Passos-Bueno MR - Search Results

1

The oldest unvaccinated Covid-19 survivors in South America.

de Castro MV, Silva MVR, Naslavsky MS, Scliar MO, Nunes K, Passos-Bueno MR, Castelli EC, Magawa JY, Adami FL, Moretti AIS, de Oliveira VL, Boscardin SB, Cunha-Neto E, Kalil J, Jouanguy E, Bastard P, Casanova JL, Quiñones-Vega M, Sosa-Acosta P, Guedes JS, de Almeida NP, Nogueira FCS, Domont GB, Santos KS, Zatz M. de Castro MV, et al. Immun Ageing. 2022 Nov 16;19(1):57. doi: 10.1186/s12979-022-00310-y. Immun Ageing. 2022. PMID: 36384671 Free PMC article.

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

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

6

Serum creatine-kinase (CK) and pyruvate-kinase (PK) activities in Duchenne (DMD) as compared with Becker (BMD) muscular dystrophy.

Zatz M, Rapaport D, Vainzof M, Passos-Bueno MR, Bortolini ER, Pavanello Rde C, Peres CA. Zatz M, et al. J Neurol Sci. 1991 Apr;102(2):190-6. doi: 10.1016/0022-510x(91)90068-i. J Neurol Sci. 1991. PMID: 2072118

7

Screening of deletions in the dystrophin gene with the cDNA probes Cf23a, Cf56a, and Cf115.

Passos-Bueno MR, Rapaport D, Love D, Flint T, Bortolini ER, Zatz M, Davies KE. Passos-Bueno MR, et al. J Med Genet. 1990 Mar;27(3):145-50. doi: 10.1136/jmg.27.3.145. J Med Genet. 1990. PMID: 2182872 Free PMC article.

8

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

9

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.

10

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.

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