Passos-Bueno MR - Search Results

1

Author Correction: Whole-genome sequencing of 1,171 elderly admixed individuals from Brazil.

Naslavsky MS, Scliar MO, Yamamoto GL, Wang JYT, Zverinova S, Karp T, Nunes K, Ceroni JRM, de Carvalho DL, da Silva Simões CE, Bozoklian D, Nonaka R, Dos Santos Brito Silva N, da Silva Souza A, de Souza Andrade H, Passos MRS, Castro CFB, Mendes-Junior CT, Mercuri RLV, Miller TLA, Buzzo JL, Rego FO, Araújo NM, Magalhães WCS, Mingroni-Netto RC, Borda V, Guio H, Rojas CP, Sanchez C, Caceres O, Dean M, Barreto ML, Lima-Costa MF, Horta BL, Tarazona-Santos E, Meyer D, Galante PAF, Guryev V, Castelli EC, Duarte YAO, Passos-Bueno MR, Zatz M. Naslavsky MS, et al. Nat Commun. 2022 Mar 30;13(1):1831. doi: 10.1038/s41467-022-29575-z. Nat Commun. 2022. PMID: 35354829 Free PMC article. No abstract available.

2

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.

3

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

4

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.

5

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

6

Apparent association of mental retardation and specific patterns of deletions screened with probes cf56a and cf23a in Duchenne muscular dystrophy.

Rapaport D, Passos-Bueno MR, Brandão L, Love D, Vainzof M, Zatz M. Rapaport D, et al. Am J Med Genet. 1991 Jun 15;39(4):437-41. doi: 10.1002/ajmg.1320390414. Am J Med Genet. 1991. PMID: 1877622

7

Estimate of the proportion of Duchenne muscular dystrophy with autosomal recessive inheritance.

Zatz M, Passos-Bueno MR, Rapaport D. Zatz M, et al. Am J Med Genet. 1989 Mar;32(3):407-10. doi: 10.1002/ajmg.1320320328. Am J Med Genet. 1989. PMID: 2658592

8

Hypothesis: the existence of embryonic and adult isoforms of mRNA dystrophin provides an explanation for unusual clinical findings.

Zatz M, Passos-Bueno MR, Vainzof M, Pavanello RC. Zatz M, et al. Am J Med Genet. 1989 Mar;32(3):438-41. doi: 10.1002/ajmg.1320320336. Am J Med Genet. 1989. PMID: 2658593 No abstract available.

9

Racial effect on serum creatine-kinase: implications for estimation of heterozygosity risks for females at-risk for Duchenne dystrophy.

Passos-Bueno MR, Rabbi-Bortolini E, Azevêdo E, Zatz M. Passos-Bueno MR, et al. Clin Chim Acta. 1989 Feb 15;179(2):163-8. doi: 10.1016/0009-8981(89)90162-9. Clin Chim Acta. 1989. PMID: 2920447 No abstract available.

10

Is dystrophin always altered in Becker muscular dystrophy patients?

Vainzof M, Passos-Bueno MR, Pavanello RC, Zatz M. Vainzof M, et al. J Neurol Sci. 1995 Jul;131(1):99-104. doi: 10.1016/0022-510x(95)00104-a. J Neurol Sci. 1995. PMID: 7561956

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