198 related articles for article (PubMed ID: 24079542)
1. 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]
2. 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]
3. 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]
4. Moniliform blepharosis in lipoid proteinosis with a homozygous ECM1 gene mutation.
Barut Selver O; Palamar M; Onay H; Furundaoturan O; Akalın T; Noyan MA
Ophthalmic Genet; 2018 Aug; 39(4):550-552. PubMed ID: 29718750
[No Abstract] [Full Text] [Related]
5. Lipoid proteinosis in two siblings: a report from south India.
Shivaswamy KN; Thappa DM; Laxmisha C; Jayanthi S
Dermatol Online J; 2003 Dec; 9(5):12. PubMed ID: 14996385
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. 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]
9. Eyelid lesions in lipoid proteinosis or Urbach-Wiethe disease: case report and review of the literature.
Callizo M; Ibáñez-Flores N; Laue J; Cuadrado V; Graell X; Sancho JM
Orbit; 2011 Oct; 30(5):242-4. PubMed ID: 21957955
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. Lipoid proteinosis: A clinical and molecular study in Egyptian patients.
Afifi HH; Amr KS; Tosson AMS; Hassan TA; Mehrez MI; El-Kamah GY
Gene; 2017 Sep; 628():308-314. PubMed ID: 28720532
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Ocular manifestations in lipoid proteinosis: A rare clinical entity.
Kamath SJ; Marthala H; Manapragada B
Indian J Ophthalmol; 2015 Oct; 63(10):793-5. PubMed ID: 26655007
[TBL] [Abstract][Full Text] [Related]
16. [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]
17. Epidermodysplasia verruciformis in lipoid proteinosis: case report and discussion of pathophysiology.
O'Blenes C; Pasternak S; Issekutz A; Gillis J; Chowdhury D; Finlayson L
Pediatr Dermatol; 2015; 32(1):118-21. PubMed ID: 23534907
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Moniliform Blepharosis of Lipoid Proteinosis.
Belliveau MJ; Alkhotani A; Ali A
JAMA Ophthalmol; 2015 Jul; 133(7):e150688. PubMed ID: 26158437
[No Abstract] [Full Text] [Related]
20. Lipoid proteinosis: phenotypic heterogeneity in Iranian families with c.507delT mutation in ECM1.
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
Exp Dermatol; 2015 Mar; 24(3):220-2. PubMed ID: 25529926
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]