Article information
Full text is only available in PDF
Bibliografía
[1.]
M.M. McGovern, R.J. Desnick.
Lipidosis.
Nelson. Tratado de Pediatría, 16.ª ed, pp. p. 444
[2.]
P.M. Coates, J.A. Cortner.
Lysosomal acid lipase deficiency: Cholesteryl ester storage disease and Wolman's disease.
Pediatric gastrointestinal disease,
[3.]
A. Abramov, S. Shorr, M. Wolman.
Generalized xanthomatosis with calcified adrenals.
Am J Dis Child, 91 (1956), pp. 282-286
[4.]
R.A. Anderson, N. Rao, R.S. Byrum, C.B. Rothschild, D.W. Bowden, R. Hayworth, et al.
In situ localization of the genetic locus encoding of the genetic encoding the lysosomal acid lipase/choleteryl esterase (LIPA) deficient in Wolman disease to chromosome 10q23.2-q23.3.
Genomics, 15 (1993), pp. 245-247
[5.]
S. Valerdiz-Casasola, R. Velasco-García, R. Rodríguez-Rodríguez.
Enfermedad de Wolman. Depósito pulmonar de lípidos.
An Esp Pediatr., 47 (1997), pp. 427-428
[6.]
D.P. Van Diggelen, H. Von Koskull, P. Ammala, G.T. Vredeveldt, H.C. Janse, W.J. Kleijer.
First trimester diagnosis of Wolman's disease.
Prenat Diagn., 8 (1988), pp. 661-663
[7.]
P. Buitrago Mata, L. Giacomin Carmiol, A. Vallejo Serrano, et al.
Enfermedad de Wolman: revisión y reporte de un caso.
Acta Pediatr Costarric., 17 (2003), pp. 46-51
[8.]
W. Krivit, C. Peters, K. Dusembery, Y. Ben-Yoseph, N.K. Ramsay, J.E. Wagner, et al.
Wolman disease successfully treated by bone marrow transplantation.
Bone Marrow Transplant., 26 (2000), pp. 567-570
[9.]
H. Du.
Enzyme therapy for lysosomal acid lipase deficieny in the mouse.
Hum Gene Ther., 10 (2002), pp. 1639-1648
Copyright © 2007. Asociación Española de Pediatría
