Cannella M - Search Results

1

Cavernous angiomas of the nervous system in Italy: clinical and genetic study.

Squitieri F, Maglione V, Buzzi MG, Nargi E, Novelletto A, Cannella M, Simonelli M, Colonnese C, Simonelli P, Innocenzi G, Gagliardi FM, Caruso R, Ragona G, Cantore GP. Squitieri F, et al. Among authors: cannella m. Neurol Sci. 2000 Jun;21(3):129-34. doi: 10.1007/s100720070087. Neurol Sci. 2000. PMID: 11076000

2

Atypical movement disorders in the early stages of Huntington's disease: clinical and genetic analysis.

Squitieri F, Berardelli A, Nargi E, Castellotti B, Mariotti C, Cannella M, Lavitrano ML, de Grazia U, Gellera C, Ruggieri S. Squitieri F, et al. Among authors: cannella m. Clin Genet. 2000 Jul;58(1):50-6. doi: 10.1034/j.1399-0004.2000.580108.x. Clin Genet. 2000. PMID: 10945661

3

Short-term effects of olanzapine in Huntington disease.

Squitieri F, Cannella M, Porcellini A, Brusa L, Simonelli M, Ruggieri S. Squitieri F, et al. Among authors: cannella m. Neuropsychiatry Neuropsychol Behav Neurol. 2001 Jan;14(1):69-72. Neuropsychiatry Neuropsychol Behav Neurol. 2001. PMID: 11234911

4

Presymptomatic tests in Huntington's disease and dominant ataxias.

Cannella M, Simonelli M, D'Alessio C, Pierelli F, Ruggieri S, Squitieri F. Cannella M, et al. Neurol Sci. 2001 Feb;22(1):55-6. doi: 10.1007/s100720170044. Neurol Sci. 2001. PMID: 11487199

5

Onset and pre-onset studies to define the Huntington's disease natural history.

Squitieri F, Cannella M, Giallonardo P, Maglione V, Mariotti C, Hayden MR. Squitieri F, et al. Among authors: cannella m. Brain Res Bull. 2001 Oct-Nov 1;56(3-4):233-8. doi: 10.1016/s0361-9230(01)00648-7. Brain Res Bull. 2001. PMID: 11719256 Review.

6

Localization of autosomal recessive early-onset parkinsonism to chromosome 1p36 (PARK7) in an independent dataset.

Bonifati V, Breedveld GJ, Squitieri F, Vanacore N, Brustenghi P, Harhangi BS, Montagna P, Cannella M, Fabbrini G, Rizzu P, van Duijn CM, Oostra BA, Meco G, Heutink P. Bonifati V, et al. Among authors: cannella m. Ann Neurol. 2002 Feb;51(2):253-6. doi: 10.1002/ana.10106. Ann Neurol. 2002. PMID: 11835383

7

CAG mutation effect on rate of progression in Huntington's disease.

Squitieri F, Cannella M, Simonelli M. Squitieri F, et al. Among authors: cannella m. Neurol Sci. 2002 Sep;23 Suppl 2:S107-8. doi: 10.1007/s100720200092. Neurol Sci. 2002. PMID: 12548366

8

Homozygosity for CAG mutation in Huntington disease is associated with a more severe clinical course.

Squitieri F, Gellera C, Cannella M, Mariotti C, Cislaghi G, Rubinsztein DC, Almqvist EW, Turner D, Bachoud-Lévi AC, Simpson SA, Delatycki M, Maglione V, Hayden MR, Donato SD. Squitieri F, et al. Among authors: cannella m. Brain. 2003 Apr;126(Pt 4):946-55. doi: 10.1093/brain/awg077. Brain. 2003. PMID: 12615650

9

Highly disabling cerebellar presentation in Huntington disease.

Squitieri F, Pustorino G, Cannella M, Toscano A, Maglione V, Morgante L, Tortorella G. Squitieri F, et al. Among authors: cannella m. Eur J Neurol. 2003 Jul;10(4):443-4. doi: 10.1046/j.1468-1331.2003.00601.x. Eur J Neurol. 2003. PMID: 12823498 No abstract available.

10

Italian Huntington disease patients--data and tissue bank.

Squitieri F, Cannella M, Gaudio L, Martino T, Maglione V, Giallonardo P, Simonelli M, Simonelli G, Mangeruga D, Ciarmiello A, Pierelli F. Squitieri F, et al. Among authors: cannella m. Neurol Sci. 2003 Oct;24(3):215-6. doi: 10.1007/s10072-003-0137-8. Neurol Sci. 2003. PMID: 14598094

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