Similar articles

• The molecular basis of lipoid proteinosis: mutations in extracellular matrix protein 1.

  Chan I, Liu L, Hamada T, Sethuraman G, McGrath JA. Chan I, et al. Exp Dermatol. 2007 Nov;16(11):881-90. doi: 10.1111/j.1600-0625.2007.00608.x. Exp Dermatol. 2007. PMID: 17927570 Review.
• Clinical and molecular abnormalities in lipoid proteinosis.

  Desmet S, Devos SA, Chan I, Hamada T, Dhooge I, McGrath JA, Naeyaert JM. Desmet S, et al. Eur J Dermatol. 2005 Sep-Oct;15(5):344-6. Eur J Dermatol. 2005. PMID: 16172042
• A novel mutation of the extracellular matrix protein 1 gene (ECM1) in a patient with lipoid proteinosis (Urbach-Wiethe disease) from Sicily.

  Lupo I, Cefalu AB, Bongiorno MR, Daniele O, Valenti V, Noto D, Camarda R, Savettieri G, Aricò M, Averna MR. Lupo I, et al. Br J Dermatol. 2005 Nov;153(5):1019-22. doi: 10.1111/j.1365-2133.2005.06842.x. Br J Dermatol. 2005. PMID: 16225617
• Three-dimensional imaging reveals major changes in skin microvasculature in lipoid proteinosis and lichen sclerosus.

  Kowalewski C, Kozłowska A, Chan I, Górska M, Woźniak K, Jabłońska S, McGrath JA. Kowalewski C, et al. J Dermatol Sci. 2005 Jun;38(3):215-24. doi: 10.1016/j.jdermsci.2005.01.012. Epub 2005 Mar 3. J Dermatol Sci. 2005. PMID: 15927815
• Lipoid proteinosis.

  Mcgrath JA. Mcgrath JA. Handb Clin Neurol. 2015;132:317-22. doi: 10.1016/B978-0-444-62702-5.00023-8. Handb Clin Neurol. 2015. PMID: 26564090 Review.