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Orphanet Journal of Rare Diseases|March 5, 2022
One year of COVID-19: infection rates and symptoms in patients with inherited metabolic diseases followed by MetabERNLaura Paneghetti, Cinzia Maria Bellettato, Annalisa Sechi, et al.
Orphanet Journal of Rare Diseases|August 4, 2021
Social and medical needs of rare metabolic patients: results from a MetabERN surveySylvia Sestini, Laura Paneghetti, Christina Lampe, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|June 14, 2017
Circulating SCCA-IgM complex is a useful biomarker to predict the outcome of therapy in hepatocellular carcinoma patientsMaria Guarino, Giovan G Di Costanzo, Andrea Gallotta, et al.
The International Journal of Biological Markers|May 2, 2018
Development of a novel diagnostic algorithm to predict NASH in HCV-positive patientsAndrea Gallotta, Laura Paneghetti, Viera Mrázová, et al.
Cancer Treatment and Research Communications|July 13, 2019
Clinical evaluation of the iXip index to reduce prostate re-biopsiesAndrea Benedetto Galosi, Lucio Dell'Atti, Alessandro Bertaccini, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|January 31, 2018
Characterization of SCCA-IgM as a biomarker of liver disease in an Asian cohort of patientsHoang Bui Huu, Nhuong Ha Thuc, Hoa Pham Thi Le, et al.
Frontiers in Medicine|March 19, 2021
Challenges in Transition From Childhood to Adulthood Care in Rare Metabolic Diseases: Results From the First Multi-Center European SurveyKarolina M Stepien, Beata Kieć-Wilk, Christina Lampe, et al.
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