MeSH Review:
Pigmentation Disorders
- Minocycline-induced immune thrombocytopenia presenting as Schamberg's disease. D'Addario, S.F., Bryan, M.E., Stringer, W.A., Johnson, S.M. Journal of drugs in dermatology : JDD. (2003)
- Regulation of tyrosinase gene expression by cAMP in B16 melanoma cells involves two CATGTG motifs surrounding the TATA box: implication of the microphthalmia gene product. Bertolotto, C., Bille, K., Ortonne, J.P., Ballotti, R. J. Cell Biol. (1996)
- SCF/c-kit signaling is required for cyclic regeneration of the hair pigmentation unit. Botchkareva, N.V., Khlgatian, M., Longley, B.J., Botchkarev, V.A., Gilchrest, B.A. FASEB J. (2001)
- Free radical reduction in the human epidermis. Schallreuter, K.U., Wood, J.M. Free Radic. Biol. Med. (1989)
- Oral pentoxifylline vs topical betamethasone in Schamberg disease: a comparative randomized investigator-blinded parallel-group trial. Panda, S., Malakar, S., Lahiri, K. Archives of dermatology. (2004)
- Should pentoxifylline be regarded as an effective treatment for Schamberg's disease? Basak, P.Y., Ergin, S. J. Am. Acad. Dermatol. (2001)
- Pentoxifylline for Schamberg's disease. Burkhart, C.G., Burkhart, K.M. J. Am. Acad. Dermatol. (1998)
- Efficacy of topical treatment of pigmentation skin disorders with plant hydroquinone glucosides as assessed by quantitative color analysis. Clarys, P., Barel, A. J. Dermatol. (1998)
- Photoprotection and skin coloring by oral carotenoids. Raab, W.P., Tronnier, H., Wiskemann, A. Dermatologica (1985)
- Successful treatment of Schamberg's disease with pentoxifylline. Kano, Y., Hirayama, K., Orihara, M., Shiohara, T. J. Am. Acad. Dermatol. (1997)
- Close association between sequence polymorphism in the KIT gene and the roan coat color in horses. Marklund, S., Moller, M., Sandberg, K., Andersson, L. Mamm. Genome (1999)
- Value of the assay for IgA-containing circulating immune complexes in Henoch-Schönlein purpura. Kawana, S., Ohta, M., Nishiyama, S. Dermatologica (1986)
- Mutation of the MITF gene in albinism-deafness syndrome (Tietz syndrome). Amiel, J., Watkin, P.M., Tassabehji, M., Read, A.P., Winter, R.M. Clin. Dysmorphol. (1998)