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6. Prevalence and Predictive Factors of Sickle Cell Emergencies Readmission in the Clinical Hematology Department of Dakar, Senegal.

Author

Diallo, Alioune Badara, Seck, Moussa, Touré, Sokhna Aissatou, Keita, Mohamed, Bousso, Elimane Seydi, Faye, Blaise Félix, Diop, Saliou, and Canatan, Duran

Subjects
*SICKLE cell anemia, *FETAL hemoglobin, *BLOOD diseases, *PATIENT readmissions, *STROKE, *PRIAPISM
Abstract

Introduction: Sickle cell emergencies are the most common cause of hospitalization for patients with sickle cell disease (SCD). Hospital readmissions represent a considerable financial burden for healthcare systems and increase patient morbidity and mortality. The aim of this study was to assess the prevalence and predictive factors of sickle cell emergencies readmission. Materials and Methods: We conducted a prospective, cross‐sectional, descriptive, and analytical study over a 4‐month period, including all adult patients admitted for an emergency related to SCD: vaso‐occlusive crisis (VOC), acute chest syndrome (ACS), severe anemia, infections, priapism, and stroke. Readmission was considered when the patient returned to the emergency within a period of <30 days, either due to recurrence, persistence of the same complication, or the occurrence of another acute complication related to SCD. Results: We recorded 151 sickle cell emergencies for 112 patients, representing 0.33 emergencies/month/patient. Fifty‐eight cases of readmission were recorded, resulting in a readmission rate of 38.41%. Among these patients, 53 (91.37%) had two admissions, and 5 (8.62%) had three admissions. The median age of the patients was 28.41 years (16–70 years), and the sex ratio was 0.57. The SS sickle cell phenotype was predominant in 97 patients (86.61%). The reasons for readmission were VOC (82.75%), ACS (13.72%), and severe anemia (3.44%). The main factors that predicted readmission were the existence of professional activity, a low fetal hemoglobin (HbF) level, the existence of neutrophilia, lymphocytosis, and/or thrombocytosis (p values of 0.0084, 0.043, and 0.020 respectively). Conclusion: The 30‐day readmission rate after a sickle cell emergency is high in our study. The main factors that predicted readmission were the existence of professional activity, a relatively low level of fetal Hb, the existence of neutrophilia, lymphocytosis, and/or thrombocytosis. [ABSTRACT FROM AUTHOR]

Published
2024
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8. Determinants of the haemoglobin level in patients with sickle cell disease living in sub‐Saharan Africa: Major impact of the country of residence and independent effects of leucocyte and platelet counts and haemolysis

Author

Rossi, Marica, primary, Belinga, Suzanne, additional, Tolo, Aissata, additional, Diop, Saliou, additional, Diagne, Ibrahima, additional, Chelo, David, additional, Wamba, Guillaume, additional, Gonzalez, Jean Paul, additional, Abough'elie, Cochise, additional, Traore, Youssouf, additional, Deme‐ly, Indou, additional, Seck, Moussa, additional, Diaw, Mor, additional, Gbonon, Valerie, additional, Boidy, Kouakou, additional, Kamara, Ismael, additional, Kitenge, Robert, additional, Jouven, Xavier, additional, Tshilolo, Léon, additional, Diallo, Dapa, additional, and Ranque, Brigitte, additional

Published
2024
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10. Management of acute pain in adults with sickle cell disease: the experience of the Clinical Hematology Department of the University of Dakar.

Author

DIALLO, Alioune Badara, SECK, Moussa, KEITA, Mohamed, TOURE', Sokhna Aissatou, BOUSSO, Elimane Seydi, NGASIA, Baron, FAYE, Blaise Félix, DIENG, Fatma, and DIOP, Saliou

Subjects
*SICKLE cell anemia, *TREATMENT effectiveness, *COMBINED modality therapy, *BLOOD diseases, *PAIN management
Abstract

