Lista de obras - Eduard J van Beers - Dominio Público Uruguay

Acute chest syndrome in sickle cell disease due to the new influenza A (H1N1) virus infection

artículo científico publicado en 2010

Addressing the diagnostic gaps in pyruvate kinase (PK) deficiency: Consensus recommendations on the diagnosis of PK deficiency

artículo científico publicado en 2018

Association of asymmetric dimethylarginine with sickle cell disease-related pulmonary hypertension

artículo científico publicado en 2008

Cardiopulmonary imaging, functional and laboratory studies in sickle cell disease associated pulmonary hypertension

artículo científico publicado en 2008

Cerebrovascular reserve capacity is impaired in patients with sickle cell disease.

artículo científico publicado en 2009

Chronic pulmonary embolism in Klippel-Trenaunay syndrome

artículo científico publicado en 2011

Circulating erythrocyte-derived microparticles are associated with coagulation activation in sickle cell disease

artículo científico publicado en 2009

Comment on "The influence of hydroxyurea on oxidative stress in sickle cell anemia"

artículo científico publicado en 2012

Comment on: Kretowski et al. (2007) Polymorphisms of the renin-angiotensin system genes predict progression of subclinical coronary atherosclerosis: Diabetes 56:863-871

artículo científico publicado en 2007

Do NSAIDs actually protect against myocardial infarction and death?

artículo científico publicado en 2009

Dynamic cerebral autoregulation in homozygous Sickle cell disease

artículo científico publicado en 2009

Effect of corruption on medical care in low-income countries

artículo científico publicado en 2011

Elevated endothelial progenitor cells during painful sickle cell crisis

artículo científico publicado en 2009

Exercise tolerance, lung function abnormalities, anemia, and cardiothoracic ratio in sickle cell patients

artículo científico publicado en 2014

Extensive slow-flow vascular malformations and pulmonary hypertension

scientific article published on 01 December 2010

Haem augments and iron chelation decreases toll-like receptor 4 mediated inflammation in monocytes from sickle cell patients

artículo científico publicado en 2017

Haematological malignancy in the intensive care unit: microbiology results and mortality.

artículo científico publicado en 2015

Imaging flow cytometry documents incomplete resistance of human sickle F-cells to ex vivo hypoxia-induced sickling

artículo científico publicado en 2014

Imaging flow cytometry for automated detection of hypoxia-induced erythrocyte shape change in sickle cell disease

artículo científico publicado en 2014

Iron overload in patients with rare hereditary hemolytic anemia: Evidence-based suggestion on whom and how to screen

scholarly article by Stephanie van Straaten et al published November 2018 in American Journal of Hematology

Iron, inflammation, and early death in adults with sickle cell disease

artículo científico publicado en 2014

Large and medium-sized pulmonary artery obstruction does not play a role of primary importance in the etiology of sickle-cell disease-associated pulmonary hypertension

scientific article published on 15 January 2008

Letter in response to: "Pulmonary thrombi are not detected by 3D magnetic resonance angiography in adults with sickle cell anemia and an elevated triscuspid regurgitant jet velocity"

artículo científico publicado en 2010

Licorice consumption as a cause of posterior reversible encephalopathy syndrome: a case report.

artículo científico publicado en 2011

N-terminal pro-B-type natriuretic peptide, tricuspid jet flow velocity, and death in adults with sickle cell disease

artículo científico publicado en 2015

No association of the hypercoagulable state with sickle cell disease related pulmonary hypertension

scientific article published on 01 May 2008

Normal sublingual microcirculation during painful crisis in sickle cell disease

artículo científico publicado en 2008

Organ involvement occurs in all forms of hereditary haemolytic anaemia

artículo científico publicado en 2018

Oxidative stress in sickle cell disease; more than a DAMP squib

artículo científico publicado en 2018

Pain rate and social circumstances rather than cumulative organ damage determine the quality of life in adults with sickle cell disease

artículo científico publicado en 2010

Patient-controlled analgesia versus continuous infusion of morphine during vaso-occlusive crisis in sickle cell disease, a randomized controlled trial

artículo científico publicado en 2007

Plasma levels of pentraxin-3, an acute phase protein, are increased during sickle cell painful crisis

article

Prospective evaluation of chronic organ damage in adult sickle cell patients: A seven-year follow-up study

artículo científico publicado en 2017

Rapid and reproducible characterization of sickling during automated deoxygenation in sickle cell disease patients

scientific article published on 08 March 2019

Screening for hemosiderosis in patients receiving multiple red blood cell transfusions.

