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Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|August 11, 1992
Abrogating chemotherapy-induced myelosuppression by recombinant granulocyte-macrophage colony-stimulating factor in patients with sarcoma: protection at the progenitor cell levelS Vadhan-Raj, H E Broxmeyer, W N Hittelman, et al.
European Journal of Neurology|September 7, 2020
Late-onset presentation and phenotypic heterogeneity of the rare R377W PSEN1 mutationM Scarioni, A Arighi, C Fenoglio, et al.
Cancer Research|March 27, 1998
Ki-ras mutation and p53 overexpression predict the clinical behavior of colorectal cancer: a Southwest Oncology Group studyD J Ahnen, P Feigl, G Quan, et al.
Cytokine|January 29, 2019
Inflammatory expression profile in peripheral blood mononuclear cells from patients with Nasu-Hakola DiseaseD Galimberti, C Fenoglio, L Ghezzi, et al.
European Journal of Neurology|November 29, 2007
Neuronal nitric oxide synthase C276T polymorphism increases the risk for frontotemporal lobar degenerationE Venturelli, C Villa, E Scarpini, et al.
European Journal of Neurology|August 30, 2008
Novel exon 1 progranulin gene variant in Alzheimer's diseaseF Cortini, C Fenoglio, I Guidi, et al.
Geroscience|February 1, 2023
Plasma microglial-derived extracellular vesicles are increased in frail patients with Mild Cognitive Impairment and exert a neurotoxic effectC Visconte, M T Golia, C Fenoglio, et al.
European Journal of Neurology|December 18, 2008
The NOS3 G894T (Glu298Asp) polymorphism is a risk factor for frontotemporal lobar degenerationE Venturelli, C Villa, C Fenoglio, et al.
European Journal of Neurology|January 14, 2010
Lack of replication of KIF1B gene in an Italian primary progressive multiple sclerosis cohortF Martinelli-Boneschi, F Esposito, D Scalabrini, et al.
European Journal of Neurology|May 29, 2009
DCUN1D1 is a risk factor for frontotemporal lobar degenerationC Villa, E Venturelli, C Fenoglio, et al.
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