767/TI_/Telethon/Italy[Grants and Funding] - Search Results

Year	Number of Results
1996	1
1997	6
1998	6
2025	0

1

Zeviani M, Tiranti V, Piantadosi C. Zeviani M, et al. Medicine (Baltimore). 1998 Jan;77(1):59-72. doi: 10.1097/00005792-199801000-00006. Medicine (Baltimore). 1998. PMID: 9465864 Free article. Review.

2

Cardiomyopathies in disorders of oxidative metabolism.

Antozzi C, Zeviani M. Antozzi C, et al. Cardiovasc Res. 1997 Aug;35(2):184-99. doi: 10.1016/s0008-6363(97)00141-7. Cardiovasc Res. 1997. PMID: 9349380 Review.

3

Identification and characterization of human cDNAs specific to BCS1, PET112, SCO1, COX15, and COX11, five genes involved in the formation and function of the mitochondrial respiratory chain.

Petruzzella V, Tiranti V, Fernandez P, Ianna P, Carrozzo R, Zeviani M. Petruzzella V, et al. Genomics. 1998 Dec 15;54(3):494-504. doi: 10.1006/geno.1998.5580. Genomics. 1998. PMID: 9878253

4

Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease.

Casari G, De Fusco M, Ciarmatori S, Zeviani M, Mora M, Fernandez P, De Michele G, Filla A, Cocozza S, Marconi R, Dürr A, Fontaine B, Ballabio A. Casari G, et al. Cell. 1998 Jun 12;93(6):973-83. doi: 10.1016/s0092-8674(00)81203-9. Cell. 1998. PMID: 9635427 Free article.

5

Disorders of mitochondria and related metabolism.

Zeviani M, Fernandez-Silva P, Tiranti V. Zeviani M, et al. Curr Opin Neurol. 1997 Apr;10(2):160-7. doi: 10.1097/00019052-199704000-00015. Curr Opin Neurol. 1997. PMID: 9146998 Review.

6

Mitochondrial disease associated with the T8993G mutation of the mitochondrial ATPase 6 gene: a clinical, biochemical, and molecular study in six families.

Uziel G, Moroni I, Lamantea E, Fratta GM, Ciceri E, Carrara F, Zeviani M. Uziel G, et al. J Neurol Neurosurg Psychiatry. 1997 Jul;63(1):16-22. doi: 10.1136/jnnp.63.1.16. J Neurol Neurosurg Psychiatry. 1997. PMID: 9221962 Free PMC article.

7

Identification of the gene encoding the human mitochondrial RNA polymerase (h-mtRPOL) by cyberscreening of the Expressed Sequence Tags database.

Tiranti V, Savoia A, Forti F, D'Apolito MF, Centra M, Rocchi M, Zeviani M. Tiranti V, et al. Hum Mol Genet. 1997 Apr;6(4):615-25. doi: 10.1093/hmg/6.4.615. Hum Mol Genet. 1997. PMID: 9097968

8

Disorders of nuclear-mitochondrial intergenomic signalling.

Zeviani M, Petruzzella V, Carrozzo R. Zeviani M, et al. J Bioenerg Biomembr. 1997 Apr;29(2):121-30. doi: 10.1023/a:1022633912917. J Bioenerg Biomembr. 1997. PMID: 9239538 Review.

9

Mutations of SURF-1 in Leigh disease associated with cytochrome c oxidase deficiency.

Tiranti V, Hoertnagel K, Carrozzo R, Galimberti C, Munaro M, Granatiero M, Zelante L, Gasparini P, Marzella R, Rocchi M, Bayona-Bafaluy MP, Enriquez JA, Uziel G, Bertini E, Dionisi-Vici C, Franco B, Meitinger T, Zeviani M. Tiranti V, et al. Am J Hum Genet. 1998 Dec;63(6):1609-21. doi: 10.1086/302150. Am J Hum Genet. 1998. PMID: 9837813 Free PMC article.

10

Cytochrome c oxidase subunit I microdeletion in a patient with motor neuron disease.

Comi GP, Bordoni A, Salani S, Franceschina L, Sciacco M, Prelle A, Fortunato F, Zeviani M, Napoli L, Bresolin N, Moggio M, Ausenda CD, Taanman JW, Scarlato G. Comi GP, et al. Ann Neurol. 1998 Jan;43(1):110-6. doi: 10.1002/ana.410430119. Ann Neurol. 1998. PMID: 9450776

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