-transparent.png){kind=logo}
This report describes the successful bone marrow transplantation of three children with thalassemia who received bone marrow, one from an HLA identical but mixed lymphocyte culture-reactive sibling, the other two from an HLA phenotypically identical parent. Evidence of engraftment was detected early (19-21 days) in all three children and only grade II acute GvHD was observed in one patient. Our report indicates that thalassemic patients can be cured by bone marrow transplantation from selected donors other than HLA genotypically identical siblings.
Related Publications
C Delfini, and
P Polchi, and
T Izzi, and
G Nicolini, and
O Paradisi, and
G Lucarelli
April 1991,
Archives of disease in childhood,
C Delfini, and
P Polchi, and
T Izzi, and
G Nicolini, and
O Paradisi, and
G Lucarelli
August 1987,
The Netherlands journal of medicine,
C Delfini, and
P Polchi, and
T Izzi, and
G Nicolini, and
O Paradisi, and
G Lucarelli
January 1980,
Haematology and blood transfusion,
C Delfini, and
P Polchi, and
T Izzi, and
G Nicolini, and
O Paradisi, and
G Lucarelli
January 1993,
Harefuah,
C Delfini, and
P Polchi, and
T Izzi, and
G Nicolini, and
O Paradisi, and
G Lucarelli
June 1990,
Hematology/oncology clinics of North America,
C Delfini, and
P Polchi, and
T Izzi, and
G Nicolini, and
O Paradisi, and
G Lucarelli
February 1981,
Human immunology,
C Delfini, and
P Polchi, and
T Izzi, and
G Nicolini, and
O Paradisi, and
G Lucarelli
September 1979,
Transplantation,
C Delfini, and
P Polchi, and
T Izzi, and
G Nicolini, and
O Paradisi, and
G Lucarelli
October 1989,
Haematologica,
C Delfini, and
P Polchi, and
T Izzi, and
G Nicolini, and
O Paradisi, and
G Lucarelli
January 1989,
Progress in clinical and biological research,
C Delfini, and
P Polchi, and
T Izzi, and
G Nicolini, and
O Paradisi, and
G Lucarelli
September 1985,
The New England journal of medicine,
