Noninvasive prenatal diagnosis of beta-thalassemia.

Mme S. Galbiati

Prenatal screening in Centro Hospitalar de Coimbra.

Mme Leticia Ribeiro

Coimbra, Portugal

Evaluation of an automated capillary electrophoresis system in the screening for hemoglobinopathies.

Mme Béatrice Gulbis

Hôpital Erasme – Université Libre de Bruxelles

Neonatal hemoglobinopathy screening in Spain.

M. J.L Vives-Corrons

Red Cell Pathology Unit , Biomedical Diagnostic Centre , Hospital Clinic. University of

Neonatal screening for sickle cell disease in France.

Mme Josiane Michau

Service de Biochimie et de génétique CHU Henri Mondor APHP

Organization of a National Network and development of National Guidelines for the treatment and care of Pediatric Sickle Cell Disease patients in a country with increasing immigration rates. The Italian experience.

Présentation du Centre International de Recherches Médicales de Franceville (CIRMF)

Présentation de la coopération Internationale Monégasque

A Genomic Approach to Phenotypic Heterogeneity of Sickle Cell Anemia.

Hypercoagulabilité, thrombose et drépanocytose

S/ ! thalassemia syndrome; an update of the molecular etiologies and the setup of a specific diagnostic tool.

Communication

Clinical heterogeneity of G6PD deficiency: New variants and correlation between genotype and phenotype, results of a five-year-survey.

Problems of adult sickle cell patients – Painful experiences in addition to painful crises.

Traitement de la Douleur

Mechanisms of pain in sickle cell disease

Table ronde