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Hledat publikace relevantní k dotazu "Genetic Diseases, Inborn"
Genetic Diseases, Inborn
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publication
Standard ECG for differential diagnosis between Anderson-Fabry disease and hypertrophic cardiomyopathy
2022 |
1. lékařská fakulta
publication
Head-to-head trial of pegunigalsidase alfa versus agalsidase beta in patients with Fabry disease and deteriorating renal function: results from the 2-year randomised phase III BALANCE study
2023 |
1. lékařská fakulta