Cerqueira A - Search Results

1

Facioscapulohumeral (FSHD1) and other forms of muscular dystrophy in the same family: is there more in muscular dystrophy than meets the eye?

Tonini MM, Passos-Bueno MR, Cerqueira A, Pavanello R, Vainzof M, Dubowitz V, Zatz M. Tonini MM, et al. Among authors: cerqueira a. Neuromuscul Disord. 2002 Aug;12(6):554-7. doi: 10.1016/s0960-8966(02)00014-7. Neuromuscul Disord. 2002. PMID: 12117479

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

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

4

Asymptomatic carriers and gender differences in facioscapulohumeral muscular dystrophy (FSHD).

Tonini MM, Passos-Bueno MR, Cerqueira A, Matioli SR, Pavanello R, Zatz M. Tonini MM, et al. Among authors: cerqueira a. Neuromuscul Disord. 2004 Jan;14(1):33-8. doi: 10.1016/j.nmd.2003.07.001. Neuromuscul Disord. 2004. PMID: 14659410

5

Milder course in Duchenne patients with nonsense mutations and no muscle dystrophin.

Zatz M, Pavanello RC, Lazar M, Yamamoto GL, Lourenço NC, Cerqueira A, Nogueira L, Vainzof M. Zatz M, et al. Among authors: cerqueira a. Neuromuscul Disord. 2014 Nov;24(11):986-9. doi: 10.1016/j.nmd.2014.06.003. Epub 2014 Jun 10. Neuromuscul Disord. 2014. PMID: 25047667

6

Transcriptional regulation differs in affected facioscapulohumeral muscular dystrophy patients compared to asymptomatic related carriers.

Arashiro P, Eisenberg I, Kho AT, Cerqueira AM, Canovas M, Silva HC, Pavanello RC, Verjovski-Almeida S, Kunkel LM, Zatz M. Arashiro P, et al. Among authors: cerqueira am. Proc Natl Acad Sci U S A. 2009 Apr 14;106(15):6220-5. doi: 10.1073/pnas.0901573106. Epub 2009 Apr 1. Proc Natl Acad Sci U S A. 2009. PMID: 19339494 Free PMC article.

7

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

8

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

9

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.

10

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.

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