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Publications by B.A. Oostra

Endoglin, a TGF-β Binding Protein of Endothelial Cells, Is the Gene for Hereditary Haemorrhagic Telangiectasia Type 1

Nature Genetics

English

HindIII/EcoRI Polymorphism in the GAA Gene

Nucleic Acids Research

English

Related publications

Estrogen Therapy for Hereditary Haemorrhagic Telangiectasia (HHT): Effects of Raloxifene, on Endoglin and ALK1 Expression in Endothelial Cells

Thrombosis and Haemostasis

English

Hereditary Haemorrhagic Telangiectasia

BMJ Case Reports

English

Hereditary Haemorrhagic Telangiectasia: Neuropathological Observations.

Journal of Neurology, Neurosurgery and Psychiatry

English

Cerebral Haemorrhage in Hereditary Haemorrhagic Telangiectasia

Archives of Disease in Childhood

English

Endoglin Mediates Fibronectin/Α5β1 Integrin and TGF-β Pathway Crosstalk in Endothelial Cells

Molecular Biology

English

The Pulmonary Vascular Complications of Hereditary Haemorrhagic Telangiectasia

European Respiratory Journal

Respiratory Medicine

English

Hereditary Haemorrhagic Telangiectasia: A Clinical and Scientific Review

European Journal of Human Genetics

English

Hereditary Haemorrhagic Telangiectasia and Pregnancy: A Review of the Literature

Orphanet Journal of Rare Diseases

English

No Live Individual Homozygous for a Novel Endoglin Mutation Was Found in a Consanguineous Arab Family With Hereditary Haemorrhagic Telangiectasia

Journal of Medical Genetics

English