Profiles
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Diego Martinelli
Bambino Gesù Children’s Research Hospital, Italy
Dr. Diego Martinelli, MD, PhD - Division of Metabolic Diseases, Department of Paediatric Subspecialties and Liver-kidney transplantation Bambino Gesù Children’s Research Hospital
Dirk Lefeber
Head of the Metabolic Disorders Research team at the Radboud University Medical Centre, Nijmegen
Prof. Dirk Lefeber - Head of the Metabolic Disorders Research team at the Radboud University Medical Centre, Nijmegen
Dominique P. Germain
Hôpitaux Universitaires Paris Ile de France Ouest, France
Dominique P Germain is Professor of Medical Genetics at the University of Versailles (UVSQ), the Director of the Research Unit “Biotherapies of Fabry disease” within the Unité Mixte de Recherche (UMR 1179) Université de Versailles / INSERM (Health and Medical Research National Institute) located at the UFR des Sciences de la Santé (Montigny), and the Head of the Division of Medical Genetics at the Raymond Poincaré Hospital (AP-HP). He is also Director of the French Referral Center for Fabry disease in Garches, France.
Dominique Roland
Institut de Pathologie et de Génétique, Génétique Humaine, département des maladies héréditaires du métabolisme, Gosselies, Belgium Center Inter Institutional for Metabolic Diseases (CIMM), Liège-Charleroi, Belgium
Dominique ROLAND, MD, paediatrician, is the Coordinator of the Center for Inborn errors of metabolism in the Institute of Pathology and Genetics which is affiliated to the CIMM She is an active administrator of Metabolics.be, the belgian association for health providers with the objective of promotion of diagnosis, study and treatment of IEM in children and adults.
Dries Dobbelaere
Lille's University Hospital
Dr Dries Dobbelaere earned his medical degree from the University of Leuven, Belgium. He completed his Postgraduate degrees in Paediatrics and Neonatology in Belgium and obtained the Inter University Postgraduate degree for Inherited Metabolic Diseases in France. He is a nominated expert to the French government for Health matters. Dr Dobbelaere obtained the label of French national reference centre on inherited metabolic diseases in children and adults for the CHRU-Lille (Centre Hospitalier Régionale Universitaire de Lille).
Dulce Quelhas MD
Centro Hospitalar do Porto, Porto, PortugalCentro Hospitalar do Porto, Porto, Portugal
Dulce Quelhas, PharmaD, MSc Is a Clinical Laboratory Geneticist specialist– ESHG at Centro de Genética Médica Jacinto de Magalhães, Centro Hospitalar do Porto
Efstathia Chronopoulou
University Hospitals Bristol NHS TRUST, Bristol Children’s Hospital
Consultant in Paediatric Inherited Metabolic Disease At the Bristol Royal Hospital for Children Division of Women’s and Children’s Services
Eileen Treacy
Biochemical Geneticist and Full Clinical Professor at University College Dublin
Prof. Eileen Treacy - Biochemical Geneticist and Full Clinical Professor at University College Dublin
Eliane Sardh
Karolinska University Hospital, Stockholm, Sweden
Eliane Sardh, MD, PhD, endocrinologist, is a member of the steering committee of European Porphyria Network an organization that promotes research in the field of porphyrias and facilitates best practice in their treatment and diagnosis. She is a senior consultant at the Center of inherited metabolic diseases and holds the lead position of the Porphyria Centre Sweden at Karolinska University hospital in Stockholm, Sweden.
Elisa Leão Teles
Centro Hospitalar de São João, Porto, Portugal
ELISA LEÃO TELES, MD, Paediatrician, Founder and Head of Metabolic Unit of Hospital S. João, Porto, Portugal (1986-2015). Currently, Senior Consultant, Head of the Multidisciplinary Team and Scientific Coordinator of the Inherited Metabolic Diseases Reference Centre of the Centro Hospitalar S. João, Porto, Portugal. Director of the post-graduate Clinical Training Program on Inherited Metabolic Diseases, approved in Portugal by legal entities.
