Marocchi A - Search Results

1

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.

2

Mutational screening of NOTCH3 gene reveals two novel mutations: complexity of CADASIL diagnosis.

Mosca L, Rivieri F, Tanel R, Bonfante A, Burlina A, Manfredini E, Primignani P, Gesu GP, Marocchi A, Penco S. Mosca L, et al. Among authors: marocchi a. J Mol Neurosci. 2014 Dec;54(4):723-9. doi: 10.1007/s12031-014-0311-x. Epub 2014 May 10. J Mol Neurosci. 2014. PMID: 24816653

3

Is the SHRSP [corrected] strain a suitable model of spontaneous CADASIL?

Penco S, Gelosa P, Pileggi S, Abbate M, Marocchi A, Guerrini U, Pignieri A, Tremoli E, Sironi L. Penco S, et al. Among authors: marocchi a. J Mol Neurosci. 2012 Feb;46(2):427-30. doi: 10.1007/s12031-011-9605-4. Epub 2011 Aug 2. J Mol Neurosci. 2012. PMID: 21809043

4

Frequency of butyrylcholinesterase gene mutations in individuals with abnormal inhibition numbers: an Italian-population study.

Lando G, Mosca A, Bonora R, Azzario F, Penco S, Marocchi A, Panteghini M, Patrosso MC. Lando G, et al. Among authors: marocchi a. Pharmacogenetics. 2003 May;13(5):265-70. doi: 10.1097/00008571-200305000-00005. Pharmacogenetics. 2003. PMID: 12724618

5

Phenotypic heterogeneity in a SOD1 G93D Italian ALS family: an example of human model to study a complex disease.

Penco S, Lunetta C, Mosca L, Maestri E, Avemaria F, Tarlarini C, Patrosso MC, Marocchi A, Corbo M. Penco S, et al. Among authors: marocchi a. J Mol Neurosci. 2011 May;44(1):25-30. doi: 10.1007/s12031-010-9480-4. Epub 2010 Dec 1. J Mol Neurosci. 2011. PMID: 21120636

6

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

7

Mutation in the senataxin gene found in a patient affected by familial ALS with juvenile onset and slow progression.

Avemaria F, Lunetta C, Tarlarini C, Mosca L, Maestri E, Marocchi A, Melazzini M, Penco S, Corbo M. Avemaria F, et al. Among authors: marocchi a. Amyotroph Lateral Scler. 2011 May;12(3):228-30. doi: 10.3109/17482968.2011.566930. Epub 2011 Mar 28. Amyotroph Lateral Scler. 2011. PMID: 21438761

8

De novo MGC4607 gene heterozygous missense variants in a child with multiple cerebral cavernous malformations.

Mosca L, Pileggi S, Avemaria F, Tarlarini C, Cigoli MS, Capra V, De Marco P, Pavanello M, Marocchi A, Penco S. Mosca L, et al. Among authors: marocchi a. J Mol Neurosci. 2012 Jul;47(3):475-80. doi: 10.1007/s12031-012-9741-5. Epub 2012 Mar 14. J Mol Neurosci. 2012. PMID: 22415356

9

New application of intelligent agents in sporadic amyotrophic lateral sclerosis identifies unexpected specific genetic background.

Penco S, Buscema M, Patrosso MC, Marocchi A, Grossi E. Penco S, et al. Among authors: marocchi a. BMC Bioinformatics. 2008 May 30;9:254. doi: 10.1186/1471-2105-9-254. BMC Bioinformatics. 2008. PMID: 18513389 Free PMC article.

10

Genetic variations within KRIT1/CCM1, MGC4607/CCM2 and PDCD10/CCM3 in a large Italian family harbouring a Krit1/CCM1 mutation.

Pileggi S, Buscone S, Ricci C, Patrosso MC, Marocchi A, Brunori P, Battistini S, Penco S. Pileggi S, et al. Among authors: marocchi a. J Mol Neurosci. 2010 Oct;42(2):235-42. doi: 10.1007/s12031-010-9360-y. Epub 2010 Apr 24. J Mol Neurosci. 2010. PMID: 20419355

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