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A Hemodynamic Study of Pulmonary Hypertension in Sickle Cell Disease

The New England journal of medicine, 2011-07, Vol.365 (1), p.44-53

2011

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Delayed hemolytic transfusion reaction in adult sickle‐cell disease: presentations, outcomes, and treatments of 99 referral center episodes

American journal of hematology, 2016-10, Vol.91 (10), p.989-994

2016

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Influence of sickle cell disease and treatment with hydroxyurea on sperm parameters and fertility of human males

Haematologica (Roma), 2008-07, Vol.93 (7), p.988-993

2008

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Complications and treatment of patients with β-thalassemia in France: results of the National Registry

Haematologica (Roma), 2010-05, Vol.95 (5), p.724-729

2010

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Estimation of the difference in HbF expression due to loss of the 5' δ-globin BCL11A binding region

Haematologica (Roma), 2013-02, Vol.98 (2), p.305-308

2013

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Aggregation of mononuclear and red blood cells through an α4β1-Lu/basal cell adhesion molecule interaction in sickle cell disease

Haematologica (Roma), 2010-11, Vol.95 (11), p.1841-1848

2010

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Population pharmacokinetics and pharmacodynamics of hydroxyurea in sickle cell anemia patients, a basis for optimizing the dosing regimen

Orphanet journal of rare diseases, 2011-05, Vol.6 (1), p.30-30, Article 30

2011

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Factors Associated With Dyspnea in Adult Patients With Sickle Cell Disease

Chest, 2005-11, Vol.128 (5), p.3336-3344

2005

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Une compilation internationale des résultats de 1 000 greffes de cellules souches pour drépanocytose

Hématologie, 2017-07, Vol.23 (4), p.227-228

Bachir, Dora

2017

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Un nomogramme diagnostique d’hémolyse retardée dans la drépanocytose : un outil indispensable à la disposition des cliniciens urgentistes

Hématologie, 2017-01, Vol.23 (1), p.21-23

Bachir, Dora

2017

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Mortalité élevée des adolescents atteints de drépanocytose homozygote avec antécédents d’accident vasculaire cérébral en rapport avec l’arrêt des programmes transfusionnels lors de la transition pédiatrie-secteur adulte aux États-Unis

Hématologie, 2016-09, Vol.22 (5), p.306-308

Bachir, Dora

2016

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Histoire naturelle de l’atteinte rénale dans la drépanocytose homozygote

Hématologie, 2016-07, Vol.22 (4), p.242-243

Bachir, Dora

2016

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La drépanocytose est passée en quarante ans d’une maladie pédiatrique mortelle à une maladie chronique de l’adulte

Hématologie, 2016-03, Vol.22 (2), p.89-91

Bachir, Dora

2016

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Le ferumoxytol (Feraheme®), nouveau fer intraveineux « minute » ?

Hématologie, 2014-07, Vol.20 (4), p.196-197

Bachir, Dora

2014

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Quel est le devenir des adultes drépanocytaires ayant un antécédent d’accident vasculaire cérébral ?

Hématologie, 2014-05, Vol.20 (3), p.140-141

Bachir, Dora

2014

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Adverse effect of hydroxyurea on spermatogenesis in patients with sickle cell anemia after 6 months of treatment

Blood, 2017-11, Vol.130 (21), p.2354-2356

2017

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Drepadom - Establishment of Home Care Services and Hospitalizations for Sickle Cell Disease Patients As Standard Care Since the Covid-19 Pandemic

Blood, 2021-11, Vol.138 (Supplement 1), p.916-916

2021

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Pyruvate Kinase (PK) Deficiency in Newborns: The Pitfalls of Diagnosis

The Journal of pediatrics, 2007-04, Vol.150 (4), p.443-445

2007

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Drepadom - Home Care Services and Hospitalizations for Sickle Cell Disease Patients during the Covid-19 Pandemic

Blood, 2020-11, Vol.136 (Supplement 1), p.12-12

2020

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Decreased sickle red blood cell adhesion to laminin by hydroxyurea is associated with inhibition of Lu/BCAM protein phosphorylation

