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Annales De Biologie Clinique
|
December 9, 2014
[Development of a laboratory test on dried blood spots for facilitating early diagnosis of alpha-1-antitrypsin deficiency]
Malika Balduyck, Colette Chapuis Cellier, Denis Roche, et al.
Journal of Clinical Medicine
|
June 2, 2021
Is Skeletal Muscle Dysfunction a Limiting Factor of Exercise Functional Capacity in Patients with Sickle Cell Disease?
Etienne Gouraud, Philippe Connes, Alexandra Gauthier-Vasserot, et al.
Clinical Hemorheology and Microcirculation
|
October 8, 2015
Importance of methodological standardization for the ektacytometric measures of red blood cell deformability in sickle cell anemia
Céline Renoux, Nermi Parrow, Camille Faes, et al.
Nucleic Acids Research
|
October 19, 2013
Updates of the HbVar database of human hemoglobin variants and thalassemia mutations
Belinda Giardine, Joseph Borg, Emmanouil Viennas, et al.
European Journal of Haematology
|
December 17, 2016
UGT1A1 (TA)<sub>n</sub> genotype is not the major risk factor of cholelithiasis in sickle cell disease children
Philippe Joly, Céline Renoux, Philippe Lacan, et al.
Frontiers in Physiology
|
October 11, 2021
Nocturnal Hypoxemia Rather Than Obstructive Sleep Apnea Is Associated With Decreased Red Blood Cell Deformability and Enhanced Hemolysis in Patients With Sickle Cell Disease
Emeric Stauffer, Solène Poutrel, Giovanna Cannas, et al.
American Journal of Hematology
|
September 2, 2022
Homozygosity for the hyperunstable hemoglobin variant Hb Agrinio (HBA2:c.89T>C) leads to severe antenatal anemia: Eight new cases in three families
Sarah Szepetowski, Claire Berger, Philippe Joly, et al.
British Journal of Haematology
|
December 22, 2022
Clinical severity and blood rheology in patients with sickle cell anaemia and co-existing autoimmune disease
Solène Poutrel, Camille Boisson, Elie Nader, et al.
European Journal of Haematology
|
June 16, 2015
G6PD deficiency and absence of α-thalassemia increase the risk for cerebral vasculopathy in children with sickle cell anemia
Philippe Joly, Nathalie Garnier, Kamila Kebaili, et al.
Haematologica
|
October 13, 2022
Variation and impact of polygenic hematologic traits in monogenic sickle cell disease
Thomas Pincez, Ken Sin Lo, Anne-Laure Pham Hung d'Alexandry D'Orengiani, et al.
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Search research articles
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Showing results (101-110 of 148) with videos related to
Sort By:
Page
of 15
Annales De Biologie Clinique
|
December 9, 2014
[Development of a laboratory test on dried blood spots for facilitating early diagnosis of alpha-1-antitrypsin deficiency]
Malika Balduyck, Colette Chapuis Cellier, Denis Roche, et al.
Journal of Clinical Medicine
|
June 2, 2021
Is Skeletal Muscle Dysfunction a Limiting Factor of Exercise Functional Capacity in Patients with Sickle Cell Disease?
Etienne Gouraud, Philippe Connes, Alexandra Gauthier-Vasserot, et al.
Clinical Hemorheology and Microcirculation
|
October 8, 2015
Importance of methodological standardization for the ektacytometric measures of red blood cell deformability in sickle cell anemia
Céline Renoux, Nermi Parrow, Camille Faes, et al.
Nucleic Acids Research
|
October 19, 2013
Updates of the HbVar database of human hemoglobin variants and thalassemia mutations
Belinda Giardine, Joseph Borg, Emmanouil Viennas, et al.
European Journal of Haematology
|
December 17, 2016
UGT1A1 (TA)<sub>n</sub> genotype is not the major risk factor of cholelithiasis in sickle cell disease children
Philippe Joly, Céline Renoux, Philippe Lacan, et al.
Frontiers in Physiology
|
October 11, 2021
Nocturnal Hypoxemia Rather Than Obstructive Sleep Apnea Is Associated With Decreased Red Blood Cell Deformability and Enhanced Hemolysis in Patients With Sickle Cell Disease
Emeric Stauffer, Solène Poutrel, Giovanna Cannas, et al.
American Journal of Hematology
|
September 2, 2022
Homozygosity for the hyperunstable hemoglobin variant Hb Agrinio (HBA2:c.89T>C) leads to severe antenatal anemia: Eight new cases in three families
Sarah Szepetowski, Claire Berger, Philippe Joly, et al.
British Journal of Haematology
|
December 22, 2022
Clinical severity and blood rheology in patients with sickle cell anaemia and co-existing autoimmune disease
Solène Poutrel, Camille Boisson, Elie Nader, et al.
European Journal of Haematology
|
June 16, 2015
G6PD deficiency and absence of α-thalassemia increase the risk for cerebral vasculopathy in children with sickle cell anemia
Philippe Joly, Nathalie Garnier, Kamila Kebaili, et al.
Haematologica
|
October 13, 2022
Variation and impact of polygenic hematologic traits in monogenic sickle cell disease
Thomas Pincez, Ken Sin Lo, Anne-Laure Pham Hung d'Alexandry D'Orengiani, et al.
Page
of 15