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The Journal of Clinical Investigation|September 5, 2008
Neural stem cell transplantation can ameliorate the phenotype of a mouse model of spinal muscular atrophyStefania Corti, Monica Nizzardo, Martina Nardini, et al.
European Journal of Neurology|February 6, 2023
Intravenous thrombolysis + endovascular thrombectomy versus thrombolysis alone in large vessel occlusion mild stroke: a propensity score matched analysisGhil Schwarz, Sara Bonato, Silvia Lanfranconi, 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.
Neurology|October 24, 2008
Mutated mitofusin 2 presents with intrafamilial variability and brain mitochondrial dysfunctionR Del Bo, M Moggio, M Rango, et al.
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.
European Journal of Neurology|February 25, 2009
TARDBP (TDP-43) sequence analysis in patients with familial and sporadic ALS: identification of two novel mutationsR Del Bo, S Ghezzi, S Corti, et al.
Carcinogenesis|November 8, 2018
Elucidating the role of Agl in bladder carcinogenesis by generation and characterization of genetically engineered miceJoseph L Sottnik, Vandana Mallaredy, Ana Chauca-Diaz, et al.
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