Dermatología  Peruana
© Círculo Dermatológico del Perú
ISSN versión electrónica 1028-7175

Dermatol. Per.     1998; 8 (1) : 33-35

MUTACIONES PROTEICAS EN LAS EPIDERMOLISIS BULOSA

Ballona Ch. Rosalía(1)

BIBLIOGRAFÍA

  1. Pearson, R.W. Clinicopathologic types of epidermolysis bullosa and their non dermatological complications. Arch. Dermatol., 1988; 124:718-725.

  1. Fine, J.D., Baver, E.A., Briggaman, R.A. y col. Revised clinical and laboratory criteria for subtypes of inherited epidermolysis bullosa. J. Am. Acad. Dermatol. 1991; 24:119-135.

  2. Begoza Garclia-Bravo. Epidermolisis bullosa hereditaria. Piel, 1997; 12:404-412.

  3. Mellerio, J.E. y col. Recesive EBS and plectin mutations: infantile respiratory complications in two unrelated cases. Br. J. Dermatol., 1997; 137:898-906.

  4. McLean, W.H.l., Lane, E.B. Intermediate filaments in disease. Curr. Opin. Cell Biol., 1995; 7:118-25.

  5. Fuchs, E. Genetic disorders of Keratins and their associated proteins. J. Dermatol. Sci., 1996; 13:181-92.

  6. Rugg, E.L., McLean, Lane, E.B. y col. A functional Knockout of human Keratin 14. Genes Der., 1995;
    8:2563-73.

  7. Jonkman, M.F. y col. Effects of Keratin 14 ablation on the clinical and cellular phenotype in a Kindred with EBS. J. Invest. Dermatol., 1996; 107:764-9.

  8. Gache, Y., Chavanas y col. Defective expression of plectin/HD1 in EBS with muscular distrophy. J Clin Invest., 1996;97: 2289-98.

  9. Smith, F.J.D., Eady, R.A.J. y col. Plectin deficiency results in muscular dystrophyy with epidermolysis bullosa. Nature Genet., 1996;13: 450-7.

  10. Patrizí, A., Di Lernia, V., Neri, L. y col. EBS associated with muscular dystrophy: a new case. Pediatr. Dermatol., 1994J1:342-5.

  11. McLean, W.H.l., Pulkkinen, L. y col. Loss of plectin causes EBS with muscular dystrophy. Genes Der. 1996; 10: 1724-35.

  12. Vidal, F., Aberdam, D., Miquel, C. y col. Integrin beta 4 mutations associated with EBJ pyloric atresia. Nature Genet., 1995;10:229-34.

  13. Pulkkinen, L., Christiano, A. y col. Mutations in the gamma 2 chain gene (LAMCZ) of Kalininllamin 5 the EBJ. Nature Genet,, 1994;6: 293-98.

  14. Allen, J. y col. Components of the basement membrana zone. Br. J. Dermatol. 1997;137: 907-915.

  15. Anderson, D.C. y col. Leukocyte adhesion deficiency. A. Rev. Med., 1987; 38: 175-194.

  16. George, J.N., Caen, J.R Glanzmann's thrombasthenia. Blood, 1990; 75: 1383-1395.

  17. Jonkrnan, M.F. y col. Expression of integrin alfa 6, beta 4 in JEB. J. invest. Dermatol. 1992; 92: 489-496.

  18. Larjava, H. y col. Vovel funtion for b1 integrina in Keratinocyte cell-cell interactions. J cell Biol 1990; 110: 803-815.

  19. Sonnenberg, A. y col. Integrin a 6 b 4 complex is located in hemidesmosomes. J. Cell Biol. 1991; 113: 907 917.

  20. Chang, Ch., y col. Py1oric atresia associated with EB. Pediatr. Pathol., 1983; 1: 449-457.

  21. Frieden, W. Aplasia cutis congenita: a clinical review and proposal for classification. J. Am. Acad. Dermatol. 1986; 14:646-660.

Texto completo | Tabla de contenido

volumenes anteriores | revistas de Salud


© 1997-2003 UNMSM. Oficina General del Sistema de Bibliotecas y Biblioteca Central
Derechos reservados