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

Year Number of Results
2002 2
2003 1
2004 1
2005 2
2006 4
2007 3
2008 2
2009 3
2010 2
2011 6
2012 3
2014 1
2017 3
2018 2
2019 1
2020 1
2024 1

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Page 1
Increase in DNA methylation in patients with amyotrophic lateral sclerosis carriers of not fully penetrant SOD1 mutations.
Coppedè F, Stoccoro A, Mosca L, Gallo R, Tarlarini C, Lunetta C, Marocchi A, Migliore L, Penco S. Coppedè F, et al. Among authors: marocchi a. Amyotroph Lateral Scler Frontotemporal Degener. 2018 Feb;19(1-2):93-101. doi: 10.1080/21678421.2017.1367401. Epub 2017 Sep 1. Amyotroph Lateral Scler Frontotemporal Degener. 2018. PMID: 28859526
Genetic variability of the fructosamine 3-kinase gene in diabetic patients.
Mosca L, Penco S, Patrosso MC, Marocchi A, Lapolla A, Sartore G, Chilelli NC, Paleari R, Mosca A. Mosca L, et al. Among authors: marocchi a. Clin Chem Lab Med. 2011 May;49(5):803-8. doi: 10.1515/CCLM.2011.133. Epub 2011 Feb 3. Clin Chem Lab Med. 2011. PMID: 21288167
The role of chromogranin A in the management of patients with phaeochromocytoma.
Grossrubatscher E, Dalino P, Vignati F, Gambacorta M, Pugliese R, Boniardi M, Rossetti O, Marocchi A, Bertuzzi M, Loli P. Grossrubatscher E, et al. Among authors: marocchi a. Clin Endocrinol (Oxf). 2006 Sep;65(3):287-93. doi: 10.1111/j.1365-2265.2006.02591.x. Clin Endocrinol (Oxf). 2006. PMID: 16918946
NOTCH3 gene mutations in subjects clinically suspected of CADASIL.
Mosca L, Marazzi R, Ciccone A, Santilli I, Bersano A, Sansone V, Grosso E, Mandrile G, Giachino DF, Adobbati L, Corengia E, Agostoni E, Fiumani A, Gallone S, Scarpini E, Guidotti M, Sterzi R, Ajmone C, Marocchi A, Penco S. Mosca L, et al. Among authors: marocchi a. J Neurol Sci. 2011 Aug 15;307(1-2):144-8. doi: 10.1016/j.jns.2011.04.019. Epub 2011 May 26. J Neurol Sci. 2011. PMID: 21616505 Free article.
35 results