Below are the most recent publications written about "Lipoid Proteinosis of Urbach and Wiethe" by people in Profiles.
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Youssefian L, Vahidnezhad H, Daneshpazhooh M, Abdollahzadeh S, Talari H, Khoshnevisan A, Chams-Davatchi C, Mobasher R, Li Q, Uitto J, Akhondzadeh S, Tabrizi M. Lipoid proteinosis: phenotypic heterogeneity in Iranian families with c.507delT mutation in ECM1. Exp Dermatol. 2015 Mar; 24(3):220-2.
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Mcgrath JA. Lipoid proteinosis. Handb Clin Neurol. 2015; 132:317-22.
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Salih MA, Abu-Amero KK, Alrasheed S, Alorainy IA, Liu L, McGrath JA, Van Maldergem L, Al-Faky YH, AlSuhaibani AH, Oystreck DT, Bosley TM. Molecular and neurological characterizations of three Saudi families with lipoid proteinosis. BMC Med Genet. 2011 Feb 24; 12:31.
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Horev L, Wollina DU, Potikha T, Hafner A, Ingber A, Liu L, McGrath JA, Zlotogorski A. Lipoid proteinosis: identification of two novel mutations in the human ECM-1 gene and lack of genotype-phenotype correlation. Acta Derm Venereol. 2009; 89(5):528-9.
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Chan I, Liu L, Hamada T, Sethuraman G, McGrath JA. The molecular basis of lipoid proteinosis: mutations in extracellular matrix protein 1. Exp Dermatol. 2007 Nov; 16(11):881-90.
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Sercu S, Poumay Y, Herphelin F, Liekens J, Beek L, Zwijsen A, Wessagowit V, Huylebroeck D, McGrath JA, Merregaert J. Functional redundancy of extracellular matrix protein 1 in epidermal differentiation. Br J Dermatol. 2007 Oct; 157(4):771-5.
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Fujimoto N, Terlizzi J, Aho S, Brittingham R, Fertala A, Oyama N, McGrath JA, Uitto J. Extracellular matrix protein 1 inhibits the activity of matrix metalloproteinase 9 through high-affinity protein/protein interactions. Exp Dermatol. 2006 Apr; 15(4):300-7.
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Kowalewski C, Kozlowska A, Chan I, G?rska M, Wozniak K, Jablonska S, McGrath JA. Three-dimensional imaging reveals major changes in skin microvasculature in lipoid proteinosis and lichen sclerosus. J Dermatol Sci. 2005 Jun; 38(3):215-24.
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Chan I, Sethuraman G, Sharma VK, Bruning E, Hamada T, McGrath JA. Molecular basis of lipoid proteinosis in two Indian siblings. J Dermatol. 2004 Sep; 31(9):764-6.
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Chan I, Bingewar G, Patil K, Nayak C, Wadhwa SL, McGrath JA. An Indian child with lipoid proteinosis resulting from a recurrent frameshift mutation (507delT) in the extracellular matrix protein 1 gene. Br J Dermatol. 2004 Sep; 151(3):726-7.