445 related articles for article (PubMed ID: 16225617)
1. 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
Br J Dermatol; 2005 Nov; 153(5):1019-22. PubMed ID: 16225617
[TBL] [Abstract][Full Text] [Related]
2. Extracellular matrix protein 1 gene (ECM1) mutations in lipoid proteinosis and genotype-phenotype correlation.
Hamada T; Wessagowit V; South AP; Ashton GH; Chan I; Oyama N; Siriwattana A; Jewhasuchin P; Charuwichitratana S; Thappa DM; Jeevankumar B; Lenane P; Krafchik B; Kulthanan K; Shimizu H; Kaya TI; Erdal ME; Paradisi M; Paller AS; Seishima M; Hashimoto T; McGrath JA
J Invest Dermatol; 2003 Mar; 120(3):345-50. PubMed ID: 12603844
[TBL] [Abstract][Full Text] [Related]
3. A novel missense mutation in exon 7 of the ECM1 gene in an Iranian lipoid proteinosis patient.
Izadi F; Mahjoubi F; Farhadi M; Tavakoli MM; Samanian S
Genet Mol Res; 2012 Nov; 11(4):3955-60. PubMed ID: 23212332
[TBL] [Abstract][Full Text] [Related]
4. Clinical and molecular characterization of lipoid proteinosis in Namaqualand, South Africa.
Van Hougenhouck-Tulleken W; Chan I; Hamada T; Thornton H; Jenkins T; McLean WH; McGrath JA; Ramsay M
Br J Dermatol; 2004 Aug; 151(2):413-23. PubMed ID: 15327549
[TBL] [Abstract][Full Text] [Related]
5. The molecular basis of lipoid proteinosis: mutations in extracellular matrix protein 1.
Chan I; Liu L; Hamada T; Sethuraman G; McGrath JA
Exp Dermatol; 2007 Nov; 16(11):881-90. PubMed ID: 17927570
[TBL] [Abstract][Full Text] [Related]
6. Clinical and molecular abnormalities in lipoid proteinosis.
Desmet S; Devos SA; Chan I; Hamada T; Dhooge I; McGrath JA; Naeyaert JM
Eur J Dermatol; 2005; 15(5):344-6. PubMed ID: 16172042
[TBL] [Abstract][Full Text] [Related]
7. Lipoid proteinosis presenting with an unusual nonsense Q32X mutation in exon 2 of the extracellular matrix protein 1 gene.
Chelvan HT; Narasimhan M; Shankaran Subramanian A; Subramaniam S
Australas J Dermatol; 2012 Nov; 53(4):e79-82. PubMed ID: 23157792
[TBL] [Abstract][Full Text] [Related]
8. Clinical and histopathological response to acitretin therapy in lipoid proteinosis.
Akoglu G; Karaduman A; Ergin S; Erkin G; Gokoz O; Unal OF; Hamada T
J Dermatolog Treat; 2011 Jun; 22(3):178-83. PubMed ID: 20666665
[TBL] [Abstract][Full Text] [Related]
9. A failure of mucocutaneous lymphangiogenesis may underlie the clinical features of lipoid proteinosis.
Uchida T; Hayashi H; Inaoki M; Miyamoto T; Fujimoto W
Br J Dermatol; 2007 Jan; 156(1):152-7. PubMed ID: 17199583
[TBL] [Abstract][Full Text] [Related]
10. A novel splice-site mutation in ECM-1 gene in a consanguineous family with lipoid proteinosis.
Horev L; Potikha T; Ayalon S; Molho-Pessach V; Ingber A; Gany MA; Edin BS; Glaser B; Zlotogorski A
Exp Dermatol; 2005 Dec; 14(12):891-7. PubMed ID: 16274456
[TBL] [Abstract][Full Text] [Related]
11. Identification of recurrent c.742G>T nonsense mutation in ECM1 in Pakistani families suffering from lipoid proteinosis.
Nasir M; Rahman SB; Sieber CM; Mir A; Latif A; Ahmad N; Malik SA; Hameed A
Mol Biol Rep; 2014; 41(4):2085-92. PubMed ID: 24413997
[TBL] [Abstract][Full Text] [Related]
12. Lipoid proteinosis: case report and review of the literature.
Di Giandomenico S; Masi R; Cassandrini D; El-Hachem M; De Vito R; Bruno C; Santorelli FM
Acta Otorhinolaryngol Ital; 2006 Jun; 26(3):162-7. PubMed ID: 17063986
[TBL] [Abstract][Full Text] [Related]
13. Molecular basis of lipoid proteinosis in a Libyan family.
Chan I; El-Zurghany A; Zendah B; Benghazil M; Oyama N; Hamada T; McGrath JA
Clin Exp Dermatol; 2003 Sep; 28(5):545-8. PubMed ID: 12950350
[TBL] [Abstract][Full Text] [Related]
14. Hyalinosis cutis et mucosae.
Vago B; Hausser I; Hennies HC; Enk A; Jappe U
J Dtsch Dermatol Ges; 2007 May; 5(5):401-5. PubMed ID: 17451385
[TBL] [Abstract][Full Text] [Related]
15. Extracellular matrix protein 1 gene (ECM1) mutations in nine Iranian families with lipoid proteinosis.
Izadi F; Mahjoubi F; Farhadi M; Kalayinia S; Bidmeshkipour A; Tavakoli MM; Samanian S
Indian J Med Res; 2016 Mar; 143(3):303-7. PubMed ID: 27241643
[TBL] [Abstract][Full Text] [Related]
16. Molecular analysis of lipoid proteinosis: identification of a novel nonsense mutation in the ECM1 gene in a Pakistani family.
Nasir M; Latif A; Ajmal M; Qamar R; Naeem M; Hameed A
Diagn Pathol; 2011 Jul; 6():69. PubMed ID: 21791056
[TBL] [Abstract][Full Text] [Related]
17. [Lipoid proteinosis of Urbach-Wiethe: a case report].
Daldon PE; Baraldi Moreira M; Talarico SR
Dermatol Online J; 2011 Nov; 17(11):8. PubMed ID: 22136864
[TBL] [Abstract][Full Text] [Related]
18. 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
J Dermatol Sci; 2005 Jun; 38(3):215-24. PubMed ID: 15927815
[TBL] [Abstract][Full Text] [Related]
19. Familial Moniliform Blepharosis: Clinical, Histopathological and Genetic Correlation.
Ranjan P; Mishra D; Plesec T; Pratap VB; Singh AD
Ophthalmic Genet; 2015 Jun; 36(2):160-4. PubMed ID: 24079542
[TBL] [Abstract][Full Text] [Related]
20. Novel human pathological mutations. Gene symbol: ECM1. Disease: Lipoid Proteinosis.
Hameed A; Nasir M; Ajmal M; Latif L
Hum Genet; 2009 Aug; 126(2):336. PubMed ID: 19694009
[No Abstract] [Full Text] [Related]
[Next] [New Search]
