about
Prevalence and Risk Factors for Complications in Patients with Nontransfusion Dependent Alpha- and Beta-Thalassemia.Optimal management of β thalassaemia intermedia.The surgeon and the patient with β-thalassaemia intermedia.The simultaneous occurrence of both hypercoagulability and hypofibrinolysis in blood and serum during systemic inflammation, and the roles of iron and fibrin(ogen).Neurological complications of beta-thalassemia.
P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on January 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
The hypercoagulable state in thalassemia intermedia.
@en
The hypercoagulable state in thalassemia intermedia.
@nl
type
label
The hypercoagulable state in thalassemia intermedia.
@en
The hypercoagulable state in thalassemia intermedia.
@nl
prefLabel
The hypercoagulable state in thalassemia intermedia.
@en
The hypercoagulable state in thalassemia intermedia.
@nl
P2093
P2860
P1433
P1476
The hypercoagulable state in thalassemia intermedia.
@en
P2093
Adlette Inati
Ali T Taher
Khaled M Musallam
P2860
P304
P356
10.3109/03630260903351619
P478
33 Suppl 1
P577
2009-01-01T00:00:00Z