Taroni F - Search Results

1

Glutamine Synthetase 1 Increases Autophagy Lysosomal Degradation of Mutant Huntingtin Aggregates in Neurons, Ameliorating Motility in a Drosophila Model for Huntington's Disease.

Vernizzi L, Paiardi C, Licata G, Vitali T, Santarelli S, Raneli M, Manelli V, Rizzetto M, Gioria M, Pasini ME, Grifoni D, Vanoni MA, Gellera C, Taroni F, Bellosta P. Vernizzi L, et al. Among authors: taroni f. Cells. 2020 Jan 13;9(1):196. doi: 10.3390/cells9010196. Cells. 2020. PMID: 31941072 Free PMC article.

2

Evidence for two distinct mitochondrial malic enzymes in human skeletal muscle: purification and properties of the NAD(P)+-dependent enzyme.

Taroni F, Gellera C, Di Donato S. Taroni F, et al. Biochim Biophys Acta. 1987 Dec 18;916(3):446-54. doi: 10.1016/0167-4838(87)90191-9. Biochim Biophys Acta. 1987. PMID: 3689803

3

Carnitine palmitoyltransferase II deficiency: structure of the gene and characterization of two novel disease-causing mutations.

Verderio E, Cavadini P, Montermini L, Wang H, Lamantea E, Finocchiaro G, DiDonato S, Gellera C, Taroni F. Verderio E, et al. Among authors: taroni f. Hum Mol Genet. 1995 Jan;4(1):19-29. doi: 10.1093/hmg/4.1.19. Hum Mol Genet. 1995. PMID: 7711730

4

Assignment of the human carnitine palmitoyltransferase II gene (CPT1) to chromosome 1p32.

Gellera C, Verderio E, Floridia G, Finocchiaro G, Montermini L, Cavadini P, Zuffardi O, Taroni F. Gellera C, et al. Among authors: taroni f. Genomics. 1994 Nov 1;24(1):195-7. doi: 10.1006/geno.1994.1605. Genomics. 1994. PMID: 7896283 No abstract available.

5

Superoxide dismutase gene mutations in Italian patients with familial and sporadic amyotrophic lateral sclerosis: identification of three novel missense mutations.

Gellera C, Castellotti B, Riggio MC, Silani V, Morandi L, Testa D, Casali C, Taroni F, Di Donato S, Zeviani M, Mariotti C. Gellera C, et al. Among authors: taroni f. Neuromuscul Disord. 2001 May;11(4):404-10. doi: 10.1016/s0960-8966(00)00215-7. Neuromuscul Disord. 2001. PMID: 11369193

6

Frataxin gene point mutations in Italian Friedreich ataxia patients.

Gellera C, Castellotti B, Mariotti C, Mineri R, Seveso V, Didonato S, Taroni F. Gellera C, et al. Among authors: taroni f. Neurogenetics. 2007 Nov;8(4):289-99. doi: 10.1007/s10048-007-0101-5. Epub 2007 Aug 17. Neurogenetics. 2007. PMID: 17703324

7

Spinocerebellar ataxia type 17 (SCA17): oculomotor phenotype and clinical characterization of 15 Italian patients.

Mariotti C, Alpini D, Fancellu R, Soliveri P, Grisoli M, Ravaglia S, Lovati C, Fetoni V, Giaccone G, Castucci A, Taroni F, Gellera C, Di Donato S. Mariotti C, et al. Among authors: taroni f. J Neurol. 2007 Nov;254(11):1538-46. doi: 10.1007/s00415-007-0579-7. Epub 2007 Oct 15. J Neurol. 2007. PMID: 17934876

8

Identification of new ANG gene mutations in a large cohort of Italian patients with amyotrophic lateral sclerosis.

Gellera C, Colombrita C, Ticozzi N, Castellotti B, Bragato C, Ratti A, Taroni F, Silani V. Gellera C, et al. Among authors: taroni f. Neurogenetics. 2008 Feb;9(1):33-40. doi: 10.1007/s10048-007-0111-3. Epub 2007 Dec 18. Neurogenetics. 2008. PMID: 18087731

9

Spinocerebellar ataxia type 28: a novel autosomal dominant cerebellar ataxia characterized by slow progression and ophthalmoparesis.

Mariotti C, Brusco A, Di Bella D, Cagnoli C, Seri M, Gellera C, Di Donato S, Taroni F. Mariotti C, et al. Among authors: taroni f. Cerebellum. 2008;7(2):184-8. doi: 10.1007/s12311-008-0053-9. Cerebellum. 2008. PMID: 18769991

10

Predictive genetic tests in neurodegenerative disorders: a methodological approach integrating psychological counseling for at-risk individuals and referring clinicians.

Mariotti C, Ferruta A, Gellera C, Nespolo C, Fancellu R, Genitrini S, Di Bella D, Panzeri M, Nanetti L, Tomasello C, Taroni F, Foresti G, Astori S. Mariotti C, et al. Among authors: taroni f. Eur Neurol. 2010;64(1):33-41. doi: 10.1159/000315033. Epub 2010 Jun 30. Eur Neurol. 2010. PMID: 20588047

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