Passos-Bueno MR - Search Results

1

Prion disease resembling frontotemporal dementia and parkinsonism linked to chromosome 17.

Nitrini R, Teixeira da Silva LS, Rosemberg S, Caramelli P, Carrilho PE, Iughetti P, Passos-Bueno MR, Zatz M, Albrecht S, LeBlanc A. Nitrini R, et al. Arq Neuropsiquiatr. 2001 Jun;59(2-A):161-4. doi: 10.1590/s0004-282x2001000200001. Arq Neuropsiquiatr. 2001. PMID: 11400017 Free article.

2

Different mosaicism frequencies for proximal and distal Duchenne muscular dystrophy (DMD) mutations indicate difference in etiology and recurrence risk.

Passos-Bueno MR, Bakker E, Kneppers AL, Takata RI, Rapaport D, den Dunnen JT, Zatz M, van Ommen GJ. Passos-Bueno MR, et al. Am J Hum Genet. 1992 Nov;51(5):1150-5. Am J Hum Genet. 1992. PMID: 1415256 Free PMC article.

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

4

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.

5

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

6

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

7

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

8

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

9

Reproductive fitness and frequency of new mutations in Becker muscular dystrophy: implications for genetic risk estimates.

Passos-Bueno MR, Zatz M. Passos-Bueno MR, et al. J Med Genet. 1991 Apr;28(4):286-7. doi: 10.1136/jmg.28.4.286. J Med Genet. 1991. PMID: 1856839 Free PMC article. No abstract available.

10

Limb-girdle syndrome: a genetic study of 22 large Brazilian families. Comparison with X-linked Duchenne and Becker dystrophies.

Passos-Bueno MR, Vainzof M, Pavanello Rde C, Pavanello-Filho I, Lima MA, Zatz M. Passos-Bueno MR, et al. J Neurol Sci. 1991 May;103(1):65-75. doi: 10.1016/0022-510x(91)90286-g. J Neurol Sci. 1991. PMID: 1865235

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