About: Maryse Étienne-Julan

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An Entity of Type : foaf:Person, within Data Space : data.idref.fr associated with source document(s)

Attributes	Values
type	Person
sameAs	Étienne-Julan, Maryse (19..-....) Étienne-Julan, Maryse (19..-....) Étienne-Julan, Maryse (19..-....)
alternative label	Étienne-Julan-Otto, Maryse
Life Event	http://www.idref.fr/143142801/birth
preferred label	Étienne-Julan, Maryse (19..-....)
name	Maryse Étienne-Julan
dbpedia-owl:citizenship	http://example.com/foo
Language	http://lexvo.org/id/iso639-3/fra
Given name	Maryse
familyName	Étienne-Julan
has biographical i...tion (Deprecated)	Médecin. Praticien hospitalier, chef de service de l'Unité Transversale - Centre de la Drépanocytose du CHU de Pointe-à-Pître en 2009
gender	female
ORCID iD	0000-0003-1339-6545
is sameAs of	Étienne-Julan, Maryse (19..-....) Étienne-Julan, Maryse (19..-....)
is Thesis advisor of	http://www.sudoc.fr/143142372/id http://www.sudoc.fr/279102038/id http://www.sudoc.fr/268696772/id
is Author of	http://www.sudoc.fr/178409227/id http://www.sudoc.fr/012098132/id Relationships between systemic vascular resistance, blood rheology and nitric oxide in children with sickle cell anemia or sickle cell-hemoglobin C disease. Decreased hematocrit-to-viscosity ratio and increased lactate dehydrogenase level in patients with sickle cell anemia and recurrent leg ulcers. 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 Is there a relationship betweenthe hematocrit-to-viscosity ratioand microvascular oxygenation in brain and muscle? High red blood cell nitric oxide synthase activation is not associated with improved vascular function and red blood cell deformability in sickle cell anaemia Association between oxidative stress and vascular reactivity in children with sickle cell anaemia and sickle haemoglobin C disease Hemorheological alterations, decreased cerebral microvascular oxygenation and cerebral vasomotion compensation in sickle cell patients. Normal muscle oxygen consumption and fatigability in sickle cell patients despite reduced microvascular oxygenation and hemorheological abnormalities. Impaired blood rheology plays a role inthe chronic disorders associated with sickle cell- hemoglobin C disease Men with Sickle Cell Anemia and Priapism Exhibit Increased Hemolytic Rate, Decreased Red Blood Cell Deformability and Increased Red Blood Cell Aggregate Strength Changes in autonomic nervous activity during vaso-occlusive crisis in patients with sickle cell anaemia Impact of eNOS polymorphisms on red blood cell aggregation in sickle cell disease Blood Thixotropy in Patients with Sickle Cell Anaemia: Role of Haematocrit and Red Blood Cell Rheological Properties Which side of the balance determines the frequency of vaso-occlusive crises in children with sickle cell anemia: Blood viscosity or microvascular dysfunction? https://hal.archives-ouvertes.fr/hal-01881713#id A medical consideration for sickle cell trait carriers in sports: example of Guadeloupe Haemolysis and abnormal haemorheology in sickle cell anaemia https://hal.archives-ouvertes.fr/hal-01881737#id Rheology of red blood cells in patients with HbC disease Proliferative retinopathy and maculopathy are two independent conditions in sickle cell disease: Is there a role of blood rheology?1 Decrease of externalized phosphatidylserine density on red blood cell-derived microparticles in SCA patients treated with hydroxycarbamide Association between relative systemic hypertension and otologic disorders in patients with sickle cell-hemoglobin C disorder Acute Moderate Exercise Does Not Further Alter the Autonomic Nervous System Activity in Patients with Sickle Cell Anemia Plasma microparticles of sickle patients during crisis or taking hydroxyurea modify endothelium inflammatory properties Design of the DREPAGREFFE trial: A prospective controlled multicenter study evaluating the benefit of genoidentical hematopoietic stem cell transplantation over chronic transfusion in sickle cell anemia children detected to be at risk of stroke by transcranial