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Hemoglobin
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September 29, 2011
α-Hemoglobin stabilizing protein: a modulating factor in thalassemias?
Henri Wajcman, Corinne Vasseur, Serge Pissard, et al.
Molecular Diagnosis : a Journal Devoted to the Understanding of Human Disease Through the Clinical Application of Molecular Biology
|
October 8, 2003
A one-step real-time PCR assay for rapid prenatal diagnosis of sickle cell disease and detection of maternal contamination
Catherine Costa, Serge Pissard, Emmanuelle Girodon, et al.
Hemoglobin
|
October 16, 2004
Compound heterozygosity for two new mutations in the beta-globin gene [codon 9 (+TA) and polyadenylation site (AATAAA-->AAAAAA)] leads to thalassemia intermedia in a Tunisian patient
Aurelia Jacquette, Geneviève Le Roux, Chantal Lacombe, et al.
Hemoglobin
|
May 26, 2016
Hb Savaria [α49(CE7)Ser→Arg; HBA2: c.150C > A]: A New Case and Complete Description
Thi Hai Yen Tran Houangkeo, Virginie Bodereau, Jean Riou, et al.
Hemoglobin
|
March 26, 2015
Genetic Modifiers of Sickle Cell Disease: A Genotype-Phenotype Relationship Study in a Cohort of 82 Children on Mayotte Island
Mathias Muszlak, Serge Pissard, Catherine Badens, et al.
Blood Cells, Molecules & Diseases
|
March 4, 2014
Variability of hemoglobin F expression in hemoglobin EE disease: hematological and molecular analysis
Naruwat Pakdee, Supawadee Yamsri, Goonnapa Fucharoen, et al.
Blood
|
April 19, 2003
Hydroxyurea can eliminate transfusion requirements in children with severe beta-thalassemia
Mohamed Bradai, Mohand Tayeb Abad, Serge Pissard, et al.
Journal of Pediatric Hematology/Oncology
|
May 20, 2026
A Rare Case of Homozygous HbE With Coinherited Alpha-Thalassemia and Hb Constant Spring in a Neonate Reveals a Mild Hematologic Phenotype
Victor Bobée, Maïssa Souissi, Cécile Dumesnil, et al.
Hemoglobin
|
March 23, 2011
A second observation of the rare frameshift mutation in the β-globin gene: codon 46 (+A) (Hbb:c.138_139insA)
Elyes Slim Ghedira, Delphine Dupin-Deguine, Denis Duffilot, et al.
American Journal of Hematology
|
January 26, 2011
Evaluation of the free α-hemoglobin pool in red blood cells: a new test providing a scale of β-thalassemia severity
Corinne Vasseur, Serge Pissard, Elisa Domingues-Hamdi, et al.
Page
of 7
Search research articles
Search
Showing results (1-10 of 63) with videos related to
Sort By:
Page
of 7
Hemoglobin
|
September 29, 2011
α-Hemoglobin stabilizing protein: a modulating factor in thalassemias?
Henri Wajcman, Corinne Vasseur, Serge Pissard, et al.
Molecular Diagnosis : a Journal Devoted to the Understanding of Human Disease Through the Clinical Application of Molecular Biology
|
October 8, 2003
A one-step real-time PCR assay for rapid prenatal diagnosis of sickle cell disease and detection of maternal contamination
Catherine Costa, Serge Pissard, Emmanuelle Girodon, et al.
Hemoglobin
|
October 16, 2004
Compound heterozygosity for two new mutations in the beta-globin gene [codon 9 (+TA) and polyadenylation site (AATAAA-->AAAAAA)] leads to thalassemia intermedia in a Tunisian patient
Aurelia Jacquette, Geneviève Le Roux, Chantal Lacombe, et al.
Hemoglobin
|
May 26, 2016
Hb Savaria [α49(CE7)Ser→Arg; HBA2: c.150C > A]: A New Case and Complete Description
Thi Hai Yen Tran Houangkeo, Virginie Bodereau, Jean Riou, et al.
Hemoglobin
|
March 26, 2015
Genetic Modifiers of Sickle Cell Disease: A Genotype-Phenotype Relationship Study in a Cohort of 82 Children on Mayotte Island
Mathias Muszlak, Serge Pissard, Catherine Badens, et al.
Blood Cells, Molecules & Diseases
|
March 4, 2014
Variability of hemoglobin F expression in hemoglobin EE disease: hematological and molecular analysis
Naruwat Pakdee, Supawadee Yamsri, Goonnapa Fucharoen, et al.
Blood
|
April 19, 2003
Hydroxyurea can eliminate transfusion requirements in children with severe beta-thalassemia
Mohamed Bradai, Mohand Tayeb Abad, Serge Pissard, et al.
Journal of Pediatric Hematology/Oncology
|
May 20, 2026
A Rare Case of Homozygous HbE With Coinherited Alpha-Thalassemia and Hb Constant Spring in a Neonate Reveals a Mild Hematologic Phenotype
Victor Bobée, Maïssa Souissi, Cécile Dumesnil, et al.
Hemoglobin
|
March 23, 2011
A second observation of the rare frameshift mutation in the β-globin gene: codon 46 (+A) (Hbb:c.138_139insA)
Elyes Slim Ghedira, Delphine Dupin-Deguine, Denis Duffilot, et al.
American Journal of Hematology
|
January 26, 2011
Evaluation of the free α-hemoglobin pool in red blood cells: a new test providing a scale of β-thalassemia severity
Corinne Vasseur, Serge Pissard, Elisa Domingues-Hamdi, et al.
Page
of 7