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Muscle & Nerve|November 16, 2019
MiRNAs as biomarkers of phenotype in neutral lipid storage disease with myopathyValentina Pegoraro, Sara Missaglia, Roberta Marozzo, et al.
European Journal of Translational Myology|June 6, 2020
Correlation between ETFDH mutations and dysregulation of serum myomiRs in MADD patientsSara Missaglia, Valentina Pegoraro, Roberta Marozzo, et al.
Orphanet Journal of Rare Diseases|February 23, 2018
Hearing impairment in MELAS: new prospective in clinical use of microRNA, a systematic reviewArianna Di Stadio, Valentina Pegoraro, Laura Giaretta, et al.
The International Journal of Neuroscience|February 22, 2020
Can miR-34a be suitable for monitoring sensorineural hearing loss in patients with mitochondrial disease? A case seriesRoberta Marozzo, Valentina Pegoraro, Laura Dipietro, et al.
Therapeutic Advances in Neurological Disorders|June 21, 2019
A new family with transportinopathy: increased clinical heterogeneityCorrado Angelini, Roberta Marozzo, Elena Pinzan, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|September 21, 2013
The MTHFR C677T polymorphism modifies age at onset in Parkinson's diseaseAnnamaria Vallelunga, Valentina Pegoraro, Manuela Pilleri, et al.
Molecular and Cellular Biochemistry|January 16, 2021
Morphological study of TNPO3 and SRSF1 interaction during myogenesis by combining confocal, structured illumination and electron microscopy analysisRoberta Costa, Maria Teresa Rodia, Nicoletta Zini, et al.
Pharmacological Research|September 17, 2018
Regulation of ER-mitochondria contacts by Parkin via Mfn2Valentina Basso, Elena Marchesan, Caterina Peggion, et al.
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