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Men with Sickle Cell Anemia and Priapism Exhibit Increased Hemolytic Rate, Decreased Red Blood Cell Deformability and Increased Red Blood Cell Aggregate Strength

PloS one, 2016, Vol.11 (5), p.e0154866-e0154866

2016

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Frequency of pain crises in sickle cell anemia and its relationship with the sympatho-vagal balance, blood viscosity and inflammation

Haematologica (Roma), 2011-11, Vol.96 (11), p.1589-1594

2011

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Editorial for Special Issue “Newborn Screening for Sickle Cell Disease and other Haemoglobinopathies”

International journal of neonatal screening, 2019-09, Vol.5 (4), p.36-36

2019

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The spectrum of cardiac anomalies in Noonan syndrome as a result of mutations in the PTPN11 gene

Pediatrics (Evanston), 2007-06, Vol.119 (6), p.e1325-e1331

2007

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Scientific Advances in Diagnosis

Hemoglobin, 2019-11, Vol.43 (6), p.317-317

Elion, Jacques

2019

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Heterozygous HbAC but not HbAS is associated with higher newborn birthweight among women with pregnancy-associated malaria

Scientific reports, 2017-05, Vol.7 (1), p.1414-8, Article 1414

2017

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Commensal Escherichia coli isolates are phylogenetically distributed among geographically distinct human populations

Microbiology (Society for General Microbiology), 2001-06, Vol.147 (Pt 6), p.1671-1676

2001

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Modulation of erythroid adhesion receptor expression by hydroxyurea in children with sickle cell disease

Haematologica (Roma), 2008-04, Vol.93 (4), p.502-510

2008

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Newborn Screening for Sickle Cell Disease in Europe

International journal of neonatal screening, 2019-02, Vol.5 (1), p.15-15

2019

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Evolutionary Implications of the Frequent Horizontal Transfer of Mismatch Repair Genes

Cell, 2000-11, Vol.103 (5), p.711-721

2000

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Differential modulation of adhesion molecule expression by hydroxycarbamide in human endothelial cells from the micro- and macrocirculation: potential implications in sickle cell disease vasoocclusive events

Haematologica (Roma), 2011-04, Vol.96 (4), p.534-542

2011

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Unsuspected glucose-6-phosphate dehydrogenase deficiency presenting as symptomatic methemoglobinemia with severe hemolysis after fava bean ingestion in a 6-year-old boy

International journal of hematology, 2011-05, Vol.93 (5), p.664-666

2011

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Pre- and postnatal phenotype of 6p25 deletions involving the FOXC1 gene

American journal of medical genetics. Part A, 2012-10, Vol.158A (10), p.2430-2438

2012

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Dominique Labie (1920-2016)

M.S. Médecine sciences, 2016-05, Vol.32 (5), p.523-526

Elion, Jacques

2016

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Fetal hemoglobin and hydroxycarbamide moduate both plasma concentration and cellular origin of circulating microparticles in sickle cell anemia children

Haematologica (Roma), 2013-06, Vol.98 (6), p.862-867

2013

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Genetic variation among major human geographic groups supports a peculiar evolutionary trend in PAX9

PloS one, 2011-01, Vol.6 (1), p.e15656-e15656

2011

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New approach to accurate interpretation of sickle cell disease newborn screening by applying multiple of median cutoffs and ratios

Pediatric blood & cancer, 2018-09, Vol.65 (9), p.e27230-n/a

2018

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The missing middle of sickle therapeutics: Multi‐agent therapy, targeting risk, using biomarkers

American journal of hematology, 2018-12, Vol.93 (12), p.1439-1443

2018

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Cellular and Molecular Effects of Hydroxycarbamide in Sickle Cell Patients

Current pharmacogenomics and personalized medicine, 2014-09, Vol.12 (2), p.114-122

2014

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Newborn screening for sickle cell disease in Europe: recommendations from a Pan‐European Consensus Conference

British journal of haematology, 2018-11, Vol.183 (4), p.648-660

2018

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Mother-to-child transmitted WT1 splice-site mutation is responsible for distinct glomerular diseases

Journal of the American Society of Nephrology, 1999-10, Vol.10 (10), p.2219-2223

1999

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Sodium phenyl butyrate downregulates endothelin‐1 expression in cultured human endothelial cells: Relevance to sickle‐cell disease

American journal of hematology, 2007-05, Vol.82 (5), p.357-362

2007

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Degree of anemia, indirect markers of hemolysis, and vascular complications of sickle cell disease in Africa

Blood, 2017-11, Vol.130 (20), p.2215-2223

2017

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Chez les drépanocytaires, le pneumocoque se joue de la prévention et s’adapte à la maladie: Conséquences vaccinales

M.S. Médecine sciences, 2014-11, Vol.30 (11), p.946-948

2014

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Sickle cell disease: pneumococcus escapes prevention and adapts to the disease. Consequences on vaccine design

M.S. Médecine sciences, 2014-11, Vol.30 (11), p.946

2014

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Men with Sickle Cell Anemia and Priapism Exhibit Increased Hemolytic Rate, Decreased Red Blood Cell Deformability and Increased Red Blood Cell Aggregate Strength

Frequency of pain crises in sickle cell anemia and its relationship with the sympatho-vagal balance, blood viscosity and inflammation

Editorial for Special Issue “Newborn Screening for Sickle Cell Disease and other Haemoglobinopathies”

The spectrum of cardiac anomalies in Noonan syndrome as a result of mutations in the PTPN11 gene

Scientific Advances in Diagnosis

Heterozygous HbAC but not HbAS is associated with higher newborn birthweight among women with pregnancy-associated malaria

Commensal Escherichia coli isolates are phylogenetically distributed among geographically distinct human populations

Modulation of erythroid adhesion receptor expression by hydroxyurea in children with sickle cell disease

Newborn Screening for Sickle Cell Disease in Europe

Evolutionary Implications of the Frequent Horizontal Transfer of Mismatch Repair Genes

Differential modulation of adhesion molecule expression by hydroxycarbamide in human endothelial cells from the micro- and macrocirculation: potential implications in sickle cell disease vasoocclusive events

Unsuspected glucose-6-phosphate dehydrogenase deficiency presenting as symptomatic methemoglobinemia with severe hemolysis after fava bean ingestion in a 6-year-old boy

Pre- and postnatal phenotype of 6p25 deletions involving the FOXC1 gene

Dominique Labie (1920-2016)

Fetal hemoglobin and hydroxycarbamide moduate both plasma concentration and cellular origin of circulating microparticles in sickle cell anemia children

Genetic variation among major human geographic groups supports a peculiar evolutionary trend in PAX9

New approach to accurate interpretation of sickle cell disease newborn screening by applying multiple of median cutoffs and ratios

The missing middle of sickle therapeutics: Multi‐agent therapy, targeting risk, using biomarkers

Cellular and Molecular Effects of Hydroxycarbamide in Sickle Cell Patients

Newborn screening for sickle cell disease in Europe: recommendations from a Pan‐European Consensus Conference

Mother-to-child transmitted WT1 splice-site mutation is responsible for distinct glomerular diseases

Sodium phenyl butyrate downregulates endothelin‐1 expression in cultured human endothelial cells: Relevance to sickle‐cell disease

Degree of anemia, indirect markers of hemolysis, and vascular complications of sickle cell disease in Africa

Chez les drépanocytaires, le pneumocoque se joue de la prévention et s’adapte à la maladie: Conséquences vaccinales

Sickle cell disease: pneumococcus escapes prevention and adapts to the disease. Consequences on vaccine design

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