Background/aim: The evolution of sickle cell disease (SCD) is marked by the occurrence of painful episodes linked to the obstruction of microvessels by sickle cells, known as vaso-occlusive crisis (VOC). The aim of this work was to report the practical aspects of the management of acute pain in adults with SCD. Recommendations based on these practices are also provided. Materials and methods: This prospective, cross-sectional, descriptive, and analytical study was conducted over a four-month period of all sickle cell patients admitted to emergency departments for VOC. The parameters studied were sociodemographic, clinicobiological, therapeutic, and evolutionary. Results: There were 118 cases of VOC identified, representing a prevalence of 78.14% of sickle cell emergencies. The mean age of the patients was 28.41 years. The SS sickle cell phenotype accounted for 86.61% of the cases. Osteoarticular pain was the reason for admission for 88.39% of the patients; it was located in the lower limbs in 39.08% and in the spine in 27.1%. Pain intensity was moderate in 6.25% of the patients, intense in 31.25%, and unbearable in 55.55%. Multimodal analgesia was the most commonly used treatment method, combining those of levels one and two (74.31%) and levels one and three (8.25%). The mean dose of morphine administered was 17.14 mg when morphine alone was prescribed for titration, 13.57 mg when paracetamol and morphine were combined, and 15.83 mg when nefopam and morphine were combined. Clinical outcome was favorable in 68.87% of the cases. Conclusion: Wide variability was observed in the modalities of analgesic treatment of sickle cell VOC. These variations reflect different views on the appropriateness of opioids. This study highlights the efficacy of multimodal analgesia in the management of acute pain in patients with SCD, particularly in regard to morphine sparing. Context-specific recommendations will be needed to harmonize practices. [ABSTRACT FROM AUTHOR]

Published
2024
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11. Lymphocytic Lymphoma Transforming into Hodgkin Lymphoma in Sub-Saharan Africa: Case Report and Literature Review.

Author

Touré, Sokhna Aïssatou, Niang, Dibor, Gueye, Serigne Mourtalla, Keita, Mohamed, Diallo, Alioune Badara, Bousso, Elimane Seydi, Dieng, Fatma, Faye, Blaise Felix, Seck, Moussa, and Diop, Saliou

Subjects
IMMUNOGLOBULIN light chains, RICHTER syndrome, CHRONIC lymphocytic leukemia, HODGKIN'S disease, LITERATURE reviews
Abstract

The Hodgkin variant Richter syndrome (HvRS) is an infrequent complication occurring in 1% of lymphocytic lymphoma/chronic lymphocytic leukemia patients. We report a case of HvRS diagnosed in Sub-Saharan Africa. A 63-year-old patient was consulted for the investigation of an abdominal mass that had been evolving for 5 years prior to admission. His history revealed night sweats, 13% weight loss in 3 months and persistent pruritis. Examination revealed bilateral cervical axillary and inguinal macroadenopathies, painless abdominal distension, pruritic lesions and WHO 2 PS. The blood count showed anemia at 9.5 g/dL. Histology revealed a lymphomatous proliferation of diffuse architecture, nodular in places, with Hodgkin and Sternberg cells associated with small lymphocytes, histiocytes and eosinophilic polymorphs. Immunohistochemistry showed CD20, PAX5, BCL2, CD5, CD23 and MYC positivity; Ki67 at 10% and cyclin D1, BCL6 and CD10 negativity; CD30 positivity on Hodgkin and Sternberg cells that remained CD20 negative; difficulty interpreting CD15; EBV positivity (EBERs); and CD3 and CD5 positivity on reactive T cells. CD138 and kappa and lambda light chains were non-contributory. The extension work-up classified the patient as Ann Arbor stage III B with a Hasenclever score of 3/7. This case illustrates the difficulties in diagnosing HvRS in our countries, where the number of haematopathologists is insufficient and the technical facilities are limited. [ABSTRACT FROM AUTHOR]

Published
2024
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12. Morbidity and Mortality Associated with COVID-19 and Acute Chest Syndrome in Sickle Cell Disease Patients.

Author

Keita, Mohamed, Seck, Moussa, Diallo, Alioune Badara, Touré, Sokhna Aissatou, Bousso, Elimane Seydi, Gueye, Serigne Mourtalla, Dieng, Nata, Dieng, Fatma, Faye, Blaise Felix, and Diop, Saliou

Subjects
*SICKLE cell anemia, *PROGNOSIS, *CHRONIC obstructive pulmonary disease, *VIRAL hepatitis, *MYOCARDIAL ischemia, *IDIOPATHIC femoral necrosis
Abstract

