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Paediatric and Perinatal Epidemiology|November 24, 2025
Genetic Diagnoses Among Congenital Anomaly Cases in Europe: Data From the EUROCAT NetworkJorieke E H Bergman, Annie Perraud, Ester Garne, et al.
Neurobiology of Disease|June 8, 2022
Systemic perturbations of the kynurenine pathway precede progression to dementia independently of amyloid-βMarcela Cespedes, Kelly R Jacobs, Paul Maruff, et al.
Acta Diabetologica|February 22, 2023
Italian translation and validation of the CGM satisfaction scale questionnaireEnza Mozzillo, Marco Marigliano, Alda Troncone, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|February 22, 2024
Satisfaction with continuous glucose monitoring is associated with quality of life in young people with type 1 diabetes regardless of metabolic control and treatment typeRoberto Franceschi, Riccardo Pertile, Marco Marigliano, et al.
Diabetes Research and Clinical Practice|September 6, 2023
Satisfaction with continuous glucose monitoring is positively correlated with time in range in children with type 1 diabetesMarco Marigliano, Riccardo Pertile, Enza Mozzillo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 2, 2018
Correction: Reproductive genetic carrier screening for cystic fibrosis, fragile X syndrome, and spinal muscular atrophy in Australia: outcomes of 12,000 testsAlison Dalton Archibald, Melanie Jane Smith, Trent Burgess, et al.
Journal of Alzheimer'S Disease : JAD|June 24, 2025
Amyloid-β protein precursor fragments in urine: Potential biomarkers for the early detection of mild cognitive impairment and dementiaJingyu Zhu, Xiao Xiao, Xiaotong Chen, et al.
Neuron|June 19, 2015
Reduction of Neuropathic and Inflammatory Pain through Inhibition of the Tetrahydrobiopterin PathwayAlban Latremoliere, Alexandra Latini, Nick Andrews, et al.
Nature Nanotechnology|July 1, 2020
Subretinally injected semiconducting polymer nanoparticles rescue vision in a rat model of retinal dystrophyJosé Fernando Maya-Vetencourt, Giovanni Manfredi, Maurizio Mete, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2017
Reproductive genetic carrier screening for cystic fibrosis, fragile X syndrome, and spinal muscular atrophy in Australia: outcomes of 12,000 testsAlison Dalton Archibald, Melanie Jane Smith, Trent Burgess, et al.
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