The landscape of Mucopolysaccharidosis in Southern and Eastern European countries: a survey from 19 specialistic centers.
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| Title: | The landscape of Mucopolysaccharidosis in Southern and Eastern European countries: a survey from 19 specialistic centers. |
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| Authors: | Tylki-Szymańska A; Department of Pediatric Nutrition and Metabolic Diseases, The Children's Memorial Health Institute, Warsaw, Poland., Almássy Z; Department of Toxicology and Metabolic Diseases, Heim Pal Children's Hospital Budapest, Budapest, Hungary., Christophidou-Anastasiadou V; Archbishop Makarios III Hospital, Nicosia, Cyprus., Avdjieva-Tzavella D; Department of Clinical Genetics, University Pediatric Hospital, Sofia, Bulgaria., Barisic I; Centre of Excellence for Reproductive and Regenerative Medicine, Children's Hospital Zagreb, Medical School University of Zagreb, Zagreb, Croatia., Cerkauskiene R; Clinic of Paediatrics, Institute of Clinical Medicine, Faculty of Medicine, Vilnius University, Vilnius, Lithuania., Cuturilo G; Faculty of Medicine, University of Belgrade, Belgrade, Serbia.; University Children's Hospital, Belgrade, Serbia., Djiordjevic M; Mother and Child Health Care Institute of Serbia, Medical University of Belgrade, Belgrade, Serbia., Gucev Z; University Children's Hospital, Skopje, North Macedonia., Hlavata A; National Institute of Children's Diseases, Department of Paediatrics, Medical Faculty Comenius University, Centre for Inherited Metabolic Disorders, Bratislava, Slovakia., Kieć-Wilk B; Unit of Rare Metabolic Diseases, Department of Metabolic Diseases, Jagiellonian University Medical College, University Hospital, Krakow, Poland., Magner M; Department of Paediatrics, University Thomayer Hospital and First Faculty of Medicine, Charles University, Prague, Czech Republic.; Department of Pediatrics, General University Hospital and First Faculty of Medicine, Charles University, Prague, Czech Republic., Pecin I; University Hospital Centre Zagreb, Department of Internal Medicine, Division of Metabolic Diseases, Zagreb School of Medicine, Zagreb, Croatia., Plaiasu V; Regional Centre of Medical Genetics, INSMC Alessandrescu-Rusescu, Bucharest, Romania., Samardzic M; Institute for Sick Children, Department of Pediatric Endocrinology and Metabolism, Medical School, University of Montenegro, Podgorica, Montenegro., Zafeiriou D; First Department of Pediatrics, Hippokratio General Hospital, Aristotle University, Thessaloniki, Greece., Zaganas I; Neurogenetics Laboratory, Neurology Department, University Hospital of Heraklion, University of Crete, Heraklion, Greece., Lampe C; Department of Child Neurology, Epileptology and Social Pediatrics, Centre for Rare Diseases, University of Giessen, Standort Giessen, Feulgenstr. 12, 35389, Giessen, Germany. christina.lampe@paediat.med.uni-giessen.de. |
| Source: | Orphanet journal of rare diseases [Orphanet J Rare Dis] 2022 Mar 24; Vol. 17 (1), pp. 136. Date of Electronic Publication: 2022 Mar 24. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172 (Electronic) Linking ISSN: 17501172 NLM ISO Abbreviation: Orphanet J Rare Dis Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| ISSN: | 1750-1172 |
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| DOI: | 10.1186/s13023-022-02285-x |