SUMMARY: COVID-19 infection has emerged as a comorbidity that can significantly increase morbidity and mortality in sickle cell patients with ACS (acute thoracic/chest syndrome). The aim of our study was to assess COVID-19-related morbidity and mortality in sickle cell patients with ACS. This was a retrospective, descriptive study of patient records followed over a 36-month period from January 2020 to December 2022. The study was conducted at the national blood transfusion center in Dakar. The sex ratio (M/F) was 0.82. The median age was 26 (17–39) years. The most represented age group was between 21 and 30 years. Factors associated with death were: at baseline, SS genotype, presence of comorbidities (asthma, chronic obstructive pulmonary disease, viral hepatitis B, ischemic heart disease), osteonecrosis of the femoral head, and use of NSAIDs (non-steroidal anti-inflammatory drugs) at diagnosis of COVID-19; at the diagnosis of ACS associated with COVID-19, respiratory distress, hypoxia (Sa02 < 92%), creatininemia >18.5 mg/l, CRP >192 mg/l, lymphopenia; the therapeutic modalities associated with death were: transfusion of RBCs (packed red blood cells) and curative anticoagulation. This study shows that patients with comorbidities and/or chronic complications of sickle cell disease can develop severe forms of ACS associated with COVID 19, leading to death. Other factors linked to death, notably diagnostic and therapeutic, were also identified in the course of this study. [ABSTRACT FROM AUTHOR]

Published
2024
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14. Degree of anemia, indirect markers of hemolysis, and vascular complications of sickle cell disease in Africa

Author

Dubert, Marie, Elion, Jacques, Tolo, Aissata, Diallo, Dapa Aly, Diop, Saliou, Diagne, Ibrahima, Sanogo, Ibrahima, Belinga, Suzanne, Guifo, Odette, Wamba, Guillaume, Ngo Sack, Françoise, Boidy, Kouakou, Kamara, Ismael, Traore, Youssouf, Diakite, Cheick Oumar, Gbonon, Valérie, Faye, Blaise Felix, Seck, Moussa, Deme Ly, Indou, Chelo, David, N'Guetta, Roland, Diop, Ibrahima Bara, Gaye, Bamba, Jouven, Xavier, and Ranque, Brigitte

Published
2017
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17. Red blood cell alloantibodies in paediatric transfusion in sub‐Saharan Africa: A new cohort and literature review

Author

Gadji, Macoura, primary, Cobar, Guéda, additional, Thiongane, Alioune, additional, Senghor, Alioune Badara, additional, Seck, Rose, additional, Faye, Blaise Félix, additional, Seck, Moussa, additional, Guéye, Youssou Bamar, additional, Sy, Diariétou, additional, Sall, Abibatou, additional, Toure, Awa Oumar, additional, Diéye, Tandakha Ndiaye, additional, and Diop, Saliou, additional

Published
2023
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18. From Lysis to Hemolysis

Author

Dieng, Mouhamed, primary, Touré, Sokhna Aïssatou, additional, Keïta, Mohamed, additional, Djiba, Boundia, additional, Ndour, Michel Assane, additional, Diedhiou, Demba, additional, Seck, Moussa, additional, and Seck, Sidy Mohamed, additional

Published
2023
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20. Biomarkers of sickle cell nephropathy in Senegal

Author

Ndour, El Hadji Malick, primary, Mnika, Khuthala, additional, Tall, Fatou Guèye, additional, Seck, Moussa, additional, Ly, Indou Dème, additional, Nembaware, Victoria, additional, Mazandu, Gaston Kuzamunu, additional, Sagna Bassène, Hélène Ange Thérèse, additional, Dione, Rokhaya, additional, Ndongo, Aliou Abdoulaye, additional, Diop, Jean Pascal Demba, additional, Barry, Nènè Oumou Kesso, additional, Djité, Moustapha, additional, Ndiaye Diallo, Rokhaya, additional, Guèye, Papa Madièye, additional, Diop, Saliou, additional, Diagne, Ibrahima, additional, Cissé, Aynina, additional, Wonkam, Ambroise, additional, and Lopez Sall, Philomène, additional

Published
2022
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21. Clinical Research in Western Africa: Efficacy and Safety of a Phase II Study of R-CHOP in First-Line DLBCL in Senegal

Author

Diop, Saliou, primary, Moulin, Charline, additional, Touré, Sokhna Aïssatou, additional, Gueye, Mourtalla, additional, Deltour, Sabine, additional, Diop, Yankhoba, additional, Ndiaye, Fatou Samba, additional, Dial, Mouhamadou Cherif, additional, Sartelet, Hervé, additional, Seck, Moussa, additional, Fall, Seynabou, additional, Senghor, Alioune Badara, additional, Touré, Awa Oumar, additional, Faye, Blaise Felix, additional, Bousso, Elimane Seydi, additional, Diallo, Alioune Badara, additional, Keita, Mohamed, additional, Niang, Elhadji Daouda, additional, Dieng, Nata, additional, Aboud, Elsa, additional, Thieblemont, Catherine, additional, Lévy, Vincent, additional, Béné, Marie C, additional, Broséus, Julien, additional, Raphael, Martine, additional, and Feugier, Pierre, additional

