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Italian Journal of Pediatrics|February 8, 2019
SIADH versus adrenal insufficiency: a life-threatening misdiagnosisStefano Pintaldi, Angela Lora, Katy Vecchiato, et al.
Journal of Human Genetics|September 12, 2019
Functional analysis of the third identified SLC25A19 mutation causative for the thiamine metabolism dysfunction syndrome 4Roberta Bottega, Maria D Perrone, Katy Vecchiato, et al.
Acta Paediatrica (Oslo, Norway : 1992)|October 22, 2013
Safety and efficacy of propofol administered by paediatricians during procedural sedation in childrenAntonio Chiaretti, Franca Benini, Filomena Pierri, et al.
Neurology. Genetics|February 3, 2026
Pilot Study of Fingolimod Treatment in Neuronal Ceroid Lipofuscinosis Type 1Martina Messina, Rebecca Whiteley, Chin Gan, et al.
Neuroimage|October 17, 2020
Scattered slice SHARD reconstruction for motion correction in multi-shell diffusion MRIDaan Christiaens, Lucilio Cordero-Grande, Maximilian Pietsch, et al.
Thorax|October 19, 2019
Differences in lung function between children with sickle cell anaemia from West Africa and EuropeMichele Arigliani, Luigi Castriotta, Ramatu Zubair, et al.
Epilepsia|December 13, 2023
Widespread, depth-dependent cortical microstructure alterations in pediatric focal epilepsyChiara Casella, Katy Vecchiato, Daniel Cromb, et al.
Brain Communications|April 16, 2021
Individualized brain development and cognitive outcome in infants with congenital heart diseaseAlexandra F Bonthrone, Ralica Dimitrova, Andrew Chew, et al.
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