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factor xi deficiency/homa

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NakalaMajaribio ya klinikiHati miliki
3 matokeo
OBJECTIVE To present a preliminary report on the feasibility, efficacy, and toxicity of irradiation (RT) and hyperthermia (HT) in patients with locally advanced, hormone-refractory prostate cancer (LAHRPC) who may or may not have received prior RT. METHODS Between 1997 and 2002, 13 consecutive

[Thrombotic thrombocytopenic purpura in children -- pathophysiologic mechanisms and their clinical significance].

Watumiaji waliosajiliwa tu ndio wanaweza kutafsiri nakala
Ingia / Ingia
Thrombotic thrombocytopenic purpura (TTP) is a severe occlusive microangiopathy characterized by thrombocytopenia, haemolytic anemia, renal dysfunction, neurological signs and fever. In most cases the disease is associated with the presence of ultra large multimers of von Willebrand factor in the

Two generations with familial thrombotic thrombocytopenic purpura.

Watumiaji waliosajiliwa tu ndio wanaweza kutafsiri nakala
Ingia / Ingia
Thrombotic thrombocytopenic purpura (TTP) is a rare multi-system disease characterised by the pentad of microangiopathic haemolytic anaemia, thrombocytopenia, renal dysfunction, fever and neurologic changes. A hereditary form of recurrent familial TTP has been described, which usually presents in
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