Lista de obras - Claire L Shovlin - Dominio Público Uruguay

7-day weighed food diaries suggest patients with hereditary hemorrhagic telangiectasia may spontaneously modify their diet to avoid nosebleed precipitants

artículo científico publicado en 2017

A double-blind, placebo controlled study of Ginkgo biloba extract ('tanakan') in elderly outpatients with mild to moderate memory impairment

artículo científico publicado en 1991

A gene for hereditary haemorrhagic telangiectasia maps to chromosome 9q3

scientific article published on 01 February 1994

A gene for primary pulmonary hypertension

scientific article published on 01 October 2000

A new locus for hereditary haemorrhagic telangiectasia (HHT3) maps to chromosome 5

artículo científico publicado en 2005

Acquired Transpleural Systemic Artery-to-Pulmonary Artery Communication Mimicking a Pulmonary Arteriovenous Malformation and Causing a False-Positive Diagnosis of a Pulmonary Embolus

artículo científico publicado en 2018

Adenosine Deaminase (ADA) Deficiency as the Unexpected Cause of CD4+ T-Lymphocytopenia in Two HIV-Negative Adult Female Siblings ⬇️

artículo científico publicado el 1 de enero de 1994

Adenosine deaminase deficiency with altered biochemical parameters in two sisters with late-onset immunodeficiency

scientific article published on 01 January 1994

Adult onset immunodeficiency caused by inherited adenosine deaminase deficiency

scientific article published on 01 September 1994

Adult presentation of adenosine deaminase deficiency

artículo científico publicado en 1993

Alveolar macrophage activity and the pulmonary complications of haematopoietic stem cell transplantation

artículo científico publicado en 2001

Antiplatelet and anticoagulant agents in hereditary hemorrhagic telangiectasia

Arterial oxygen content is precisely maintained by graded erythrocytotic responses in settings of high/normal serum iron levels, and predicts exercise capacity: an observational study of hypoxaemic patients with pulmonary arteriovenous malformations

artículo científico publicado en 2014

British Thoracic Society Clinical Statement on Pulmonary Arteriovenous Malformations.

artículo científico publicado en 2017

COVID-19 genomic susceptibility: Definition of ACE2 variants relevant to human infection with SARS-CoV-2 in the context of ACMG/AMP Guidance

artículo científico publicado en 2020

Can Iron Treatments Aggravate Epistaxis in Some Patients With Hereditary Hemorrhagic Telangiectasia?

scientific article published on 23 April 2016

Cancer and hereditary haemorrhagic telangiectasia

artículo científico publicado en 2016

Cardiopulmonary exercise testing demonstrates maintenance of exercise capacity in patients with hypoxemia and pulmonary arteriovenous malformations

artículo científico publicado en 2014

Cerebral Abscess Associated With Odontogenic Bacteremias, Hypoxemia, and Iron Loading in Immunocompetent Patients With Right-to-Left Shunting Through Pulmonary Arteriovenous Malformations

artículo científico publicado en 2017

Characterization of endoglin and identification of novel mutations in hereditary hemorrhagic telangiectasia

artículo científico publicado en 1997

Circulatory contributors to the phenotype in hereditary hemorrhagic telangiectasia

artículo científico publicado en 2015

Contributors

Development and implementation of a COVID-19 near real-time traffic light system in an acute hospital setting

scientific article published on 18 September 2020

Dietary supplement use and nosebleeds in hereditary haemorrhagic telangiectasia - an observational study

artículo científico publicado en 2016

Directional next-generation RNA sequencing and examination of premature termination codon mutations in endoglin/hereditary haemorrhagic telangiectasia

artículo científico publicado en 2013

Early detection of severe COVID-19 disease patterns define near real-time personalised care, bioseverity in males, and decelerating mortality rates.

artículo científico publicado en 2020

Elevated factor VIII in hereditary haemorrhagic telangiectasia (HHT): association with venous thromboembolism

artículo científico publicado en 2007

Embolisation of PAVMs reported to improve nosebleeds by a subgroup of patients with hereditary haemorrhagic telangiectasia

artículo científico publicado en 2016

Embolisation of pulmonary arteriovenous malformations: no consistent effect on pulmonary artery pressure

artículo científico publicado en 2008

Embolization of pulmonary arteriovenous malformations using the Amplatzer vascular plug: successful treatment of 69 consecutive patients

artículo científico publicado en 2010

Endothelial cell processing and alternatively spliced transcripts of factor VIII: potential implications for coagulation cascades and pulmonary hypertension

artículo científico publicado en 2010

Estimates of maternal risks of pregnancy for women with hereditary haemorrhagic telangiectasia (Osler-Weber-Rendu syndrome): suggested approach for obstetric services.

