Tomaino C - Search Results

1

The parkin gene is not a major susceptibility locus for typical late-onset Parkinson's disease.

Oliveri RL, Zappia M, Annesi G, Annesi F, Spadafora P, Pasqua AA, Tomaino C, Nicoletti G, Bosco D, Messina D, Logroscino G, Manobianca G, Epifanio A, Morgante L, Savettieri G, Quattrone A. Oliveri RL, et al. Among authors: tomaino c. Neurol Sci. 2001 Feb;22(1):73-4. doi: 10.1007/s100720170053. Neurol Sci. 2001. PMID: 11487208

2

The parkin gene is not involved in late-onset Parkinson's disease.

Oliveri RL, Zappia M, Annesi G, Bosco D, Annesi F, Spadafora P, Pasqua AA, Tomaino C, Nicoletti G, Pirritano D, Labate A, Gambardella A, Logroscino G, Manobianca G, Epifanio A, Morgante L, Savettieri G, Quattrone A. Oliveri RL, et al. Among authors: tomaino c. Neurology. 2001 Jul 24;57(2):359-62. doi: 10.1212/wnl.57.2.359. Neurology. 2001. PMID: 11468333

3

No evidence of association between the alpha-2 macroglobulin gene and Parkinson's disease in a case-control sample.

Nicoletti G, Annesi G, Tomaino C, Spadafora P, Pasqua AA, Annesi F, Serra P, Caracciolo M, Messina D, Zappia M, Quattrone A. Nicoletti G, et al. Among authors: tomaino c. Neurosci Lett. 2002 Aug 2;328(1):65-7. doi: 10.1016/s0304-3940(02)00003-4. Neurosci Lett. 2002. PMID: 12123860

4

Association of the 5-HT6 receptor gene polymorphism C267T with Parkinson's disease.

Messina D, Annesi G, Serra P, Nicoletti G, Pasqua A, Annesi F, Tomaino C, Cirò-Candiano IC, Carrideo S, Caracciolo M, Spadafora P, Zappia M, Savettieri G, Quattrone A. Messina D, et al. Among authors: tomaino c. Neurology. 2002 Mar 12;58(5):828-9. doi: 10.1212/wnl.58.5.828. Neurology. 2002. PMID: 11889255 No abstract available.

5

Familial essential tremor is not associated with SCA-12 mutation in southern Italy.

Nicoletti G, Annesi G, Carrideo S, Tomaino C, Di Costanzo A, Zappia M, Quattrone A. Nicoletti G, et al. Among authors: tomaino c. Mov Disord. 2002 Jul;17(4):837-8. doi: 10.1002/mds.10191. Mov Disord. 2002. PMID: 12210890

6

AbetaPP A713T mutation in late onset Alzheimer's disease with cerebrovascular lesions.

Bernardi L, Geracitano S, Colao R, Puccio G, Gallo M, Anfossi M, Frangipane F, Curcio SA, Mirabelli M, Tomaino C, Vasso F, Smirne N, Maletta R, Bruni AC. Bernardi L, et al. Among authors: tomaino c. J Alzheimers Dis. 2009;17(2):383-9. doi: 10.3233/JAD-2009-1061. J Alzheimers Dis. 2009. PMID: 19363265

7

Novel MAPT Val75Ala mutation and PSEN2 Arg62Hys in two siblings with frontotemporal dementia.

Gallo M, Tomaino C, Puccio G, Frangipane F, Curcio SA, Bernardi L, Geracitano S, Anfossi M, Mirabelli M, Colao R, Vasso F, Smirne N, Maletta RG, Bruni AC. Gallo M, et al. Among authors: tomaino c. Neurol Sci. 2010 Feb;31(1):65-70. doi: 10.1007/s10072-009-0132-9. Epub 2009 Sep 19. Neurol Sci. 2010. PMID: 19768372

8

A procedure for cloning genomic DNA fragments with increasing thermoresistance.

Bellizzi D, Cartolano AS, Annesi F, Tomaino C, Sgaramella V, Losso MA. Bellizzi D, et al. Among authors: tomaino c. Gene. 1998 Sep 28;219(1-2):63-71. doi: 10.1016/s0378-1119(98)00377-1. Gene. 1998. PMID: 9756997

9

Novel PSEN1 and PGRN mutations in early-onset familial frontotemporal dementia.

Bernardi L, Tomaino C, Anfossi M, Gallo M, Geracitano S, Costanzo A, Colao R, Puccio G, Frangipane F, Curcio SA, Mirabelli M, Smirne N, Iapaolo D, Maletta RG, Bruni AC. Bernardi L, et al. Among authors: tomaino c. Neurobiol Aging. 2009 Nov;30(11):1825-33. doi: 10.1016/j.neurobiolaging.2008.01.005. Epub 2008 Mar 7. Neurobiol Aging. 2009. PMID: 18314228

10

Apolipoprotein(a) null phenotype is related to a delayed age at onset of Alzheimer's disease.

Emanuele E, Peros E, Tomaino C, Feudatari E, Bernardi L, Binetti G, Maletta R, D'Angelo A, Montagna L, Bruni AC, Geroldi D. Emanuele E, et al. Among authors: tomaino c. Neurosci Lett. 2004 Feb 26;357(1):45-8. doi: 10.1016/j.neulet.2003.12.043. Neurosci Lett. 2004. PMID: 15036610

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