Optimal treatment strategies for severe aplasticanaemia remain to be determined.
2
Then they were given the devastating diagnosis of aplasticanaemia.
3
We present here a patient treated for aplasticanaemia, who developed fungal arthritis of the hip and systemic candidaemia.
4
Aims: To review 10 years of local experience in treating severe aplasticanaemia with BMT and immunosuppressive therapy with emphasis on long-term outcomes.
5
These results suggest that while rIL-1 alpha can be safely administered, no significant haematologic improvement was observed in patients with severe aplasticanaemia.
1
It can cause aplasticanemia and other effects on immune system cells.
2
Conclusions: Survivors of aplasticanemia are at high risk for subsequent malignant conditions.
3
The expression of these apoptotic genes was also investigated in aplasticanemia patients.
4
In conclusion, ALG-based IS therapy was effective for aplasticanemia in Chinese patients.
5
We examined whether mutations in the perforin gene occurred in acquired aplasticanemia.
6
Results in myelodysplasia and aplasticanemia have been less encouraging.
7
Associations of genotypes and alleles with aplasticanemia were analyzed.
8
This preoperative regimen is extremely effective in decreasing rejection following transplantation for severe aplasticanemia.
9
Whether these abnormalities are relevant to the pathogenesis of aplasticanemia remains to be determined.
10
In aplasticanemia, predictive markers of response to immunosuppressive therapy have not been well defined.
11
A significant excess was also found for aplasticanemia.
12
The incidence of aplasticanemia in Bangkok is higher than that reported in recent European studies.
13
Speculates that Lee agreed to the show because she'd been diagnosed with aplasticanemia in 2000.
14
ATG was administered to only one case of aplasticanemia and ALG was administered to the remainder.
15
Objective: To determine the outcome of transplanting bone marrow from genetically identical twins into patients with aplasticanemia.
16
In vitro cultures of hemopoietic precursor cells and clinical studies have partly clarified the pathogenesis of aplasticanemia.