Vainzof M - Search Results

1

Relation between height and clinical course in Duchenne muscular dystrophy.

Zatz M, Rapaport D, Vainzof M, Rocha JM, Pavanello Rde C, Colletto GM, Peres CA. Zatz M, et al. Among authors: vainzof m. Am J Med Genet. 1988 Feb;29(2):405-10. doi: 10.1002/ajmg.1320290223. Am J Med Genet. 1988. PMID: 3354613

2

Steroids in Duchenne muscular dystrophy.

Zatz M, Pavanello Rde C, Vainzof M, Passos-Bueno MR. Zatz M, et al. Among authors: vainzof m. Neuromuscul Disord. 1992;2(1):59. doi: 10.1016/0960-8966(92)90028-5. Neuromuscul Disord. 1992. PMID: 1356047 No abstract available.

3

Screening of glycerol kinase deficiency in patients affected by Duchenne and Becker muscular dystrophy.

Schreiber R, Passas-Bueno MR, Rapaport D, Pavanello Rde C, Vainzof M, Fernandes ME, Zootz M. Schreiber R, et al. Among authors: vainzof m. Clin Chim Acta. 1992 Jul 31;209(1-2):103-4. doi: 10.1016/0009-8981(92)90339-r. Clin Chim Acta. 1992. PMID: 1395032 No abstract available.

4

A deletion including the brain promoter of the Duchenne muscular dystrophy gene is not associated with mental retardation.

Rapaport D, Passos-Bueno MR, Takata RI, Campiotto S, Eggers S, Vainzof M, Makover A, Nudel U, Yaffe D, Zatz M. Rapaport D, et al. Among authors: vainzof m. Neuromuscul Disord. 1992;2(2):117-20. doi: 10.1016/0960-8966(92)90043-6. Neuromuscul Disord. 1992. PMID: 1422198

5

Additional dystrophin fragment in Becker muscular dystrophy patients: correlation with the pattern of DNA deletion.

Vainzof M, Passos-Bueno MR, Rapaport D, Pavanello RC, Zatz M, Bulman DE. Vainzof M, et al. Am J Med Genet. 1992 Oct 1;44(3):382-4. doi: 10.1002/ajmg.1320440323. Am J Med Genet. 1992. PMID: 1488991 No abstract available.

6

A model to estimate the expression of the dystrophin gene in muscle from female Becker muscular dystrophy carriers.

Vainzof M, Passos-Bueno MR, Pavanello RC, Schreiber R, Zatz M. Vainzof M, et al. J Med Genet. 1992 Jul;29(7):476-9. J Med Genet. 1992. PMID: 1640426 Free PMC article.

7

Dystrophin immunostaining in muscles from patients with different types of muscular dystrophy: a Brazilian study.

Vainzof M, Pavanello RC, Pavanello Filho I, Passos-Bueno MR, Rapaport D, Hsi CT, Zatz M. Vainzof M, et al. J Neurol Sci. 1990 Sep;98(2-3):221-33. doi: 10.1016/0022-510x(90)90263-m. J Neurol Sci. 1990. PMID: 1700808

8

Immunofluorescence dystrophin study in Duchenne dystrophy through the concomitant use of two antibodies directed against the carboxy-terminal and the amino-terminal region of the protein.

Vainzof M, Zubrzycka-Gaarn EE, Rapaport D, Passos-Bueno MR, Pavanello RC, Pavanello-Filho I, Zatz M. Vainzof M, et al. J Neurol Sci. 1991 Feb;101(2):141-7. doi: 10.1016/0022-510x(91)90038-9. J Neurol Sci. 1991. PMID: 1709683

9

Estimate of the intrafamilial correlation for serum creatine kinase and pyruvate kinase in females at risk for Duchenne and Becker muscular dystrophies.

Rabbi-Bortolini E, Dal Colletto GM, Passos-Bueno MR, Vainzof M, Rapaport D, Zatz M. Rabbi-Bortolini E, et al. Among authors: vainzof m. Hum Hered. 1991;41(6):370-8. doi: 10.1159/000154029. Hum Hered. 1991. PMID: 1797630

10

Dystrophin immunofluorescence pattern in manifesting and asymptomatic carriers of Duchenne's and Becker muscular dystrophies of different ages.

Vainzof M, Pavanello RC, Pavanello I, Tsanaclis AM, Levy JA, Passos-Bueno MR, Rapaport D, Zatz M. Vainzof M, et al. Neuromuscul Disord. 1991;1(3):177-83. doi: 10.1016/0960-8966(91)90022-k. Neuromuscul Disord. 1991. PMID: 1822792

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