Profiles
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Kurt Ullrich
University Medical Center Hamburg-Eppendorf
Training in pathology, biochemistry and pediatrics/inborn errors of metabolism (University of Freiburg, Münster, Germany).
Labrune Philippe
Assistance Publique-Hôpitaux de Paris, Hôpital Antoine-Béclère - France
Philippe Labrune, MD, PhD, pediatrician-geneticist, is Chief of the Pediatric Unit in Antoine-Béclère Hospital (Assistance Publique Hôpitaux de Paris,France), Director of the Centre for Inherited Metabolic Hepatic Diseases, and Co-director of the “Rare Diseases Platform - Paris Sud”, France. He is a members of SFEIM and SSIEM (learned societies).
Laurent Gouya
Hôpitaux Universitaires Paris Nord Val de Seine (HUPNVS), Hôpital Louis‐Mourier
Laurent Gouya MD, PhD Co-head of INSERM team “Heme iron and inflammatory diseases” U1149, CRI: research center on inflammation; Pôle de Recherche et d'Enseignement Supérieur, Sorbonne Paris-Cité, Paris, France. Our team belongs to the laboratory of excellence GREx. Our main research interest focuses on heme biosynthesis and iron metabolism in physiological and pathological conditions.
Luc Regal
Metabolic Centre ULB-VUB, Brussels, Belgium
Dr. Luc Regal - Metabolic Centre ULB-VUB, Brussels, Belgium
Luis Aldámiz-Echevarría
Hospital Universitario Cruces, Barakaldo, Spain
Medical Doctor in the Department of Paediatrics at Cruces University Hospital, where he is responsible for the Unit of Rare Hereditary Metabolic Diseases. Principal Investigator of the Inherited Metabolic Diseases Research Group at BioCruces Health Research Institute. Associate Professor in the Faculty of Medicine at the University of the Basque Country (UPV/EHU).
Luísa Diogo
Centro Hospitalar Universitário de Coimbra and Faculty of Medicine, University of Coimbra,Portugal
Dr. Luísa Diogo received her Ph.D. degree under the scope of “Mitochondrial disorders in children: evaluation of diagnosis criteria in a cohort of children” from the Faculty of Medicine of the University of Coimbra in 2010. Prior to that, in 1982 she completed her MD degree at the Medicine Faculty, University of Coimbra.
Madara Auzenbaha
Leading researcher in Riga Stradins University Scientific Laboratory of Molecular Genetics; Head of Rare Diseases Coordination Center, Children’s Clinical University hospital of Riga
Dr. Madara Auzenbaha, PhD, MD. Leading researcher in Riga Stradins University Scientific Laboratory of Molecular Genetics; Head of Rare Diseases Coordination Center and ERN BoMS member at the Children’s Clinical University hospital of Riga
Madara Masinska
Children’s Clinical University hospital of Riga, Latvia
Dr. Madara Masinska - Children’s Clinical University hospital of Riga, Latvia
Maja Di Rocco
Giannina Gaslini Institute
Maja Di Rocco is Head of the Unit of Rare Disease and Adjunct Professor of Metabolic Diseases at the Postgraduate School of Paediatrics, Medical Genetics and Paediatric Neurology and Psychiatry at the University of Genoa
Manuel Schiff
Assistance Publique Hôpitaux de Paris- University Hospital Robert-Debré, France
Associate Professor of Pediatrics since Nov. 2013 Coordinator and Head of the Reference Center for Inborn Errors of Metabolism since Jan. 2015 Robert Debré University Hospital, Paris, France
Marcello Bellusci MD
Metabolic paeditrician and HCP representative
Metabolic paeditrician and HCP representative, Hospital Universitario 12 de Octubre, Madrid - Spain