artículo científico publicado en 2017

Sickle Cell Imaging Flow Cytometry Assay (SIFCA).

artículo científico publicado en 2016

Sickle cell patients are characterized by a reduced glycocalyx volume

artículo científico publicado en 2008

The clinical spectrum of pyruvate kinase deficiency: data from the Pyruvate Kinase Deficiency Natural History Study.

artículo científico publicado en 2018

Worldwide study of hematopoietic allogeneic stem cell transplantation in pyruvate kinase deficiency.

artículo científico publicado en 2017

Lista de obras de Eduard J van Beers

Acute chest syndrome in sickle cell disease due to the new influenza A (H1N1) virus infection

Addressing the diagnostic gaps in pyruvate kinase (PK) deficiency: Consensus recommendations on the diagnosis of PK deficiency

Association of asymmetric dimethylarginine with sickle cell disease-related pulmonary hypertension

Cardiopulmonary imaging, functional and laboratory studies in sickle cell disease associated pulmonary hypertension

Cerebrovascular reserve capacity is impaired in patients with sickle cell disease.

Chronic pulmonary embolism in Klippel-Trenaunay syndrome

Circulating erythrocyte-derived microparticles are associated with coagulation activation in sickle cell disease

Comment on "The influence of hydroxyurea on oxidative stress in sickle cell anemia"

Comment on: Kretowski et al. (2007) Polymorphisms of the renin-angiotensin system genes predict progression of subclinical coronary atherosclerosis: Diabetes 56:863-871

Do NSAIDs actually protect against myocardial infarction and death?

Dynamic cerebral autoregulation in homozygous Sickle cell disease

Effect of corruption on medical care in low-income countries

Elevated endothelial progenitor cells during painful sickle cell crisis

Exercise tolerance, lung function abnormalities, anemia, and cardiothoracic ratio in sickle cell patients

Extensive slow-flow vascular malformations and pulmonary hypertension

Haem augments and iron chelation decreases toll-like receptor 4 mediated inflammation in monocytes from sickle cell patients

Haematological malignancy in the intensive care unit: microbiology results and mortality.

Imaging flow cytometry documents incomplete resistance of human sickle F-cells to ex vivo hypoxia-induced sickling

Imaging flow cytometry for automated detection of hypoxia-induced erythrocyte shape change in sickle cell disease

Iron overload in patients with rare hereditary hemolytic anemia: Evidence-based suggestion on whom and how to screen

Iron, inflammation, and early death in adults with sickle cell disease

Large and medium-sized pulmonary artery obstruction does not play a role of primary importance in the etiology of sickle-cell disease-associated pulmonary hypertension

Letter in response to: "Pulmonary thrombi are not detected by 3D magnetic resonance angiography in adults with sickle cell anemia and an elevated triscuspid regurgitant jet velocity"

Licorice consumption as a cause of posterior reversible encephalopathy syndrome: a case report.

N-terminal pro-B-type natriuretic peptide, tricuspid jet flow velocity, and death in adults with sickle cell disease

No association of the hypercoagulable state with sickle cell disease related pulmonary hypertension

Normal sublingual microcirculation during painful crisis in sickle cell disease

Organ involvement occurs in all forms of hereditary haemolytic anaemia

Oxidative stress in sickle cell disease; more than a DAMP squib

Pain rate and social circumstances rather than cumulative organ damage determine the quality of life in adults with sickle cell disease

Patient-controlled analgesia versus continuous infusion of morphine during vaso-occlusive crisis in sickle cell disease, a randomized controlled trial

Plasma levels of pentraxin-3, an acute phase protein, are increased during sickle cell painful crisis

Prospective evaluation of chronic organ damage in adult sickle cell patients: A seven-year follow-up study

Rapid and reproducible characterization of sickling during automated deoxygenation in sickle cell disease patients

Screening for hemosiderosis in patients receiving multiple red blood cell transfusions.

Sickle Cell Imaging Flow Cytometry Assay (SIFCA).

Sickle cell patients are characterized by a reduced glycocalyx volume

The clinical spectrum of pyruvate kinase deficiency: data from the Pyruvate Kinase Deficiency Natural History Study.

Worldwide study of hematopoietic allogeneic stem cell transplantation in pyruvate kinase deficiency.