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Journal Articles

Studying the Determinant of Sickle Cell Disease Vasculopathy in Sub-Saharan Africa : The Biocadre Study

Brigitte Ranque, Abdoul Karim Dembele, MD, Mor Diaw, PhD, Claudine Lapoumeroulie, PhD, Lucile Offredo, MS, Dapa Aly Diallo, MD, Diop Saliou, MD, Yves Colin Aronovicz, PhD, Olivier Blanc Brude, PhD, Philippe Connes, PhD, Pierre-Louis Tharaux, MD PhD, Marc Romana, PhD, Xavier Jouven, MD PhD, Caroline Le Van Kim, PhD

Blood (2019) 134 (Supplement_1): 2310.

https://doi.org/10.1182/blood-2019-126713

Published: 2019

Journal Articles

CELL-Derived Microparticles and Sickle CELL Disease Chronic Vasculopathy in Sub-Saharan Africa

Abdoul Karim Dembele, MD, Claudine Lapoumeroulie, PhD, Mor Diaw, PhD, Oumar Tessougué, MD, Lucile Offredo, MS, Dapa Aly Diallo, MD, Saliou Diop, MD MSc, Jacques Elion, MD PhD, Yves Colin Aronovicz, Pierre Louis Tharaux, MD PhD, Xavier Jouven, MD PhD, Marc Romana, PhD, Brigitte Ranque, MD PhD, Caroline Le Van Kim, PhD

Blood (2019) 134 (Supplement_1): 3568.

https://doi.org/10.1182/blood-2019-121334

Published: 2019

Journal Articles

Long Range Sequencing Shows Improved Resolution in the Detection of Beta Globin Cluster Variants

Aruna Rangan, MD, Molly S. Hein, Tejaswi Koganti, William G. Jenkinson, Christopher A. Hilker, Joseph H. Blommel, Tavanna R. Porter, MS, LCGC, Jin Jen, Nicole Hoppman, Rong He, MD, David S. Viswanatha, Ross Aleff, James D. Hoyer, MD, Eric Wieben, Eric W. Klee, PhD, Benjamin R. Kipp, Jennifer L. Oliveira, MD

Blood (2019) 134 (Supplement_1): 3548.

https://doi.org/10.1182/blood-2019-130652

Published: 2019

Journal Articles

Polymorphisms in Inflammatory Genes Modulate the Occurrence of Clinical Complications in Patients with Sickle Cell Disease

Blood (2019) 134 (Supplement_1): 4825.

https://doi.org/10.1182/blood-2019-124218

Published: 2019

Journal Articles

Structural Variation within the Beta-Globin Gene Cluster Among HbS Haplotype Groups

Pamela Lurie, MS, Bamidele Tayo, PhD, Richard S. Cooper, MD, Guillame Lettre, PhD, Ambroise Wonkman, MD PhD, George Ayodo, Stephen K. Obaro, MD PhD, Titilola S. Akingbola, MBBS, FWACP, Neil Hanchard, MD PhD

Blood (2018) 132 (Supplement 1): 2365.

https://doi.org/10.1182/blood-2018-99-119824

Published: 2018

Journal Articles

A Polymorphism in Toll-like Receptor 2 Gene Is Associated with Occurrence of Bacterial Infections in Sickle Cell Disease Patients

Blood (2018) 132 (Supplement 1): 3652.

https://doi.org/10.1182/blood-2018-99-112296

Published: 2018

Journal Articles

Spatial Distribution of Invasive Pneumococcal Serotypes in West Africa: A Retrospective Analysis to Inform Immunization in Persons with Sickle Cell Disease

Thomas Carsillo, PhD, Kokou Hefoume Amegan-Aho, MD, Andrea Feller, PhD, Avery McIntosh, PhD, Jonathan Spector, MD MPH, Stephen K. Obaro, MD PhD

Blood (2018) 132 (Supplement 1): 3668.

https://doi.org/10.1182/blood-2018-99-119406

Published: 2018

Journal Articles

Risk-Benefit and Cost-Effectiveness of Universal Iron Interventions for Public Health Control of Anemia in Young Children in 78 Countries: A Microsimulation Study

Sant-Rayn Pasricha, MD PhD, Adrian Gheorghe, PhD, Fayrouz Ashour, Amrita Arcot, BS, Laura E Murray-Kolb, PhD, Parmi Suchdev, MD MPH, Michael Bode, PhD

Blood (2018) 132 (Supplement 1): 2276.

https://doi.org/10.1182/blood-2018-99-117611

Published: 2018

Journal Articles

Prevalence and Correlates of Growth Failure in African Patients with Sickle Cell Disease: A Multinational Study

Laure Alexandre, Msc, Dapa Diallo, Prof, Aissata Tolo, Prof, Saliou Diop, Prof, Ibrahima Sanogo, Prof, Ibrahima Diagne, Prof, Guillaume Wamba, MD, Kouakou Boidy, MD, Indou Deme Ly, MD, Abdoul Karim Dembele, MD, Suzanne Belinga, MD, Marie Dubert, Msc, Xavier Jouven, Prof, Brigitte Ranque, MD PhD

