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12,868 results
  • Repigmentation in vitiligo universalis after starting dialysis-could they be related? [Journal Article]
    Clin Kidney J 2019; 12(5):735-736Farahbakhsh N, Nielson C, Gillihan R
  • Vitiligo is an acquired disorder of pigmentation characterized by the development of white macules and patches on the skin. Although multiple theories have been proposed to understand the underlying pathophysiology behind the pigment loss, the exact etiology remains unknown. Vitiligo universalis is an extremely rare variant that causes nearly complete depigmentation of the entire body surface. Tr…
  • Therapeutic effects of iNOS inhibition against vitiligo in an animal model. [Journal Article]
    Eur J Transl Myol 2019; 29(3):8383Mansourpour H, Ziari K, … Poor AH
  • Nitric oxide (NO) is involved in several biological processes, but its role in human melanogenesis and vitiligo need further studies. Previous studies revealed that exposure to UVA and UVB were capable of the inducing nitric oxide production in keratinocytes and melanocytes through the activation of constitutive nitric oxide synthase, whereas inducible nitric oxide synthase overexpression has bee…
  • Clinical & ultrastructural evaluation of the effect of fractional CO2 laser on facial melasma. [Journal Article]
    Ultrastruct Pathol 2019; :1-10El-Sinbawy ZG, Abdelnabi NM, … Elgarhy LH
  • Melasma represents the most obvious and disfiguring change of the face leading to psychological problems especially in females. Ablative lasers have also been used by many professionals to treat melasma, although there is few scientific data supporting this indication. The exact mechanism of action of ablative lasers in melasma is not yet clear enough. We aimed to evaluate the ultrastructural eff…
  • Waardenburg syndrome with dry eyes: A rare association. [Case Reports]
    Taiwan J Ophthalmol 2019 Jul-Sep; 9(3):198-201Shrinkhal , Singh A, … Yadav P
  • Waardenburg syndrome (WS) is a rare congenital disorder primarily characterized by characteristic facial abnormalities as dystopia canthorum and synophrys; depigmentation of the hair, skin (premature graying of hair), and/or the iris of both eyes; and/or congenital deafness. Here, we report a rare case of WS with associated dry eyes. A 4-year-old female presented with blue eyes and no tear and na…
  • Café noir spots: A Feature of Familial Progressive Hyper- and Hypopigmentation. [Letter]
    J Eur Acad Dermatol Venereol 2019Gülseren D, Güleray N, … Ersoy-Evans S
  • Familial progressive hyper- and hypopigmentation (FPHH) is a rare genodermatosis characterized by multiple café au lait spots and hypopigmented ash-leaf macules intermingled with blotchy hyperpigmentation (1,2). Herein, we describe a Turkish FPHH patient with café-noir spots. A 16-year-old male presented to our Pediatric Dermatology Clinic, with extensive hyperpigmentation, irregular brown patche…
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