De Vivo DC - Search Results

1

Mitochondrial defects of brain and muscle.

De Vivo DC, DiMauro S. De Vivo DC, et al. Biol Neonate. 1990;58 Suppl 1:54-69. doi: 10.1159/000243300. Biol Neonate. 1990. PMID: 2265220 Review.

2

Clinical syndromes associated with ragged red fibers.

Rowland LP, Blake DM, Hirano M, Di Mauro S, Schon EA, Hays AP, Devivo DC. Rowland LP, et al. Rev Neurol (Paris). 1991;147(6-7):467-73. Rev Neurol (Paris). 1991. PMID: 1962052

3

Cytochrome c oxidase deficiency.

DiMauro S, Lombes A, Nakase H, Mita S, Fabrizi GM, Tritschler HJ, Bonilla E, Miranda AF, DeVivo DC, Schon EA. DiMauro S, et al. Pediatr Res. 1990 Nov;28(5):536-41. doi: 10.1203/00006450-199011000-00025. Pediatr Res. 1990. PMID: 2175026 Review.

4

Mitochondrial diseases.

Zeviani M, Bonilla E, DeVivo DC, DiMauro S. Zeviani M, et al. Neurol Clin. 1989 Feb;7(1):123-56. Neurol Clin. 1989. PMID: 2646519 Review.

5

Mitochondrial myopathies.

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

6

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

7

Clinical heterogeneity associated with the mitochondrial DNA T8993C point mutation.

Santorelli FM, Mak SC, Vazquez-Memije ME, Shanske S, Kranz-Eble P, Jain KD, Bluestone DL, De Vivo DC, DiMauro S. Santorelli FM, et al. Among authors: de vivo dc. Pediatr Res. 1996 May;39(5):914-7. doi: 10.1203/00006450-199605000-00028. Pediatr Res. 1996. PMID: 8726250

8

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

9

Clinical manifestations of mitochondrial DNA depletion.

Vu TH, Sciacco M, Tanji K, Nichter C, Bonilla E, Chatkupt S, Maertens P, Shanske S, Mendell J, Koenigsberger MR, Sharer L, Schon EA, DiMauro S, DeVivo DC. Vu TH, et al. Neurology. 1998 Jun;50(6):1783-90. doi: 10.1212/wnl.50.6.1783. Neurology. 1998. PMID: 9633728

10

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

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