Zatz M - Search Results

1

Recurrence of COVID-19 associated with reduced T-cell responses in a monozygotic twin pair.

de Castro MV, Santos KS, Apostolico JS, Fernandes ER, Almeida RR, Levin G, Magawa JY, Nunes JPS, Bruni M, Yamamoto MM, Lima AC, Silva MVR, Matos LRB, Coria VR, Castelli EC, Scliar MO, Kuramoto A, Bruno FR, Jacintho LC, Nunes K, Wang JYT, Coelho VP, Neto MM, Maciel RMB, Naslavsky MS, Passos-Bueno MR, Boscardin SB, Rosa DS, Kalil J, Zatz M, Cunha-Neto E. de Castro MV, et al. Among authors: zatz m. Open Biol. 2022 Feb;12(2):210240. doi: 10.1098/rsob.210240. Epub 2022 Feb 2. Open Biol. 2022. PMID: 35104433 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. Among authors: zatz m. J Med Genet. 1992 Jul;29(7):476-9. J Med Genet. 1992. PMID: 1640426 Free PMC article.

3

Immunofluorescence dystrophin study in Duchenne dystrophy through the concomitant use of two antibodies directed against the carboxy-terminal and the amino-terminal region of the protein.

Vainzof M, Zubrzycka-Gaarn EE, Rapaport D, Passos-Bueno MR, Pavanello RC, Pavanello-Filho I, Zatz M. Vainzof M, et al. Among authors: zatz m. J Neurol Sci. 1991 Feb;101(2):141-7. doi: 10.1016/0022-510x(91)90038-9. J Neurol Sci. 1991. PMID: 1709683

4

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

5

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. Among authors: zatz m. 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.

6

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. Among authors: zatz m. J Neurol Sci. 1991 May;103(1):65-75. doi: 10.1016/0022-510x(91)90286-g. J Neurol Sci. 1991. PMID: 1865235

7

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. Among authors: zatz m. Am J Med Genet. 1991 Jun 15;39(4):437-41. doi: 10.1002/ajmg.1320390414. Am J Med Genet. 1991. PMID: 1877622

8

Linkage analysis in families with autosomal recessive limb-girdle muscular dystrophy (LGMD) and 6q probes flanking the dystrophin-related sequence.

Passos-Bueno MR, Terwilliger J, Ott J, Vainzof M, Love DR, Davies KE, Zatz M. Passos-Bueno MR, et al. Among authors: zatz m. Am J Med Genet. 1991 Jan;38(1):140-6. doi: 10.1002/ajmg.1320380130. Am J Med Genet. 1991. PMID: 2012126

9

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

10

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. Among authors: zatz m. 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.

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