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Cephalalgia : an International Journal of Headache|March 16, 2013
The role of tyrosine metabolism in the pathogenesis of chronic migraineGiovanni D'Andrea, Domenico D'Amico, Gennaro Bussone, et al.
Neurogenetics|April 23, 2024
Early-onset dysphagia and severe neurodevelopmental disorder as early signs in a patient with two novel variants in NARS1: a case report and brief review of the literatureCarlo Alberto Cesaroni, Gianluca Contrò, Carlotta Spagnoli, et al.
Drugs & Aging|June 11, 2008
Glutathione S-transferase P1 Ile105Val polymorphism is associated with haematological toxicity in elderly rectal cancer patients receiving preoperative chemoradiotherapyMarco Agostini, Lara Maria Pasetto, Salvatore Pucciarelli, et al.
The Journal of Pharmacology and Experimental Therapeutics|September 27, 2007
1-(3',4'-Dichloro-2-fluoro[1,1'-biphenyl]-4-yl)-cyclopropanecarboxylic acid (CHF5074), a novel gamma-secretase modulator, reduces brain beta-amyloid pathology in a transgenic mouse model of Alzheimer's disease without causing peripheral toxicityBruno P Imbimbo, Elda Del Giudice, Davide Colavito, et al.
Brain : a Journal of Neurology|July 28, 2006
Longitudinal analysis of immune cell phenotypes in early stage multiple sclerosis: distinctive patterns characterize MRI-active patientsLuciano Rinaldi, Paolo Gallo, Massimiliano Calabrese, et al.
American Journal of Medical Genetics. Part A|September 5, 2024
Two novel compound heterozygous HOXB1 variants in congenital facial palsy: A case report and a brief review of the literatureChiara Brugnoli, Susanna Rizzi, Carlo Alberto Cesaroni, et al.
European Journal of Neurology|February 3, 2023
Evaluating the contribution of the gene TARDBP in Italian patients with amyotrophic lateral sclerosisSerena Lattante, Mario Sabatelli, Giulia Bisogni, et al.
Gut|March 26, 2013
Amniotic fluid stem cells improve survival and enhance repair of damaged intestine in necrotising enterocolitis via a COX-2 dependent mechanismAugusto Zani, Mara Cananzi, Francesco Fascetti-Leon, et al.
Scientific Reports|March 16, 2021
Novel CARMIL2 loss-of-function variants are associated with pediatric inflammatory bowel diseaseLuca Bosa, Vritika Batura, Davide Colavito, et al.
Annals of the New York Academy of Sciences|April 27, 2007
Genetics of healthy aging in Europe: the EU-integrated project GEHA (GEnetics of Healthy Aging)Claudio Franceschi, Vladyslav Bezrukov, Hélène Blanché, et al.
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