Profiles
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Simona Bucerzan
Assistant Professor at “Iuliu Hațieganu” University of Medicine and Pharmacy, Cluj-Napoca and senior doctor in Pediatrics and Medical Genetics at the Medical Genetics Department of Emergency Clinical Hospital for Children.
Dr. Simona Bucerzan - Assistant Professor at “Iuliu Hațieganu” University of Medicine and Pharmacy, Cluj-Napoca and senior doctor in Pediatrics and Medical Genetics at the Medical Genetics Department of Emergency Clinical Hospital for Children
Simona Tárnoková
Department of Laboratory medicine, Center for inherited metabolic disorders (CIMD), National Institute of Children's Diseases and Comenius University, Faculty of Medicine, Bratislava, Slovakia
Dr. Simona Tárnoková - Department of Laboratory medicine, Center for inherited metabolic disorders (CIMD), National Institute of Children's Diseases and Comenius University, Faculty of Medicine, Bratislava, Slovakia
Stefan Kölker, MD
Centre for Pediatric and Adolescent Medicine, University Hospital Heidelberg, Germany
Prof. Dr. Stefan KÖLKER, MD, Pediatrician with certified specializations in Pediatric Metabolic Medicine and Pediatric Neurology and Professor in Translational Metabolic Medicine and Pediatric Neurology is Head of the Division of Pediatric Neurology and Metabolic Medicine at the University Children’s Hospital in Heidelberg, Germany.
Suresch Vijay
Birmingham Children’s Hospital NHS Foundation Trust
Consultant in Paediatric Inherited Metabolic diseases (IMDs) at Birmingham Children's Hospital NHS Foundation Trust
Sverre Sandberg
Professor at the Norwegian Porphyria Centre (NAPOS), Helse Bergen HF, Haukeland University Hospital, Bergen Norway
Sverre Sandberg, MD, PhD, Specialist in Biological Chemistry (Clinical Chemistry), is the founder and former Director of the Norwegian Porphyria Centre (NAPOS). He is Director of the Norwegian Quality Improvement of Laboratory Examinations (NOKLUS) and past president of the European Federation of Clinical Chemistry and Laboratory Medicine (EFLM). He is Professor at the Institute of Global Health and Primary Health Care, University of Bergen, Norway.
Svetlana Lajic
Karolinska University Hospital, Stockholm, Sweden
Svetlana Lajic, MD, PhD, Pediatric endocrinologist, is a senior consultant at the Astrid Lindgrens´s Children´s Hospital, Karolinska University Hospital and Team lead of the pediatric metabolic unit. She is an Associate professor at the Department of Women´s and Children´s Health, Karolinska Institutet. She is the pediatric chair of the Adrenal sub-theme in the EndoERN network and member of the Steering committee of EndoERN.
Tarekegn G. Hiwot
University Hospital of Birmingham NHS Foundation Trust
Institute of Metabolism and Systems Research Honorary Reader in Inherited Metabolic Disorders University of Birmingham
Terry Derks
University of Groningen UMC Groningen, the Netherlands
Terry Derks, MD/PhD, pediatrician consultant metabolic medicine University of Groningen UMC Groningen Beatrix Children’s Hospital Section of Metabolic Diseases Hanzeplein 1 9700 RB Groningen the Netherlands Expert in Inborn errors of metabolism Neonatal screening Hepatic glycogen storage diseases (GSD) Medium-chain acyl-CoA dehydrogenase deficiency (MCADD) Multiple acyl-CoA dehydrogenase deficiency (MADD)
Thomas Opladen
University Hospital Heidelberg, Heidelberg, Germany
Associate Professor, Division of Pediatric Neurology and Metabolic Medicine, Centre for Pediatric and Adolescent Medicine
Tomáš Honzík
Charles University and General University Hospital in Prague, • Department of Pediatrics and Adolescent Medicine (1. LF), Czech Republic
Associate professor of Paediatrics, MD, Ph.D. • Inst. of Inherited Metabolic Disorders, 1st Faculty of Medicine, Charles University and General University Hospital, Prague • Dept. of Paediatrics and Adolescent Medicine, 1st Faculty of Medicine Charles University and General University Hospital, Prague