Published
2022
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22. Clinical Research in Africa: Collaborative Project between Senegal and France to Improve the Diagnosis and Therapeutic Management of Adult Lymphoma Patients

Author

Toure, Sokhna Aïssatou, primary, Moulin, Charline, additional, Diop, Yankhoba, additional, Gueye, Mourtalla, additional, Dial, Mouhamadou Cherif, additional, Sartelet, Hervé, additional, Ndiaye, Fatou Samba, additional, Seck, Moussa, additional, Fall, Seynabou, additional, Senghor, Alioune Badara, additional, Touré, Awa Oumar, additional, Deltour, Sabine, additional, Faye, Blaise Felix, additional, Bousso, Elimane Seydi, additional, Diallo, Alioune Badara, additional, Keita, Mohamed, additional, Niang, Elhadji Daouda, additional, Dieng, Nata, additional, Thieblemont, Catherine, additional, Broséus, Julien, additional, Raphael, Martine, additional, Feugier, Pierre, additional, and Diop, Saliou, additional

Published
2022
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24. Compressive Myeloradiculopathies in Multiple Myeloma: Clinical and Radiological Characteristics of a Series of 29 Patients

Author

Faye Atoumane, Ndiaye Fatou Samba Diago, El Hadji Daouda Niang, Mbodji Ahmadou Bamba, Bousso Elimane, Sarr Khadim, Fall Seynabou, Mbaye Khalifa Ababacar, Ka Mamadou, Diop Saliou, Ndiaye Moustapha, and Seck Moussa

Subjects
medicine.medical_specialty, Series (stratigraphy), business.industry, Radiological weapon, medicine, Radiology, business, medicine.disease, Multiple myeloma
Published
2021
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25. Effects of Senegal haplotype (Xmn1-rs7412844), alpha-thalassemia (3.7kb HBA1/HBA2 deletion), NPRL3-rs11248850 and BCL11A-rs4671393 variants on sickle cell nephropathy

Author

Ndour, El Hadji Malick, Mnika, Khuthala, Guèye Tall, Fatou, Seck, Moussa, Dème Ly, Indou, Nembaware, Victoria, Sagna-Bassène, Hélène Ange Thérèse, Dione, Rokhaya, Ndongo, Aliou Abdoulaye, Diop, Jean Pascal Demba, Barry, Nènè Oumou Kesso, Djité, Moustapha, Ndiaye Diallo, Rokhaya, Guèye, Papa Madièye, Diop, Saliou, Diagne, Ibrahima, Cissé, Aynina, Wonkam, Ambroise, and Lopez Sall, Philomène

Subjects
Original Article
Abstract

Objective: Sickle cell anemia (SCA) can cause substantial kidney dysfunction resulting in sickle cell nephropathy, which may be affected by the presence of modifier genes. This study evaluates the effects of some modifier genes on sickle cell nephropathy. Methods: Patients living with SCA were recruited. Alpha-thalassemia (3.7kb HBA1/HBA2 deletion) was genotyped using gap PCR multiplex. Senegal haplotype (Xmn1-rs7412844), BCL11A-rs4671393 and NPRL3-rs11248850 were genotyped using Mass Array. The effects of variants on kidney dysfunction were then evaluated using multivariate analysis. Results: The number of patients living with SCA included in this study was 162 with a median age of 20 years [minimum-maximum: 4-57] and a female frequency of 53.21%. Senegal haplotype, BCL11A-rs4671393 variant were protective factors against albuminuria stage A2 with an odds ratio (OR) of 0.22 (95% CI 0.05-0.90) and 0.27 (95% CI 0.08-0.96) respectively. The combination NPRL3-rs11248850 variant - 3.7kb HBA1/HBA2 deletion was a protective factor against albuminuria stage A2 (OR = 0.087, 95% Cl 0.01-0.78) but it was a risk factor for glomerular hyperfiltration (OR = 17.69, 95% CI 1.85-169.31). Conclusions: All four variants displayed a protective effect against albuminuria stage A2. The combination alpha-thalassemia - NPRL3-rs11248850 variant is a risk factor for glomerular hyperfiltration.

