Latest papers

Intramedullary spinal cord hemorrhage (hematomyelia).

A web-based clinical record 'xl'Emofilia' for outpatients with haemophilia and allied disorders in the Region of Emilia-Romagna: features and pilot use.

Familial multiple coagulation factor deficiencies - chance associations and distinct clinical disorders.

The spectrum of inherited bleeding disorders in pediatrics.

[Congenital coagulopathies and coagulation factor inhibitors].

Deficiency of the human complement regulatory protein factor h associated with low levels of component C9.

Mechanisms of the factor V Leiden paradox.

Insulin resistance, obesity, hypofibrinolysis, hyperandrogenism, and coronary heart disease risk factors in 25 pre-perimenarchal girls age or =14 years, 13 with precocious puberty, 23 with a first-degree relative with polycystic ovary syndrome.

Nonstroke arterial thrombosis in children: Hacettepe experience.

Cryptogenic stroke in a boy with atrial septal defect and hyperhomocysteinemia.

Spectrum of changes in endogenous thrombin potential due to heritable disorders of coagulation.

Use of intravenous tissue plasminogen activator in a 16-year-old patient with basilar occlusion.

Prophylaxis of bleeding episodes and surgical interventions in patients with rare inherited coagulation disorders.

Prophylaxis in congenital coagulation disorders: past, present and future.

National and international registries of rare bleeding disorders.

Intracranial haemorrhage in patients with congenital haemostatic defects.

Thrombophilic dimension of recurrent fetal loss in Indian patients.

Rare bleeding disorders.

Guideline on the selection and use of therapeutic products to treat haemophilia and other hereditary bleeding disorders. A United Kingdom Haemophilia Center Doctors' Organisation (UKHCDO) guideline approved by the British Committee for Standards in Haematology.

Inherited bleeding disorders: results from the Italian Regional Haemophilia Centre of Pescara.