Bresolin N - Search Results

1

Association of neuronal nitric oxide synthase C276T polymorphism with Alzheimer's disease.

Galimberti D, Venturelli E, Gatti A, Lovati C, Fenoglio C, Mariani C, Forloni G, Bresolin N, Scarpini E. Galimberti D, et al. Among authors: bresolin n. J Neurol. 2005 Aug;252(8):985-6. doi: 10.1007/s00415-005-0783-2. Epub 2005 Mar 17. J Neurol. 2005. PMID: 15765269 No abstract available.

2

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

3

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

4

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

5

MCP-1 in Alzheimer's disease patients: A-2518G polymorphism and serum levels.

Fenoglio C, Galimberti D, Lovati C, Guidi I, Gatti A, Fogliarino S, Tiriticco M, Mariani C, Forloni G, Pettenati C, Baron P, Conti G, Bresolin N, Scarpini E. Fenoglio C, et al. Among authors: bresolin n. Neurobiol Aging. 2004 Oct;25(9):1169-73. doi: 10.1016/j.neurobiolaging.2003.11.008. Neurobiol Aging. 2004. PMID: 15312962

6

CCR2-64I polymorphism and CCR5Delta32 deletion in patients with Alzheimer's disease.

Galimberti D, Fenoglio C, Lovati C, Gatti A, Guidi I, Venturelli E, Cutter GR, Mariani C, Forloni G, Pettenati C, Baron P, Conti G, Bresolin N, Scarpini E. Galimberti D, et al. Among authors: bresolin n. J Neurol Sci. 2004 Oct 15;225(1-2):79-83. doi: 10.1016/j.jns.2004.07.005. J Neurol Sci. 2004. PMID: 15465089

7

Influence of the Glu298Asp polymorphism of NOS3 on age at onset and homocysteine levels in AD patients.

Guidi I, Galimberti D, Venturelli E, Lovati C, Del Bo R, Fenoglio C, Gatti A, Dominici R, Galbiati S, Virgilio R, Pomati S, Comi GP, Mariani C, Forloni G, Bresolin N, Scarpini E. Guidi I, et al. Among authors: bresolin n. Neurobiol Aging. 2005 Jun;26(6):789-94. doi: 10.1016/j.neurobiolaging.2004.07.003. Neurobiol Aging. 2005. PMID: 15718036 Clinical Trial.

8

Vascular endothelial growth factor gene variability is associated with increased risk for AD.

Del Bo R, Scarlato M, Ghezzi S, Martinelli Boneschi F, Fenoglio C, Galbiati S, Virgilio R, Galimberti D, Galimberti G, Crimi M, Ferrarese C, Scarpini E, Bresolin N, Comi GP. Del Bo R, et al. Among authors: bresolin n. Ann Neurol. 2005 Mar;57(3):373-80. doi: 10.1002/ana.20390. Ann Neurol. 2005. PMID: 15732116

9

Chemokine network in multiple sclerosis: role in pathogenesis and targeting for future treatments.

Galimberti D, Bresolin N, Scarpini E. Galimberti D, et al. Among authors: bresolin n. Expert Rev Neurother. 2004 May;4(3):439-53. doi: 10.1586/14737175.4.3.439. Expert Rev Neurother. 2004. PMID: 15853541 Review.

10

The T-786C NOS3 polymorphism in Alzheimer's disease: association and influence on gene expression.

Venturelli E, Galimberti D, Lovati C, Fenoglio C, Scalabrini D, Mariani C, Forloni G, Bresolin N, Scarpini E. Venturelli E, et al. Among authors: bresolin n. Neurosci Lett. 2005 Jul 15;382(3):300-3. doi: 10.1016/j.neulet.2005.03.032. Epub 2005 Apr 7. Neurosci Lett. 2005. PMID: 15925107

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