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Nereo Bresolin

Showing results (281-290 of 346) with videos related to

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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.
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.
Blood|July 1, 2006
VCAM-1 expression on dystrophic muscle vessels has a critical role in the recruitment of human blood-derived CD133+ stem cells after intra-arterial transplantationManuela Gavina, Marzia Belicchi, Barbara Rossi, et al.
Frontiers in Neurology|February 16, 2019
Can Intestinal Pseudo-Obstruction Drive Recurrent Stroke-Like Episodes in Late-Onset MELAS Syndrome? A Case Report and Review of the LiteratureDelia Gagliardi, Eleonora Mauri, Francesca Magri, et al.
BMC Neurology|September 15, 2012
Quantitative muscle strength assessment in duchenne muscular dystrophy: longitudinal study and correlation with functional measuresAlberto Lerario, Serena Bonfiglio, MariaPia Sormani, et al.
Pageof 35

Showing results (281-290 of 346) with videos related to

Sort By:
Pageof 35
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.
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.
Blood|July 1, 2006
VCAM-1 expression on dystrophic muscle vessels has a critical role in the recruitment of human blood-derived CD133+ stem cells after intra-arterial transplantationManuela Gavina, Marzia Belicchi, Barbara Rossi, et al.
Frontiers in Neurology|February 16, 2019
Can Intestinal Pseudo-Obstruction Drive Recurrent Stroke-Like Episodes in Late-Onset MELAS Syndrome? A Case Report and Review of the LiteratureDelia Gagliardi, Eleonora Mauri, Francesca Magri, et al.
BMC Neurology|September 15, 2012
Quantitative muscle strength assessment in duchenne muscular dystrophy: longitudinal study and correlation with functional measuresAlberto Lerario, Serena Bonfiglio, MariaPia Sormani, et al.
Pageof 35