Zobrazeno 1 - 10
of 40
pro vyhledávání: '"L A Parapia"'
Publikováno v:
Leukemialymphoma. 2(3-4)
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 3(4)
We have studied the number of patients registered with congenital bleeding disorders at the Haemophilia Centre, Bradford, UK, according to ethnic group. The large Pakistani population in Bradford presents a different spectrum of disorders compared wi
Autor:
L. A. Parapia, E. Johnson
Publikováno v:
European Journal of Haematology. 39:278-281
6 patients with refractory anaemia with excess blasts (RAEB) were treated with a new oral anthracycline, idarubicin. 3 patients achieved complete remission, and the remaining 3 achieved partial remission. These responses were maintained for 8-60 wk,
Autor:
Carolyn Jackson, L. A. Parapia
Publikováno v:
British Journal of Haematology. 141:32-35
Ehlers-Danlos syndrome is an inherited heterogeneous group of connective tissue disorders, characterized by abnormal collagen synthesis, affecting skin, ligaments, joints, blood vessels and other organs. It is one of the oldest known causes of bruisi
Autor:
L. A. Parapia
Publikováno v:
British Journal of Haematology. 139:14-19
Trepanning of bone is the oldest known procedure carried out by man and yet it is only in the last 100 years that we have made use of the technique to diagnose and treat haematological disorders. These advances have been made possible by improvements
Autor:
R. J. Grace, J. Stone, D. L. Barnard, N. S. A. Stuart, A. V. Simmons, D. Parker, G. J. Dovey, J. Tucker, J. A. Child, M. Morgan, D. R. Norfolk, John Fletcher, L. A. Parapia
Publikováno v:
Hematological Oncology. 9:235-244
Fifty-seven patients, initially diagnosed as having advanced high grade non-Hodgkin's lymphoma (NHL) or Hodgkin's disease (HD) refractory to first-line treatment or in relapse, were treated with ifosfamide 6 g/m2, infused over 48 h, followed by mitox
Autor:
L. A. Parapia, P. Prabu
Publikováno v:
Clinical and Laboratory Haematology. 28:198-201
Bernard-Soulier syndrome (BSS) is a rare autosomal recessively inherited bleeding disorder. Pregnancy in patients with BSS is characterized by ante-, intra-, or postpartum haemorrhage, which may be delayed and severe. There is no consensus in the man
Autor:
B. A. McVerry, P. Moreton, J. A. Child, M. R. Howard, G. M. Smith, S. Bolam, Gareth J. Morgan, D. Gilson, J. M. Davies, M. J. Mackie, S. S. Jalihal, L. A. Parapia, A. T. Williams
Publikováno v:
Cancer Chemotherapy and Pharmacology. 53:324-328
We have developed and evaluated a CNS-targeted chemotherapy regimen based on the pharmacokinetic properties of the individual drugs in the combination.In a twin-track study, 16 patients with secondary CNS lymphoma (SCNSL) and 8 with primary CNS lymph
Publikováno v:
American Journal of Hematology. 75:195-199
The clinical behavior and optimal treatment of patients presenting with skin infiltration by B-cell lymphoma have not been established. To clarify this we assessed the clinical and laboratory features of 51 patients presenting with cutaneous infiltra
Publikováno v:
Transfusion Medicine. 11:371-375
As clinical governance moves from concept to practice, it is emerging as a realistic strategy to promote and improve quality within the National Health Service, as well as satisfying the demand for external accountability. In the context of blood tra