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Journal of Forensic Sciences|August 8, 2015
A Practical Guide for the Formulation of Propositions in the Bayesian Approach to DNA Evidence Interpretation in an Adversarial EnvironmentSimone Gittelson, Tim Kalafut, Steven Myers, et al.Journal of Neuromuscular Diseases|May 6, 2026
Clinical and pathological findings in two Italian siblings of Romani ancestry with charcot-marie-tooth type 4D and review of the current literatureElena Abati, Carola Rita Ferrari Aggradi, Stefania Magri, et al.Frontiers in Genetics|December 27, 2016
Evaluation of Forensic DNA Traces When Propositions of Interest Relate to Activities: Analysis and Discussion of Recurrent ConcernsAlex Biedermann, Christophe Champod, Graham Jackson, et al.Journal of Neurochemistry|March 16, 2026
Neurotrophic Modulation Restores Motor and Developmental Defects in Zebrafish Models of ints11 DeficiencyAnna Pistocchi, Elena Chiricozzi, Matilde Molteni, et al.Experimental Neurology|March 18, 2009
A majority of Huntington's disease patients may be treatable by individualized allele-specific RNA interferenceMaria Stella Lombardi, Leonie Jaspers, Christine Spronkmans, et al.Clinical Parkinsonism & Related Disorders|January 29, 2025
Novel NOTCH3 mutation c.1564 T > A (p.Cys522Ser) presenting with early-onset Parkinsonism and white matter lesionsNicola Rifino, Silvia Baratta, Esteban Zacarias, et al.Neuromuscular Disorders : NMD|July 27, 2007
Identification of the infant-type R631C mutation in patients with the benign muscular form of CPT2 deficiencyOlimpia Musumeci, Mohammed Aguennouz, Giacomo Pietro Comi, et al.Neuromuscular Disorders : NMD|October 19, 2010
Co-occurrence of amyotrophic lateral sclerosis and Charcot-Marie-Tooth disease type 2A in a patient with a novel mutation in the mitofusin-2 geneChiara Marchesi, Claudia Ciano, Ettore Salsano, et al.Journal of the Peripheral Nervous System : JPNS|May 28, 2016
Screening for SH3TC2 gene mutations in a series of demyelinating recessive Charcot-Marie-Tooth disease (CMT4)Giuseppe Piscosquito, Paola Saveri, Stefania Magri, et al.Journal of the Peripheral Nervous System : JPNS|December 17, 2016
Hereditary gelsolin amyloidosis (HGA): a neglected cause of bilateral progressive or recurrent facial palsyAnna Sagnelli, Giuseppe Piscosquito, Daniela Di Bella, et al.Pageof 18