Cerqueira A - Search Results

1

Analysis of the CTG repeat in skeletal muscle of young and adult myotonic dystrophy patients: when does the expansion occur?

Zatz M, Passos-Bueno MR, Cerqueira A, Marie SK, Vainzof M, Pavanello RC. Zatz M, et al. Among authors: cerqueira a. Hum Mol Genet. 1995 Mar;4(3):401-6. doi: 10.1093/hmg/4.3.401. Hum Mol Genet. 1995. PMID: 7795594

2

Equal proportions of affected cells in muscle and blood of a mosaic carrier of facioscapulohumeral muscular dystrophy.

Tonini MM, Lemmers RJ, Pavanello RC, Cerqueira AM, Frants RR, van der Maarel SM, Zatz M. Tonini MM, et al. Hum Genet. 2006 Mar;119(1-2):23-8. doi: 10.1007/s00439-005-0100-2. Epub 2005 Dec 8. Hum Genet. 2006. PMID: 16341710

3

Absence of correlation between skewed X inactivation in blood and serum creatine-kinase levels in Duchenne/Becker female carriers.

Sumita DR, Vainzof M, Campiotto S, Cerqueira AM, Cánovas M, Otto PA, Passos-Bueno MR, Zatz M. Sumita DR, et al. Among authors: cerqueira am. Am J Med Genet. 1998 Dec 4;80(4):356-61. Am J Med Genet. 1998. PMID: 9856563

4

[Myotonic dystrophy: study of clinico-genetic correlation in a pair of relatives (father-son)].

Reed UC, Passos-Bueno MR, Nagahashi-Marie SK, Cerqueira A, Mendonça LI, Levy JA, Diament A, Zatz M. Reed UC, et al. Among authors: cerqueira a. Arq Neuropsiquiatr. 1994 Dec;52(4):545-8. doi: 10.1590/s0004-282x1994000400015. Arq Neuropsiquiatr. 1994. PMID: 7611950 Portuguese.

5

High proportion of new mutations and possible anticipation in Brazilian facioscapulohumeral muscular dystrophy families.

Zatz M, Marie SK, Passos-Bueno MR, Vainzof M, Campiotto S, Cerqueira A, Wijmenga C, Padberg G, Frants R. Zatz M, et al. Among authors: cerqueira a. Am J Hum Genet. 1995 Jan;56(1):99-105. Am J Hum Genet. 1995. PMID: 7825608 Free PMC article.

6

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. Among authors: cerqueira a. 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.

7

CTG repeat length in muscle from patients affected with myotonic dystrophy (DM).

Zatz M, Passos-Bueno MR, Cerqueira A, Vainzof M. Zatz M, et al. Among authors: cerqueira a. J Med Genet. 1996 Feb;33(2):173. doi: 10.1136/jmg.33.2.173-a. J Med Genet. 1996. PMID: 8929960 Free PMC article. No abstract available.

8

The facioscapulohumeral muscular dystrophy (FSHD1) gene affects males more severely and more frequently than females.

Zatz M, Marie SK, Cerqueira A, Vainzof M, Pavanello RC, Passos-Bueno MR. Zatz M, et al. Among authors: cerqueira a. Am J Med Genet. 1998 May 1;77(2):155-61. Am J Med Genet. 1998. PMID: 9605290

9

Segregation distortion of the CTG repeats at the myotonic dystrophy (DM) locus: new data from Brazilian DM families.

Zatz M, Cerqueira A, Vainzof M, Passos-Bueno MR. Zatz M, et al. Among authors: cerqueira a. J Med Genet. 1997 Sep;34(9):790-1. doi: 10.1136/jmg.34.9.790. J Med Genet. 1997. PMID: 9321774 Free PMC article. No abstract available.

10

Paternal inheritance or different mutations in maternally related patients occur in about 3% of Duchenne familial cases.

Zatz M, Sumita D, Campiotto S, Canovas M, Cerqueira A, Vainzof M, Passos-Bueno MR. Zatz M, et al. Among authors: cerqueira a. Am J Med Genet. 1998 Jul 24;78(4):361-5. doi: 10.1002/(sici)1096-8628(19980724)78:4<361::aid-ajmg11>3.0.co;2-g. Am J Med Genet. 1998. PMID: 9714440

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