artículo científico publicado en 2008

European Reference Network For Rare Vascular Diseases (VASCERN) Outcome Measures For Hereditary Haemorrhagic Telangiectasia (HHT)

European Reference Network for Rare Vascular Diseases (VASCERN) position statement on cerebral screening in adults and children with hereditary haemorrhagic telangiectasia (HHT)

artículo científico publicado en 2020

Executive summary of the 12th HHT international scientific conference.

artículo científico publicado en 2017

Exercise capacity reflects airflow limitation rather than hypoxaemia in patients with pulmonary arteriovenous malformations

artículo científico publicado en 2019

Fine mapping of the hereditary haemorrhagic telangiectasia (HHT)3 locus on chromosome 5 excludes VE-Cadherin-2, Sprouty4 and other interval genes

artículo científico publicado en 2010

Flight-related complications are infrequent in patients with hereditary haemorrhagic telangiectasia/pulmonary arteriovenous malformations, despite low oxygen saturations and anaemia

scientific article published on 26 September 2011

Genetic analysis of susceptibility to experimental autoimmune encephalomyelitis in a cross between SJL/J and B10.S mice

artículo científico publicado en 1996

Hemoglobin Is a Vital Determinant of Arterial Oxygen Content in Hypoxemic Patients with Pulmonary Arteriovenous Malformations

artículo científico publicado en 2017

Hemorrhage-adjusted iron requirements, hematinics and hepcidin define hereditary hemorrhagic telangiectasia as a model of hemorrhagic iron deficiency

artículo científico publicado en 2013

Hereditary haemorrhagic telangiectasia (Osler-Weber-Rendu syndrome): a view from the 21st century.

artículo científico publicado en 2003

Hereditary haemorrhagic telangiectasia: Pathophysiology, diagnosis and treatment ⬇️

artículo científico publicado el 25 de septiembre de 2010

Hereditary haemorrhagic telangiectasia: a clinical and scientific review

artículo científico publicado en 2009

Hypoxaemia, sport and polycythaemia: a case from Imperial College London

artículo científico publicado en 2015

Implications for COVID-19 triage from the ICNARC report of 2204 COVID-19 cases managed in UK adult intensive care units

scientific article published on 04 May 2020

Increase in COVID-19 inpatient survival following detection of Thromboembolic and Cytokine storm risk from the point of admission to hospital by a near real time Traffic-light System (TraCe-Tic)

artículo científico publicado en 2020

Injections of Intravenous Contrast for Computerized Tomography Scans Precipitate Migraines in Hereditary Hemorrhagic Telangiectasia Subjects at Risk of Paradoxical Emboli: Implications for Right-to-Left Shunt Risks

artículo científico publicado en 2016

Iron deficiency, ischaemic strokes, and right-to-left shunts: From pulmonary arteriovenous malformations to patent foramen ovale?

artículo científico publicado en 2014

Ischaemic strokes in patients with pulmonary arteriovenous malformations and hereditary hemorrhagic telangiectasia: associations with iron deficiency and platelets

artículo científico publicado en 2014

Lifestyle and dietary influences on nosebleed severity in hereditary hemorrhagic telangiectasia

artículo científico publicado en 2013

Long-term outcomes of patients with pulmonary arteriovenous malformations considered for lung transplantation, compared with similarly hypoxaemic cohorts

artículo científico publicado en 2017

Low Dose Iron Treatments Induce a DNA Damage Response in Human Endothelial Cells within Minutes

artículo científico publicado en 2016

Low grade mosaicism in hereditary haemorrhagic telangiectasia identified by bidirectional whole genome sequencing reads through the 100,000 Genomes Project clinical diagnostic pipeline

artículo científico publicado en 2020

Low serum haptoglobin and blood films suggest intravascular haemolysis contributes to severe anaemia in hereditary haemorrhagic telangiectasia

scholarly article by Lieze Thielemans et al published 18 October 2018 in Haematologica

Low serum iron levels are associated with elevated plasma levels of coagulation factor VIII and pulmonary emboli/deep venous thromboses in replicate cohorts of patients with hereditary haemorrhagic telangiectasia.

artículo científico publicado en 2011

Management of pulmonary arteriovenous malformations in pulmonary hypertensive patients: a pressure to embolise?

