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Cortex; a Journal Devoted to the Study of the Nervous System and Behavior|August 25, 2015
No effects of 20 Hz-rTMS of the primary motor cortex in vegetative state: A randomised, sham-controlled studyMassimo Cincotta, Fabio Giovannelli, Roberta Chiaramonti, et al.British Journal of Haematology|April 7, 1999
Diamond-Blackfan anaemia in the Italian populationU Ramenghi, E Garelli, S Valtolina, et al.Cells|June 19, 2024
A Focus on the Pathophysiology of Adrenomedullin Expression: Endothelitis and Organ Damage in Severe Viral and Bacterial InfectionsSilvia Spoto, Stefania Basili, Roberto Cangemi, et al.Journal of Clinical Medicine|May 13, 2023
Assessment and Monitoring of the Quality of Clinical Pathways in Patients with Depressive Disorders: Results from a Multiregional Italian Investigation on Mental Health Care Quality (the QUADIM Project)Matteo Monzio Compagnoni, Giulia Caggiu, Liliana Allevi, et al.Frontiers in Medicine|November 17, 2022
Synergistic effect of myocardial injury and mid-regional proAdrenomedullin elevation in determining clinical outcomes of SARS-CoV-2 patientsSilvia Spoto, Fabio Mangiacapra, Giorgio D'Avanzo, et al.BMC Psychiatry|June 13, 2023
The quality of mental health care for people with bipolar disorders in the Italian mental health system: the QUADIM projectBarbara D'Avanzo, Angelo Barbato, Matteo Monzio Compagnoni, et al.Cancer Letters|March 25, 2021
Pharmacological inhibition of 17β-hydroxysteroid dehydrogenase impairs human endometrial cancer growth in an orthotopic xenograft mouse modelSofia Xanthoulea, Gonda F J Konings, Niina Saarinen, et al.American Journal of Medical Genetics. Part A|June 20, 2012
The Coffin-Siris syndrome: a proposed diagnostic approach and assessment of 15 overlapping casesSamantha A Schrier, Joann N Bodurtha, Barbara Burton, et al.Nature|December 22, 2006
An enigmatic long-lasting gamma-ray burst not accompanied by a bright supernovaM Della Valle, G Chincarini, N Panagia, et al.Human Mutation|August 13, 2021
Molecular basis of mucopolysaccharidosis IVA (Morquio A syndrome): A review and classification of GALNS gene variants and reporting of 68 novel variantsAlessandra Zanetti, Francesca D'Avanzo, Moeenaldeen AlSayed, et al.Pageof 47