Servidei S - Search Results

1

Nucleus-driven multiple large-scale deletions of the human mitochondrial genome: a new autosomal dominant disease.

Zeviani M, Bresolin N, Gellera C, Bordoni A, Pannacci M, Amati P, Moggio M, Servidei S, Scarlato G, DiDonato S. Zeviani M, et al. Among authors: servidei s. Am J Hum Genet. 1990 Dec;47(6):904-14. Am J Hum Genet. 1990. PMID: 1978558 Free PMC article.

2

Dominantly inherited mitochondrial myopathy with multiple deletions of mitochondrial DNA: clinical, morphologic, and biochemical studies.

Servidei S, Zeviani M, Manfredi G, Ricci E, Silvestri G, Bertini E, Gellera C, Di Mauro S, Di Donato S, Tonali P. Servidei S, et al. Neurology. 1991 Jul;41(7):1053-9. doi: 10.1212/wnl.41.7.1053. Neurology. 1991. PMID: 2067633

3

Tissue distribution and transmission of mitochondrial DNA deletions in mitochondrial myopathies.

Zeviani M, Gellera C, Pannacci M, Uziel G, Prelle A, Servidei S, DiDonato S. Zeviani M, et al. Among authors: servidei s. Ann Neurol. 1990 Jul;28(1):94-7. doi: 10.1002/ana.410280118. Ann Neurol. 1990. PMID: 2375642

4

Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome.

Moraes CT, DiMauro S, Zeviani M, Lombes A, Shanske S, Miranda AF, Nakase H, Bonilla E, Werneck LC, Servidei S, et al. Moraes CT, et al. Among authors: servidei s. N Engl J Med. 1989 May 18;320(20):1293-9. doi: 10.1056/NEJM198905183202001. N Engl J Med. 1989. PMID: 2541333

5

An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region.

Zeviani M, Servidei S, Gellera C, Bertini E, DiMauro S, DiDonato S. Zeviani M, et al. Among authors: servidei s. Nature. 1989 May 25;339(6222):309-11. doi: 10.1038/339309a0. Nature. 1989. PMID: 2725645

6

Mitochondrial myopathies.

DiMauro S, Bonilla E, Zeviani M, Servidei S, DeVivo DC, Schon EA. DiMauro S, et al. Among authors: servidei s. J Inherit Metab Dis. 1987;10 Suppl 1:113-28. doi: 10.1007/BF01812852. J Inherit Metab Dis. 1987. PMID: 2824920 Review.

7

Biochemical and molecular aspects of cytochrome C oxidase deficiency.

DiMauro S, Zeviani M, Servidei S, Prelle A, Miranda AF, Bonilla E, Schon EA. DiMauro S, et al. Among authors: servidei s. Adv Neurol. 1988;48:93-105. Adv Neurol. 1988. PMID: 2825476 Review. No abstract available.

8

Cytochrome c oxidase deficiency in Leigh syndrome.

DiMauro S, Servidei S, Zeviani M, DiRocco M, DeVivo DC, DiDonato S, Uziel G, Berry K, Hoganson G, Johnsen SD, et al. DiMauro S, et al. Among authors: servidei s. Ann Neurol. 1987 Oct;22(4):498-506. doi: 10.1002/ana.410220409. Ann Neurol. 1987. PMID: 2829705

9

Metabolic myopathies.

DiMauro S, Miranda AF, Sakoda S, Schon EA, Servidei S, Shanske S, Zeviani M. DiMauro S, et al. Among authors: servidei s. Am J Med Genet. 1986 Dec;25(4):635-51. doi: 10.1002/ajmg.1320250406. Am J Med Genet. 1986. PMID: 2878616

10

Myopathy and fatal cardiopathy due to cytochrome c oxidase deficiency.

Zeviani M, Van Dyke DH, Servidei S, Bauserman SC, Bonilla E, Beaumont ET, Sharda J, VanderLaan K, DiMauro S. Zeviani M, et al. Among authors: servidei s. Arch Neurol. 1986 Nov;43(11):1198-202. doi: 10.1001/archneur.1986.00520110084025. Arch Neurol. 1986. PMID: 3022695

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

296 results

Search Page

Filters