Lista de obras - Maryse Etienne-Julan - Dominio Público Uruguay

Acute moderate exercise does not further alter the autonomic nervous system activity in patients with sickle cell anemia

artículo científico publicado en 2014

Alpha thalassemia protects sickle cell anemia patients from macro-albuminuria through its effects on red blood cell rheological properties

artículo científico publicado en 2014

Association between relative systemic hypertension and otologic disorders in patients with sickle cell-hemoglobin C disorder

Association of adenylyl cyclase 6 rs3730070 polymorphism and hemolytic level in patients with sickle cell anemia

artículo científico publicado en 2016

Blood thixotropy in patients with sickle cell anaemia: role of haematocrit and red blood cell rheological properties

artículo científico publicado en 2014

CAREST--Multilingual Regional Integration for Health Promotion and Research on Sickle Cell Disease and Thalassemia.

artículo científico publicado en 2016

Cardiorespiratory responses during three repeated incremental exercise tests in sickle cell trait carriers.

artículo científico publicado en 2007

Changes in autonomic nervous activity during vaso-occlusive crisis in patients with sickle cell anaemia.

artículo científico publicado en 2016

Concerted evolution in the GAPDH family of retrotransposed pseudogenes

artículo científico publicado en 1993

Cord blood transplantation and the potential for gene therapy. Gene transduction using a recombinant adeno-associated viral vector.

artículo científico publicado en 1995

Decreased hematocrit-to-viscosity ratio and increased lactate dehydrogenase level in patients with sickle cell anemia and recurrent leg ulcers

artículo científico publicado en 2013

Delayed beneficial effect of acute exercise on red blood cell aggregate strength in patients with sickle cell anemia

artículo científico publicado en 2012

Does higher red blood cell (RBC) lactate transporter activity explain impaired RBC deformability in sickle cell trait?

artículo científico publicado en 2005

Does increased red blood cell deformability raise the risk for osteonecrosis in sickle cell anemia?

artículo científico publicado en 2013

Does the pattern of repeated sprint ability differ between sickle cell trait carriers and healthy subjects

artículo científico publicado en 2006

Early onset dactylitis associated with the occurrence of severe events in children with sickle cell anaemia. The Paediatric Cohort of Guadeloupe (1984-99)

scientific article published on 01 January 2006

Effect of Age on Blood Rheology in Sickle Cell Anaemia and Sickle Cell Haemoglobin C Disease: A Cross-Sectional Study

artículo científico publicado en 2016

Exacerbation of oxidative stress during sickle vaso-occlusive crisis is associated with decreased anti-band 3 autoantibodies rate and increased red blood cell-derived microparticle level: a prospective study

artículo científico publicado en 2016

Haemolysis and abnormal haemorheology in sickle cell anaemia

artículo científico publicado en 2014

Hematologic and hemorheological determinants of resting and exercise-induced hemoglobin oxygen desaturation in children with sickle cell disease

artículo científico publicado en 2013

Hematological and hemorheological determinants of the six-minute walk test performance in children with sickle cell anemia

artículo científico publicado en 2013

Hematopoietic colony formation from human growth factor-dependent TF1 cells and human cord blood myeloid progenitor cells depends on SHP2 phosphatase function

artículo científico publicado en 2012

Hemorheological alterations, decreased cerebral microvascular oxygenation and cerebral vasomotion compensation in sickle cell patients

artículo científico publicado en 2012

Hemorheological risk factors of acute chest syndrome and painful vaso-occlusive crisis in children with sickle cell disease

artículo científico publicado en 2012

High red blood cell nitric oxide synthase activation is not associated with improved vascular function and red blood cell deformability in sickle cell anaemia

artículo científico publicado en 2014

Hydroxyurea treatment does not increase blood viscosity and improves red blood cell rheology in sickle cell anemia

artículo científico publicado en 2015

Impact of eNOS polymorphisms on red blood cell aggregation in sickle cell disease

artículo científico publicado en 2015

Impaired blood rheology plays a role in the chronic disorders associated with sickle cell-hemoglobin C disease

artículo científico publicado en 2014

Impaired oxygen uptake efficiency slope and off-transient kinetics of pulmonary oxygen uptake in sickle cell anemia are associated with hemorheological abnormalities

artículo científico publicado en 2014

Increased blood viscosity and red blood cell aggregation in a patient with sickle cell anemia and smoldering myeloma.

