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Showing 49 to 52 of 52 entries
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Histamine Regulates the Inflammatory Profile of SOD1-G93A Microglia and the Histaminergic System Is Dysregulated in Amyotrophic Lateral Sclerosis.

Frontiers in immunology

Apolloni S, Fabbrizio P, Amadio S, Napoli G, Verdile V, Morello G, Iemmolo R, Aronica E, Cavallaro S, Volonté C.
PMID: 29250069
Front Immunol. 2017 Nov 30;8:1689. doi: 10.3389/fimmu.2017.01689. eCollection 2017.

Amyotrophic lateral sclerosis (ALS) is a late-onset motor neuron disease where activated glia release pro-inflammatory cytokines that trigger a vicious cycle of neurodegeneration in the absence of resolution of inflammation. Given the well-established role of histamine as a neuron-to-glia...

Three-electron auger process from beam-foil excited multiply charged ions.

Physical review letters

De Filippo E, Lanzanò G, Rothard H, Volant C.
PMID: 18643496
Phys Rev Lett. 2008 Jun 13;100(23):233202. doi: 10.1103/PhysRevLett.100.233202. Epub 2008 Jun 13.

Electron emission from collisions of C3+ ions (22.7 A MeV) with carbon foils (21, 49 and 90 microg/cm(2)) was studied by the time-of-flight method. Two prominent emission patterns can be readily identified as "binary encounter" electrons and "cusp" electrons....

Drug Repurposing: A Network-based Approach to Amyotrophic Lateral Sclerosis.

Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics

Fiscon G, Conte F, Amadio S, Volonté C, Paci P.
PMID: 33987813
Neurotherapeutics. 2021 Jul;18(3):1678-1691. doi: 10.1007/s13311-021-01064-z. Epub 2021 May 13.

The continuous adherence to the conventional "one target, one drug" paradigm has failed so far to provide effective therapeutic solutions for heterogeneous and multifactorial diseases as amyotrophic lateral sclerosis (ALS), a rare progressive and chronic, debilitating neurological disease for...

Repurposing of Trimetazidine for amyotrophic lateral sclerosis: A study in SOD1.

British journal of pharmacology

Scaricamazza S, Salvatori I, Amadio S, Nesci V, Torcinaro A, Giacovazzo G, Primiano A, Gloriani M, Candelise N, Pieroni L, Loeffler JP, Renè F, Quessada C, Tefera TW, Wang H, Steyn FJ, Ngo ST, Dobrowolny G, Lepore E, Urbani A, Musarò A, Volonté C, Ferraro E, Coccurello R, Valle C, Ferri A.
PMID: 34783031
Br J Pharmacol. 2021 Nov 16; doi: 10.1111/bph.15738. Epub 2021 Nov 16.

BACKGROUND AND PURPOSE: Amyotrophic lateral sclerosis (ALS), a neurodegenerative disease characterized by the degeneration of upper and lower motor neurons, progressive wasting and paralysis of voluntary muscles and is currently incurable. Although considered to be a pure motor neuron...

Showing 49 to 52 of 52 entries