Doppler (NCT 01340404) Multifocal electroretinogram findings in sickle cell maculopathy Severe proliferative retinopathy is associated with blood hyperviscosity in sickle cell hemoglobin-C disease but not in sickle cell anemia. Concerted evolution in the GAPDH family of retrotransposed pseudogenes. Relationships between systemic vascular resistance, blood rheology and nitric oxide in children with sickle cell anemia or sickle cell-hemoglobin C disease. Sickle cell anemia in Guadeloupean children: pattern and prevalence of acute clinical events Does increased red blood cell deformability raise the risk for osteonecrosis in sickle cell anemia? Patterns of exercise-related inflammatory response in sickle cell trait carriers Acute Moderate Exercise Does Not Further Alter the Autonomic Nervous System Activity in Patients with Sickle Cell Anemia Hematologic and hemorheological determinants of resting and exercise-induced hemoglobin oxygen desaturation in children with sickle cell disease. Hemorheological risk factors of acute chest syndrome and painful vaso-occlusive crisis in children with sickle cell disease. UGT1A1 polymorphism outweighs the modest effect of deletional (−3.7 kb) α-thalassemia on cholelithogenesis in sickle cell anemia Micro- and macrovascular function in children with sickle cell anaemia and sickle cell haemoglobin C disease Red blood cell nitric oxide synthase activation is increased in patients with sickle cell hemoglobin C disease 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 Central retinal vein occlusion in a sickle cell trait carrier after a cycling race. Lipid profiles in French West Indies sickle cell disease cohorts, and their general population Association of adenylyl cyclase 6 rs3730070 polymorphism and hemolytic level in patients with sickle cell anemia Is there a relationship between the hematocrit-to-viscosity ratio and microvascular oxygenation in brain and muscle? Cerebral and muscle microvascular oxygenation in children with sickle cell disease: Influence of hematology, hemorheology and vasomotion. Drépanocytose et priapisme : rôle des paramètres hématologiques et hémorhéologiques Impaired oxygen uptake efficiency slope and off-transient kinetics of pulmonary oxygen uptake in sickle cell anemia are associated with hemorheological abnormalities Measuring workload with electrodermal activity during common braking actions Effect of Age on Blood Rheology in Sickle Cell Anaemia and Sickle Cell Haemoglobin C Disease: A Cross-Sectional Study Alpha-thalassaemia promotes frequent vaso-occlusive crises in children with sickle cell anaemia through haemorheological changes CAREST—Multilingual Regional Integration for Health Promotion and Research on Sickle Cell Disease and Thalassemia Alpha thalassemia protects sickle cell anemia patients from macro-albuminuria through its effects on red blood cell rheological properties. Male gender, increased blood viscosity, body mass index and triglyceride levels are independently associated with systemic relative hypertension in sickle cell anemia. Concerted evolution in the GAPDH family of retrotransposed pseudogenes Design of the DREPAGREFFE trial: A prospective controlled multicenter study evaluating the benefit of genoidentical hematopoietic stem cell transplantation over chronic transfusion in sickle cell anemia children detected to be at risk of stroke by transcranial Doppler (NCT 01340404) https://hal.archives-ouvertes.fr/hal-01881536#id Effects of hydroxyurea on blood rheology in sickle cell anemia: A two-years follow-up study Differences of microparticle patterns between sickle cell anemia and hemoglobin SC patients Sickle Cell Maculopathy: Microstructural Analysis Using OCTA and Identification of Genetic, Systemic, and Biological Risk Factors http://www.sudoc.fr/273638947/id Hematological and hemorheological determinants of the six-minute walk test performance in children with sickle cell anemia.
is primary topic of	http://www.idref.fr/143142801
is Opponent of	http://www.sudoc.fr/262690748/id

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