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FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|July 18, 2019
A novel mutation in <i>SPART</i> gene causes a severe neurodevelopmental delay due to mitochondrial dysfunction with complex I impairments and altered pyruvate metabolismChiara Diquigiovanni, Christian Bergamini, Rebeca Diaz, et al.
European Journal of Pediatrics|October 27, 2015
Epidemiology of haemolytic uremic syndrome in children. Data from the North Italian HUS networkGianluigi Ardissino, Stefania Salardi, Elisa Colombo, et al.
Human Molecular Genetics|April 17, 2021
A rare missense variant in the ATP2C2 gene is associated with language impairment and related measuresAngela Martinelli, Mabel L Rice, Joel B Talcott, et al.
Translational Psychiatry|July 26, 2017
The DCDC2 deletion is not a risk factor for dyslexiaT S Scerri, E Macpherson, A Martinelli, et al.
The Science of the Total Environment|September 19, 2024
Development of new RT-PCR assays for the specific detection of BA.2.86 SARS-CoV-2 and its descendent sublineagesKatja Spiess, Mauro Petrillo, Valentina Paracchini, et al.
Water Research|October 5, 2013
EU-wide monitoring survey on emerging polar organic contaminants in wastewater treatment plant effluentsRobert Loos, Raquel Carvalho, Diana C António, et al.
Cells|December 7, 2019
Transcriptional Characterization of Stage I Epithelial Ovarian Cancer: A Multicentric StudyEnrica Calura, Matteo Ciciani, Andrea Sambugaro, et al.
Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin|August 22, 2025
Novel (d)PCR assays for influenza A(H5Nx) viruses clade 2.3.4.4b surveillanceGerhard Buttinger, Mauro Petrillo, Viviana Valastro, et al.
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