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Clinical Hemorheology and Microcirculation
|
November 20, 2020
HbF-promoting polymorphisms may specifically reduce the residual risk of cerebral vasculopathy in SCA children with alpha-thalassemia
Philippe Joly, Nathalie Bonello-Palot, Catherine Badens, et al.
Haematologica
|
January 12, 2005
Severe hemolytic anemia in a Vietnamese family, associated with novel mutations in the gene encoding for pyruvate kinase
Catherine Costa, Juliette Albuisson, Thi Hao Le, et al.
British Journal of Haematology
|
May 18, 2006
Pyruvate kinase deficiency in France: a 3-year study reveals 27 new mutations
Serge Pissard, Isabelle Max-Audit, Laurent Skopinski, et al.
Nucleic Acids Research
|
October 30, 2020
Clinically relevant updates of the HbVar database of human hemoglobin variants and thalassemia mutations
Belinda M Giardine, Philippe Joly, Serge Pissard, et al.
The Journal of Biological Chemistry
|
April 8, 2010
Alpha-hemoglobin stabilizing protein (AHSP), a kinetic scheme of the action of a human mutant, AHSPV56G
Thomas Brillet, Véronique Baudin-Creuza, Corinne Vasseur, et al.
Annales De Biologie Clinique
|
May 9, 2012
[Molecular diagnosis of HFE mutations in routine laboratories. Results of a survey from reference laboratories in France]
Anne-Marie Jouanolle, Victoria Gérolami, Cécile Ged, et al.
Transfusion
|
November 9, 2022
Prenatal management of fetal anemia due to pyruvate kinase deficiency: A case report
Emeline Maisonneuve, Marlène Sohier Lepine, Paul Maurice, et al.
Hemoglobin
|
November 17, 2010
A dyserythropoietic anemia associated with homozygous Hb Plasencia [α125(H8)Leu→Arg (α2)] (HBA2:c.377T>G), a variant with an unstable α chain
Loïc Garçon, Achille Iolascon, Serge Pissard, et al.
Annales De Biologie Clinique
|
January 7, 2017
Diagnostic approach to hemoglobins with high oxygen affinity: experience from France and Belgium and review of the literature
Corentin Orvain, Philippe Joly, Serge Pissard, et al.
Haematologica
|
July 28, 2011
Variants in genetic modifiers of β-thalassemia can help to predict the major or intermedia type of the disease
Catherine Badens, Philippe Joly, Imane Agouti, et al.
Page
of 7
Search research articles
Search
Showing results (31-40 of 63) with videos related to
Sort By:
Page
of 7
Clinical Hemorheology and Microcirculation
|
November 20, 2020
HbF-promoting polymorphisms may specifically reduce the residual risk of cerebral vasculopathy in SCA children with alpha-thalassemia
Philippe Joly, Nathalie Bonello-Palot, Catherine Badens, et al.
Haematologica
|
January 12, 2005
Severe hemolytic anemia in a Vietnamese family, associated with novel mutations in the gene encoding for pyruvate kinase
Catherine Costa, Juliette Albuisson, Thi Hao Le, et al.
British Journal of Haematology
|
May 18, 2006
Pyruvate kinase deficiency in France: a 3-year study reveals 27 new mutations
Serge Pissard, Isabelle Max-Audit, Laurent Skopinski, et al.
Nucleic Acids Research
|
October 30, 2020
Clinically relevant updates of the HbVar database of human hemoglobin variants and thalassemia mutations
Belinda M Giardine, Philippe Joly, Serge Pissard, et al.
The Journal of Biological Chemistry
|
April 8, 2010
Alpha-hemoglobin stabilizing protein (AHSP), a kinetic scheme of the action of a human mutant, AHSPV56G
Thomas Brillet, Véronique Baudin-Creuza, Corinne Vasseur, et al.
Annales De Biologie Clinique
|
May 9, 2012
[Molecular diagnosis of HFE mutations in routine laboratories. Results of a survey from reference laboratories in France]
Anne-Marie Jouanolle, Victoria Gérolami, Cécile Ged, et al.
Transfusion
|
November 9, 2022
Prenatal management of fetal anemia due to pyruvate kinase deficiency: A case report
Emeline Maisonneuve, Marlène Sohier Lepine, Paul Maurice, et al.
Hemoglobin
|
November 17, 2010
A dyserythropoietic anemia associated with homozygous Hb Plasencia [α125(H8)Leu→Arg (α2)] (HBA2:c.377T>G), a variant with an unstable α chain
Loïc Garçon, Achille Iolascon, Serge Pissard, et al.
Annales De Biologie Clinique
|
January 7, 2017
Diagnostic approach to hemoglobins with high oxygen affinity: experience from France and Belgium and review of the literature
Corentin Orvain, Philippe Joly, Serge Pissard, et al.
Haematologica
|
July 28, 2011
Variants in genetic modifiers of β-thalassemia can help to predict the major or intermedia type of the disease
Catherine Badens, Philippe Joly, Imane Agouti, et al.
Page
of 7