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个人简介
Dr Morava did her specialty trainings in Europe and also in the US, as pediatrician, geneticist and metabolic specialist. Her major clinical expertise is inborn errors of metabolism. She has decades of experience in the diagnostics, follow-up and treatment in IEM, especially in mitochondrial disorders and congenital disorders of glycosylation.
Dr Morava is actively involved in developing novel therapies in genetic disorders. She is involved in clinical trials. Currently she focusses on clinical trials in congenital disorders of glycosylation (CDG). She is also the main PI of the multicenter study on the Natural history of congenital disorders of glycosylation.
研究兴趣
论文共 334 篇作者统计合作学者相似作者
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Proteomicspp.e2400012-e2400012, (2024)
Molecular genetics and metabolismno. 1 (2024): 108126-108126
Silvia Radenkovic,Rohit Budhraja, Teun Klein-Gunnewiek,Alexia Tyler King,Tarun N. Bhatia,Anna N. Ligezka, Karen Driesen, Rameen Shah,Bart Ghesquière, Akhilesh Pandey,Nael Nadif Kasri,Steven A. Sloan,
Cell Reportsno. 3 (2024): 113883-113883
GENETICS IN MEDICINEno. 2 (2024)
Genetics in medicine : official journal of the American College of Medical Geneticsno. 2 (2024): 101027-101027
Wirginia Krzyściak,Marta Szwajca, Natalia Śmierciak, Robert Chrzan,Aleksander Turek,Paulina Karcz, Amira Bryll,Maciej Pilecki,Eva Morava,Anna Ligęzka,Tamas Kozicz,Paulina Mazur,
Scientific Reportsno. 1 (2024): 1-13
AMERICAN JOURNAL OF MEDICAL GENETICS PART Ano. 6 (2023): 1626-1631
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCEno. 8 (2023)
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Silvia Radenkovic,Christin Johnsen,Andreas Schulze, Gurnoor Lail, Laura Guilder,Kaitlin Schwartz,Matthew Schultz,Saadet Mercimek-Andrews,Suzanne Boyer,Eva Morava
Therapeutic advances in rare disease (2023): 26330040221150269-263300402211502
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