Search research articles
Contact Us
Filters
Showing results (11-20 of 14) with videos related to
Page
of 2
Sort By:
You have reached the last page of results.
This site can display upto 14 results.
Blood Cells, Molecules & Diseases
|
February 3, 2019
Reprogramming of bone marrow derived mesenchymal stromal cells to human induced pluripotent stem cells from pediatric patients with hematological diseases using a commercial mRNA kit
Irene Sfougataki, Ioannis Grafakos, Ioanna Varela, et al.
Expert Review of Molecular Diagnostics
|
September 27, 2023
Retrospective analysis of persistent HyperCKemia with or without muscle weakness in a case series from Greece highlights vast <i>DMD</i> variant heterogeneity
Kyriaki Kekou, Maria Svingou, Nikos Vogiatzakis, et al.
Expert Review of Molecular Diagnostics
|
January 30, 2023
Combined exome analysis and exome depth assessment achieve a high diagnostic yield in an epilepsy case series, revealing significant genomic heterogeneity and novel mechanisms
Danai Veltra, Faidon-Nikolaos Tilemis, Nikolaos M Marinakis, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
October 18, 2025
"Tuberous sclerosis in Greece: A national cohort study on clinical features and rare manifestations"
Maria Spanou, Vasileios Skoutelis, Zacharias Dimitriadis, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 14) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 14 results.
Blood Cells, Molecules & Diseases
|
February 3, 2019
Reprogramming of bone marrow derived mesenchymal stromal cells to human induced pluripotent stem cells from pediatric patients with hematological diseases using a commercial mRNA kit
Irene Sfougataki, Ioannis Grafakos, Ioanna Varela, et al.
Expert Review of Molecular Diagnostics
|
September 27, 2023
Retrospective analysis of persistent HyperCKemia with or without muscle weakness in a case series from Greece highlights vast <i>DMD</i> variant heterogeneity
Kyriaki Kekou, Maria Svingou, Nikos Vogiatzakis, et al.
Expert Review of Molecular Diagnostics
|
January 30, 2023
Combined exome analysis and exome depth assessment achieve a high diagnostic yield in an epilepsy case series, revealing significant genomic heterogeneity and novel mechanisms
Danai Veltra, Faidon-Nikolaos Tilemis, Nikolaos M Marinakis, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
October 18, 2025
"Tuberous sclerosis in Greece: A national cohort study on clinical features and rare manifestations"
Maria Spanou, Vasileios Skoutelis, Zacharias Dimitriadis, et al.
Page
of 2