DeVivo DC - Search Results

1

Comparative biochemical studies of ATPases in cells from patients with the T8993G or T8993C mitochondrial DNA mutations.

Vázquez-Memije ME, Shanske S, Santorelli FM, Kranz-Eble P, DeVivo DC, DiMauro S. Vázquez-Memije ME, et al. Among authors: devivo dc. J Inherit Metab Dis. 1998 Dec;21(8):829-36. doi: 10.1023/a:1005418718299. J Inherit Metab Dis. 1998. PMID: 9870208

2

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. Among authors: devivo dc. J Inherit Metab Dis. 1996;19(1):43-50. doi: 10.1007/BF01799347. J Inherit Metab Dis. 1996. PMID: 8830176

3

Mitochondrial myopathies.

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

4

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. Among authors: devivo dc. Ann Neurol. 1993 Dec;34(6):827-34. doi: 10.1002/ana.410340612. Ann Neurol. 1993. PMID: 8250532

5

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. Pediatr Res. 1996 May;39(5):914-7. doi: 10.1203/00006450-199605000-00028. Pediatr Res. 1996. PMID: 8726250

6

Measurement of ATP production in mitochondrial disorders.

Shepherd RK, Checcarelli N, Naini A, De Vivo DC, DiMauro S, Sue CM. Shepherd RK, et al. J Inherit Metab Dis. 2006 Feb;29(1):86-91. doi: 10.1007/s10545-006-0148-8. J Inherit Metab Dis. 2006. PMID: 16601873

7

Skin fibroblast carnitine uptake in secondary carnitine deficiency disorders.

Tein I, De Vivo DC, Ranucci D, DiMauro S. Tein I, et al. J Inherit Metab Dis. 1993;16(1):135-46. doi: 10.1007/BF00711327. J Inherit Metab Dis. 1993. PMID: 8387612

8

Oligomycin induces a decrease in the cellular content of a pathogenic mutation in the human mitochondrial ATPase 6 gene.

Manfredi G, Gupta N, Vazquez-Memije ME, Sadlock JE, Spinazzola A, De Vivo DC, Schon EA. Manfredi G, et al. J Biol Chem. 1999 Apr 2;274(14):9386-91. doi: 10.1074/jbc.274.14.9386. J Biol Chem. 1999. PMID: 10092618 Free article.

9

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.

10

Mitochondrial diseases.

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

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