Quattrone A - Search Results

1

Motor-sensory neuropathy without minifascicles in a patient with 46XY gonadal dysgenesis.

Malandrini A, Gambelli S, Muglia M, Berti G, Gaudiano C, Patitucci A, Sugie K, Umehara F, Quattrone A, Dotti MT, Federico A. Malandrini A, et al. Among authors: quattrone a. Brain Dev. 2008 Apr;30(4):291-4. doi: 10.1016/j.braindev.2007.07.010. Epub 2007 Sep 4. Brain Dev. 2008. PMID: 17768021

2

A novel point mutation in PMP22 gene in an Italian family with hereditary neuropathy with liability to pressure palsies.

Muglia M, Patitucci A, Rizzi R, Ungaro C, Conforti FL, Gabriele AL, Magariello A, Mazzei R, Motti L, Sabadini R, Sprovieri T, Marcello N, Quattrone A. Muglia M, et al. Among authors: quattrone a. J Neurol Sci. 2007 Dec 15;263(1-2):194-7. doi: 10.1016/j.jns.2007.05.034. Epub 2007 Aug 20. J Neurol Sci. 2007. PMID: 17707409

3

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

4

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.

5

A novel founder mutation in the MFN2 gene associated with variable Charcot-Marie-Tooth type 2 phenotype in two families from Southern Italy.

Muglia M, Vazza G, Patitucci A, Milani M, Pareyson D, Taroni F, Quattrone A, Mostacciuolo ML. Muglia M, et al. Among authors: quattrone a. BMJ Case Rep. 2009;2009:bcr08.2008.0652. doi: 10.1136/bcr.08.2008.0652. Epub 2009 Jan 23. BMJ Case Rep. 2009. PMID: 21686698 Free PMC article.

6

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

7

Putative role of specific JAG1 gene exons in modulating clinical features in patients with leukoencephalopathy.

Ungaro C, Sprovieri T, Conforti FL, Muglia M, Patitucci A, Magariello A, Gabriele AL, Quattrone A, Mazzei R. Ungaro C, et al. Among authors: quattrone a. Neurosci Lett. 2007 May 11;418(1):1-3. doi: 10.1016/j.neulet.2007.02.059. Epub 2007 Mar 1. Neurosci Lett. 2007. PMID: 17368936

8

Spastic paraplegia with thinning of the corpus callosum and white matter abnormalities: further mutations and relative frequency in ZFYVE26/SPG15 in the Italian population.

Denora PS, Muglia M, Casali C, Truchetto J, Silvestri G, Messina D, Boukrhis A, Magariello A, Modoni A, Masciullo M, Malandrini A, Morelli M, de Leva MF, Villanova M, Giugni E, Citrigno L, Rizza T, Federico A, Pierallini A, Quattrone A, Filla A, Brice A, Stevanin G, Santorelli FM. Denora PS, et al. Among authors: quattrone a. J Neurol Sci. 2009 Feb 15;277(1-2):22-5. doi: 10.1016/j.jns.2008.09.039. Epub 2008 Dec 13. J Neurol Sci. 2009. PMID: 19084844

9

Mutation analysis of the SPG4 gene in Italian patients with pure and complicated forms of spastic paraplegia.

Magariello A, Muglia M, Patitucci A, Ungaro C, Mazzei R, Gabriele AL, Sprovieri T, Citrigno L, Conforti FL, Liguori M, Gambardella A, Bono F, Piccoli T, Patti F, Zappia M, Mancuso M, Iemolo F, Quattrone A. Magariello A, et al. Among authors: quattrone a. J Neurol Sci. 2010 Jan 15;288(1-2):96-100. doi: 10.1016/j.jns.2009.09.025. Epub 2009 Oct 28. J Neurol Sci. 2010. PMID: 19875132

10

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

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

915 results

Search Page

Filters