artículo científico publicado en 2012

Is there a relationship between the hematocrit-to-viscosity ratio and microvascular oxygenation in brain and muscle?

artículo científico publicado en 2015

Lactic response in sickle cell trait carriers in comparison with subjects with normal hemoglobin.

artículo científico publicado en 2003

Male gender, increased blood viscosity, body mass index and triglyceride levels are independently associated with systemic relative hypertension in sickle cell anemia

artículo científico publicado en 2013

Micro- and macrovascular function in children with sickle cell anaemia and sickle cell haemoglobin C disease.

artículo científico publicado en 2017

Normal muscle oxygen consumption and fatigability in sickle cell patients despite reduced microvascular oxygenation and hemorheological abnormalities

artículo científico publicado en 2012

Patterns of exercise-related inflammatory response in sickle cell trait carriers

artículo científico publicado en 2008

Physical activity level is not a determinant of autonomic nervous system activity and clinical severity in children/adolescents with sickle cell anemia: A pilot study

artículo científico publicado en 2015

Pulmonary hypertension in an adult sickle cell population in Guadeloupe

artículo científico publicado en 2008

Red blood cell aggregation, aggregate strength and oxygen transport potential of blood are abnormal in both homozygous sickle cell anemia and sickle-hemoglobin C disease.

artículo científico publicado en 2009

Red blood cell nitric oxide synthase activation is increased in patients with sickle cell hemoglobin C disease

artículo científico publicado en 2015

Relationships between systemic vascular resistance, blood rheology and nitric oxide in children with sickle cell anemia or sickle cell-hemoglobin C disease

artículo científico publicado en 2014

Rheology of red blood cells in patients with HbC disease

artículo científico publicado en 2014

Risk factors and impact of orthopaedic monitoring on the outcome of avascular necrosis of the femoral head in adults with sickle cell disease: 215 patients case study with control group

artículo científico publicado en 2011

Severe proliferative retinopathy is associated with blood hyperviscosity in sickle cell hemoglobin-C disease but not in sickle cell anemia

scientific article published on January 2013

Sickle cell anemia in Guadeloupean children: pattern and prevalence of acute clinical events

artículo científico publicado en 2006

Sickle cell trait in French West Indian elite sprint athletes

artículo científico publicado en 2005

UGT1A1 polymorphism outweighs the modest effect of deletional (-3.7 kb) alpha-thalassemia on cholelithogenesis in sickle cell anemia

artículo científico publicado en 2006

Uncommon Posterior Reversible Encephalopathy Syndrome in a Sickle-Cell Patient.

artículo científico publicado en 2015

Universal newborn screening for haemoglobinopathies in Guadeloupe (French West Indies): a 27-year experience

artículo científico publicado en 2013

Ventilatory and lactic thresholds in subjects with sickle cell trait

artículo científico publicado en 2007

Which side of the balance determines the frequency of vaso-occlusive crises in children with sickle cell anemia: Blood viscosity or microvascular dysfunction?

artículo científico publicado en 2015

[Analysis of hospitalization of adult sickle-cell patients in Guadeloupe]

artículo científico publicado en 2000

Lista de obras de Maryse Etienne-Julan

Acute moderate exercise does not further alter the autonomic nervous system activity in patients with sickle cell anemia

Alpha thalassemia protects sickle cell anemia patients from macro-albuminuria through its effects on red blood cell rheological properties

Association between relative systemic hypertension and otologic disorders in patients with sickle cell-hemoglobin C disorder

Association of adenylyl cyclase 6 rs3730070 polymorphism and hemolytic level in patients with sickle cell anemia

Blood thixotropy in patients with sickle cell anaemia: role of haematocrit and red blood cell rheological properties

CAREST--Multilingual Regional Integration for Health Promotion and Research on Sickle Cell Disease and Thalassemia.

Cardiorespiratory responses during three repeated incremental exercise tests in sickle cell trait carriers.

Changes in autonomic nervous activity during vaso-occlusive crisis in patients with sickle cell anaemia.

Concerted evolution in the GAPDH family of retrotransposed pseudogenes

Cord blood transplantation and the potential for gene therapy. Gene transduction using a recombinant adeno-associated viral vector.

Decreased hematocrit-to-viscosity ratio and increased lactate dehydrogenase level in patients with sickle cell anemia and recurrent leg ulcers

Delayed beneficial effect of acute exercise on red blood cell aggregate strength in patients with sickle cell anemia

Does higher red blood cell (RBC) lactate transporter activity explain impaired RBC deformability in sickle cell trait?

