Quattrone A - Search Results

1

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

2

Body weight influences pharmacokinetics of levodopa in Parkinson's disease.

Zappia M, Crescibene L, Arabia G, Nicoletti G, Bagalà A, Bastone L, Caracciolo M, Bonavita S, Di Costanzo A, Scornaienchi M, Gambardella A, Quattrone A. Zappia M, et al. Among authors: quattrone a. Clin Neuropharmacol. 2002 Mar-Apr;25(2):79-82. doi: 10.1097/00002826-200203000-00004. Clin Neuropharmacol. 2002. PMID: 11981233

3

Further evidence that SPG3A gene mutations cause autosomal dominant hereditary spastic paraplegia.

Muglia M, Magariello A, Nicoletti G, Patitucci A, Gabriele AL, Conforti FL, Mazzei R, Caracciolo M, Ardito B, Lastilla M, Tedeschi G, Quattrone A. Muglia M, et al. Among authors: quattrone a. Ann Neurol. 2002 Jun;51(6):794-5. doi: 10.1002/ana.10185. Ann Neurol. 2002. PMID: 12112092 No abstract available.

4

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

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

6

A novel mutation in the CLN1 gene in a patient with juvenile neuronal ceroid lipofuscinosis.

Mazzei R, Conforti FL, Magariello A, Bravaccio C, Militerni R, Gabriele AL, Sampaolo S, Patitucci A, Di Iorio G, Muglia M, Quattrone A. Mazzei R, et al. Among authors: quattrone a. J Neurol. 2002 Oct;249(10):1398-400. doi: 10.1007/s00415-002-0849-3. J Neurol. 2002. PMID: 12382155

7

Mutation analysis of the MECP2 gene in patients with Rett syndrome.

Conforti FL, Mazzei R, Magariello A, Patitucci A, Gabriele AL, Muglia M, Quattrone A, Fiumara A, Barone R, Pavone L, Nisticò R, Mangone L. Conforti FL, et al. Among authors: quattrone a. Am J Med Genet A. 2003 Mar 1;117A(2):184-7. doi: 10.1002/ajmg.a.10898. Am J Med Genet A. 2003. PMID: 12567420 No abstract available.

8

A simple method for diagnosis of autosomal recessive spinal muscular atrophy by denaturing high-performance liquid chromatography.

Mazzei R, Conforti FL, Muglia M, Sprovieri T, Patitucci A, Magariello A, Gabriele AL, Quattrone A. Mazzei R, et al. Among authors: quattrone a. J Child Neurol. 2003 Apr;18(4):269-71. doi: 10.1177/08830738030180041301. J Child Neurol. 2003. PMID: 12760430

9

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.

10

Temporal lobe epilepsy as a unique manifestation of multiple sclerosis.

Gambardella A, Valentino P, Labate A, Sibilia G, Ruscica F, Colosimo E, Nisticò R, Messina D, Zappia M, Quattrone A. Gambardella A, et al. Among authors: quattrone a. Can J Neurol Sci. 2003 Aug;30(3):228-32. doi: 10.1017/s031716710000264x. Can J Neurol Sci. 2003. PMID: 12945947

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