Quattrone A - Search Results

1

An axon regeneration signature in a Charcot-Marie-Tooth disease type 2 patient.

Cavalcanti F, Kidd T, Patitucci A, Valentino P, Bono F, Nisticò R, Quattrone A. Cavalcanti F, et al. Among authors: quattrone a. J Neurogenet. 2009;23(3):324-8. doi: 10.1080/01677060802447585. J Neurogenet. 2009. PMID: 19657941 Free PMC article.

2

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

3

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

4

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.

5

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

6

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

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

Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A.

Züchner S, Mersiyanova IV, Muglia M, Bissar-Tadmouri N, Rochelle J, Dadali EL, Zappia M, Nelis E, Patitucci A, Senderek J, Parman Y, Evgrafov O, Jonghe PD, Takahashi Y, Tsuji S, Pericak-Vance MA, Quattrone A, Battaloglu E, Polyakov AV, Timmerman V, Schröder JM, Vance JM. Züchner S, et al. Among authors: quattrone a. Nat Genet. 2004 May;36(5):449-51. doi: 10.1038/ng1341. Epub 2004 Apr 4. Nat Genet. 2004. PMID: 15064763 No abstract available.

9

Further evidence of genetic heterogeneity in autosomal dominant distal motor neuronopathy.

Passamonti L, Muglia M, Magariello A, Bellesi M, Conforti FL, Mazzei R, Patitucci A, Gabriele AL, Sprovieri T, Peluso G, Caracciolo M, Medici E, Logullo F, Provinciali L, Quattrone A. Passamonti L, et al. Among authors: quattrone a. Neuromuscul Disord. 2004 Nov;14(11):705-10. doi: 10.1016/j.nmd.2004.07.004. Neuromuscul Disord. 2004. PMID: 15482954

10

Could mitochondrial haplogroups play a role in sporadic amyotrophic lateral sclerosis?

Mancuso M, Conforti FL, Rocchi A, Tessitore A, Muglia M, Tedeschi G, Panza D, Monsurrò M, Sola P, Mandrioli J, Choub A, DelCorona A, Manca ML, Mazzei R, Sprovieri T, Filosto M, Salviati A, Valentino P, Bono F, Caracciolo M, Simone IL, La Bella V, Majorana G, Siciliano G, Murri L, Quattrone A. Mancuso M, et al. Among authors: quattrone a. Neurosci Lett. 2004 Nov 23;371(2-3):158-62. doi: 10.1016/j.neulet.2004.08.060. Neurosci Lett. 2004. PMID: 15519748

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