3.4, n=7.2-16.9 g/l; IgA 0.1, n=0.69-3.82 g/l and IgM 0.1, n=0.63-2.77 g/l) and deficient T cell function. Histopathologic examination of a skin nodule showed well demarcated areas of fibrinoid degeneration of collagen that stain homogeneously and are surrounded by histiocytes in a palisading arrangement, suggestive of granuloma annulare. No microorganisms could be detected. Serology for rheumatoid factor and HIV infection has been persistently negative. Although most infections, including common warts responded well to intravenous immunoglobulin replacement thrapy (12 g/i.v., every 2 weeks) and oral board spectrum antibiotic therapy, the subcutaneous nodules persisted. The vitiliginous patch responded favorably and disappeared within 24 local PUVA sessions. Since skin nodules are asymptomatic, no further treatment was given. [censored]
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/articles/dermatology/S1545961615P0279X: | |
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A Phase I Safety and Pharmacokinetic Study of ATX-101: Injectable, Synthetic Deoxycholic Acid for Submental Contouring: Scientific, Peer-Reviewed Dermatology Article Indexed with MEDLINE/PubMed |
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Scientific, peer-reviewed Dermatology article, indexed with MEDLINE/PubMed: A Phase I Safety and Pharmacokinetic Study of ATX-101: Injectable, Synthetic Deoxycholic Acid for Submental Contouring : ATX-101 (deoxycholic acid [DCA] injection) is a proprietary formulation of pure synthetic DCA. When injected into subcutaneous fat, ATX-101 results in focal adipocytolysis, the targeted destruction of fat cells. ATX-101 is undergoing investigation as an injectable drug for contouring the submental area by reducing submental fat (SMF). The purpose of this study was to evaluate the safety and pharmacokinetics (PK) of the maximal the utic dose of ATX-101 (100 mg total dose). Following PK evaluation of endogenous DCA, subjects (N = 24) received subcutaneous injections of ATX-101 (2 mg/cm2, with or without 0.9% benzyl alcohol) into SMF; PK evaluation was repeated periodically over 24 hours. Endogenous DCA plasma concentrations measured prior to injection were highly variable within and between subjects. Similarly, following ATX-101 injection, DCA plasma concentrations were highly variable, peaked rapidly, and returned to the range observed for endogenous values by 24 hours postdose. All subjects experienced at least 1 adverse event (AE). No death, serious AE, or AE-related discontinuations occurred. The majority of AEs were transient, ociated with the area treated, and of mild or moderate severity. No clinically significant changes were reported for laboratory test results, vital signs, or Holter electrocardiograms postdosing. These data support the favorable safety and efficacy observations of ATX-101 as an injectable drug to reduce SMF. J Drugs Dermatol. 2015;14(3):279-284. [censored]
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