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ON THE VERSATILITY OF VON WILLEBRAND FACTOR
2958PDF: 1213HTML: 11427 -
VON WILLEBRAND FACTOR, ANGIODYSPLASIA AND ANGIOGENESIS
3916PDF: 1663HTML: 8248Randi Fig: 224 -
EFFECTS OF FACTOR XIII DEFICIENCY ON THROMBOELASTOGRAPHY. THROMBELASTOGRAPHY WITH CALCIUM AND LYSIS BY ADDITION OF STREPTOKINASE IS MORE SENSITIVE THAN SOLUBILITY TESTS
3213PDF: 1043HTML: 1962Untitled: 207Untitled: 226Untitled: 212Untitled: 225Untitled: 211 -
CIRCUMCISION IN MALES WITH BLEEDING DISORDERS
2052PDF: 978HTML: 6835Cover letter: 203 -
HIV-ASSOCIATED VENOUS THROMBOEMBOLISM
4638PDF: 1550HTML: 8546 -
DYNAMIC MONITORING OF ADAMTS 13 ACTIVITY FOR DIFFERENTIAL DIAGNOSIS ACROSS THE SPECTRUM OF SEPSIS ASSOCIATED WITH THROMBOTIC MICROANGIOPATIES Adamts 13 and Sepsis Associated with Thrombotic Thrombocytopenic Purpura
905PDF: 777HTML: 242 -
THE PROTHROMBOTIC STATE ASSOCIATED WITH SARS-COV-2 INFECTION: PATHOPHYSIOLOGICAL ASPECTS COVID and Thrombosis
2489PDF: 870HTML: 484 -
Guest Editor: G. Castaman GENE THERAPY FOR HEMOPHILIA: FACTS AND QUANDARIES IN THE 21ST CENTURY GENE THERAPY FOR HEMOPHILIA
2279PDF: 2008HTML: 529 -
MILD BLEEDERS: DIAGNOSIS IS ELUSIVE IN LARGE NUMBER OF PATIENTS
3410PDF: 775HTML: 770Figure 1 Distribution of the various causes of mild bleeding (in %) in males and females: 235Figure 2 Age and Sex distribution of patients with Bleeding disorders- Unclassified: 236Table : Distribution of the sites of bleeding and their causes: 219 -
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SARS-CoV-2 INFECTED PATIENTS: FROM A HEMATOLOGIST PERSPECTIVE COVID-19 and Hematology
1559PDF: 1017HTML: 450 -
MOLECULAR MECHANISMS OF INHIBITOR DEVELOPMENT IN HEMOPHILIA Guest Editor: Giancarlo Costaman
3548PDF: 1681HTML: 710 -
PATHOGENESIS AND TREATMENT OF THROMBOHEMORRHAGIC DIATHESIS IN ACUTE PROMYELOCYTIC LEUKEMIA
1972PDF: 879HTML: 10363Figures 1,2,3: 254 -
VASCULAR ENDOTHELIAL GROWTH FACTOR IN CHILDREN WITH THALASSEMIA MAJOR PDF
1408PDF: 923HTML: 1143Figure 1 the correlation between frequency of blood transfusion and serum vascular endothelial growth factor (VEGF).: 226 -
MUTATIONAL PROFILES OF F8 AND F9 IN A COHORT OF HAEMOPHILIA A AND HAEMOPHILIA B PATIENTS IN THE MULTI-ETHNIC MALAYSIAN POPULATION
2173PDF: 1123HTML: 975Figure 1: 210Figure 2: 232 -
FAMILIAL MEDITERRANEAN FEVER AND HYPERCOAGULABILITY
1311PDF: 763HTML: 1265 -
TOXICITIES ASSOCIATED WITH CAR-T CELL THERAPIES CAR-T Cell Toxicity
2646PDF: 1788HTML: 696 -
PATHOGENESIS OF MALARIA IN TISSUES AND BLOOD
4743PDF: 2025HTML: 18192 -
NEW THERAPEUTIC OPTIONS FOR THE TREATMENT OF SICKLE CELL DISEASE Guest Editor: Raffaella Origa
7145PDF: 3797HTML: 839 -
Idiopathic pulmonary embolism in a case of severe family ANKRD26 thrombocytopenia
2360PDF: 895HTML: 974Patient’s family tree: 220 -
THALASSEMIA AND VENOUS THROMBOEMBOLISM
3095PDF: 1190HTML: 4701 -
Refractory Immune Thrombocytopenic Purpura and Cytomegalovirus Infection: A Call for a Change in the Current Guidelines
4460PDF: 1261HTML: 2427Figure 1: 217 -
COAGULOPATHY IN BETA-THALASSEMIA: CURRENT UNDERSTANDING AND FUTURE PERSPECTIVES
1360PDF: 525HTML: 8354 -
Microangiopathic Anemia of Acute Brucellosis – is it a True TTP?
1264PDF: 841HTML: 1795
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