De Vivo DC - Search Results

1

Genetic heterogeneity in Leigh syndrome.

DiMauro S, De Vivo DC. DiMauro S, et al. Among authors: de vivo dc. Ann Neurol. 1996 Jul;40(1):5-7. doi: 10.1002/ana.410400104. Ann Neurol. 1996. PMID: 8687192 No abstract available.

2

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. Ann Neurol. 1987 Oct;22(4):498-506. doi: 10.1002/ana.410220409. Ann Neurol. 1987. PMID: 2829705

3

The mutation at nt 8993 of mitochondrial DNA is a common cause of Leigh's syndrome.

Santorelli FM, Shanske S, Macaya A, DeVivo DC, DiMauro S. Santorelli FM, et al. Ann Neurol. 1993 Dec;34(6):827-34. doi: 10.1002/ana.410340612. Ann Neurol. 1993. PMID: 8250532

4

The mitochondrial DNA A8344G mutation in Leigh syndrome revealed by analysis in paraffin-embedded sections: revisiting the past.

Santorelli FM, Tanji K, Shanske S, Krishna S, Schmidt RE, Greenwood RS, DiMauro S, De Vivo DC. Santorelli FM, et al. Among authors: de vivo dc. Ann Neurol. 1998 Dec;44(6):962-4. doi: 10.1002/ana.410440616. Ann Neurol. 1998. PMID: 9851442

5

Biochemical and molecular analysis of cytochrome c oxidase deficiency in Leigh's syndrome.

Lombes A, Nakase H, Tritschler HJ, Kadenbach B, Bonilla E, DeVivo DC, Schon EA, DiMauro S. Lombes A, et al. Neurology. 1991 Apr;41(4):491-8. doi: 10.1212/wnl.41.4.491. Neurology. 1991. PMID: 1849240

6

Mitochondrial myopathies.

DiMauro S, Bonilla E, Zeviani M, Nakagawa M, DeVivo DC. DiMauro S, et al. Ann Neurol. 1985 Jun;17(6):521-38. doi: 10.1002/ana.410170602. Ann Neurol. 1985. PMID: 3927817 Review.

7

Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: a distinctive clinical syndrome.

Pavlakis SG, Phillips PC, DiMauro S, De Vivo DC, Rowland LP. Pavlakis SG, et al. Among authors: de vivo dc. Ann Neurol. 1984 Oct;16(4):481-8. doi: 10.1002/ana.410160409. Ann Neurol. 1984. PMID: 6093682

8

Comparative biochemical studies in fibroblasts from patients with different forms of Leigh syndrome.

Vazquez-Memije ME, Shanske S, Santorelli FM, Kranz-Eble P, Davidson E, DeVivo DC, DiMauro S. Vazquez-Memije ME, et al. J Inherit Metab Dis. 1996;19(1):43-50. doi: 10.1007/BF01799347. J Inherit Metab Dis. 1996. PMID: 8830176

9

Maternally inherited encephalopathy associated with a single-base insertion in the mitochondrial tRNATrp gene.

Santorelli FM, Tanji K, Sano M, Shanske S, El-Shahawi M, Kranz-Eble P, DiMauro S, De Vivo DC. Santorelli FM, et al. Among authors: de vivo dc. Ann Neurol. 1997 Aug;42(2):256-60. doi: 10.1002/ana.410420220. Ann Neurol. 1997. PMID: 9266739

10

Differential features of patients with mutations in two COX assembly genes, SURF-1 and SCO2.

Sue CM, Karadimas C, Checcarelli N, Tanji K, Papadopoulou LC, Pallotti F, Guo FL, Shanske S, Hirano M, De Vivo DC, Van Coster R, Kaplan P, Bonilla E, DiMauro S. Sue CM, et al. Among authors: de vivo dc. Ann Neurol. 2000 May;47(5):589-95. Ann Neurol. 2000. PMID: 10805329

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