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M. Halabi-Tawil, F. Lionnet, R. Girot, C. Bachmeyer, P. Lévy and S. Aractingi, “Sickle Cell Leg Ulcers: A Frequently Disabling Complication and a Marker of Severity,” British Journal of Dermatology, Vol. 158, No. 2, 2008, pp. 339-344. doi:10.1111/j.1365-2133.2007.08323.x

has been cited by the following article:

• TITLE: Cutaneous Manifestations of Sickle Cell Disease

  AUTHORS: Heather Jones, Morey Blinder, Milan Anadkat

  KEYWORDS: Sickle Cell Disease; Leg Ulcers; Pseudoxanthoma Elasticum; Nitric Oxide Deficiency; Hydroxyurea

  JOURNAL NAME: Open Journal of Blood Diseases, Vol.3 No.3, September 16, 2013

  ABSTRACT: Sickle cell disease is an inherited erythrocyte disorder affecting multiple organ systems. As individuals are living well into middle age due to advances in diagnosis and treatment, further disease-related complications are being recognized. This article reviews the cutaneous manifestations of sickle cell disease including leg ulcers and acquired pseudoxanthoma elasticum.