Published
2022

30. Determination of microglucosuria v1

Author

Hadji Malick Ndour, El, primary, Mnika, Khuthala, additional, Gueye Tall, Fatou, additional, Seck, Moussa, additional, Deme Ly, Indou, additional, Nembaware, Victoria, additional, Kuzamunu Mazandu, Gaston, additional, Ange Therese Sagna-Bassene, Helene, additional, Dione, Rokhaya, additional, Abdoulaye Ndongo, Aliou, additional, Pascal Demba Diop, Jean, additional, Oumou Kesso Barry, Nene, additional, Djite, Moustapha, additional, Ndiaye Diallo, Rokhaya, additional, Madieye Gueye, Papa, additional, Diop, Saliou, additional, Diagne, Ibrahima, additional, Cisse, Aynina, additional, Wonkam, Ambroise, additional, and Lopez Sall, Philomene, additional

Published
2022
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31. Détermination du débit de filtration glomérulaire au cours de la drépanocytose au Sénégal: Schwartz, Cockcroft et Gault, MDRD, CKD-EPI ou JSCCS ?

Author

Djite, Moustapha, primary, Sall, Philomène Lopez, additional, Wonkam, Ambroise, additional, Cisse, Aynina, additional, Diagne, Ibrahima, additional, Diop, Saliou, additional, Gueye, Papa Madièye, additional, Diallo, Rokhaya Ndiaye, additional, Aidara, Souleymane, additional, Mara, Sokhna, additional, Keita, Younoussa, additional, Toure, Aïssatou, additional, Ndour, El Hadji Malick, additional, Barry, Nènè Oumou kesso, additional, Diop, Jean Pascal Demba, additional, Ndongo, Aliou Abdoulaye, additional, Sagna-Bassene, Hélène Ange Thérèse, additional, Nembaware, Victoria, additional, Ly, Indou Dème, additional, Seck, Moussa, additional, Mnika, Khuthala, additional, Mazandu, Gaston Kuzamunu, additional, Tall, Fatou Guèye, additional, and Dione, Rokhaya, additional

Published
2022
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33. TRANSFUSION PRACTICE, POST-TRANSFUSION COMPLICATIONS AND RISK FACTORS IN SICKLE CELL DISEASE IN SENEGAL, WEST AFRICA.

Author

Seck, Moussa, primary, Senghor, Alioune Badara, additional, Loum, Mossane, additional, Touré, Sokhna Aissatou, additional, Faye, Blaise Félix, additional, Diallo, Alioune Badara, additional, Keita, Mohamed, additional, Bousso, Elimane Seydi, additional, Guèye, Sérigne Mourtalla, additional, Gadji, Macoura, additional, Sall, Abibatou, additional, Touré, Awa Oumar, additional, and Diop, Saliou, additional

Published
2022
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38. Analyse des effets liés à la pollution atmosphérique au Sénégal, le cas de Dakar

Author

Seck, Moussa, Olivier, Marc-J, Seck, Moussa, and Olivier, Marc-J

Abstract

L’objectif principal est de déterminer l’impact des effets négatifs liés à la pollution atmosphérique au Sénégal, particulièrement à Dakar, sur l’environnement, la santé et l’économie. La pollution atmosphérique a des impacts irréversibles sur la santé publique, l’environnement et l’économie en lien aux activités quotidiennes des Dakarois. En effet, les améliorations recherchées peuvent s’appliquer à Dakar et dans la sous-région. Elles doivent être mises en place telles que proposées. Les données empiriques relevées sur le terrain et celles obtenues à partir des recherches effectuées ont d’une part, facilité l’identification des impacts négatifs des polluants atmosphériques à Dakar. D’autre part, elles ont permis de déterminer les sources génératrices d’impacts négatifs suivants : la vétusté du parc automobile, la mauvaise gestion des huiles usées, l’incinération de matières dangereuses, l’utilisation du bois comme combustibles urbain, les activités de l’industrie de raffinage et de la cimenterie, la poussière provenant du désert du Sahara et un manque d’éducation lié à l’environnement. Pour lutter contre ces impacts, le gouvernement a mis en place des stratégies axées au développement durable, en vain jusqu’à ce jour. Les perspectives suggérées se fondent sur l’analyse critériée de pertinence. Celles-ci se rapportent aux principes de développement durable. Il s’agit notamment de renforcer : les moyens du système de santé, déployer les moyens logistiques liés à la gestion de la qualité de l’air, investir dans la formation et à l’éveil des consciences, des programmes axés au développement socioéconomique, inclure les citoyens au processus de prise de décision, renforcer les capacités de la collecte des matières résiduelles, resserrer sa politique d’importation de véhicules usagés, mettre en place des entreprises de recyclage et de valorisation de l’acier des vieilles voitures, la revitalisation des forêts et des milieux humides, mettre en application une taxe verte

