Alimonti D - Search Results

1

The rare G93D mutation causes a slowly progressing lower motor neuron disease.

Restagno G, Lombardo F, Sbaiz L, Mari C, Gellera C, Alimonti D, Calvo A, Tarenzi L, Chiò A. Restagno G, et al. Among authors: alimonti d. Amyotroph Lateral Scler. 2008;9(1):35-9. doi: 10.1080/17482960701788198. Amyotroph Lateral Scler. 2008. PMID: 18273717

2

SOD1 activity and protective factors in familial ALS patients with L84F SOD1 mutation.

Curti D, Rognoni F, Alimonti D, Malaspina A, Feletti F, Tessera S, Finotti N, Rehak L, Mazzini L, Zerbi F, Poloni TE, Ceroni M. Curti D, et al. Among authors: alimonti d. Amyotroph Lateral Scler Other Motor Neuron Disord. 2002 Sep;3(3):115-22. doi: 10.1080/146608202760834111. Amyotroph Lateral Scler Other Motor Neuron Disord. 2002. PMID: 12495572

3

The epidemiology and treatment of ALS: focus on the heterogeneity of the disease and critical appraisal of therapeutic trials.

Beghi E, Chiò A, Couratier P, Esteban J, Hardiman O, Logroscino G, Millul A, Mitchell D, Preux PM, Pupillo E, Stevic Z, Swingler R, Traynor BJ, Van den Berg LH, Veldink JH, Zoccolella S; Eurals Consortium. Beghi E, et al. Amyotroph Lateral Scler. 2011 Jan;12(1):1-10. doi: 10.3109/17482968.2010.502940. Epub 2010 Aug 11. Amyotroph Lateral Scler. 2011. PMID: 20698807 Free PMC article. Review.

4

Clustering of ALS patients in central Italy due to the occurrence of the L84F SOD1 gene mutation.

Ceroni M, Malaspina A, Poloni TE, Alimonti D, Rognoni F, Habgood J, Imbesi F, Antonelli P, Alfonsi E, Curti D, deBelleroche J. Ceroni M, et al. Among authors: alimonti d. Neurology. 1999 Sep 22;53(5):1064-71. doi: 10.1212/wnl.53.5.1064. Neurology. 1999. PMID: 10496267

5

Increased incidence of FMO1 gene single nucleotide polymorphisms in sporadic amyotrophic lateral sclerosis.

Cereda C, Gabanti E, Corato M, de Silvestri A, Alimonti D, Cova E, Malaspina A, Ceroni M. Cereda C, et al. Among authors: alimonti d. Amyotroph Lateral Scler. 2006 Dec;7(4):227-34. doi: 10.1080/17482960600864413. Amyotroph Lateral Scler. 2006. PMID: 17127561

6

Disease clustering: the example of ALS, PD, dementia and hereditary ataxias in Italy.

Malaspina A, Alimonti D, Poloni TE, Ceroni M. Malaspina A, et al. Among authors: alimonti d. Funct Neurol. 2002 Oct-Dec;17(4):177-82. Funct Neurol. 2002. PMID: 12675260 Review.

7

Renal tubular impairment during riluzole therapy.

Poloni TE, Alimonti D, Montagna G, Segagni S, Imbesi F, Malaspina A, Ceroni M. Poloni TE, et al. Among authors: alimonti d. Neurology. 1999 Feb;52(3):670. doi: 10.1212/wnl.52.3.670-a. Neurology. 1999. PMID: 10025816 No abstract available.

8

Genotype-phenotype correlation in familial amyotrophic lateral sclerosis with SOD1 mutation.

Alimonti D, Malaspina A, Poloni TE, Ceroni M. Alimonti D, et al. Funct Neurol. 2000 Jul-Sep;15(3):177-91. Funct Neurol. 2000. PMID: 11062847 Review. No abstract available.

9

Amyotrophic lateral sclerosis and SOD1 gene: an overview.

Ceroni M, Curti D, Alimonti D. Ceroni M, et al. Among authors: alimonti d. Funct Neurol. 2001;16(4 Suppl):171-80. Funct Neurol. 2001. PMID: 11996514 Review. No abstract available.

10

Migraine with aura and white matter abnormalities: Notch3 mutation.

Ceroni M, Poloni TE, Tonietti S, Fabozzi D, Uggetti C, Frediani F, Simonetti F, Malaspina A, Alimonti D, Celano M, Ferrari M, Carrera P. Ceroni M, et al. Among authors: alimonti d. Neurology. 2000 May 9;54(9):1869-71. doi: 10.1212/wnl.54.9.1869. Neurology. 2000. PMID: 10802804

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