BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

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]
    of 10.