Blood (2017) 130 (Supplement 1): 971.

https://doi.org/10.1182/blood.V130.Suppl_1.971.971

Published: 2017

Journal Articles

Impact of α-Gene Deletions and β-Globin Cluster Haplotypes on Biological Parameters at Baseline and on Hydroxyurea in Children with Sickle Cell Anemia

Francoise Bernaudin, MD, Cécile Arnaud, MD, Annie Kamdem, MD, Serge Pissard, MD PhD, Isabelle Hau, MD, Ralph Epaud, MD PhD, Corinne Pondarré, MD PhD

Blood (2016) 128 (22): 10.

https://doi.org/10.1182/blood.V128.22.10.10

Published: 2016

Journal Articles

Polymorphisms Associated with the Arab-Indian Haplotype of Sickle Cell Anemia Are Candidate Fetal Hemoglobin Gene Modulators

Vinod Vathipadiekal, PhD, Abdulrahman Alsultan, MD, John Farrell, PhD, A.M Al-Rubaish, Fahad Al-Muhanna, Z Naserullah, A Alsuliman, P.K. Patra, Jacqueline Milton, Lindsay Farrer, David H.K. Chui, MD, Amein Al-Ali, Paola Sebastiani, PhD, Martin H. Steinberg, MD

Blood (2015) 126 (23): 3388.

https://doi.org/10.1182/blood.V126.23.3388.3388

Published: 2015

Journal Articles

A Candidate Trans-Acting Modulator of Fetal Hemoglobin Gene Expression in the Arab-Indian Haplotype of Sickle Cell Anemia

Blood (2015) 126 (23): 409.

https://doi.org/10.1182/blood.V126.23.409.409

Published: 2015

Journal Articles

BCL11A enhancer Haplotypes Are Associated with the Distribution of HbF in Arab-Indian and African Haplotype Sickle Cell Anemia but Not the Different Population Levels of HbF

Paola Sebastiani, PhD, John J. Farrell, PhD, Shuai Wang, MS, Heather L Edward, BA, Heather M. Shappell, BS, Harold T. Bae, PhD, Clinton T. Baldwin, PhD, A. M. Al-Rubaish, MD, Zaki Naserullah, MD, Ahmed Alsuliman, MD, Pradeep K. Patra, PhD, Lindsay A. Farrer, PhD, David H.K. Chui, MD, Abdulrahman Alsultan, MD, Duyen A. Ngo, MD, Haifa Kathrin Al-Ali, MD, Martin H. Steinberg, MD

Blood (2014) 124 (21): 4066.

https://doi.org/10.1182/blood.V124.21.4066.4066

Published: 2014

Journal Articles

Characteristics Of Chronic Lymphocytic Leukemia (CLL) In Senegal. Clinical Features, Cytology, Immunophenotype, Cytogenetic Abnormalities and Altered Expression Of Micro-RNA

Abibatou Sall Fall, MD, Tandakha Ndiaye Dieye, MD PhD, Fatou Samba Ndiaye, Saliou Diop, MD, MSC, Claire Mathiot, MD, Charles-Henri Gattiolat, PhD, Evelyne May, Sr., PhD, Joëlle Wiels, Sr., PhD, Saloua Trojani, MD PhD, Awa Toure, Sr., MD PhD, Martine Raphael, Sr., MD PhD

Blood (2013) 122 (21): 5283.

https://doi.org/10.1182/blood.V122.21.5283.5283

Published: 2013

Journal Articles

Early Clinical Manifestations, Presence Of a Single Bantou Haplotype and High Baseline Reticulocyte Count Predict Severity In a Sickle Cell Anemia Newborn Cohort

Corinne Pondarre, MD, PHD, Annie Kamdem, MD, Cécile Arnaud, MD, Serge Pissard, PhD, Josiane Michau, PHD, Clément Tassel, MD, Isabelle Hau, MD, Ralph Epaud, MD, PHD, Francoise Bernaudin, MD

Blood (2013) 122 (21): 2213.

https://doi.org/10.1182/blood.V122.21.2213.2213

Published: 2013

Journal Articles

Determinants Of Mortality and Survival In Children With Sickle Cell Disease (SCD) In Sub Saharan Africa

Tom Adamkiewicz, MD, MSCR, FRCP(C), Adel Driss, PhD, MSc, BSc, Hyacinth I Hyacinth, MBBS, MPH, Jacqueline Hibbert, PhD, Jonathan K Stiles, PhD

Blood (2013) 122 (21): 4676.

https://doi.org/10.1182/blood.V122.21.4676.4676

Published: 2013

Journal Articles

Sickle Cell Disease Glomerulopathy In Five Subsaharian African Countries: Results Of The Cadre Study

Brigitte Ranque, MD, PhD, Marie Michèle Thiam, MD, Msc, Dapa Aly Diallo, MD, Saliou Diop, MD, MSC, Ibrahima Diagne, MD, Ibrahima Sanogo, MD, Gustave Koffi, MD, Kouakou Boidy, MD, Luc Sica, MD, Guillaume Wamba, MD, Suzanne Belinga, MD, Pierre Louis Tharaux, MD, PhD, Xavier Jouven, MD, PhD

