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

Year Number of Results
1990 1
1991 1
1993 1
1996 1
1997 1
2000 1
2001 3
2007 1
2009 1
2010 2
2013 1
2014 1
2022 1
2024 0

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15 results

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Page 1
Mitochondrial Diseases in Childhood.
Ardissone A, Lamantea E, Invernizzi F, Zeviani M, Genitrini S, Moroni I, Uziel G. Ardissone A, et al. Among authors: genitrini s. Curr Mol Med. 2014;14(8):1069-1078. doi: 10.2174/1566524014666141010155317. Curr Mol Med. 2014. PMID: 25323866
Early-onset Parkinson's disease.
Giovannini P, Piccolo I, Genitrini S, Soliveri P, Girotti F, Geminiani G, Scigliano G, Caraceni T. Giovannini P, et al. Among authors: genitrini s. Mov Disord. 1991;6(1):36-42. doi: 10.1002/mds.870060107. Mov Disord. 1991. PMID: 2005920
Validation of the Italian version of the pediatric CMT quality of life outcome measure.
Moroni I, Danti FR, Pareyson D, Pagliano E, Piscosquito G, Foscan M, Marchi A, Ardissone A, Genitrini S, Wu TT, Shy ME, Ramchandren S. Moroni I, et al. Among authors: genitrini s. J Peripher Nerv Syst. 2022 Jun;27(2):127-130. doi: 10.1111/jns.12494. Epub 2022 May 3. J Peripher Nerv Syst. 2022. PMID: 35416371 Free PMC article.
Non-motor effects of deep brain stimulation of the subthalamic nucleus in Parkinson's disease: preliminary physiological results.
Priori A, Cinnante C, Genitrini S, Pesenti A, Tortora G, Bencini C, Barelli MV, Buonamici V, Carella F, Girotti F, Soliveri P, Magrini F, Morganti A, Albanese A, Broggi S, Scarlato G, Barbieri S. Priori A, et al. Among authors: genitrini s. Neurol Sci. 2001 Feb;22(1):85-6. doi: 10.1007/s100720170059. Neurol Sci. 2001. PMID: 11487214
Response to L-DOPA in multiple system atrophy.
Parati EA, Fetoni V, Geminiani GC, Soliveri P, Giovannini P, Testa D, Genitrini S, Caraceni T, Girotti F. Parati EA, et al. Among authors: genitrini s. Clin Neuropharmacol. 1993 Apr;16(2):139-44. doi: 10.1097/00002826-199304000-00006. Clin Neuropharmacol. 1993. PMID: 8477409
Predictive genetic tests in neurodegenerative disorders: a methodological approach integrating psychological counseling for at-risk individuals and referring clinicians.
Mariotti C, Ferruta A, Gellera C, Nespolo C, Fancellu R, Genitrini S, Di Bella D, Panzeri M, Nanetti L, Tomasello C, Taroni F, Foresti G, Astori S. Mariotti C, et al. Among authors: genitrini s. Eur Neurol. 2010;64(1):33-41. doi: 10.1159/000315033. Epub 2010 Jun 30. Eur Neurol. 2010. PMID: 20588047
Severe deficiency of the fatty acid amide hydrolase (FAAH) activity segregates with the Huntington's disease mutation in peripheral lymphocytes.
Battista N, Bari M, Tarditi A, Mariotti C, Bachoud-Lévi AC, Zuccato C, Finazzi-Agrò A, Genitrini S, Peschanski M, Di Donato S, Cattaneo E, Maccarrone M. Battista N, et al. Among authors: genitrini s. Neurobiol Dis. 2007 Jul;27(1):108-16. doi: 10.1016/j.nbd.2007.04.012. Epub 2007 May 6. Neurobiol Dis. 2007. PMID: 17553686
15 results