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Year Number of Results
2002 1
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2017 4
2018 8
2019 7
2020 4
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2023 2
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Page 1
Human blood lipid profiles after dietary supplementation of different omega 3 ethyl esters formulations.
Donnarumma D, Di Salle A, Micalizzi G, Vento F, La Tella R, Iannotta P, Trovato E, Melone MAB, Rigano F, Donato P, Mondello L, Peluso G. Donnarumma D, et al. Among authors: melone mab. J Chromatogr B Analyt Technol Biomed Life Sci. 2023 Dec 1;1231:123922. doi: 10.1016/j.jchromb.2023.123922. Epub 2023 Nov 4. J Chromatogr B Analyt Technol Biomed Life Sci. 2023. PMID: 37976941 Free article.
A Translational Approach to Spinal Neurofibromatosis: Clinical and Molecular Insights from a Wide Italian Cohort.
Paterra R, Bettinaglio P, Borghi A, Mangano E, Tritto V, Cesaretti C, Schettino C, Bordoni R, Santoro C, Avignone S, Moscatelli M, Melone MAB, Saletti V, Piluso G, Natacci F, Riva P, Eoli M. Paterra R, et al. Among authors: melone mab. Cancers (Basel). 2022 Dec 22;15(1):59. doi: 10.3390/cancers15010059. Cancers (Basel). 2022. PMID: 36612057 Free PMC article.
Genotype-Phenotype Correlations in Neurofibromatosis Type 1: Identification of Novel and Recurrent NF1 Gene Variants and Correlations with Neurocognitive Phenotype.
Napolitano F, Dell'Aquila M, Terracciano C, Franzese G, Gentile MT, Piluso G, Santoro C, Colavito D, Patanè A, De Blasiis P, Sampaolo S, Paladino S, Melone MAB. Napolitano F, et al. Among authors: melone mab. Genes (Basel). 2022 Jun 23;13(7):1130. doi: 10.3390/genes13071130. Genes (Basel). 2022. PMID: 35885913 Free PMC article.
Down Syndrome Fetal Fibroblasts Display Alterations of Endosomal Trafficking Possibly due to SYNJ1 Overexpression.
De Rosa L, Fasano D, Zerillo L, Valente V, Izzo A, Mollo N, Amodio G, Polishchuk E, Polishchuk R, Melone MAB, Criscuolo C, Conti A, Nitsch L, Remondelli P, Pierantoni GM, Paladino S. De Rosa L, et al. Among authors: melone mab. Front Genet. 2022 May 13;13:867989. doi: 10.3389/fgene.2022.867989. eCollection 2022. Front Genet. 2022. PMID: 35646085 Free PMC article.
Fighting the Huntington's Disease with a G-Quadruplex-Forming Aptamer Specifically Binding to Mutant Huntingtin Protein: Biophysical Characterization, In Vitro and In Vivo Studies.
Riccardi C, D'Aria F, Digilio FA, Carillo MR, Amato J, Fasano D, De Rosa L, Paladino S, Melone MAB, Montesarchio D, Giancola C. Riccardi C, et al. Among authors: melone mab. Int J Mol Sci. 2022 Apr 27;23(9):4804. doi: 10.3390/ijms23094804. Int J Mol Sci. 2022. PMID: 35563194 Free PMC article.
Clinical-Genetic Features Influencing Disability in Spastic Paraplegia Type 4: A Cross-sectional Study by the Italian DAISY Network.
Rossi S, Rubegni A, Riso V, Barghigiani M, Bassi MT, Battini R, Bertini E, Cereda C, Cioffi E, Criscuolo C, Dal Fabbro B, Dato C, D'Angelo MG, Di Muzio A, Diamanti L, Dotti MT, Filla A, Gioiosa V, Liguori R, Martinuzzi A, Massa R, Mignarri A, Moroni R, Musumeci O, Nicita F, Orologio I, Orsi L, Pegoraro E, Petrucci A, Plumari M, Ricca I, Rizzo G, Romano S, Rumore R, Sampaolo S, Scarlato M, Seri M, Stefan C, Straccia G, Tessa A, Travaglini L, Trovato R, Ulgheri L, Vazza G, Orlacchio A, Silvestri G, Santorelli FM, Melone MAB, Casali C. Rossi S, et al. Among authors: melone mab. Neurol Genet. 2022 Mar 30;8(2):e664. doi: 10.1212/NXG.0000000000000664. eCollection 2022 Apr. Neurol Genet. 2022. PMID: 35372684 Free PMC article.
POLR3A variants in hereditary spastic paraparesis and ataxia: clinical, genetic, and neuroradiological findings in a cohort of Italian patients.
Di Donato I, Gallo A, Ricca I, Fini N, Silvestri G, Gurrieri F, Cirillo M, Cerase A, Natale G, Matrone F, Riso V, Melone MAB, Tessa A, De Michele G, Federico A, Filla A, Dotti MT, Santorelli FM. Di Donato I, et al. Among authors: melone mab. Neurol Sci. 2022 Feb;43(2):1071-1077. doi: 10.1007/s10072-021-05462-1. Epub 2021 Jul 23. Neurol Sci. 2022. PMID: 34296356 Free PMC article.
39 results