Passos-Bueno MR - Search Results

1

Optimal population-specific HLA imputation with dimension reduction.

Douillard V, Dos Santos Brito Silva N, Bourguiba-Hachemi S, Naslavsky MS, Scliar MO, Duarte YAO, Zatz M, Passos-Bueno MR, Limou S, Gourraud PA, Launay É, Castelli EC, Vince N; SNP-HLA Reference Consortium (SHLARC). Douillard V, et al. Among authors: passos bueno mr. HLA. 2024 Jan;103(1):e15282. doi: 10.1111/tan.15282. Epub 2023 Nov 11. HLA. 2024. PMID: 37950640

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

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

6

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

7

Myotonic dystrophy: genetic, clinical, and molecular analysis of patients from 41 Brazilian families.

Passos-Bueno MR, Cerqueira A, Vainzof M, Marie SK, Zatz M. Passos-Bueno MR, et al. J Med Genet. 1995 Jan;32(1):14-8. doi: 10.1136/jmg.32.1.14. J Med Genet. 1995. PMID: 7897620 Free PMC article.

8

Facioscapulohumeral muscular dystrophy: aspects of genetic counselling, acceptance of preclinical diagnosis, and fitness.

Eggers S, Passos-Bueno MR, Zatz M. Eggers S, et al. J Med Genet. 1993 Jul;30(7):589-92. doi: 10.1136/jmg.30.7.589. J Med Genet. 1993. PMID: 8411033 Free PMC article.

9

Absence of correlation between utrophin localization and quantity and the clinical severity in Duchenne/Becker dystrophies.

Vainzof M, Passos-Bueno MR, Man N, Zatz M. Vainzof M, et al. Am J Med Genet. 1995 Sep 25;58(4):305-9. doi: 10.1002/ajmg.1320580403. Am J Med Genet. 1995. PMID: 8533838

10

Seven autosomal recessive limb-girdle muscular dystrophies in the Brazilian population: from LGMD2A to LGMD2G.

Passos-Bueno MR, Vainzof M, Moreira ES, Zatz M. Passos-Bueno MR, et al. Am J Med Genet. 1999 Feb 19;82(5):392-8. doi: 10.1002/(sici)1096-8628(19990219)82:5<392::aid-ajmg7>3.0.co;2-0. Am J Med Genet. 1999. PMID: 10069710

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