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Publications by A Karabegovic

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

Related publications

Hereditary Haemorrhagic Telangiectasia

BMJ Case Reports

English

Characterization of a Family Mutation in the 5’ Untranslated Region of the Endoglin Gene Causative of Hereditary Hemorrhagic Telangiectasia

Journal of Human Genetics

English

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

Nature Genetics

English

Cerebral Haemorrhage in Hereditary Haemorrhagic Telangiectasia

Archives of Disease in Childhood

English

Hereditary Haemorrhagic Telangiectasia: Neuropathological Observations.

Journal of Neurology, Neurosurgery and Psychiatry

English

Hereditary Haemorrhagic Telangiectasia: A Clinical and Scientific Review

European Journal of Human Genetics

English

Novel Homozygous PANK2 Mutation Identified in a Consanguineous Chinese Pedigree With Pantothenate Kinase-Associated Neurodegeneration

Biomedical Reports

Molecular Biology

English

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

Thrombosis and Haemostasis

English

Primary Pulmonary Hypertension in Families With Hereditary Haemorrhagic Telangiectasia

European Respiratory Journal

Respiratory Medicine

English