Blood, 2010-09, Vol.116 (12), p.2152-2159

2010

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Improvements in haemolysis and indicators of erythrocyte survival do not correlate with acute vaso‐occlusive crises in patients with sickle cell disease: a phase III randomized, placebo‐controlled, double‐blind study of the gardos channel blocker senicapoc (ICA‐17043)

British journal of haematology, 2011-04, Vol.153 (1), p.92-104

2011

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Delayed hemolytic transfusion reaction in sickle cell disease patients: evidence of an emerging syndrome with suicidal red blood cell death

Transfusion (Philadelphia, Pa.), 2009-09, Vol.49 (9), p.1785-1792

2009

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Predictive Factors for Survival in Sickle Cell Disease: A Cohort Study Using Etendard Data

Blood, 2018-11, Vol.132 (Supplement 1), p.7-7

2018

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The liver in sickle cell disease

La Presse médicale (1983), 2023-12, Vol.52 (4), p.104212-104212, Article 104212

2023

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Transfusion requirements and complication rate in β‐thalassemia intermedia due to heterozygous β‐globin gene mutation and triplicated α‐globin genes

European journal of haematology, 2023-11, Vol.111 (5), p.742-747

2023

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A Hemodynamic Study of Pulmonary Hypertension in Sickle Cell Disease

Delayed hemolytic transfusion reaction in adult sickle‐cell disease: presentations, outcomes, and treatments of 99 referral center episodes

Influence of sickle cell disease and treatment with hydroxyurea on sperm parameters and fertility of human males

Complications and treatment of patients with β-thalassemia in France: results of the National Registry

Estimation of the difference in HbF expression due to loss of the 5' δ-globin BCL11A binding region

Aggregation of mononuclear and red blood cells through an α4β1-Lu/basal cell adhesion molecule interaction in sickle cell disease

Population pharmacokinetics and pharmacodynamics of hydroxyurea in sickle cell anemia patients, a basis for optimizing the dosing regimen

Factors Associated With Dyspnea in Adult Patients With Sickle Cell Disease

Une compilation internationale des résultats de 1 000 greffes de cellules souches pour drépanocytose

Un nomogramme diagnostique d’hémolyse retardée dans la drépanocytose : un outil indispensable à la disposition des cliniciens urgentistes

Mortalité élevée des adolescents atteints de drépanocytose homozygote avec antécédents d’accident vasculaire cérébral en rapport avec l’arrêt des programmes transfusionnels lors de la transition pédiatrie-secteur adulte aux États-Unis

Histoire naturelle de l’atteinte rénale dans la drépanocytose homozygote

La drépanocytose est passée en quarante ans d’une maladie pédiatrique mortelle à une maladie chronique de l’adulte

Le ferumoxytol (Feraheme®), nouveau fer intraveineux « minute » ?

Quel est le devenir des adultes drépanocytaires ayant un antécédent d’accident vasculaire cérébral ?

Adverse effect of hydroxyurea on spermatogenesis in patients with sickle cell anemia after 6 months of treatment

Drepadom - Establishment of Home Care Services and Hospitalizations for Sickle Cell Disease Patients As Standard Care Since the Covid-19 Pandemic

Pyruvate Kinase (PK) Deficiency in Newborns: The Pitfalls of Diagnosis

Drepadom - Home Care Services and Hospitalizations for Sickle Cell Disease Patients during the Covid-19 Pandemic

Decreased sickle red blood cell adhesion to laminin by hydroxyurea is associated with inhibition of Lu/BCAM protein phosphorylation

Improvements in haemolysis and indicators of erythrocyte survival do not correlate with acute vaso‐occlusive crises in patients with sickle cell disease: a phase III randomized, placebo‐controlled, double‐blind study of the gardos channel blocker senicapoc (ICA‐17043)

Delayed hemolytic transfusion reaction in sickle cell disease patients: evidence of an emerging syndrome with suicidal red blood cell death

Predictive Factors for Survival in Sickle Cell Disease: A Cohort Study Using Etendard Data

The liver in sickle cell disease

Transfusion requirements and complication rate in β‐thalassemia intermedia due to heterozygous β‐globin gene mutation and triplicated α‐globin genes

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