artículo científico publicado en 2009

Managing passengers with stable respiratory disease planning air travel: British Thoracic Society recommendations

artículo científico publicado en 2011

Medical complications of pregnancy in hereditary haemorrhagic telangiectasia

artículo científico publicado en 1995

Mutational and phenotypic characterisation of hereditary hemorrhagic telangiectasia

artículo científico publicado en 2020

Orthodeoxia and postural orthostatic tachycardia in patients with pulmonary arteriovenous malformations: a prospective 8-year series

artículo científico publicado en 2014

Patients with in-situ metallic coils and Amplatzer vascular plugs used to treat pulmonary arteriovenous malformations since 1984 can safely undergo magnetic resonance imaging

scientific article published on 24 April 2019

Post-NICE 2008: Antibiotic prophylaxis prior to dental procedures for patients with pulmonary arteriovenous malformations (PAVMs) and hereditary haemorrhagic telangiectasia

artículo científico publicado en 2008

Prevention of serious infections in hereditary hemorrhagic telangiectasia: roles for prophylactic antibiotics, the pulmonary capillaries-but not vaccination

scholarly article by Claire Shovlin et al published February 2019 in Haematologica

Pulmonary Thromboemboli Modifying the Natural History of Pulmonary Arteriovenous Malformations

artículo científico publicado en 2011

Pulmonary arteriovenous malformations

artículo científico publicado en 2014

Pulmonary arteriovenous malformations and their mimics.

artículo científico publicado en 2014

Pulmonary arteriovenous malformations emerge from the shadows

artículo científico publicado en 2017

Pulmonary arteriovenous malformations: effect of embolization on right-to-left shunt, hypoxemia, and exercise tolerance in 66 patients

scientific article published on 01 August 2002

Pulmonary arteriovenous malformations: evidence of physician under-education

artículo científico publicado en 2017

Pulmonary toxicity of malaria prophylaxis.

artículo científico publicado en 1988

Relationships between epistaxis, migraines, and triggers in hereditary hemorrhagic telangiectasia

artículo científico publicado en 2014

Reply to Bianca et al.

artículo científico publicado en 2009

Reply to Fernández-Fernández.

artículo científico publicado en 2009

Reported cardiac phenotypes in hereditary hemorrhagic telangiectasia emphasize burdens from arrhythmias, anemia and its treatments, but suggest reduced rates of myocardial infarction

artículo científico publicado en 2016

Safety of direct oral anticoagulants in patients with hereditary hemorrhagic telangiectasia

scientific article published on 28 August 2019

Safety of thalidomide and bevacizumab in patients with hereditary hemorrhagic telangiectasia

artículo científico publicado en 2019

Second International Guidelines for the Diagnosis and Management of Hereditary Hemorrhagic Telangiectasia

artículo científico publicado en 2020

Should asymptomatic patients with hereditary haemorrhagic telangiectasia (HHT) be screened for cerebral vascular malformations? Data from 22,061 years of HHT patient life

artículo científico publicado en 2003

Specific cancer rates may differ in patients with hereditary haemorrhagic telangiectasia compared to controls

scientific article published on 20 December 2013

Supermodels and disease: insights from the HHT mice.

artículo científico publicado en 1999

The Lung in Hereditary Hemorrhagic Telangiectasia.

artículo científico publicado en 2017

Top dietary iron sources in the UK.

artículo científico publicado en 2014

Triage assessment of cardiorespiratory risk status based on measurement of the anaerobic threshold, and estimation by activity limitation in patients with pulmonary arteriovenous malformations and hereditary haemorrhagic telangiectasia

artículo científico publicado en 2020

Uptake and radiological findings of screening cerebral magnetic resonance scans in patients with hereditary haemorrhagic telangiectasia

scientific article published on 01 November 2018

Vascular inflammation and endothelial injury in SARS-CoV-2 infection: The overlooked regulatory cascades implicated by the ACE2 gene cluster

artículo científico publicado en 2020

Veterans Specific Activity Questionnaire (VSAQ): a new and efficient method of assessing exercise capacity in patients with pulmonary arteriovenous malformations

Lista de obras de Claire L Shovlin

7-day weighed food diaries suggest patients with hereditary hemorrhagic telangiectasia may spontaneously modify their diet to avoid nosebleed precipitants

A double-blind, placebo controlled study of Ginkgo biloba extract ('tanakan') in elderly outpatients with mild to moderate memory impairment

