Results 81 to 90 of about 1,636 (159)
A Caucasian boy, born to unrelated parents, and with no family history of psoriasis or atopy, developed chronic psoriasiform dermatitis on the palmar surface of the fingers when he was a year old.
R. Grimalt +3 more
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Sjogren-Larsson syndrome: biochemical defects and follow up in three cases
Sjogren-Larsson syndrome is a rare disorder that consists of congenital ichthyosis and neurological symptoms due to an enzymatic defect of fatty aldehyde dehydrogenase in the fatty alcohol cycle. We report three cases of Sjogren-Larsson syndrome in which
Taube, MBP +4 more
core
Kepeğe karşı etkili şampuan formüllerinin hazırlanması ve etkinliklerinin değerlendirilmesi
1. ÖZET Saçtaki kepek problemi, pekçok nedene bağlı olsa da, en önemli nedenlerinden biri Malassezia furfur' un neden olduğu mantar enfeksiyonudur.
Gökçay, Esin
core
BACKGROUND: The aim of this study is to evaluate efficacy and tolerability of a complete skin care line consisting of an oral supplement in two distinct formulations for males and females, and a topical cream device in the treatment of mild and moderate ...
Potenza C. +8 more
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Laser and Light Therapies for Acne
Acne vulgaris is a very common cutaneous disorder which can cause permanent scarring and disfigurement.Acne is a multifactorial disorder of pilosebaceous units and affects the areas of skin with the greatest concentration of sebaceous follicles such as ...
Rajabi-Estarabadi, Ali +5 more
core +1 more source
A Rare Case of Hereditary Ichthyosis: Case Report
Hereditary ichthyosis is a group of genetic skin disorders characterized by dry, scaly skin. These conditions vary widely in severity and are often classified based on genetic and clinical features.
Mwagobele, Lusajo +4 more
core +1 more source
Formulation and Evaluation of a Medicated Nail Lacquer for the Treatment of Onychomycosis [PDF]
INTRODUCTION:Over the last decades the treatment of illness has been accomplished by administrating drugs to human body via various routes namely oral, parental, topical, inhalation etc.
Aswani, V M
core
Papillon-Lefèvre syndrome: from then until now
Papillon-Lefévre syndrome (PLS) is a very rare autosomal recessive trait characterized by palmoplantar hyperkeratosis and severe generalized early-onset periodontitis leading to premature loss of both primary and permanent dentitions.
Hattab, Faiez N.
core
The Effectiveness of Topical Keratolytics (Alpha Hydroxy Acids/Beta Hydroxy Acids/Urea) in Treating Keratosis Pilaris: A Review of the Literature. [PDF]
Dampa E.
europepmc +1 more source
Long follow-up treating CHILD nevi with topical cholesterol and statins. [PDF]
Ferradoza MTN +5 more
europepmc +1 more source

