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Aasne Karine Aarsand
Director of the Norwegian Porphyria Centre (NAPOS), Helse Bergen HF, Haukeland University Hospital, Bergen Norway
Aasne Karine Aarsand, MD, PhD, Specialist in Biological Chemistry (Clinical Chemistry), is the Director of the Norwegian Porphyria Centre (NAPOS). She is also a Consultant at the Laboratory of Clinical Biochemistry and the Norwegian Quality Improvement of Laboratory Examinations (NOKLUS).
Ahmad Ardeshir Monavari
Clinical Lead of the National Centre for Inherited Metabolic Disorders, Dublin
Prof. Ahmad Ardeshir Monavari - Clinical Lead of the National Centre for Inherited Metabolic Disorders, Dublin
Alberto Burlina
University Hospital of Padova, Italy
Director of the Division of Inborn Errors of Metabolism, Department of Pediatrics, University Hospital of Padova, Padua, Italy and Expanded Neonatal Screening Center of North East of Italy.
Alberto Piperno
San Gerardo Hostpital Monza, Italy
Head of the Unit of Medical Genetics, S.Gerardo Hospital, Monza. Full Professor of Genetics University of Milano-Bicocca; Director of the Centre for Rare Disorders (Disorders of Iron Metabolism, Hereditary anemia, Hereditary Metabolic disorders), San Gerardo Hospital, Monza, Italy and EDUCATION
Alessandro Salviati
Department of Neuroscience, Biomedicine and Movement University of Verona
Alessandro Salviati, MD, PhD, Neurologist and Medical Geneticist, is the Head of the Laboratory for Biochemical and Molecular Diagnosis of Lysosomal Storage Disorders and Neurogenetic Unit at the University of Verona, Italy.
Algirdas Utkus
Vilnius University Hospital Santariskiu klinikos
Prof. Algirdas Utkus is the Head of the Centre for Medical Genetics in Vilnius University Hospital Santaros Klinikos.
Allan M. Lund MD
Consultant Metabolic Paediatrician, Head, Center for Inherited Metabolic Diseases, Departments of Paediatrics and Clinical Genetics, Copenhagen University Hospital, Rigshospitalet, Denmark.
Dr. Allan M. Lund MD, DMSc., Paediatrician, Head for Center for Inherited Metabolic Diseases. Responsible for diagnosis and treatment of metabolic diseases on a national basis; chairs the Committee for Clinical Genetics and Screening (The Danish Pediatric Society) and the Committee for MS/MS-Screening – supervising the extended neonatal screening for IEM in Denmark. Advisor to the National Health Authorities on rare diseases and neonatal screening.
Ana Cristina Ferreira
Coordinator of the Reference Center for Hereditary Metabolic Diseases - Centro Hospitalar Universitário de Lisboa Central
Dr. Ana Cristina Ferreira - Coordinator of the Reference Center for Hereditary Metabolic Diseases - Centro Hospitalar Universitário de Lisboa Central
