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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1988 1
1989 1
1990 2
1998 1
2000 1
2002 1
2004 1
2007 1
2008 3
2009 2
2010 2
2012 3
2013 1
2014 2
2015 1
2016 1
2017 2
2018 4
2019 8
2020 5
2021 11
2022 4
2023 2
2024 2

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55 results

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Page 1
A New Vision of IgA Nephropathy: The Missing Link.
Sallustio F, Curci C, Di Leo V, Gallone A, Pesce F, Gesualdo L. Sallustio F, et al. Among authors: gallone a. Int J Mol Sci. 2019 Dec 26;21(1):189. doi: 10.3390/ijms21010189. Int J Mol Sci. 2019. PMID: 31888082 Free PMC article. Review.
PLIN4-related myopathy: clinical, histological and imaging data in a large cohort of patients.
Maggi L, Gibertini S, Iannibelli E, Gallone A, Bonanno S, Cazzato D, Gerevini S, Moscatelli M, Blasevich F, Riolo G, Mantegazza R, Ruggieri A. Maggi L, et al. Among authors: gallone a. J Neurol. 2023 Sep;270(9):4538-4543. doi: 10.1007/s00415-023-11729-8. Epub 2023 May 5. J Neurol. 2023. PMID: 37145156 Free PMC article. No abstract available.
Anoctamin-5 related muscle disease: clinical and genetic findings in a large European cohort.
de Bruyn A, Montagnese F, Holm-Yildiz S, Scharff Poulsen N, Stojkovic T, Behin A, Palmio J, Jokela M, De Bleecker JL, de Visser M, van der Kooi AJ, Ten Dam L, Domínguez González C, Maggi L, Gallone A, Kostera-Pruszczyk A, Macias A, Łusakowska A, Nedkova V, Olive M, Álvarez-Velasco R, Wanschitz J, Paradas C, Mavillard F, Querin G, Fernández-Eulate G, Quinlivan R, Walter MC, Depuydt CE, Udd B, Vissing J, Schoser B, Claeys KG. de Bruyn A, et al. Among authors: gallone a. Brain. 2023 Sep 1;146(9):3800-3815. doi: 10.1093/brain/awad088. Brain. 2023. PMID: 36913258
A transcriptomics study of hereditary angioedema attacks.
Castellano G, Divella C, Sallustio F, Montinaro V, Curci C, Zanichelli A, Bonanni E, Suffritti C, Caccia S, Bossi F, Gallone A, Schena FP, Gesualdo L, Cicardi M. Castellano G, et al. Among authors: gallone a. J Allergy Clin Immunol. 2018 Sep;142(3):883-891. doi: 10.1016/j.jaci.2018.03.016. Epub 2018 May 4. J Allergy Clin Immunol. 2018. PMID: 29729940 Free article.
Renal progenitor cells revert LPS-induced endothelial-to-mesenchymal transition by secreting CXCL6, SAA4, and BPIFA2 antiseptic peptides.
Sallustio F, Stasi A, Curci C, Divella C, Picerno A, Franzin R, De Palma G, Rutigliano M, Lucarelli G, Battaglia M, Staffieri F, Crovace A, Pertosa GB, Castellano G, Gallone A, Gesualdo L. Sallustio F, et al. Among authors: gallone a. FASEB J. 2019 Oct;33(10):10753-10766. doi: 10.1096/fj.201900351R. Epub 2019 Jul 3. FASEB J. 2019. PMID: 31268775
Screening of mutations of hemophilia A in 40 Italian patients: a novel G-to-A mutation in intron 10 of the F8 gene as a putative cause of mild hemophilia A in southern Italy.
Santacroce R, Santoro R, Sessa F, Iannaccaro P, Sarno M, Longo V, Gallone A, Vecchione G, Muleo G, Margaglione M. Santacroce R, et al. Among authors: gallone a. Blood Coagul Fibrinolysis. 2008 Apr;19(3):197-202. doi: 10.1097/MBC.0b013e3282f234ab. Blood Coagul Fibrinolysis. 2008. PMID: 18388498
Next-generation sequencing application to investigate skeletal muscle channelopathies in a large cohort of Italian patients.
Brugnoni R, Maggi L, Canioni E, Verde F, Gallone A, Ariatti A, Filosto M, Petrelli C, Logullo FO, Esposito M, Ruggiero L, Tonin P, Riguzzi P, Pegoraro E, Torri F, Ricci G, Siciliano G, Silani V, Merlini L, De Pasqua S, Liguori R, Pini A, Mariotti C, Moroni I, Imbrici P, Desaphy JF, Mantegazza R, Bernasconi P. Brugnoni R, et al. Among authors: gallone a. Neuromuscul Disord. 2021 Apr;31(4):336-347. doi: 10.1016/j.nmd.2020.12.003. Epub 2020 Dec 14. Neuromuscul Disord. 2021. PMID: 33573884
55 results