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Journal Articles

Cumulative Incidences and Risk Factors for Intra and Extracranial Cerebral Arteriopathy in Sickle Cell Disease Children

Francoise Bernaudin, MD, Suzanne Verlhac, MD, Cécile Arnaud, MD, Annie Kamdem, MD, Isabelle Hau, MD, Fouad Madhi, MD, Ralph Epaud, MDPhD, Camille Jung, MD, Corinne Pondarré, MD PhD

Blood (2020) 136 (Supplement 1): 56–57.

https://doi.org/10.1182/blood-2020-136089

Published: 2020

Journal Articles

Immune Reconstitution in 107 Children with Sickle Cell Anemia Transplanted with Bone Marrow or Cord Blood from a Matched-Sibling Donor after Myeloablative Conditioning Regimen Including 20mg/Kg ATG

Francoise Bernaudin, MD, Azadeh Djavidi, MD, Cécile Arnaud, MD, Annie Kamdem, MD, Isabelle Hau, MD, Corinne Pondarré, MD PhD, Jean-Paul Vernant, MD, Mathieu Kuentz, MD, Nathalie Dhedin, MD, Jean-Hugues Dalle, MD PhD, Eliane Gluckman, Gerard Socie, MD PhD

Blood (2019) 134 (Supplement_1): 2253.

https://doi.org/10.1182/blood-2019-125316

Published: 2019

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

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

High LDH Level, G6PD Deficiency and Absence of alpha-Thalassemia Are Significant Independent Risk Factors of Abnormally High Cerebral Velocities in Patients with Sickle Cell Anemia.

Francoise Bernaudin, MD, Suzanne Verlhac, MD, Lena Coïc, MD, Cecile Arnaud, MD, Annie Kamdem, MD, Isabelle Hau, MD, M.G. Neonato, PHD, Christophe Delacourt, MD

Blood (2007) 110 (11): 430.

https://doi.org/10.1182/blood.V110.11.430.430

Published: 2007

NARROW

Cumulative Incidences and Risk Factors for Intra and Extracranial Cerebral Arteriopathy in Sickle Cell Disease Children

Immune Reconstitution in 107 Children with Sickle Cell Anemia Transplanted with Bone Marrow or Cord Blood from a Matched-Sibling Donor after Myeloablative Conditioning Regimen Including 20mg/Kg ATG

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

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

High LDH Level, G6PD Deficiency and Absence of alpha-Thalassemia Are Significant Independent Risk Factors of Abnormally High Cerebral Velocities in Patients with Sickle Cell Anemia.

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ASH Publications

American Society of Hematology

Cumulative Incidences and Risk Factors for Intra and Extracranial Cerebral Arteriopathy in Sickle Cell Disease Children

Immune Reconstitution in 107 Children with Sickle Cell Anemia Transplanted with Bone Marrow or Cord Blood from a Matched-Sibling Donor after Myeloablative Conditioning Regimen Including 20mg/Kg ATG

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

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

High LDH Level, G6PD Deficiency and Absence of alpha-Thalassemia Are Significant Independent Risk Factors of Abnormally High Cerebral Velocities in Patients with Sickle Cell Anemia.

Email alerts

ASH Publications

American Society of Hematology

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