Published
2021

44. Subclinical Cardiac Dysfunction Is Associated With Extracardiac Organ Damages

Author

Menet, Aymeric, primary, Ranque, Brigitte, additional, Diop, Ibrahima Bara, additional, Kingue, Samuel, additional, N'guetta, Roland, additional, Diarra, Mamadou, additional, Diallo, Dapa, additional, Diop, Saliou, additional, Diagne, Ibrahima, additional, Sanogo, Ibrahima, additional, Chelo, David, additional, Wamba, Guillaume, additional, Deme-Ly, Indou, additional, Faye, Blaise Felix, additional, Seck, Moussa, additional, Tolo, Aissata, additional, Boidy, Kouakou, additional, Koffi, Gustave, additional, Abough, Eli Cochise, additional, Diakite, Cheick Oumar, additional, Traore, Youssouf, additional, Legueun, Gaëlle, additional, Kamara, Ismael, additional, Offredo, Lucile, additional, Marechaux, Sylvestre, additional, Mirabel, Mariana, additional, and Jouven, Xavier, additional

Published
2018
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45. Pulse wave velocity is lower in trained than in untrained sickle cell trait carriers

Author

Ouédraogo, Valentin, primary, Connes, Philippe, additional, Tripette, Julien, additional, Tiendrébéogo, Arnaud Jean Florent, additional, Sow, Abdou Khadir, additional, Diaw, Mor, additional, Seck, Moussa, additional, Diop, Mountaga, additional, Hallab, Magid, additional, Belue, Rhonda, additional, Samb, Abdoulaye, additional, Ba, Abdoulaye, additional, and Lefthériotis, Georges, additional

Published
2018
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46. Profil biochimique et hématologique des patients drépanocytaires homozygotes en phase stationnaire au centre National de Transfusion Sanguine de Dakar

Author

Doupa, Dominique, primary, Djite, Moustapha, additional, Gueye, Pape Madieye, additional, Seck, Moussa, additional, Faye, Blaise Felix, additional, Seck, Sidy Mohamed, additional, Diallo, Fatou, additional, Ndiaye, Arame, additional, Samba, Abdourahmane, additional, Cisse, Fatou, additional, Diatta, Alassane, additional, Diagne, Ibrahima, additional, and Diop, Saliou, additional

Published
2017
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47. Évaluation de la technique par chimiluminescence pour le dépistage des agents viraux VHB, VHC et VIH dans les dons de sang au centre national de transfusion sanguine de Dakar

Author

Gadji, Macoura, primary, Guéye, Youssou Bamar, additional, Ba, Aissata, additional, Senghor, Alioune Badara, additional, Seck, Rose, additional, Faye, Blaise Felix, additional, Seck, Moussa, additional, Sy, Diarietou, additional, Diéye, Tandakha Ndiaye, additional, and Diop, Saliou, additional

Published
2017
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49. Séroprévalence virale et allo-immunisation post-transfusionnelle chez les patients suivis pour syndrome drépanocytaire majeur

Author

Senghor, Alioune Badara, primary, Seck, Moussa, additional, Faye, Blaise Felix, additional, Gadji, Macoura, additional, Gueye, Youssou Bamar, additional, Seck, Rose, additional, Sy, Diarriatou, additional, Dieng, Nata, additional, Touré, Sokhna Aicha, additional, Dieye, Tandakh Ndiaye, additional, and Diop, Saliou, additional

Published
2017
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50. Évaluation externe de la qualité des banques de sang au Sénégal

Author

Senghor, Alioune Badara, primary, Sow, Thérèse Odou, additional, Gadji, Macoura, additional, Gueye, Youssou Bamar, additional, Seck, Moussa, additional, Faye, Blaise Félix, additional, Seck, Rose, additional, Derneville, Marie Madeleine, additional, Sy, Diarriatou, additional, Dieye, Tandakha Ndiaye, additional, and Diop, Saliou, additional

Published
2017
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