Miranda AF - Search Results

1

Partial dystrophin deficiency in monozygous twin carriers of the Duchenne gene discordant for clinical myopathy.

Bonilla E, Younger DS, Chang HW, Tantravahi U, Miranda AF, Medori R, DiMauro S, Warburton D, Rowland LP. Bonilla E, et al. Among authors: miranda af. Neurology. 1990 Aug;40(8):1267-70. doi: 10.1212/wnl.40.8.1267. Neurology. 1990. PMID: 2199849

2

Differential diagnosis of fatal and benign cytochrome c oxidase-deficient myopathies of infancy: an immunohistochemical approach.

Tritschler HJ, Bonilla E, Lombes A, Andreetta F, Servidei S, Schneyder B, Miranda AF, Schon EA, Kadenbach B, DiMauro S. Tritschler HJ, et al. Among authors: miranda af. Neurology. 1991 Feb;41(2 ( Pt 1)):300-5. doi: 10.1212/wnl.41.2_part_1.300. Neurology. 1991. PMID: 1846953

3

Widespread tissue distribution of mitochondrial DNA deletions in Kearns-Sayre syndrome.

Shanske S, Moraes CT, Lombes A, Miranda AF, Bonilla E, Lewis P, Whelan MA, Ellsworth CA, DiMauro S. Shanske S, et al. Among authors: miranda af. Neurology. 1990 Jan;40(1):24-8. doi: 10.1212/wnl.40.1.24. Neurology. 1990. PMID: 2296377

4

Cytochrome c oxidase deficiency in Leigh's syndrome: genetic evidence for a nuclear DNA-encoded mutation.

Miranda AF, Ishii S, DiMauro S, Shay JW. Miranda AF, et al. Neurology. 1989 May;39(5):697-702. doi: 10.1212/wnl.39.5.697. Neurology. 1989. PMID: 2540452

5

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: miranda af. Adv Neurol. 1988;48:93-105. Adv Neurol. 1988. PMID: 2825476 Review. No abstract available.

6

Duchenne muscular dystrophy: deficiency of dystrophin at the muscle cell surface.

Bonilla E, Samitt CE, Miranda AF, Hays AP, Salviati G, DiMauro S, Kunkel LM, Hoffman EP, Rowland LP. Bonilla E, et al. Among authors: miranda af. Cell. 1988 Aug 12;54(4):447-52. doi: 10.1016/0092-8674(88)90065-7. Cell. 1988. PMID: 3042151

7

Immunocytochemical study of dystrophin in muscle cultures from patients with Duchenne muscular dystrophy and unaffected control patients.

Miranda AF, Bonilla E, Martucci G, Moraes CT, Hays AP, Dimauro S. Miranda AF, et al. Am J Pathol. 1988 Sep;132(3):410-6. Am J Pathol. 1988. PMID: 3046367 Free PMC article.

8

Normal and dystrophin-deficient muscle fibers in carriers of the gene for Duchenne muscular dystrophy.

Bonilla E, Schmidt B, Samitt CE, Miranda AF, Hays AP, de Oliveira AB, Chang HW, Servidei S, Ricci E, Younger DS, et al. Bonilla E, et al. Among authors: miranda af. Am J Pathol. 1988 Dec;133(3):440-5. Am J Pathol. 1988. PMID: 3059802 Free PMC article.

9

Immunocytochemical study of nebulin in Duchenne muscular dystrophy.

Bonilla E, Miranda AF, Prelle A, Salviati G, Betto R, Zeviani M, Schon EA, DiMauro S, Rowland LP. Bonilla E, et al. Among authors: miranda af. Neurology. 1988 Oct;38(10):1600-3. doi: 10.1212/wnl.38.10.1600. Neurology. 1988. PMID: 3419605

10

Phosphoglycerate kinase deficiency: biochemical and molecular genetic studies in a new myopathic variant (PGK Alberta).

Tonin P, Shanske S, Miranda AF, Brownell AK, Wyse JP, Tsujino S, DiMauro S. Tonin P, et al. Among authors: miranda af. Neurology. 1993 Feb;43(2):387-91. doi: 10.1212/wnl.43.2.387. Neurology. 1993. PMID: 7679780

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