A gene for hereditary haemorrhagic telangiectasia maps to chromosome 9q3

A gene for primary pulmonary hypertension

A new locus for hereditary haemorrhagic telangiectasia (HHT3) maps to chromosome 5

Acquired Transpleural Systemic Artery-to-Pulmonary Artery Communication Mimicking a Pulmonary Arteriovenous Malformation and Causing a False-Positive Diagnosis of a Pulmonary Embolus

Adenosine Deaminase (ADA) Deficiency as the Unexpected Cause of CD4+ T-Lymphocytopenia in Two HIV-Negative Adult Female Siblings ⬇️

Adenosine deaminase deficiency with altered biochemical parameters in two sisters with late-onset immunodeficiency

Adult onset immunodeficiency caused by inherited adenosine deaminase deficiency

Adult presentation of adenosine deaminase deficiency

Alveolar macrophage activity and the pulmonary complications of haematopoietic stem cell transplantation

Antiplatelet and anticoagulant agents in hereditary hemorrhagic telangiectasia

Arterial oxygen content is precisely maintained by graded erythrocytotic responses in settings of high/normal serum iron levels, and predicts exercise capacity: an observational study of hypoxaemic patients with pulmonary arteriovenous malformations

British Thoracic Society Clinical Statement on Pulmonary Arteriovenous Malformations.

COVID-19 genomic susceptibility: Definition of ACE2 variants relevant to human infection with SARS-CoV-2 in the context of ACMG/AMP Guidance

Can Iron Treatments Aggravate Epistaxis in Some Patients With Hereditary Hemorrhagic Telangiectasia?

Cancer and hereditary haemorrhagic telangiectasia

Cardiopulmonary exercise testing demonstrates maintenance of exercise capacity in patients with hypoxemia and pulmonary arteriovenous malformations

Cerebral Abscess Associated With Odontogenic Bacteremias, Hypoxemia, and Iron Loading in Immunocompetent Patients With Right-to-Left Shunting Through Pulmonary Arteriovenous Malformations

Characterization of endoglin and identification of novel mutations in hereditary hemorrhagic telangiectasia

Circulatory contributors to the phenotype in hereditary hemorrhagic telangiectasia

Contributors

Development and implementation of a COVID-19 near real-time traffic light system in an acute hospital setting

Dietary supplement use and nosebleeds in hereditary haemorrhagic telangiectasia - an observational study

Directional next-generation RNA sequencing and examination of premature termination codon mutations in endoglin/hereditary haemorrhagic telangiectasia

Early detection of severe COVID-19 disease patterns define near real-time personalised care, bioseverity in males, and decelerating mortality rates.

Elevated factor VIII in hereditary haemorrhagic telangiectasia (HHT): association with venous thromboembolism

Embolisation of PAVMs reported to improve nosebleeds by a subgroup of patients with hereditary haemorrhagic telangiectasia

Embolisation of pulmonary arteriovenous malformations: no consistent effect on pulmonary artery pressure

Embolization of pulmonary arteriovenous malformations using the Amplatzer vascular plug: successful treatment of 69 consecutive patients

Endothelial cell processing and alternatively spliced transcripts of factor VIII: potential implications for coagulation cascades and pulmonary hypertension

Estimates of maternal risks of pregnancy for women with hereditary haemorrhagic telangiectasia (Osler-Weber-Rendu syndrome): suggested approach for obstetric services.

European Reference Network For Rare Vascular Diseases (VASCERN) Outcome Measures For Hereditary Haemorrhagic Telangiectasia (HHT)

European Reference Network for Rare Vascular Diseases (VASCERN) position statement on cerebral screening in adults and children with hereditary haemorrhagic telangiectasia (HHT)

Executive summary of the 12th HHT international scientific conference.

Exercise capacity reflects airflow limitation rather than hypoxaemia in patients with pulmonary arteriovenous malformations

Fine mapping of the hereditary haemorrhagic telangiectasia (HHT)3 locus on chromosome 5 excludes VE-Cadherin-2, Sprouty4 and other interval genes

Flight-related complications are infrequent in patients with hereditary haemorrhagic telangiectasia/pulmonary arteriovenous malformations, despite low oxygen saturations and anaemia

Genetic analysis of susceptibility to experimental autoimmune encephalomyelitis in a cross between SJL/J and B10.S mice

Hemoglobin Is a Vital Determinant of Arterial Oxygen Content in Hypoxemic Patients with Pulmonary Arteriovenous Malformations

Hemorrhage-adjusted iron requirements, hematinics and hepcidin define hereditary hemorrhagic telangiectasia as a model of hemorrhagic iron deficiency

Hereditary haemorrhagic telangiectasia (Osler-Weber-Rendu syndrome): a view from the 21st century.

