Quattrone A - Search Results

1

Association study between four polymorphisms in the HFE, TF and TFR genes and Parkinson's disease in southern Italy.

Greco V, De Marco EV, Rocca FE, Annesi F, Civitelli D, Provenzano G, Tarantino P, Scornaienchi V, Pucci F, Salsone M, Novellino F, Morelli M, Paglionico S, Gambardella A, Quattrone A, Annesi G. Greco V, et al. Among authors: quattrone a. Neurol Sci. 2011 Jun;32(3):525-7. doi: 10.1007/s10072-011-0504-9. Epub 2011 Mar 8. Neurol Sci. 2011. PMID: 21384276

2

Association study of dopamine D2, D3 receptor gene polymorphisms with motor fluctuations in PD.

Zappia M, Annesi G, Quattrone A. Zappia M, et al. Among authors: quattrone a. Neurology. 2002 Mar 12;58(5):837; author reply 837-8. doi: 10.1212/wnl.58.5.837-a. Neurology. 2002. PMID: 11889264 No abstract available.

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: quattrone a. Neurosci Lett. 2002 Aug 2;328(1):65-7. doi: 10.1016/s0304-3940(02)00003-4. Neurosci Lett. 2002. PMID: 12123860

4

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: quattrone a. Mov Disord. 2002 Jul;17(4):837-8. doi: 10.1002/mds.10191. Mov Disord. 2002. PMID: 12210890

5

A large family with pure autosomal dominant hereditary spastic paraplegia from southern Italy mapping to chromosome 14q11.2-q24.3.

Muglia M, Magariello A, Nicoletti G, Patitucci A, Gabriele AL, Conforti FL, Mazzei R, Caracciolo M, Casari G, Ardito B, Lastilla M, Gambardella A, Quattrone A. Muglia M, et al. Among authors: quattrone a. J Neurol. 2002 Oct;249(10):1413-6. doi: 10.1007/s00415-002-0856-4. J Neurol. 2002. PMID: 12382159

6

Two novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus.

Annesi G, Gambardella A, Carrideo S, Incorpora G, Labate A, Pasqua AA, Civitelli D, Polizzi A, Annesi F, Spadafora P, Tarantino P, Cirò Candiano IC, Romeo N, De Marco EV, Ventura P, LePiane E, Zappia M, Aguglia U, Pavone L, Quattrone A. Annesi G, et al. Among authors: quattrone a. Epilepsia. 2003 Sep;44(9):1257-8. doi: 10.1046/j.1528-1157.2003.22503.x. Epilepsia. 2003. PMID: 12919402 Free article. No abstract available.

7

Association between Synapsin III gene promoter polymorphisms and multiple sclerosis.

Liguori M, Cittadella R, Manna I, Valentino P, La Russa A, Serra P, Trojano M, Messina D, Ruscica F, Andreoli V, Romeo N, Livrea P, Quattrone A. Liguori M, et al. Among authors: quattrone a. J Neurol. 2004 Feb;251(2):165-70. doi: 10.1007/s00415-004-0293-7. J Neurol. 2004. PMID: 14991350

8

A novel exon 1 mutation in a patient with atypical lafora progressive myoclonus epilepsy seen as childhood-onset cognitive deficit.

Annesi G, Sofia V, Gambardella A, Candiano IC, Spadafora P, Annesi F, Cutuli N, De Marco EV, Civitelli D, Carrideo S, Tarantino P, Barone R, Zappia M, Quattrone A. Annesi G, et al. Among authors: quattrone a. Epilepsia. 2004 Mar;45(3):294-5. doi: 10.1111/j.0013-9580.2004.33203.x. Epilepsia. 2004. PMID: 15009235 Free article. No abstract available.

9

Increased risk for Alzheimer disease with the interaction of MPO and A2M polymorphisms.

Zappia M, Manna I, Serra P, Cittadella R, Andreoli V, La Russa A, Annesi F, Spadafora P, Romeo N, Nicoletti G, Messina D, Gambardella A, Quattrone A. Zappia M, et al. Among authors: quattrone a. Arch Neurol. 2004 Mar;61(3):341-4. doi: 10.1001/archneur.61.3.341. Arch Neurol. 2004. PMID: 15023809

10

Startle epilepsy complicating aspartylglucosaminuria.

Labate A, Barone R, Gambardella A, Civitelli D, Fiumara A, Annesi G, Zappia M, Pavone L, Quattrone A. Labate A, et al. Among authors: quattrone a. Brain Dev. 2004 Mar;26(2):130-3. doi: 10.1016/S0387-7604(03)00069-X. Brain Dev. 2004. PMID: 15036433

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