Bresolin N - Search Results

1

Neuronal nitric oxide synthase C276T polymorphism increases the risk for frontotemporal lobar degeneration.

Venturelli E, Villa C, Scarpini E, Fenoglio C, Guidi I, Lovati C, Marcone A, Cortini F, Scalabrini D, Clerici F, Bresolin N, Mariani C, Cappa S, Galimberti D. Venturelli E, et al. Among authors: bresolin n. Eur J Neurol. 2008 Jan;15(1):77-81. doi: 10.1111/j.1468-1331.2007.02007.x. Epub 2007 Nov 27. Eur J Neurol. 2008. PMID: 18042235

2

Muscle biopsy in Alzheimer's disease: morphological and biochemical findings.

Mariani C, Bresolin N, Farina E, Moggio M, Ferrante C, Ciafaloni E, Sertorelli S, Ciccone A, Scarlato G. Mariani C, et al. Among authors: bresolin n. Clin Neuropathol. 1991 Jul-Aug;10(4):171-6. Clin Neuropathol. 1991. PMID: 1884524

3

Treatment of anxiety with ketazolam in elderly patients.

Bresolin N, Monza G, Scarpini E, Scarlato G, Straneo G, Martinazzoli A, Benincà G, Cattoni C, De Candia R, Belloni G, et al. Bresolin N, et al. Clin Ther. 1988;10(5):536-42. Clin Ther. 1988. PMID: 2908803 Clinical Trial.

4

Biochemical and immunologic studies in a case of congenital myopathy with unusual morphologic features.

Biral D, Damiani E, Scarpini E, Bet L, Bresolin N, Moggio M, Pellegrini G, Barbieri S, Scarlato G. Biral D, et al. Among authors: bresolin n. Neurology. 1987 Oct;37(10):1658-62. doi: 10.1212/wnl.37.10.1658. Neurology. 1987. PMID: 3309721

5

Multiple sclerosis and mitochondrial myopathy: an unusual combination of diseases.

Bet L, Moggio M, Comi GP, Mariani C, Prelle A, Checcarelli N, Bordoni A, Bresolin N, Scarpini E, Scarlato G. Bet L, et al. Among authors: bresolin n. J Neurol. 1994 Jul;241(8):511-6. doi: 10.1007/BF00919714. J Neurol. 1994. PMID: 7964921

6

Retrospective study of a large population of patients affected with mitochondrial disorders: clinical, morphological and molecular genetic evaluation.

Sciacco M, Prelle A, Comi GP, Napoli L, Battistel A, Bresolin N, Tancredi L, Lamperti C, Bordoni A, Fagiolari G, Ciscato P, Chiveri L, Perini MP, Fortunato F, Adobbati L, Messina S, Toscano A, Martinelli-Boneschi F, Papadimitriou A, Scarlato G, Moggio M. Sciacco M, et al. Among authors: bresolin n. J Neurol. 2001 Sep;248(9):778-88. doi: 10.1007/s004150170094. J Neurol. 2001. PMID: 11596783

7

A mitochondrial tRNA(His) gene mutation causing pigmentary retinopathy and neurosensorial deafness.

Crimi M, Galbiati S, Perini MP, Bordoni A, Malferrari G, Sciacco M, Biunno I, Strazzer S, Moggio M, Bresolin N, Comi GP. Crimi M, et al. Among authors: bresolin n. Neurology. 2003 Apr 8;60(7):1200-3. doi: 10.1212/01.wnl.0000055865.30580.39. Neurology. 2003. PMID: 12682337

8

The 129 codon polymorphism of the prion protein gene influences earlier cognitive performance in Down syndrome subjects.

Del Bo R, Comi GP, Giorda R, Crimi M, Locatelli F, Martinelli-Boneschi F, Pozzoli U, Castelli E, Bresolin N, Scarlato G. Del Bo R, et al. Among authors: bresolin n. J Neurol. 2003 Jun;250(6):688-92. doi: 10.1007/s00415-003-1057-5. J Neurol. 2003. PMID: 12796830

9

Remarkable infidelity of polymerase gammaA associated with mutations in POLG1 exonuclease domain.

Del Bo R, Bordoni A, Sciacco M, Di Fonzo A, Galbiati S, Crimi M, Bresolin N, Comi GP. Del Bo R, et al. Among authors: bresolin n. Neurology. 2003 Oct 14;61(7):903-8. doi: 10.1212/01.wnl.0000092303.13864.be. Neurology. 2003. PMID: 14557557

10

Inducible nitric oxide synthase (iNOS) in immune-mediated demyelination and Wallerian degeneration of the rat peripheral nervous system.

Conti G, Rostami A, Scarpini E, Baron P, Galimberti D, Bresolin N, Contri M, Palumbo C, De Pol A. Conti G, et al. Among authors: bresolin n. Exp Neurol. 2004 Jun;187(2):350-8. doi: 10.1016/j.expneurol.2004.01.026. Exp Neurol. 2004. PMID: 15144861

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