Zatz M - Search Results

1

A normal life without muscle dystrophin.

Zatz M, Vieira NM, Zucconi E, Pelatti M, Gomes J, Vainzof M, Martins-Bach AB, Garcia Otaduy MC, Bento dos Santos G, Amaro E Jr, Landini V, Andrade T. Zatz M, et al. Neuromuscul Disord. 2015 May;25(5):371-4. doi: 10.1016/j.nmd.2015.02.007. Epub 2015 Feb 24. Neuromuscul Disord. 2015. PMID: 25770920

2

Steroids in Duchenne muscular dystrophy.

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

3

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: zatz m. Neuromuscul Disord. 1992;2(2):117-20. doi: 10.1016/0960-8966(92)90043-6. Neuromuscul Disord. 1992. PMID: 1422198

4

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. Among authors: zatz m. 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.

5

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. Among authors: zatz m. J Med Genet. 1992 Jul;29(7):476-9. J Med Genet. 1992. PMID: 1640426 Free PMC article.

6

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. Among authors: zatz m. J Neurol Sci. 1990 Sep;98(2-3):221-33. doi: 10.1016/0022-510x(90)90263-m. J Neurol Sci. 1990. PMID: 1700808

7

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. Among authors: zatz m. J Neurol Sci. 1991 Feb;101(2):141-7. doi: 10.1016/0022-510x(91)90038-9. J Neurol Sci. 1991. PMID: 1709683

8

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. Among authors: zatz m. Neuromuscul Disord. 1991;1(3):177-83. doi: 10.1016/0960-8966(91)90022-k. Neuromuscul Disord. 1991. PMID: 1822792

9

Short stature in Duchenne muscular dystrophy.

Rapaport D, Colletto GM, Vainzof M, Duaik MC, Zatz M. Rapaport D, et al. Among authors: zatz m. Growth Regul. 1991 Mar;1(1):11-5. Growth Regul. 1991. PMID: 1842555

10

Familial occurrence of Duchenne dystrophy through paternal lines in four families.

Zatz M, Passos-Bueno MR, Rapaport D, Vainzof M. Zatz M, et al. Am J Med Genet. 1991 Jan;38(1):80-4. doi: 10.1002/ajmg.1320380118. Am J Med Genet. 1991. PMID: 1849353

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