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Journal of Community Genetics|March 19, 2021
Rare disease care pathways in the EU: from odysseys and labyrinths towards highwaysBirute Tumiene, Holm GraessnerMedicina (Kaunas, Lithuania)|December 6, 2007
[Fabry's disease: a clinical case and literature review]Rasa Dobrovolskiene, Algirdas Utkus, Birute Tumiene, et al.Clinical Nutrition (Edinburgh, Scotland)|March 19, 2020
Nutritional and immune impairments and their effects on outcomes in early pancreatic cancer patients undergoing pancreatoduodenectomyJaroslav Tumas, Birute Tumiene, Jolita Jurkeviciene, et al.Genes|March 25, 2022
2022 Overview of Metabolic EpilepsiesBirute Tumiene, Carlos R Ferreira, Clara D M van KarnebeekJournal of Applied Genetics|September 22, 2017
Phenotype comparison confirms ZMYND11 as a critical gene for 10p15.3 microdeletion syndromeBirute Tumiene, Ž Čiuladaitė, E Preikšaitienė, et al.American Journal of Medical Genetics. Part A|April 13, 2012
Clinical and molecular characterization of a second case of 7p22.1 microduplicationEgle Preiksaitiene, Jurate Kasnauskiene, Zivile Ciuladaite, et al.Journal of Community Genetics|March 18, 2021
European Reference Networks: challenges and opportunitiesBirute Tumiene, Holm Graessner, Irene Mj Mathijssen, et al.European Journal of Public Health|June 15, 2026
Identifying barriers and policy priorities for rare disease research in underrepresented European countriesBaiba Lace, Inna Inashkina, Dorica Dan, et al.Healthcare (Basel, Switzerland)|September 23, 2022
Making Sure That Orphan Incentives Tip the Right Way in EuropeDenis Horgan, Jasmina Koeva-Balabanova, Ettore Capoluongo, et al.Biomedicine Hub|February 10, 2021
Digitalisation and COVID-19: The Perfect StormDenis Horgan, Joanne Hackett, C Benedikt Westphalen, et al.Pageof 2