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Biochemical and Biophysical Research Communications|August 9, 2011
Unusual adult-onset Leigh syndrome presentation due to the mitochondrial m.9176T>C mutationDario Ronchi, Andreina Bordoni, Alessandra Cosi, et al.
Pediatric Neurology|March 1, 2006
New mutations in TK2 gene associated with mitochondrial DNA depletionSara Galbiati, Andreina Bordoni, Dimitra Papadimitriou, et al.
Journal of Neurology|May 8, 2002
Retrospective study of a large population of patients with asymptomatic or minimally symptomatic raised serum creatine kinase levelsAlessandro Prelle, Lucia Tancredi, Monica Sciacco, et al.
Brain : a Journal of Neurology|January 17, 2019
Key role of SMN/SYNCRIP and RNA-Motif 7 in spinal muscular atrophy: RNA-Seq and motif analysis of human motor neuronsFederica Rizzo, Monica Nizzardo, Shikha Vashisht, et al.
Archives of Neurology|July 14, 2010
Mitochondrial respiratory chain dysfunction in muscle from patients with amyotrophic lateral sclerosisVeronica Crugnola, Costanza Lamperti, Valeria Lucchini, et al.
Annals of Neurology|January 16, 2021
A Novel Homozygous VPS11 Variant May Cause Generalized DystoniaEdoardo Monfrini, Filippo Cogiamanian, Sabrina Salani, et al.
Neurobiology of Aging|February 19, 2005
Influence of the Glu298Asp polymorphism of NOS3 on age at onset and homocysteine levels in AD patientsIlaria Guidi, Daniela Galimberti, Eliana Venturelli, et al.
Journal of the Neurological Sciences|June 22, 2011
Two novel mutations in PEO1 (twinkle) gene associated with chronic external ophthalmoplegiaDario Ronchi, Elisa Fassone, Andreina Bordoni, et al.
Scientific Reports|January 12, 2018
Paroxysmal Nocturnal Hemoglobinuria (Pnh): Brain Mri Ischemic Lesions In Neurologically Asymtomatic PatientsWilma Barcellini, Elisa Scola, Silvia Lanfranconi, et al.
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