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The American Journal of Surgical Pathology|September 26, 2003
Malignant pancreatic endocrine tumor in a child with tuberous sclerosisPaola Francalanci, Francesca Diomedi-Camassei, Cristina Purificato, et al.International Journal of Molecular Sciences|May 14, 2025
Mitochondrial Dysfunction in Genetic and Non-Genetic Parkinson's DiseaseMartina Lucchesi, Letizia Biso, Marco Bonaso, et al.Frontiers in Neurology|September 8, 2022
Cardiac magnetic resonance findings in neuronal ceroid lipofuscinosis: A case reportGiancarlo Todiere, Stefania Della Vecchia, Maria Aurora Morales, et al.Scientific Reports|July 14, 2025
Long-term benefits of TUDCA supplement in ARSACS zebrafish modelValentina Naef, Stefania Della Vecchia, Michela Giacich, et al.Genes|February 24, 2024
KLHL40-Related Myopathy: A Systematic Review and Insight into a Follow-up Biomarker via a New Case ReportBianca Buchignani, Gemma Marinella, Rosa Pasquariello, et al.Neurogenetics|December 11, 2025
Gastrointestinal symptoms in neuronal ceroid lipofuscinoses (NCLs): an observational study on prevalence, timing of progression, and impact on quality of lifeStefania Della Vecchia, Alessandro Simonati, Maria Laura Manca, et al.Scientific Reports|August 17, 2019
Functional Transcriptome Analysis in ARSACS KO Cell Model Reveals a Role of Sacsin in AutophagyFederica Morani, Stefano Doccini, Roberto Sirica, et al.The International Journal of Neuroscience|August 24, 2013
Diffusion tensor imaging in SPG11- and SPG4-linked hereditary spastic paraplegiaFrancesco Garaci, Nicola Toschi, Simona Lanzafame, et al.Frontiers in Neuroscience|October 9, 2024
Expanding the molecular landscape of childhood apraxia of speech: evidence from a single-center experienceDaniela Formicola, Irina Podda, Elia Dirupo, et al.Pharmacological Research|June 23, 2025
Naringenin and SMER28 target lysosomal reformation and rescue SPG11 and SPG15 hereditary spastic paraplegia phenotypesChiara Vantaggiato, Giulia Guarato, Francesca Brivio, et al.Pageof 20