Blood (2013) 122 (21): 779.

https://doi.org/10.1182/blood.V122.21.779.779

Published: 2013

Journal Articles

Severe Impairment of γ-Globin Gene Silencing in an Asymptomatic Adult Patient Homozygous for the Codon 8 (–AA) Frame-Shift β 0 -Thalassemia Mutation

Andrew Campbell, MD, Hong-yuan Luo, Katherine Benson, Lance Davis, Patrick G. Gallagher, MD, Martin H. Steinberg, MD, Peter Fraser, PhD, Bernard G. Forget, MD, David H.K. Chui, MD

Blood (2012) 120 (21): 1022.

https://doi.org/10.1182/blood.V120.21.1022.1022

Published: 2012

Journal Articles

Mutations Identified in Thrombocytopenia THC2 Are Likely to Dysregulate ANKRD26 Expression

Chiara Gnan, MSc, Patrizia Noris, MD, Felisa C. Molinas, MD, PhD, Shinji Kunishima, PhD, Paula Graciela Heller, M.D., Ph.D, Akihiro Iguchi, MD, PhD, Alessandro Pecci, MD, Erica Valencic, PhD, Seri Marco, MD, Silverio Perrotta, MD, Carlo Luigi Balduini, MD, Anna Savoia, PhD

Blood (2011) 118 (21): 708.

https://doi.org/10.1182/blood.V118.21.708.708

Published: 2011

Journal Articles

Fetal Hemoglobin In Sickle Cell Anemia: Molecular Characterization of Saudi Patients From the Southwestern Province.

Abdulrahman Alsultan, MD, Nadia Solovieff, Aamer Aleem, MBBS, Farjah H. AlGahtani, MBBS, Ali Al-Shehri, MBBS, Mohamed Elfaki Osman, MBBS, Kadijah Kurban, MBBS, Hasan Bahakim, MD, Abdul Kareem Al-Momen, MBBS, FRCPC, David H.K. Chui, MD, Martin H. Steinberg, MD

Blood (2010) 116 (21): 1621.

https://doi.org/10.1182/blood.V116.21.1621.1621

Published: 2010

NARROW

Studying the Determinant of Sickle Cell Disease Vasculopathy in Sub-Saharan Africa : The Biocadre Study

CELL-Derived Microparticles and Sickle CELL Disease Chronic Vasculopathy in Sub-Saharan Africa

Long Range Sequencing Shows Improved Resolution in the Detection of Beta Globin Cluster Variants

Polymorphisms in Inflammatory Genes Modulate the Occurrence of Clinical Complications in Patients with Sickle Cell Disease

Structural Variation within the Beta-Globin Gene Cluster Among HbS Haplotype Groups

A Polymorphism in Toll-like Receptor 2 Gene Is Associated with Occurrence of Bacterial Infections in Sickle Cell Disease Patients

Spatial Distribution of Invasive Pneumococcal Serotypes in West Africa: A Retrospective Analysis to Inform Immunization in Persons with Sickle Cell Disease

Risk-Benefit and Cost-Effectiveness of Universal Iron Interventions for Public Health Control of Anemia in Young Children in 78 Countries: A Microsimulation Study

Prevalence and Correlates of Growth Failure in African Patients with Sickle Cell Disease: A Multinational Study

Impact of α-Gene Deletions and β-Globin Cluster Haplotypes on Biological Parameters at Baseline and on Hydroxyurea in Children with Sickle Cell Anemia

Polymorphisms Associated with the Arab-Indian Haplotype of Sickle Cell Anemia Are Candidate Fetal Hemoglobin Gene Modulators

A Candidate Trans-Acting Modulator of Fetal Hemoglobin Gene Expression in the Arab-Indian Haplotype of Sickle Cell Anemia

BCL11A enhancer Haplotypes Are Associated with the Distribution of HbF in Arab-Indian and African Haplotype Sickle Cell Anemia but Not the Different Population Levels of HbF

Characteristics Of Chronic Lymphocytic Leukemia (CLL) In Senegal. Clinical Features, Cytology, Immunophenotype, Cytogenetic Abnormalities and Altered Expression Of Micro-RNA

Early Clinical Manifestations, Presence Of a Single Bantou Haplotype and High Baseline Reticulocyte Count Predict Severity In a Sickle Cell Anemia Newborn Cohort

Determinants Of Mortality and Survival In Children With Sickle Cell Disease (SCD) In Sub Saharan Africa

Sickle Cell Disease Glomerulopathy In Five Subsaharian African Countries: Results Of The Cadre Study

Severe Impairment of γ-Globin Gene Silencing in an Asymptomatic Adult Patient Homozygous for the Codon 8 (–AA) Frame-Shift β 0 -Thalassemia Mutation

Mutations Identified in Thrombocytopenia THC2 Are Likely to Dysregulate ANKRD26 Expression

Fetal Hemoglobin In Sickle Cell Anemia: Molecular Characterization of Saudi Patients From the Southwestern Province.

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American Society of Hematology

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American Society of Hematology

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