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C L Shovlin

Showing results (1-10 of 32) with videos related to

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Clinical Science (London, England : 1979)|June 9, 1998
Glaxo/MRS Young Investigator Medal. Molecular studies on adenosine deaminase deficiency and hereditary haemorrhagic telangiectasiaC L Shovlin
Thrombosis and Haemostasis|July 1, 1997
Molecular defects in rare bleeding disorders: hereditary haemorrhagic telangiectasiaC L Shovlin
Interventional Neuroradiology : Journal of Peritherapeutic Neuroradiology, Surgical Procedures and Related Neurosciences|July 30, 2010
Genetic aspects of cerebrovascular malformationsC L Shovlin
Annual Review of Physiology|January 1, 1996
Inherited diseases of the vasculatureC L Shovlin, J Scott
QJM : Monthly Journal of the Association of Physicians|August 11, 2020
Vascular inflammation and endothelial injury in SARS-CoV-2 infection: the overlooked regulatory cascades implicated by the ACE2 gene clusterC L Shovlin, M P Vizcaychipi
Thorax|July 19, 2000
A hereditary haemorrhagic telangiectasia family with pulmonary involvement is unlinked to the known HHT genes, endoglin and ALK-1G M Wallace, C L Shovlin
Journal of Cancer Research and Clinical Oncology|November 13, 2016
Cancer and hereditary haemorrhagic telangiectasiaA E Hosman, C L Shovlin
Respiration; International Review of Thoracic Diseases|August 30, 2017
The Lung in Hereditary Hemorrhagic TelangiectasiaSophie Dupuis-Girod, Vincent Cottin, C L Shovlin
Clinical Radiology|April 27, 2021
Transpleural systemic artery-to-pulmonary artery communications in the absence of chronic inflammatory lung disease. A case series and review of the literatureA Alsafi, C L Shovlin, J E Jackson
Rhinology|August 14, 2012
Silent threat? A retrospective study of screening practices for pulmonary arteriovenous malformations in patients with hereditary haemorrhagic telangiectasiaM M Verkerk, C L Shovlin, V J Lund
Pageof 4

Showing results (1-10 of 32) with videos related to

Sort By:
Pageof 4
Clinical Science (London, England : 1979)|June 9, 1998
Glaxo/MRS Young Investigator Medal. Molecular studies on adenosine deaminase deficiency and hereditary haemorrhagic telangiectasiaC L Shovlin
Thrombosis and Haemostasis|July 1, 1997
Molecular defects in rare bleeding disorders: hereditary haemorrhagic telangiectasiaC L Shovlin
Interventional Neuroradiology : Journal of Peritherapeutic Neuroradiology, Surgical Procedures and Related Neurosciences|July 30, 2010
Genetic aspects of cerebrovascular malformationsC L Shovlin
Annual Review of Physiology|January 1, 1996
Inherited diseases of the vasculatureC L Shovlin, J Scott
QJM : Monthly Journal of the Association of Physicians|August 11, 2020
Vascular inflammation and endothelial injury in SARS-CoV-2 infection: the overlooked regulatory cascades implicated by the ACE2 gene clusterC L Shovlin, M P Vizcaychipi
Thorax|July 19, 2000
A hereditary haemorrhagic telangiectasia family with pulmonary involvement is unlinked to the known HHT genes, endoglin and ALK-1G M Wallace, C L Shovlin
Journal of Cancer Research and Clinical Oncology|November 13, 2016
Cancer and hereditary haemorrhagic telangiectasiaA E Hosman, C L Shovlin
Respiration; International Review of Thoracic Diseases|August 30, 2017
The Lung in Hereditary Hemorrhagic TelangiectasiaSophie Dupuis-Girod, Vincent Cottin, C L Shovlin
Clinical Radiology|April 27, 2021
Transpleural systemic artery-to-pulmonary artery communications in the absence of chronic inflammatory lung disease. A case series and review of the literatureA Alsafi, C L Shovlin, J E Jackson
Rhinology|August 14, 2012
Silent threat? A retrospective study of screening practices for pulmonary arteriovenous malformations in patients with hereditary haemorrhagic telangiectasiaM M Verkerk, C L Shovlin, V J Lund
Pageof 4