Hereditary haemorrhagic telangiectasia: Pathophysiology, diagnosis and treatment ⬇️

Hereditary haemorrhagic telangiectasia: a clinical and scientific review

Hypoxaemia, sport and polycythaemia: a case from Imperial College London

Implications for COVID-19 triage from the ICNARC report of 2204 COVID-19 cases managed in UK adult intensive care units

Increase in COVID-19 inpatient survival following detection of Thromboembolic and Cytokine storm risk from the point of admission to hospital by a near real time Traffic-light System (TraCe-Tic)

Injections of Intravenous Contrast for Computerized Tomography Scans Precipitate Migraines in Hereditary Hemorrhagic Telangiectasia Subjects at Risk of Paradoxical Emboli: Implications for Right-to-Left Shunt Risks

Iron deficiency, ischaemic strokes, and right-to-left shunts: From pulmonary arteriovenous malformations to patent foramen ovale?

Ischaemic strokes in patients with pulmonary arteriovenous malformations and hereditary hemorrhagic telangiectasia: associations with iron deficiency and platelets

Lifestyle and dietary influences on nosebleed severity in hereditary hemorrhagic telangiectasia

Long-term outcomes of patients with pulmonary arteriovenous malformations considered for lung transplantation, compared with similarly hypoxaemic cohorts

Low Dose Iron Treatments Induce a DNA Damage Response in Human Endothelial Cells within Minutes

Low grade mosaicism in hereditary haemorrhagic telangiectasia identified by bidirectional whole genome sequencing reads through the 100,000 Genomes Project clinical diagnostic pipeline

Low serum haptoglobin and blood films suggest intravascular haemolysis contributes to severe anaemia in hereditary haemorrhagic telangiectasia

Low serum iron levels are associated with elevated plasma levels of coagulation factor VIII and pulmonary emboli/deep venous thromboses in replicate cohorts of patients with hereditary haemorrhagic telangiectasia.

Management of pulmonary arteriovenous malformations in pulmonary hypertensive patients: a pressure to embolise?

Managing passengers with stable respiratory disease planning air travel: British Thoracic Society recommendations

Medical complications of pregnancy in hereditary haemorrhagic telangiectasia

Mutational and phenotypic characterisation of hereditary hemorrhagic telangiectasia

Orthodeoxia and postural orthostatic tachycardia in patients with pulmonary arteriovenous malformations: a prospective 8-year series

Patients with in-situ metallic coils and Amplatzer vascular plugs used to treat pulmonary arteriovenous malformations since 1984 can safely undergo magnetic resonance imaging

Post-NICE 2008: Antibiotic prophylaxis prior to dental procedures for patients with pulmonary arteriovenous malformations (PAVMs) and hereditary haemorrhagic telangiectasia

Prevention of serious infections in hereditary hemorrhagic telangiectasia: roles for prophylactic antibiotics, the pulmonary capillaries-but not vaccination

Pulmonary Thromboemboli Modifying the Natural History of Pulmonary Arteriovenous Malformations

Pulmonary arteriovenous malformations

Pulmonary arteriovenous malformations and their mimics.

Pulmonary arteriovenous malformations emerge from the shadows

Pulmonary arteriovenous malformations: effect of embolization on right-to-left shunt, hypoxemia, and exercise tolerance in 66 patients

Pulmonary arteriovenous malformations: evidence of physician under-education

Pulmonary toxicity of malaria prophylaxis.

Relationships between epistaxis, migraines, and triggers in hereditary hemorrhagic telangiectasia

Reply to Bianca et al.

Reply to Fernández-Fernández.

Reported cardiac phenotypes in hereditary hemorrhagic telangiectasia emphasize burdens from arrhythmias, anemia and its treatments, but suggest reduced rates of myocardial infarction

Safety of direct oral anticoagulants in patients with hereditary hemorrhagic telangiectasia

Safety of thalidomide and bevacizumab in patients with hereditary hemorrhagic telangiectasia

Second International Guidelines for the Diagnosis and Management of Hereditary Hemorrhagic Telangiectasia

Should asymptomatic patients with hereditary haemorrhagic telangiectasia (HHT) be screened for cerebral vascular malformations? Data from 22,061 years of HHT patient life