Does increased red blood cell deformability raise the risk for osteonecrosis in sickle cell anemia?

Does the pattern of repeated sprint ability differ between sickle cell trait carriers and healthy subjects

Early onset dactylitis associated with the occurrence of severe events in children with sickle cell anaemia. The Paediatric Cohort of Guadeloupe (1984-99)

Effect of Age on Blood Rheology in Sickle Cell Anaemia and Sickle Cell Haemoglobin C Disease: A Cross-Sectional Study

Exacerbation of oxidative stress during sickle vaso-occlusive crisis is associated with decreased anti-band 3 autoantibodies rate and increased red blood cell-derived microparticle level: a prospective study

Haemolysis and abnormal haemorheology in sickle cell anaemia

Hematologic and hemorheological determinants of resting and exercise-induced hemoglobin oxygen desaturation in children with sickle cell disease

Hematological and hemorheological determinants of the six-minute walk test performance in children with sickle cell anemia

Hematopoietic colony formation from human growth factor-dependent TF1 cells and human cord blood myeloid progenitor cells depends on SHP2 phosphatase function

Hemorheological alterations, decreased cerebral microvascular oxygenation and cerebral vasomotion compensation in sickle cell patients

Hemorheological risk factors of acute chest syndrome and painful vaso-occlusive crisis in children with sickle cell disease

High red blood cell nitric oxide synthase activation is not associated with improved vascular function and red blood cell deformability in sickle cell anaemia

Hydroxyurea treatment does not increase blood viscosity and improves red blood cell rheology in sickle cell anemia

Impact of eNOS polymorphisms on red blood cell aggregation in sickle cell disease

Impaired blood rheology plays a role in the chronic disorders associated with sickle cell-hemoglobin C disease

Impaired oxygen uptake efficiency slope and off-transient kinetics of pulmonary oxygen uptake in sickle cell anemia are associated with hemorheological abnormalities

Increased blood viscosity and red blood cell aggregation in a patient with sickle cell anemia and smoldering myeloma.

Is there a relationship between the hematocrit-to-viscosity ratio and microvascular oxygenation in brain and muscle?

Lactic response in sickle cell trait carriers in comparison with subjects with normal hemoglobin.

Male gender, increased blood viscosity, body mass index and triglyceride levels are independently associated with systemic relative hypertension in sickle cell anemia

Micro- and macrovascular function in children with sickle cell anaemia and sickle cell haemoglobin C disease.

Normal muscle oxygen consumption and fatigability in sickle cell patients despite reduced microvascular oxygenation and hemorheological abnormalities

Patterns of exercise-related inflammatory response in sickle cell trait carriers

Physical activity level is not a determinant of autonomic nervous system activity and clinical severity in children/adolescents with sickle cell anemia: A pilot study

Pulmonary hypertension in an adult sickle cell population in Guadeloupe

Red blood cell aggregation, aggregate strength and oxygen transport potential of blood are abnormal in both homozygous sickle cell anemia and sickle-hemoglobin C disease.

Red blood cell nitric oxide synthase activation is increased in patients with sickle cell hemoglobin C disease

Relationships between systemic vascular resistance, blood rheology and nitric oxide in children with sickle cell anemia or sickle cell-hemoglobin C disease

Rheology of red blood cells in patients with HbC disease

Risk factors and impact of orthopaedic monitoring on the outcome of avascular necrosis of the femoral head in adults with sickle cell disease: 215 patients case study with control group

Severe proliferative retinopathy is associated with blood hyperviscosity in sickle cell hemoglobin-C disease but not in sickle cell anemia

Sickle cell anemia in Guadeloupean children: pattern and prevalence of acute clinical events

Sickle cell trait in French West Indian elite sprint athletes

UGT1A1 polymorphism outweighs the modest effect of deletional (-3.7 kb) alpha-thalassemia on cholelithogenesis in sickle cell anemia

Uncommon Posterior Reversible Encephalopathy Syndrome in a Sickle-Cell Patient.

Universal newborn screening for haemoglobinopathies in Guadeloupe (French West Indies): a 27-year experience

Ventilatory and lactic thresholds in subjects with sickle cell trait

Which side of the balance determines the frequency of vaso-occlusive crises in children with sickle cell anemia: Blood viscosity or microvascular dysfunction?

[Analysis of hospitalization of adult sickle-cell patients in Guadeloupe]