La greffe de moelle dans les maladies héréditaires.


Autoria(s): Buján-Boza, Willem A.; Ferster, Alina; Devalck, Christine; Vamos, Eszter; Mascart, Françoise; Denis, Robert; Azzi, Nadira; Vergauwen, P; Sariban, Eric
Data(s)

01/06/1992

Resumo

Since 1968, bone marrow transplantation became the first line therapy for selected metabolic and immunological hereditary disorders. Actually, advances in the supportive care in bone marrow transplantation and a better knowledge of the immunology of BMT complications has been associated with a better disease correction and an increase in long term survival. New approaches are under investigation and include: hematopoietic growth factors, enzymatic replacement and gene therapy. However at the present time BMT is still the only curative treatment for selected hereditary disorders.

English Abstract

Journal Article

info:eu-repo/semantics/published

Formato

No full-text files

Identificador

uri/info:pmid/1631420

local/0026873292

http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/96565

Idioma(s)

fr

Fonte

Revue médicale de Bruxelles, 13 (6

Palavras-Chave #Pédiatrie #Cancérologie #Hématologie #Wiskott-Aldrich Syndrome -- therapy
Tipo

info:eu-repo/semantics/article

info:ulb-repo/semantics/articlePeerReview

info:ulb-repo/semantics/openurl/article