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Multicenter evaluation of xpert MTB/RIF ultra tests reporting detection of "Trace" of Mycobacterium tuberculosis DNA.
Mazzola E, Monte PD, Piersimoni C, Giudice AD, Camaggi A, Pedrotti C, Gurrieri F, Russo C, Farina C, Lombardi A, Viggiani P, Cenci E, Nisticò S, Rognoni V, Sala E, Cichero P, Frizzera E, Monzillo V, Morini F, Scarparo C, Borroni E, Cirillo DM, Tortoli E. Mazzola E, et al. Among authors: gurrieri f. Int J Mycobacteriol. 2021 Jan-Mar;10(1):101-103. doi: 10.4103/ijmy.ijmy_200_20. Int J Mycobacteriol. 2021. PMID: 33707382 No abstract available.
First Italian report of a liver abscess and metastatic endogenous endophthalmitis caused by ST-23 hypervirulent Klebsiella pneumoniae in an immunocompetent individual.
De Francesco MA, Tiecco G, Scaltriti E, Piccinelli G, Corbellini S, Gurrieri F, Crosato V, Moioli G, Marchese V, Focà E, Bertelli DA, Castelli F, Caruso A. De Francesco MA, et al. Among authors: gurrieri f. Infection. 2023 Feb;51(1):271-276. doi: 10.1007/s15010-022-01879-8. Epub 2022 Jul 8. Infection. 2023. PMID: 35802342 Free PMC article.
Strongyloides stercoralis infection: an underlying cause of invasive bacterial infections of enteric origin. Results from a prospective cross-sectional study of a northern Italian tertiary hospital.
Gardini G, Froeschl G, Gurrieri F, De Francesco MA, Cattaneo C, Marchese V, Piccinelli G, Corbellini S, Pagani C, Santagiuliana M, Fumarola B, Gulletta M, Perandin F, Castelli F, Matteelli A. Gardini G, et al. Among authors: gurrieri f. Infection. 2023 Oct;51(5):1541-1548. doi: 10.1007/s15010-023-02072-1. Epub 2023 Jul 18. Infection. 2023. PMID: 37462896 Free PMC article.
A pathogenic variant in the FLCN gene presenting with pure dementia: is autophagy at the intersection between neurodegeneration and cancer?
Bottillo I, Laino L, Azzarà A, Lintas C, Cassano I, Di Lazzaro V, Ursini F, Motolese F, Bargiacchi S, Formicola D, Grammatico P, Gurrieri F. Bottillo I, et al. Among authors: gurrieri f. Front Neurosci. 2024 Jan 5;17:1304080. doi: 10.3389/fnins.2023.1304080. eCollection 2023. Front Neurosci. 2024. PMID: 38249578 Free PMC article.
Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative gene.
Panagiotakaki E, Tiziano FD, Mikati MA, Vijfhuizen LS, Nicole S, Lesca G, Abiusi E, Novelli A, Di Pietro L; I.B.AHC Consortium; IAHCRC Consortium; Harder AVE, Walley NM, De Grandis E, Poulat AL, Portes VD, Lépine A, Nassogne MC, Arzimanoglou A, Vavassori R, Koenderink J, Thompson CH, George AL Jr, Gurrieri F, van den Maagdenberg AMJM, Heinzen EL. Panagiotakaki E, et al. Among authors: gurrieri f. Eur J Hum Genet. 2024 Feb;32(2):224-231. doi: 10.1038/s41431-023-01489-4. Epub 2023 Dec 14. Eur J Hum Genet. 2024. PMID: 38097767
110 results